PMCCPMCCPMCC

Search tips
Search criteria 

Advanced

 
Logo of currneuroLink to Publisher's site
 
Curr Neuropharmacol. 2016 October; 14(7): 674–687.
Published online 2016 October. doi:  10.2174/1570159X14666160115130414
PMCID: PMC5050395

Inflammation and Immune Regulation as Potential Drug Targets in Antidepressant Treatment

Abstract

Growing evidence supports a mutual relationship between inflammation and major depression. A variety of mechanisms are outlined, indicating how inflammation may be involved in the pathogenesis, course and treatment of major depression. In particular, this review addresses 1) inflammatory cytokines as markers of depression and potential predictors of treatment response, 2) findings that cytokines interact with antidepressants and non-pharmacological antidepressive therapies, such as electroconvulsive therapy, deep brain stimulation and physical activity, 3) the influence of cytokines on the cytochrome (CYP) p450-system and drug efflux transporters, and 4) how cascades of inflammation might serve as antidepressant drug targets. A number of clinical trials have focused on agents with immunmodulatory properties in the treatment of depression, of which this review covers nonsteroidal anti-inflammatory drugs (NSAIDs), cytokine inhibitors, ketamine, polyunsaturated fatty acids, statins and curcumin. A perspective is also provided on possible future immune targets for antidepressant therapy, such as toll-like receptor-inhibitors, glycogen synthase kinase-3 inhibitors, oleanolic acid analogs and minocycline. Concluding from the available data, markers of inflammation may become relevant factors for more personalised planning and prediction of response of antidepressant treatment strategies. Agents with anti-inflammatory properties have the potential to serve as clinically relevant antidepressants. Further studies are required to better define and identify subgroups of patients responsive to inflammatory agents as well as to define optimal time points for treatment onset and duration.

Keywords: Biomarker, cytokines, curcumin, depression, infliximab, ketamine, treatment prediction

1. Introduction

Major depression is a severe, potentially life threatening, high prevalence disorder, which is a leading cause of medical and economic disease related burden worldwide [1-3]. Currently, no more than half of the patients treated show a response, even less achieve remission from the depressive episode [4, 5]. Hence, intensified research on the neuro-
biology of depressive disorders and identification of factors relevant for therapeutic advances are vital for the improvement and addition of antidepressant treatment options. As one of the most rapidly growing fields in psychiatric research, mounting evidence supports a central involvement of the inflammatory system in the etiopathogenesis of depressive disorders. Increased knowledge about the regulation of pro- and anti-inflammatory cytokines as central mediators of the inflammatory response may support the development of immunity-based antidepressant agents, as alternatives to present day more transmitter-focused pharmacological approaches. Targeting cytokine regulation as a candidate mechanism in depression may further lead to improved prediction of therapeutic outcomes and the discovery of susceptibility factors for non-response. In addition to a comprehensive summary of current knowledge of molecular mechanisms of cytokine involvement in depression, this review provides an overview of the relationship between inflammation, pharmacokinetics and pharmacodynamics of drugs as well as the connection between cytokines, mechanisms of action of antidepressants and antidepressant treatment outcome. An overview of present immuno-
modulators as antidepressant agents is also presented. Potential future immunological agents in antidepressant therapy for which only experimental or little clinical data exist are discussed. Emphasis is given to the molecular basis of findings (Fig. 1).

2. Pathomechanisms of cytokines in depression

The “inflammation hypothesis” in depression is substantiated by findings that predominantly pro-inflammatory cytokines are over-expressed in the blood of depressed subjects [6-9]. Simultaneously, prolonged high concentrations of cytokines, up-regulated by different environmental, somatic and socio-behavioural factors, may increase the risk for the development of a depressive episode [10, 11]. Given that these relationships are not unequivocal, since not all subjects with high cytokine concentrations develop depressive symptoms and not all depressive patients exhibit elevated pro-inflammatory mediators, an inflammation and cytokine-associated subtype of depression has been recently proposed [12]. In subjects predisposed to depression, cytokines may exert pro-depressive effects in a number of ways: Cytokines induce indolamine-2,3-dioxygenase (IDO), which is involved in the metabolism of tryptophan to kynurenine and the increased transformation of kynurenine to neurotoxic quinolinic acid. A shift of tryptophan metabolism to kynurenine simultaneously reduces serotonin (5-HT) synthesis by tryptophan hydroxylase [13, 14]. Correspondingly, lipopolysaccharide (LPS)-induced inflammation results in both increase in IDO and depressive-like-behaviour whereas the blockade of IDO-activation prevents the development of depressive-like-behaviour [15]. Pro-inflammatory cytokines further negatively influence the active 5-HT fraction by up-regulating the activity and expression of antidepressant-sensitive serotonin transporters (SERT) [16, 17]. Cytokines lead to a disruption of the negative feedback loop of the HPA axis by stimulating the excessive release of corticotrophin-releasing hormone (CRH) and by facilitating glucocorticoid resistance [18, 19], with antidepressant response restoring the disturbed interaction between cytokines and the HPA-axis [20]. Cytokines also contribute to increased redox signalling of nitric oxide (NO) and NO synthase (NOS) which impairs antioxidant defence cascades relevant in depression [21, 22]. Cytokines may further be involved in decreased neuroplasticity and suppression of neurotrophic factors [23] and also related to cerebral structural alterations in depression [24].

3. The influence of cytokines on pharma-
cokinetics and -dynamics

The pharmacokinetic and -dynamic properties of an antidepressant drug are fundamental for its efficacy. Among the various responses to inflammation, cytokines have been shown to significantly affect drug metabolism as well as the transmission of drugs between cells and cell systems, especially the crossing of the blood brain barrier. In this section, we provide a selective overview of the connection between cytokines and the cytochrome p-450 (CYP) system and trans-membrane drug transport.

3.1. Inflammation and the Cytochrome p-450 System

The metabolism of the majority of antidepressants through deactivation and bioactivation relies on CYP enzymes, which are mainly located in hepatic and circulating peripheral blood mononuclear cells (PBMC) [25]. The variability of CYP-activity depends on several endogenous factors such as genetics, gender, age and morbidity as well as exogenous factors like smoking, co-medication and food components. Moreover, the inflammation-state of an organism influences the expression and activity of CYP proteins. Since antidepressants are mainly metabolised by CYP enzymes 2D6, 1A2, 3A4 and 2C19 [26], the grade of inflammation may therefore impact on the bioavailability of a drug. Influencing PBMC could affect intracellular and systemic drug concentrations and bioavailability. In-vitro, the pro-inflammatory cytokines IL-2, IL-12 and IFN-γ lead to decreased expression of CYP2D6 and CYP3A4 in PBMC. Bertilsson and colleagues also showed that pro-inflammatory cytokines and macrophages decreased the mRNA expression of CYP3A4 [27]. Combined and separate application of IL-1ß, TNF-α and IFN-γ led to a marked decrease in CYP expression via activation of NO [28]. Further, an inverse relationship was found between the concentrations of TNF-α and IL-6 on the one side and CYP 2C19 on the other [29]. Based on the finding that these effects could be blocked by inhibitors of NOS and initiated by NO donors [30], it was concluded that NOS is one of the main contributor to the effects of the cytokines on the CYP system. Cytokines and cytokine modulators may act by alterations of transcription factor activity for CYP enzyme expression as well as changes in CYP enzyme stability [31]. As a limitation concerning the relevance of these findings in depression, the majority of studies on humans included patients with chronic inflammatory diseases or cardiovascular diseases who exhibit higher levels of pro-inflammatory cytokines than depressed subjects. Since the majority of studies revealed a cytokine-mediated blockade of CYP and since CYP mostly facilitates depletion rather than bioactivation of the majority of antidepressants, an increase in drug concentrations in depression may be expected. One exception is that the half-life of fluoxetine was significantly reduced when peginterferon-α-2b was added, indicating an accelerated depletion of fluoxetine [32]. Another recent investigation also did not detect an influence of inflammation, as defined by CRP blood levels, on serum concentrations of citalopram or venlafaxine [33]. However, overall few studies have addressed the relationship of cytokines, antidepressants and drug metabolism, limiting the transferability of the aforementioned results in the context of affective disorders and antidepressant treatment. Due to a lack of data, the assumption that altered CYP-activation may be of relevance for depressed patients with inflammatory co-morbidities, by being associated with more side effects during treatment with antidepressants [34, 35] remains hypothetical.

3.2. Impact of Inflammation on Trans-membrane Drug Transport

The blood brain barrier (BBB) is the largest obstacle to antidepressant drugs entering the central nervous system (CNS), amongst other mechanisms due to trans-membranous drug efflux transporters, which unload xenobiotics from endothelial cells back into the bloodstream. It is not well understood how cytokines influence the permeability of the BBB. In addition to involvement in the modification of tight junction structures, cytokines regulate endothelial signalling and the activity and expression of drug efflux transporters [36]. Variants of P-glycoprotein (P-gp), a product of the ATP-binding cassette (ABC) sub-family B (ABCB1)-transporter, pivotal for the transport of drugs and molecules across intra- and extra-cellular membranes, have been shown to be of relevance in antidepressant treatment outcome [37]. The expression of ABCB1-mRNA and -protein was found to be increased following cytokine stimulation, leading to reduced cellular accumulation of drugs [38, 39]. The expression of breast cancer related protein (BCRP), another important drug efflux transporter expressed on the BBB, was found reduced by IL-1ß, IL-6 and TNF-α [40]. Long-term stimulation with TNF-α increased the expression and activity of P-gp via nuclear factor kappa-light-chain-enhancer of activated B-cells (NF-κB), whereas short-term stimulation with a lower concentration of TNF-α led to a decrease of P-gp functioning [41]. IL-1 in contrast led to a continuous decrease in protein expression of both P-gp and BCRP [42]. The evidence that cytokines may affect drug efflux transporters, and also regulate P-gp drug-transporters in a time-and dose-dependent manner, is of potential relevance in antidepressant treatment strategies. This evidence suggests that both duration of depression and extent of inflammation influence the bioavailability of antidepressants.

4. The relationship between cytokines and depression, antidepressant treat-
ments, and prediction of antidepressant drug response

The following paragraphs summarise clinical and preclinical data indicating cytokine levels are altered in depressed subjects, relate to certain symptoms and symptom dimensions of depression, respond to drug administration, and are related to (and possibly predict) treatment outcome of antidepressant therapies.

4.1. Cytokine Levels and Depression

A large body of studies suggests both pro- and anti-inflammatory cytokines are up-regulated in depressive disorders. A number of cytokines have been investigated and found elevated, amongst them IL-2, IL-5, IL-6, IL-7, IL-8, IL-10, IL-12, IL-13, IFN-γ and granulocyte colony-stimulating factor (GM-CSF) [8, 43, 44]. Within the broad range of cytokines, the most extensively studied mediators are IL-1, IL-6 and TNF-α. Yet for these cytokines positive findings vary with two recent meta-analyses confirming higher levels of IL-6 and C-reactive protein (CRP) in patients with major depression and in patients at risk for depression [6, 45], whereas the association between TNF-α, IL-1β and major depression was not consistent [6]. A previous meta-analysis with medical co-morbidity as an exclusion criteria reported that blood levels of both IL-6 and TNF-α were elevated in depressed subjects [7]. Despite these reported increases in cytokines in selective populations, one may not infer that depression is associated with inflammation in all patients [46] but more probably a subtype of patients suffering from major depression [12]. There is no evidence of an across the board relationship between inflammation, depression and depressive symptoms given that the majority of patients suffering from inflammation do not exhibit a depressive syndrome and given the increased incidence for depression following treatment with cytokine-analogs [46, 47].

4.2. Antidepressants and Cytokines

Evidence is mounting that antidepressants not only exert their effect on depression by regulating neurotransmitters but also have immunosuppressive and anti-inflammatory properties. Lines of evidence suggest that pro-inflammatory cytokine production is affected by antidepressant treatment. A recent meta-analysis revealed that persistent elevations of TNF-α were associated with poorer clinical outcome of antidepressant treatment in depressed subjects [48]. It was further concluded that antidepressant therapy leads to a decrease of IL-6 independent of clinical outcome, pointing towards a general and clinically non-specific suppression of inflammatory activity during therapy [48]. At variance with these results, a previous meta-analysis found significant changes, not in TNF-α, but in IL-1 and IL-6 during therapy [49]. After 12-weeks treatment, levels of various cytokines significantly decreased, with no greater difference in those patients achieving remission from depression compared to non-depressed subjects [43]. A possible explanation was proposed based on findings that antidepressant treatment induced the up-regulation of regulatory T cells that may in turn down-regulate cytokine production, as observed by decreases in IL-1 levels [50]. Another mode of action could be the modulation of IDO during antidepressant therapy. The changes in IDO further correlated with improvement in depression severity [14]. Several preclinical studies supported the impact of a range of drugs on pro-inflammatory cytokines: In rats, imipramine and fluoxetine administration led to decreased TNF-α and IL-1ß levels as well as TNF-α and IL-1ß mRNA expression in microglia cultures [51]. Paroxetine administration reduced microglia-mediated neurotoxicity, potentially by reducing the activity of NOS and by reducing levels and mRNA of TNF-α and IL-1ß [52]. Amitryptiline further reduced NO production, TNF-α and IL-1ß-levels [53]. Chronic stress and LPS-stimulation in rats led to increased expression of TNF-α and IL-6 that could be reversed by mianserin [54]. Despite these observations of predominantly drug-induced reductions, venlafaxine administration reduced concentrations of pro-inflammatory cytokines, whereas sertraline increased the concentrations of IFN-α and IL-6. Further, irrespective of whether they led to increased or decreased concentrations of pro-inflammatory cytokines, both antidepressants induced decreased activity
of NF-κB [55]. In-vitro-analyses of human blood samples also showed that antidepressants as a class did not unidirectionally lower cytokine concentrations but variously increased or decreased cytokine levels, depending on the antidepressant administered [56]. The mood-stabilizer lithium, alone and in combination with antidepressants, was shown to lead to an increased secretion of pro-inflammatory cytokines, which may possibly contribute to side effects of the drug and to the beneficial effects in diseases associated with immunological deficits [57]. The incubation of stimulated whole blood with different antidepressants further showed anti-inflammatory immunoregulatory effects of antidepressants through inhibition of IFN-γ and stimulation of IL-10 release [58].

4.3. Cytokines, Depressive Symptoms and Severities

There is little evidence of a relationship between cytokines and the severity of depression in humans [59], the majority of studies reporting negative findings [8, 43, 60]. IL-2-receptor and TNF-α were found positively related
to decreased activity in depressed patients [61]. Only
for suicidality enough data exists to draw preliminary conclusions. A meta-analysis reported that levels of IL-1β and IL-6 were significantly increased in blood and postmortem brain samples of patients with suicidality compared to non-suicidal depressive and healthy subjects [62], another review also supporting IL-2, IL-8 and TFN-α [63]. The majority of studies on this topic come from animal models of depression. Of these, one may conclude that the administration of IFN-α (and other pro-inflammatory cytokines) increased depression-like features in mice [64] and that anhedonia after chronic mild stress is followed by increases of cytokines, such as TFN-α, IL-6 and IL-10 [54]. Behavioural despair in isolated rats was further accompanied by elevated levels of TNF-α, IL-4 and IL-10 [65]. However, findings from these studies can only very limited be referenced to major depression, as much as effects of cytokine alterations on sickness behavior, a temporary, reactive syndrome with partial symptom-overlap with major depression [66].

4.4. Cytokines and Treatment Outcome

Concerning the question whether cytokines could be related to and may predict treatment outcome, data trend towards elevated levels of pro-inflammatory cytokines relating to poorer clinical response [67]. A recent investigation demonstrated that response to antidepressant treatment was differentially related to baseline CRP levels, with a better response to the serotonin reuptake inhibitor escitalopram in those patients with lower CRP levels and a better response to the norepinephrine reuptake inhibitor nortriptyline when serum levels of CRP were higher [68]. High baseline levels of TNF-α and IL-6 were associated with treatment resistance [48, 61, 69-71]. Levels of pro-and anti-inflammatory cytokines normalised after treatment only in those patients recovering from a depressive episode [43].
IL-1-polymorphisms were associated with reduced response to antidepressants [72]. Moreover, specific IL-1 genotypes were associated with treatment resistant depression [72]. In preclinical studies, mice with an astrocyte-specific deletion of TNF-α showed a lack of behavioural response to antidepressant administration [73].

5. Anti-inflammatory agents in anti-
depressant treatment strategies

Besides conventional antidepressants, anti-inflammatory agents have potential antidepressant properties. These include a group (NSAID, cytokine-inhibitors) with direct impact on cytokines, and active substances, primarily prescribed for non-affective disorders, but which showed antidepressant effects via immune-modulation (Fig. 11).

Fig. (1)
Model of relevant pathomechanisms of inflammation and antidepressive drug targets in depressive disorders. Legend: ASA=acetylsalicylic acid, BDNF=brain-derived neurotrophic factor, COX=cyclooxygenase, CYP=cytochrome p-450 system, GSK- 3=glycogen synthase ...

5.1. Nonsteroidal Anti-inflammatory Drugs (NSAIDs)

Treatment with NSAIDs, a group of anti-inflammatory agents inhibiting the activity of cyclooxygenase (COX)-1 and -2, has been investigated in depth in a number of trials. A recent meta-analysis provides evidence that NSAIDs, especially the COX-2-selective inhibitor celecoxib, have a positive effect on antidepressant treatment outcome [74]. However in a recent [75] and another large study, no antidepressant effects of celecoxib or naproxen monotherapy in elderly subjects were detected [76]. Moreover, NSAIDs were reported to attenuate antidepressant effects of SSRI’s in both animal models for depression as well as in STAR*D trial participants [77]. A selective review moreover inferred an aggravation of the pathophysiology of depression and an increased risk for cardiovascular diseases in depression [78]. Corresponding to the latter, a retrospective analysis showed that a combination of antidepressants with NSAIDs, except low-dose acetylsalicylic acid (ASA), in general increased the risk for later psychiatric counselling [79]. ASA may mediate its antidepressant effects by stimulating the endogenous production of anti-inflammatory mediators, by reducing oxidative stress [80] and by inhibiting the STAT6 signalling pathways that are mediated by IL-4 and IL-13 [81]. As both IL-4 and IL-13 are found associated with depression [8], regulation by ASA of cytokine-induced intracellular transcriptional cascades could explain the improvement of treatment outcome when ASA was added to treatment with antidepressants in mice [82]. In combination with antidepressants, ASA may further exert antidepressant features by inhibiting the phosphorylation of NF-κB, the expression of the indoleamine 2,3-dioxygenase (IDO) enzyme and the depletion of 5-HT [83].

5.2. Cytokine Inhibitors

Inhibiting the effects of cytokines with monoclonal antibodies is a promising therapeutic approach, though at present associated with the risk of potentially serious side-effects [84]. TNF-α blockers such as etanercept, fusing the TNF-receptor with the antibody, were demonstrated to reduce depressive symptoms in patients primarily suffering from psoriasis [85]. The administration of etanercept reduced depressive-like behaviour equivalent to imipramine in rats [86] and etanercept monotherapy in patients with treatment-resistant depression partially improved depression severity [87]. Long-term treatment with infliximab, a chimeric monoclonal antibody binding with high affinity to free and membrane-bound TNF-α, reduced overall severity of depression in those treatment-resistant patients with higher inflammatory activity, as shown by higher baseline CRP levels, but not in those patients with normal CRP-levels [88]. Also, infliximab led to improvement in sleep and arousal regulation in depressed patients [89], systems dysregulated in major depression, which were found associated with alterations in serum cytokine levels [90]. Animal studies further support an antidepressant-like effect of infliximab in rat models [91] potentially by preventing reductions in levels of hippocampal brain-derived neurotrophic factor (BDNF). For adalimumab, another monoclonal anti-TNF α-antibody, and ustekinumab, a monoclonal anti-IL-12 and anti-23-antibody, positive effects on depressive symptoms again were observed in psoriatic patients [92, 93]. Despite these initial outcomes, randomised trials in patients with major depression, other than those characterised as non-responders, are lacking.

5.3. Ketamine

The N-methyl-D-aspartate (NMDA) receptor antagonist ketamine has rapid antidepressant effects, serving as a potential antidepressant in severe and chronic forms of depression [94]. Assumed modes of action range from BDNF-derived synaptogenesis in the prefrontal cortex, inhibition of glycogen synthase kinase-3 beta (GSK-3β) and activation of mammalian target of rapamycin (mTOR) [95]. Further anti-inflammatory properties are found in reducing the release of pro-inflammatory cytokines like TNF-α and IL-6 [96, 97]. Currently it is not known if ketamine’s antidepressant effect may be linked to its anti-inflammatory effect, however there is some data prompting investigation of this topic. In an animal model of depression, administration of ketamine lowered levels of IL-1β, IL-6, TNF-α, IDO and the kynurenine/tryptophan ratio within the rats’ hippocampus [98]. In addition to the attenuation of levels of pro-inflammatory mediators, ketamine also suppressed the depression-related nuclear translocation of NF-κB [99]. Moreover, levels of IL-6 were shown to potentially serve as a biomarker in predicting those subjects with a therapeutic benefit of ketamine [100]. Anti-suicidal effects of ketamine were suggested to be linked to interruption of the kynurenine pathway and modulating pro-inflammatory cytokines [101]. Finally, memory impairment and increases of IL-1β and TNF-α following electro-
convulsive shock in rats were both positively attenuated by ketamine [102].

5.4. Polyunsaturated Fatty Acids (PUFAs)

Evidence supports specific dietary supplements having both antidepressant and anti-inflammatory properties. In depression, abnormal fatty acid profile and high co-morbidity with the metabolic syndrome are associated with increased levels of pro-inflammatory cytokines [8, 103]. Significantly reduced concentrations of PUFAs have been repeatedly demonstrated [104]. Studies demonstrated a positive effect of PUFAs on antidepressant outcome and symptom reduction [105] that was reduced for omega-3 fatty acids when controlling for the heterogeneity of the studies and publication bias [106]. Also, differing PUFA diets in heterogeneous study samples may account for the equivocal results [107, 108]. The antidepressant effect of treatment with PUFA supplements was found to depend on the proportion of eicosapentaenoic acids (EPA) to docosahexaenoic acid (DHA) in the diet [109]. EPA were shown to have a cytokine-suppressing effect [110] but also the administration of DHA reduced the expression of TNF-α and interleukin-6 [111]. The central target for the PUFA-mediated anti-inflammatory and antidepressant effects is NF-κB [112], by intracellular translocation of NF-κB [111], activation of the transcriptional factor peroxisome proliferator-activated receptors (PPAR)-γ [112] and the suppression of COX-2 expression by modulation of toll-like receptor 4 (TLR4) signalling pathways [113].

5.5. Statins

In contrast to studies suggesting PUFA diets to be of moderate antidepressant effect, contradictory findings emerged for statins, a family of HMG-CoA-reductase-inhibitors involved in the regulation of hyperlipidaemia. An effect as an add-on in acute depression has been found [114, 115]. However, long-term administration of statins did not lower the incidence of major depression during a five-year period, indicating no preventive role for statins in depression [116]. Contradicting data point towards a depressogenic effect of statins in the long-term, with recommendations
that this risk should be declared when prescribing a statin [117, 118]. Pathways of statins’ anti-inflammatory and antidepressant properties are not resolved. On the one
hand statins reduce the monocyte expression of TNF-α
and IL-1β [119], levels of TNF-α and IL-6 [120] as
well as chemoattractant protein-1 relevant for the activation of NF-κB [121]. On the other hand, statins stimulate the expression of NOS [122], a critical agent in inflammation in depression.

5.6. Curcumin

A further supplemental agent with anti-inflammatory and antidepressive features is curcumin, a diarylheptanoid and the principal of curcuma longa. Besides the potential to increase concentrations of biogenic amines within the cortex and hippocampus [123], curcuma administration led to the inhibition of COX-2, lipoxygenase (LOX), and NOS [124] and to reductions in circulating levels of TNF-α, IL-1 and NF-κB [125-127]. These mechanisms may in part account for antidepressant effects observed in preclinical investigations (for an overview see [128]). A clinical trial with curcumin monotherapy further reported an effect in antidepressant therapy when compared to placebo [129]. An add-on therapy adjunctive to a SSRI led to a slightly more favourable outcome compared to antidepressant monotherapy [130].

6. Inflammation and non-pharmacological antidepressant treatment

In this section, evidence for the relationships between non-pharmacological therapeutic approaches, their benefit in treatment outcome and the immune system are presented. These therapies are predominately applied as add-ons to drug administration, used in treatment-resistant depression, or are currently under investigation for their clinical efficacy.

6.1. Electroconvulsive Therapy (ECT)

ECT has consistently been reported one of the most effective treatment strategies for major depression, especially in treatment-resistant depression [131]. ECT led to a partly stimulus-dose dependent rapid increase of pro-inflammatory cytokines, suggesting neuronal depolarization as a mechanism of cytokine release [132, 133]. ECT further increased lipopolysaccharide-stimulated production of pro-inflammatory IL-6 and TNF-α, whereas cytokines with anti-inflammatory properties IL-4 and IL-10 were found unaffected [134]. After initial increase in levels, repeated ECTs led to a normalization of TNF-α in depressed patients [135]. Another study showed that ECT led to an up-regulation of IL-1β and TNF-α as well as an increase in memory impairment that were both reversed by ketamine [136]. Based on these as well as on findings of an ECT-mediated activation of microglia and an up-regulation of neurotrophins that simultaneously act as immunotrophins, the intriguing conclusion was made that ECT-induced “potentiation, rather than suppression, of inflammatory responses may be of therapeutic relevance to chronically depressed patients or a subgroup thereof” [137].

6.2. Deep Brain Stimulation (DBS)

Research on DBS as a therapy in depression has been subject to limitations of study design [138, 139]. At the same time, connections between DBS and the immune system,
and relevance to antidepressant treatment, are as yet unclear. Preclinical studies suggest that DBS may lead to alterations in immunity, with findings of increased levels of pro-inflammatory IL-1, IL-6, TNF-α and IFN-γ following DBS of the ventromedial hypothalamic nucleus in rats [140]. Another study suggests that inflammation may mediate the effect of DBS, potentially related to the immediate but not long-lasting improvements after implantation in some subjects, associated with a regional inflammation that was reversed by anti-inflammatory drugs [141]. Blockade of this inflammation was hypothesised to account for poorer anti-depressive response in both DBS patients and animals treated with anti-inflammatory drugs.

6.3. Physical Activity and Sleep Deprivation

Several studies have revealed evidence for the beneficial effects of regular exercises on depressive symptoms [142-144]. Modulation of inflammation could be one of the underlying influences, since physical activity reduces the levels of circulating inflammatory mediators [145]. Less physical activity, in both depression and obesity, was associated with increased expression of cytokines, whereas moderate daily physical activity was connected to the expression of anti-inflammatory IL-10 [8]. There is evidence that cytokines, even if they do not change under exercise, could predict therapy response. Thus, higher levels of TNF-α at the beginning of an exercise-based treatment were associated with a distinct reduction of depressive symptoms, though cytokine levels did not significantly change during 12 weeks of treatment [146].

Inflammatory cytokines have effects on sleep-wake-regulation, as deduced from the impact of cytokines on sleep duration, sleep stage fractions and arousal regulation [90, 147]. Levels of wake-promoting cytokines peak during daytime [148], levels of IL-10 reduce during sleep [149], and narcoleptic and insomniac humans show higher levels of IL-4 than controls [32, 150]. Sleep deprivation (SD) is an effective treatment option in depression with rapid, but mostly not sustained, antidepressive effects. Whereas SD led to increased levels of TNF-α in healthy subjects and sleep restriction led to an increase in IL-4-to-IL-2-ratio [151, 152], SD and the recovery night differentially affected cytokine levels in depressive patients and controls [153]. Related to therapeutic outcome, high baseline levels of IL-6 were related to worse response to SD [154]. Given these two interventions where higher levels of cytokines at the beginning of treatment point towards better (physical activity) and worse (SD) therapy response, cytokines as potential markers for prediction of therapy response could thus be used for a tailored choice of the appropriate therapy.

7. Immune targets for future anti-depressant therapy

The following section presents a selection of drug targets with antidepressant potential, supported by theoretical considerations and preclinical findings. Except for minocycline, these substances are some distance away from examination in clinical trials but worth consideration in perspectives of antidepressant treatment (Fig. 1).

7.1. Toll-like Receptor-inhibitors

Toll-like receptors (TLRs), especially TLR4, are a class of membrane-spanning proteins which recognize pathogen-associated molecular patterns (PAMP) and lead to the expression of cytokines. Expression of TLRs was increased in the dorsolateral prefrontal cortex in depression [155] and the expression of TLR4 was associated with the development of depressive symptoms especially in the context of a high-cholesterol-diet [156]. The TLR4-specific inhibitor TAK-242 prevented the increase of COX-2, NOS and IL-1β mRNA in the frontal cortex [157]. Modulators of TLR4, such as eritoran, have recently been generated and hypothetically may become new antidepressant agents though not enough data are yet available to support this assumption [158].

7.2. Glycogen Synthase Kinase-3-inhibitors

Glycogen synthase kinase-3 (GSK-3) is a serine/
threonine protein kinase regulating a large group of transcription factors and transcriptional modulators as well as 5-HT-receptors, whose activity was found impaired both in the cortex and in PBMC of depressed subjects [159]. Via stimulation of TLRs, GSK-3 leads to the up-regulation of pro-inflammatory cytokines [160], whereas blockade of GSK-3 leads to significant reductions in cytokine modulation [161]. GSK-3 can be inhibited by several antidepressants and mood stabilizers [158] and blockade of GSK-3 has been demonstrated as a central element in the antidepressant and neuroprotective effect of the more than 50 identified GSK-3-modulators [162]. The regulation of inflammation by GSK-3 may contribute to both the therapeutic actions of mood stabilizers, antidepressants and ketamine as well as to novel antidepressant drug targets that inhibit GSK3.

7.3. Oleanolic Acids

The triterpenoids or oleanolic acids, present in nutritional supplements and medicinal plants, have anti-inflammatory properties through up-regulating anti-oxidants and inhibiting pro-inflammatory signalling. Analogs are currently under investigation for the treatment of several chronic diseases and different forms of cancer. Concerning depression, no clinical trial has yet been reported. However, in animal models oleanolic acid analogs showed antidepressant effects attributed to high intrinsic activity on 5-HT-receptors [163] and by up-regulation of BDNF-related phosphorylation and activation of extracellular signal-regulated kinases [164, 165]. These preclinical data could make oleanolic acids worth considering as a part of trials searching for alternative antidepressive compounds.

7.4. Minocycline

The tetracycline derivative minocycline, an antibiotic able to cross the blood-brain barrier, may exert antidepressant properties by attenuating the expression of pro-inflammatory cytokines by LPS and by normalization of the kynurenine/tryptophan ratio as demonstrated in animals showing depressive-like behaviour [166, 167]. Minocyline may further inhibit the decreased hippocampal neurogenesis caused by up-regulated cytokines [64]. A small open-label trial with minocycline adjunctive to conventional anti-
depressants showed significant improvement and no serious adverse events [168]. Randomised, double-blind studies to further elucidate the efficacy of minocycline are currently in progress [169].

8. Discussion

Mounting evidence supports a central involvement of inflammation in the pathogenesis of depressive disorders. This is substantiated by high rates of comorbidities between depression and inflammatory diseases as well as an increased risk for the development of depression after sustained inflammation and treatment with pro-inflammatory agents [170]. Results of a variety of trials reporting on cytokines in depression [8, 43] allow the conclusion of increased concentrations of cytokines in patients suffering from major depression [6, 7], which supports the existence of an inflammatory cytokine-associated depressive sub-type [12]. Assumptions of an inflammatory form of depression further concur with findings showing that levels of cytokines at baseline inform prediction of antidepressant outcome. This review suggests that increased levels of cytokines could imply both beneficial and poor treatment outcome. Whereas the majority of studies report a worse outcome in those subjects with higher baseline inflammation [69, 70], an interplay between CRP levels and specific antidepressants on treatment outcome has recently been reported [68], pointing towards a relationship between the grade of inflammation, the antidepressant applied and the therapeutic outcome. In support of the latter, higher levels of IL-6 were generally associated with poor outcome when treated with conventional antidepressants but found beneficial for response when patients were treated with a NSAID [171]. In contrast to the majority of studies on pharmacotherapy, higher levels of cytokines were associated with beneficial clinical outcome of non-pharmacological ECT, DBS and physical activity [135, 141, 146]. Thus, these results suggest that the relationship between levels of cytokines and antidepressive outcome is not unequivocal but relate to the method applied. Further, the findings support the inclusion of cytokine and CRP-levels in pre-treatment investigations to guide the most appropriate and effective therapeutic strategy. Findings of associations with cytokine levels, predominantly in those patients responding to treatment [43, 149] strengthens the notion that cytokines are a mediator of effective antidepressant properties. However, in the majority of trials changes in cytokines during therapy were independent of clinical outcome (see 4.4). Hence, data point towards a cytokine-depleting effect during therapy, independent of any changes in the behavioural dimension. Relevant to this, reviewing the available data on the role of cytokines in depressive severity and separate symptoms, we did not establish a relationship between cytokines and clinical features. Nevertheless, intensified research is needed in this area, given that the majority of studies were not performed in humans or did not report on this topic.

Molecular mechanisms of the interaction between inflammation and depression include modulations of IDO, NO and NOS expression, different transmitter receptors and neurotrophic factors. Since it is of central relevance for the effectiveness of antidepressant drugs this review further addressed the impact of cytokines on CYP enzymes and transmembranous drug transporters. Pro-inflammatory cytokines were mainly shown to down-regulate the CYP-system which in consequence possibly leads to 1) minor depletion of antidepressant drugs followed by accumulation in the organism, potentially provoking side effects or exceeding the threshold for toxicity, and 2) decreased levels of active metabolites of antidepressant drugs which are incorporated as a prodrug, e.g. amitriptylinoxid, and need the CYP system to become pharmacologically active. Thus, the changes in CYP-system might result in decreased or increased bioavailability of several antidepressant drugs. Several pro-inflammatory cytokines were further found to activate transmembranous drug transporters, which decreases transport of antidepressant drugs between tissues, especially migration into the CNS through the BBB. As inflammation may reduce the drugs’ bioavailability and dispersibility within the organs, inclusion of markers of inflammation in combinations with drug monitoring could help optimising antidepressant treatment.

For NSAIDs, data indicate their administration during a depressive episode to have positive effects on severity and outcome, especially when combined with conventional antidepressants [74, 77]. Efficacy of NSAIDS is not demonstrated in long-term treatment, maintenance therapy or prevention of depression. There is equivocal data on the occurrence of side-effects [78, 79]. Thus caution is required in the use of NSAIDs with constant appraisement of the benefit. Data indicate cytokine inhibitors to have antidepressive properties, however the lack of randomised trials make definite conclusions impossible at this time [85, 88]. Obstacles for their clinical use will include the potential of serious side effects, though not yet statistically quantified [74, 84], which could presumably restrict the indication to treatment-resistant depressive patients failing to respond to conventional therapies. The latter may also apply to ketamine as a future treatment option in treatment-resistant depression and suicidality. With fewer side effects than the aforementioned, supplemental PUFAs have proven efficacy in major depression, especially in those diets with positive EPA/DHA and omega 3/omega 6 fatty acids ratios [109]. For statins, benefits for short-term-use during an acute depressive episode were shown [115], however concerns for a depressogenic effect in the long-run were raised [117]. For curcumin, first results on its antidepressant effect are promising and its role will require further investigation in future trials. To summarise, on the data available, the anti-inflammatory agents in this section have all shown effects in depression and in somatic diseases highly comorbid with depression. For the prospective agents, animal studies are promising. However, not enough data are yet available to judge if antidepressive agents may be realised on the basis of these protein-inhibitors and antibiotics, given the potential of severe side-effects and the non-specificity of the anti-inflammatory modes of action.

9. Conclusion

Current antidepressants as well as non-pharmacological therapies exert antidepressant effects most probably in part by modulation of inflammatory cascades. Recent findings support the inclusion of cytokine- and CRP-levels into pre-treatment considerations to select the most appropriate and effective therapeutic strategy. Current immunomodulators like NSAIDs, cytokine blockers, PUFAs and curcuma are promising approaches to extend the spectrum of anti-
depressant therapy, especially in the subgroup of depressive patients showing a cytokine-related depression or in those with immunity-associated comorbidities. The range of antidepressants may increase in the future if promising initial data on GSK-3, TLR-4 and oleanolic acids is verified in upcoming clinical trials.

ACKNOWLEDGEMENTs

Declared none.

CONFLICT OF INTEREST

The authors confirm that this article content has no conflict of interest.

REFERENCES

1. WHO. Facts sheep No 369 Depression. http://www.who.int/ mediacentre/factsheets/fs369/en/ 2012. October; [Accessed August 15, 2015]
2. Kupfer D.J., Frank E., Phillips M.L. Major depressive disorder: new clinical, neurobiological, and treatment perspectives. Lancet. 2012;379(9820):1045–1055. [http://dx.doi.org/10.1016/S0140-6736(11)60602-8]. [PMID: 22189047]. [PMC free article] [PubMed]
3. Greenberg P.E., Fournier A.A., Sisitsky T., Pike C.T., Kessler R.C. The economic burden of adults with major depressive disorder in the United States (2005 and 2010). J. Clin. Psychiatry. 2015;76(2):155–162. [http://dx.doi.org/10.4088/JCP.14m09298]. [PMID: 25742202]. [PubMed]
4. Rush A.J., Trivedi M.H., Wisniewski S.R., Nierenberg A.A., Stewart J.W., Warden D., Niederehe G., Thase M.E., Lavori P.W., Lebowitz B.D., McGrath P.J., Rosenbaum J.F., Sackeim H.A., Kupfer D.J., Luther J., Fava M. Acute and longer-term outcomes in depressed outpatients requiring one or several treatment steps: a STAR*D report. Am. J. Psychiatry. 2006;163(11):1905–1917. [http://dx.doi.org/10.1176/ajp.2006.163.11. 1905]. [PMID: 17074942]. [PubMed]
5. Gibbons R.D., Hur K., Brown C.H., Davis J.M., Mann J.J. Benefits from antidepressants: synthesis of 6-week patient-level outcomes from double-blind placebo-controlled randomized trials of fluoxetine and venlafaxine. Arch. Gen. Psychiatry. 2012;69(6):572–579. [http://dx.doi.org/10.1001/archgenpsychiatry.2011.2044]. [PMID: 22393205]. [PMC free article] [PubMed]
6. Haapakoski R., Mathieu J., Ebmeier K.P., Alenius H., Kivimäki M. Cumulative meta-analysis of interleukins 6 and 1β, tumour necrosis factor α and C-reactive protein in patients with major depressive disorder. Brain Behav. Immun. 2015;49:206–215. [http://dx.doi.org/10.1016/j.bbi.2015.06.001]. [PMID: 26065825]. [PMC free article] [PubMed]
7. Dowlati Y., Herrmann N., Swardfager W., Liu H., Sham L., Reim E.K., Lanctôt K.L. A meta-analysis of cytokines in major depression. Biol. Psychiatry. 2010;67(5):446–457. [http://dx.doi.
org/10.1016/j.biopsych.2009.09.033]. [PMID: 20015486]. [PubMed]
8. Schmidt F.M., Lichtblau N., Minkwitz J., Chittka T., Thormann J., Kirkby K.C., Sander C., Mergl R., Faßhauer M., Stumvoll M., Holdt L.M., Teupser D., Hegerl U., Himmerich H. Cytokine levels in depressed and non-depressed subjects, and masking effects of obesity. J. Psychiatr. Res. 2014;55:29–34. [http://dx. doi.org/10.1016/j.jpsychires.2014.04.021]. [PMID: 24838047]. [PubMed]
9. Eller T., Vasar V., Shlik J., Maron E. Pro-inflammatory cytokines and treatment response to escitalopram in major depressive disorder. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2008;32(2):445–450. [http://dx.doi.org/10.1016/j.pnpbp.2007.09. 015]. [PMID: 17976882]. [PubMed]
10. Berk M., Williams L.J., Jacka F.N., O’Neil A., Pasco J.A., Moylan S., Allen N.B., Stuart A.L., Hayley A.C., Byrne M.L., Maes M. So depression is an inflammatory disease, but where does the inflammation come from? BMC Med. 2013;11:200. [http://dx.doi.org/10.1186/1741-7015-11-200]. [PMID: 24228900]. [PMC free article] [PubMed]
11. Felger J.C., Lotrich F.E. Inflammatory cytokines in depression: neurobiological mechanisms and therapeutic implications. Neuroscience. 2013;246:199–229. [http://dx.doi.org/10.1016/ j.neuroscience.2013.04.060]. [PMID: 23644052]. [PMC free article] [PubMed]
12. Lotrich F.E. Inflammatory cytokine-associated depression. Brain Res. 2015;1617:113–125. [http://dx.doi.org/10.1016/j.brainres. 2014.06.032]. [PMID: 25003554]. [PMC free article] [PubMed]
13. Müller N., Schwarz M.J. The immune-mediated alteration of serotonin and glutamate: towards an integrated view of depression. Mol. Psychiatry. 2007;12(11):988–1000. [http://dx.doi.org/10. 1038/sj.mp.4002006]. [PMID: 17457312]. [PubMed]
14. Zoga M., Oulis P., Chatzipanagiotou S., Masdrakis V.G., Pliatsika P., Boufidou F., Foteli S., Soldatos C.R., Nikolaou C., Papageorgiou C. Indoleamine 2,3-dioxygenase and immune changes under antidepressive treatment in major depression in females. In Vivo. 2014;28(4):633–638. [PMID: 24982234]. [PubMed]
15. O’Connor J.C., Lawson M.A., André C., Moreau M., Lestage J., Castanon N., Kelley K.W., Dantzer R. Lipopolysaccharide-induced depressive-like behavior is mediated by indoleamine 2,3-dioxygenase activation in mice. Mol. Psychiatry. 2009;14(5):511–522. [http://dx.doi.org/10.1038/sj.mp.4002148]. [PMID: 18195714]. [PMC free article] [PubMed]
16. Malynn S., Campos-Torres A., Moynagh P., Haase J. The pro-inflammatory cytokine TNF-α regulates the activity and expression of the serotonin transporter (SERT) in astrocytes. Neurochem. Res. 2013;38(4):694–704. [http://dx.doi.org/10.1007/s11064-012-0967-y]. [PMID: 23338678]. [PubMed]
17. Ferrés-Coy A., Galofré M., Pilar-Cuéllar F., Vidal R., Paz V., Ruiz-Bronchal E., Campa L., Pazos Á., Caso J.R., Leza J.C., Alvarado G., Montefeltro A., Valdizán E.M., Artigas F., Bortolozzi A. Therapeutic antidepressant potential of a conjugated siRNA silencing the serotonin transporter after intranasal administration. Mol. Psychiatry. 2015 [Epub ahead of print]. [http://dx.doi.org/10.1038/mp.2015.80]. [PMID: 26100539]. [PMC free article] [PubMed]
18. Dunn A.J. Cytokine activation of the HPA axis. Ann. N. Y. Acad. Sci. 2000;917:608–617. [http://dx.doi.org/10.1111/j.1749-6632.2000.tb05426.x]. [PMID: 11268389]. [PubMed]
19. Zunszain P.A., Anacker C., Cattaneo A., Carvalho L.A., Pariante C.M. Glucocorticoids, cytokines and brain abnormalities in depression. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2011;35(3):722–729. [http://dx.doi.org/10.1016/j.pnpbp.2010.04. 011]. [PMID: 20406665]. [PMC free article] [PubMed]
20. Himmerich H., Binder E.B., Künzel H.E., Schuld A., Lucae S., Uhr M., Pollmächer T., Holsboer F., Ising M. Successful antidepressant therapy restores the disturbed interplay between TNF-alpha system and HPA axis. Biol. Psychiatry. 2006;60(8):882–888. [http://dx.doi.org/10.1016/j.biopsych.2006.03.075]. [PMID: 16989778]. [PubMed]
21. Moylan S., Berk M., Dean O.M., Samuni Y., Williams L.J., O’Neil A., Hayley A.C., Pasco J.A., Anderson G., Jacka F.N., Maes M. Oxidative & nitrosative stress in depression: why so much stress? Neurosci. Biobehav. Rev. 2014;45:46–62. [http://dx. doi.org/10.1016/j.neubiorev.2014.05.007]. [PMID: 24858007]. [PubMed]
22. Vaváková M., Ďuračková Z., Trebatická J. Markers of Oxidative Stress and Neuroprogression in Depression Disorder. Oxid. Med.Cell. Longev. 2015 898393. [PMC free article] [PubMed]
23. Eyre H., Baune B.T. Neuroplastic changes in depression: a role for the immune system. Psychoneuroendocrinology. 2012;37(9):1397–1416. [http://dx.doi.org/10.1016/j.psyneuen.2012.03.019]. [PMID: 22525700]. [PubMed]
24. Frodl T., Amico F. Is there an association between peripheral immune markers and structural/functional neuroimaging findings? Prog. Neuropsychopharmacol. Biol. Psychiatry. 2014;48:295–303. [http://dx.doi.org/10.1016/j.pnpbp.2012.12.013]. [PMID: 23313563]. [PubMed]
25. Haas C.E., Brazeau D., Cloen D., Booker B.M., Frerichs V., Zaranek C., Frye R.F., Kufel T. Cytochrome P450 mRNA expression in peripheral blood lymphocytes as a predictor of enzyme induction. Eur. J. Clin. Pharmacol. 2005;61(8):583–593. [http://dx.doi.org/10.1007/s00228-005-0971-0]. [PMID: 16041547]. [PubMed]
26. Hiemke C., Baumann P., Bergemann N., Conca A., Dietmaier O., Egberts K., Fric M., Gerlach M., Greiner C., Gründer G., Haen E., Havemann-Reinecke U., Jaquenoud Sirot E., Kirchherr H., Laux G., Lutz U.C., Messer T., Müller M.J., Pfuhlmann B., Rambeck B., Riederer P., Schoppek B., Stingl J., Uhr M., Ulrich S., Waschgler R., Zernig G. AGNP consensus guidelines for therapeutic drug monitoring in psychiatry: update 2011. Pharmacopsychiatry. 2011;44:195–235. [http://dx.doi.org/10. 1055/s-0031-1286287]. [PubMed]
27. Bertilsson P.M., Olsson P., Magnusson K.E. Cytokines influence mRNA expression of cytochrome P450 3A4 and MDRI in intestinal cells. J. Pharm. Sci. 2001;90(5):638–646. [http://dx.doi.org/10. 1002/1520-6017(200105)90:5<638:AID-JPS1020>3.0.CO;2-L]. [PMID: 11288108]. [PubMed]
28. Carlson T.J., Billings R.E. Role of nitric oxide in the cytokine-mediated regulation of cytochrome P-450. Mol. Pharmacol. 1996;49:796–801. [PubMed]
29. Frye R.F., Schneider V.M., Frye C.S., Feldman A.M. Plasma levels of TNF-alpha and IL-6 are inversely related to cytochrome P450-dependent drug metabolism in patients with congestive heart failure. J. Card. Fail. 2002;8(5):315–319. [http://dx.doi.org/
10.1054/jcaf.2002.127773]. [PMID: 12411982]. [PubMed]
30. Aitken A.E., Lee C.M., Morgan E.T. Roles of nitric oxide in inflammatory downregulation of human cytochromes P450. Free Radic. Biol. Med. 2008;44(6):1161–1168. [http://dx.doi.org/10. 1016/j.freeradbiomed.2007.12.010]. [PMID: 18206661]. [PMC free article] [PubMed]
31. Lee J.I., Zhang L., Men A.Y., Kenna L.A., Huang S.M. CYP-mediated therapeutic protein-drug interactions: clinical findings, proposed mechanisms and regulatory implications. Clin. Pharmacokinet. 2010;49(5):295–310. [http://dx.doi.org/10.2165/ 11319980-000000000-00000]. [PMID: 20384392]. [PubMed]
32. Furlanut M., Soardo G., Donnini D., Sechi L., Franceschi L. Fluoxetine disposition in patients with chronic hepatitis C treated with interferon-α. Clin. Pharmacokinet. 2010;49(11):767–772. [http://dx.doi.org/10.2165/11534720-000000000-00000]. [PMID: 20923249]. [PubMed]
33. Hefner G., Shams M.E., Unterecker S., Falter T., Hiemke C. Retrospective pilot study for analysis of antidepressant serum concentrations of citalopram and venlafaxine during inflammation. Pharmacopsychiatry. 2015;48(6):215–218. [http://dx.doi.org/10. 1055/s-0035-1559666]. [PMID: 26335759]. [PubMed]
34. Koch M.W., Glazenborg A., Uyttenboogaart M., Mostert J., De Keyser J. Pharmacologic treatment of depression in multiple sclerosis. Cochrane Database Syst. Rev. 2011;(2):CD007295. [PMID: 21328292]. [PubMed]
35. Bird H., Broggini M. Paroxetine versus amitriptyline for treatment of depression associated with rheumatoid arthritis: a randomized, double blind, parallel group study. J. Rheumatol. 2000;27(12):2791–2797. [PMID: 11128665]. [PubMed]
36. Pan W., Stone K.P., Hsuchou H., Manda V.K., Zhang Y., Kastin A.J. Cytokine signaling modulates blood-brain barrier function. Curr. Pharm. Des. 2011;17(33):3729–3740. [http://dx. doi.org/10.2174/138161211798220918]. [PMID: 21834767]. [PMC free article] [PubMed]
37. Breitenstein B., Brückl T.M., Ising M., Müller-Myhsok B., Holsboer F., Czamara D. ABCB1 gene variants and antidepressant treatment outcome: A meta-analysis. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 2015;168B(4):274–283. [http://dx.doi.org/
10.1002/ajmg.b.32309]. [PMID: 25847751]. [PubMed]
38. Liptrott N.J., Penny M., Bray P.G., Sathish J., Khoo S.H., Back D.J., Owen A. The impact of cytokines on the expression of drug transporters, cytochrome P450 enzymes and chemokine receptors in human PBMC. Br. J. Pharmacol. 2009;156(3):497–508. [http://
dx.doi.org/10.1111/j.1476-5381.2008.00050.x]. [PMID: 19154420]. [PMC free article] [PubMed]
39. Yu C., Kastin A.J., Tu H., Waters S., Pan W. TNF activates P-glycoprotein in cerebral microvascular endothelial cells. Cell. Physiol. Biochem. 2007;20(6):853–858. [http://dx.doi.org/
10.1159/000110445]. [PMID: 17982267]. [PubMed]
40. Poller B., Drewe J., Krähenbühl S., Huwyler J., Gutmann H. Regulation of BCRP (ABCG2) and P-glycoprotein (ABCB1) by cytokines in a model of the human blood-brain barrier. Cell. Mol. Neurobiol. 2010;30(1):63–70. [http://dx.doi.org/10.1007/s10571-009-9431-1]. [PMID: 19629677]. [PubMed]
41. Bauer B., Hartz A.M., Miller D.S. Tumor necrosis factor alpha and endothelin-1 increase P-glycoprotein expression and transport activity at the blood-brain barrier. Mol. Pharmacol. 2007;71(3):667–675. [http://dx.doi.org/10.1124/mol.106.029512]. [PMID: 17132686]. [PubMed]
42. von Wedel-Parlow M., Wölte P., Galla H.J. Regulation of major efflux transporters under inflammatory conditions at the blood-brain barrier in vitro. J. Neurochem. 2009;111(1):111–118. [http://
dx.doi.org/10.1111/j.1471-4159.2009.06305.x]. [PMID: 19656257]. [PubMed]
43. Dahl J., Ormstad H., Aass H.C., Malt U.F., Bendz L.T., Sandvik L., Brundin L., Andreassen O.A. The plasma levels of various cytokines are increased during ongoing depression and are reduced to normal levels after recovery. Psychoneuroendocrinology. 2014;45:77–86. [http://dx.doi.org/10.1016/j.psyneuen.2014.03. 019]. [PMID: 24845179]. [PubMed]
44. Simon N.M., McNamara K., Chow C.W., Maser R.S., Papakostas G.I., Pollack M.H., Nierenberg A.A., Fava M., Wong K.K. A detailed examination of cytokine abnormalities in Major Depressive Disorder. Eur. Neuropsychopharmacol. 2008;18(3):230–233. [http://dx.doi.org/10.1016/j.euroneuro.2007.06. 004]. [PMID: 17681762]. [PMC free article] [PubMed]
45. Valkanova V., Ebmeier K.P., Allan C.L. CRP, IL-6 and depression: a systematic review and meta-analysis of longitudinal studies. J. Affect. Disord. 2013;150(3):736–744. [http://dx.doi.
org/10.1016/j.jad.2013.06.004]. [PMID: 23870425]. [PubMed]
46. Marques-Deak A.H., Neto F.L., Dominguez W.V., Solis A.C., Kurcgant D., Sato F., Ross J.M., Prado E.B. Cytokine profiles in women with different subtypes of major depressive disorder. J. Psychiatr. Res. 2007;41(1-2):152–159. [http://dx.doi.org/10.1016/ j.jpsychires.2005.11.003]. [PMID: 16375926]. [PubMed]
47. Asnis G.M., De La Garza R.I. Interferon-induced depression in chronic hepatitis C: a review of its prevalence, risk factors, biology, and treatment approaches. J. Clin. Gastroenterol. 2006;40(4):322–335. [http://dx.doi.org/10.1097/01.mcg.0000210099.36500.fe]. [PMID: 16633105]. [PubMed]
48. Strawbridge R., Arnone D., Danese A., Papadopoulos A., Herane Vives A., Cleare A.J. Inflammation and clinical response to treatment in depression: A meta-analysis. Eur. Neuropsychopharmacol. 2015;25(10):1532–1543. [Epub ahead of print]. [http://
dx.doi.org/10.1016/j.euroneuro.2015.06.007]. [PMID: 26169573]. [PubMed]
49. Hannestad J., DellaGioia N., Bloch M. The effect of antidepressant medication treatment on serum levels of inflammatory cytokines: a meta-analysis. Neuropsychopharmacology. 2011;36(12):2452–2459. [http://dx.doi.org/10.1038/npp.2011.132]. [PMID: 21796103]. [PMC free article] [PubMed]
50. Himmerich H., Milenović S., Fulda S., Plümäkers B., Sheldrick A.J., Michel T.M., Kircher T., Rink L. Regulatory T cells increased while IL-1β decreased during antidepressant therapy. J. Psychiatr. Res. 2010;44(15):1052–1057. [http://dx.doi.org/10. 1016/j.jpsychires.2010.03.005]. [PMID: 20413130]. [PubMed]
51. Obuchowicz E., Bielecka A.M., Paul-Samojedny M., Pudełko A., Kowalski J. Imipramine and fluoxetine inhibit LPS-induced activation and affect morphology of microglial cells in the rat glial culture. Pharmacol. Rep. 2014;66(1):34–43. [http://dx.doi.org/
10.1016/j.pharep.2013.08.002]. [PMID: 24905304]. [PubMed]
52. Liu R.P., Zou M., Wang J.Y., Zhu J.J., Lai J.M., Zhou L.L., Chen S.F., Zhang X., Zhu J.H. Paroxetine ameliorates lipopolysaccharide-induced microglia activation via differential regulation of MAPK signaling. J. Neuroinflammation. 2014;11:47. [http://dx.doi.org/10.1186/1742-2094-11-47]. [PMID: 24618100]. [PMC free article] [PubMed]
53. Vismari L., Alves G.J., Muscará M.N., Palermo-Neto J. A possible role to nitric oxide in the anti-inflammatory effects of amitriptyline. Immunopharmacol. Immunotoxicol. 2012;34(4):578–585. [http://dx.doi.org/10.3109/08923973.2011.638305]. [PMID: 22208160]. [PubMed]
54. Manikowska K., Mikołajczyk M., Mikołajczak P.Ł., Bobkiewicz-Kozłowska T. The influence of mianserin on TNF-α, IL-6 and IL-10 serum levels in rats under chronic mild stress. Pharmacol. Rep. 2014;66(1):22–27. [http://dx.doi.org/10.1016/j. pharep.2013.06.003]. [PMID: 24905302]. [PubMed]
55. Horowitz M.A., Wertz J., Zhu D., Cattaneo A., Musaelyan K., Nikkheslat N., Thuret S., Pariante C.M., Zunszain P.A. Antidepressant compounds can be both pro- and anti-inflammatory in human hippocampal cells. Int. J. Neuropsychopharmacol. 2015;18(3):18. [http://dx.doi.org/10.1093/ijnp/pyu076]. [PMID: 25522414]. [PMC free article] [PubMed]
56. Munzer A., Sack U., Mergl R., Schönherr J., Petersein C., Bartsch S., Kirkby K.C., Bauer K., Himmerich H. Impact of antidepressants on cytokine production of depressed patients in vitro. Toxins (Basel) 2013;5(11):2227–2240. [http://dx.doi.org/
10.3390/toxins5112227]. [PMID: 24257035]. [PMC free article] [PubMed]
57. Petersein C., Sack U., Mergl R., Schönherr J., Schmidt F.M., Lichtblau N., Kirkby K.C., Bauer K., Himmerich H. Impact of lithium alone and in combination with antidepressants on cytokine production in vitro. J Neural Transm (Vienna) 2015;122(1):109–122. [http://dx.doi.org/10.1007/s00702-014-1328-6]. [PMID: 25377522]. [PubMed]
58. Maes M., Song C., Lin A.H., Bonaccorso S., Kenis G., De Jongh R., Bosmans E., Scharpé S. Negative immunoregulatory effects of antidepressants: inhibition of interferon-gamma and stimulation of interleukin-10 secretion. Neuropsychopharmacology. 1999;20(4):370–379. [http://dx.doi.org/10.1016/S0893-133X(98) 00088-8]. [PMID: 10088138]. [PubMed]
59. Thomas A.J., Davis S., Morris C., Jackson E., Harrison R., O’Brien J.T. Increase in interleukin-1beta in late-life depression. Am. J. Psychiatry. 2005;162(1):175–177. [http://dx.doi.org/
10.1176/appi.ajp.162.1.175]. [PMID: 15625217]. [PubMed]
60. Steptoe A., Kunz-Ebrecht S.R., Owen N. Lack of association between depressive symptoms and markers of immune and vascular inflammation in middle-aged men and women. Psychol. Med. 2003;33(4):667–674. [http://dx.doi.org/10.1017/ S0033291702007250]. [PMID: 12785468]. [PubMed]
61. Eller T., Aluoja A., Maron E., Vasar V. Soluble interleukin-2 receptor and tumor necrosis factor levels in depressed patients in Estonia. Medicina (Kaunas) 2009;45(12):971–977. [PMID: 20173400]. [PubMed]
62. Black C., Miller B.J. Meta-Analysis of Cytokines and Chemokines in Suicidality: Distinguishing Suicidal Versus Nonsuicidal Patients. Biol. Psychiatry. 2015;78(1):28–37. [http://dx.doi.org/10.1016/ j.biopsych.2014.10.014]. [PMID: 25541493]. [PubMed]
63. Serafini G., Pompili M., Elena Seretti M., Stefani H., Palermo M., Coryell W., Girardi P. The role of inflammatory cytokines in suicidal behavior: a systematic review. Eur. Neuropsychopharmacol. 2013;23(12):1672–1686. [http://dx.doi.org/10.1016/ j.euroneuro.2013.06.002]. [PMID: 23896009]. [PubMed]
64. Zheng L.S., Kaneko N., Sawamoto K. Minocycline treatment ameliorates interferon-alpha- induced neurogenic defects and depression-like behaviors in mice. Front. Cell. Neurosci. 2015;9:5. [http://dx.doi.org/10.3389/fncel.2015.00005]. [PMID: 25674053]. [PMC free article] [PubMed]
65. Krügel U., Fischer J., Bauer K., Sack U., Himmerich H. The impact of social isolation on immunological parameters in rats. Arch. Toxicol. 2014;88(3):853–855. [PMID: 24500571]. [PubMed]
66. Maes M., Berk M., Goehler L., Song C., Anderson G., Gałecki P., Leonard B. Depression and sickness behavior are Janus-faced responses to shared inflammatory pathways. BMC Med. 2012;10:66. [http://dx.doi.org/10.1186/1741-7015-10-66]. [PMID: 22747645]. [PMC free article] [PubMed]
67. Janssen D.G., Caniato R.N., Verster J.C., Baune B.T. A psychoneuroimmunological review on cytokines involved in antidepressant treatment response. Hum. Psychopharmacol. 2010;25(3):201–215. [http://dx.doi.org/10.1002/hup.1103]. [PMID: 20373471]. [PubMed]
68. Uher R., Tansey K.E., Dew T., Maier W., Mors O., Hauser J., Dernovsek M.Z., Henigsberg N., Souery D., Farmer A., McGuffin P. An inflammatory biomarker as a differential predictor of outcome of depression treatment with escitalopram and nortriptyline. Am. J. Psychiatry. 2014;171(12):1278–1286. [http://
dx.doi.org/10.1176/appi.ajp.2014.14010094]. [PMID: 25017001]. [PubMed]
69. Yoshimura R., Hori H., Ikenouchi-Sugita A., Umene-Nakano W., Ueda N., Nakamura J. Higher plasma interleukin-6 (IL-6) level is associated with SSRI- or SNRI-refractory depression. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2009;33(4):722–726. [http://dx.doi.org/10.1016/j.pnpbp.2009.03.020]. [PMID: 19332097]. [PubMed]
70. Lanquillon S., Krieg J.C., Bening-Abu-Shach U., Vedder H. Cytokine production and treatment response in major depressive disorder. Neuropsychopharmacology. 2000;22(4):370–379. [http://
dx.doi.org/10.1016/S0893-133X(99)00134-7]. [PMID: 10700656]. [PubMed]
71. Maes M., Bosmans E., De Jongh R., Kenis G., Vandoolaeghe E., Neels H. Increased serum IL-6 and IL-1 receptor antagonist concentrations in major depression and treatment resistant depression. Cytokine. 1997;9(11):853–858. [http://dx.doi.org/10.1006/cyto. 1997.0238]. [PMID: 9367546]. [PubMed]
72. Baune B.T., Dannlowski U., Domschke K., Janssen D.G., Jordan M.A., Ohrmann P., Bauer J., Biros E., Arolt V., Kugel H., Baxter A.G., Suslow T. The interleukin 1 beta (IL1B) gene is associated with failure to achieve remission and impaired emotion processing in major depression. Biol. Psychiatry. 2010;67(6):543–549. [http://dx.doi.org/10.1016/j.biopsych.2009.11.004]. [PMID: 20044070]. [PubMed]
73. Duseja R., Heir R., Lewitus G.M., Altimimi H.F., Stellwagen D. Astrocytic TNFα regulates the behavioral response to anti- depressants. Brain Behav. Immun. 2015;44:187–194. [http://dx. doi.org/10.1016/j.bbi.2014.09.012]. [PMID: 25300923]. [PubMed]
74. Köhler O., Benros M.E., Nordentoft M., Farkouh M.E., Iyengar R.L., Mors O., Krogh J. Effect of anti-inflammatory treatment on depression, depressive symptoms, and adverse effects: a systematic review and meta-analysis of randomized clinical trials. JAMA Psychiatry. 2014;71(12):1381–1391. [http://dx.doi.org/10.1001/ jamapsychiatry.2014.1611]. [PMID: 25322082]. [PubMed]
75. Eyre H.A., Air T., Proctor S., Rositano S., Baune B.T. A critical review of the efficacy of non-steroidal anti-inflammatory drugs in depression. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2015;57(57):11–16. [http://dx.doi.org/10.1016/j.pnpbp.2014.10.003]. [PMID: 25455584]. [PubMed]
76. Fields C., Drye L., Vaidya V., Lyketsos C. Celecoxib or naproxen treatment does not benefit depressive symptoms in persons age 70 and older: findings from a randomized controlled trial. Am. J. Geriatr. Psychiatry. 2012;20(6):505–513. [http://dx. doi.org/10.1097/JGP.0b013e318227f4da]. [PMID: 21775876]. [PMC free article] [PubMed]
77. Warner-Schmidt J.L., Vanover K.E., Chen E.Y., Marshall J.J., Greengard P. Antidepressant effects of selective serotonin reuptake inhibitors (SSRIs) are attenuated by antiinflammatory drugs in mice and humans. Proc. Natl. Acad. Sci. USA. 2011;108(22):9262–9267. [http://dx.doi.org/10.1073/pnas.1104836108]. [PMID: 21518864]. [PubMed]
78. Maes M. Targeting cyclooxygenase-2 in depression is not a viable therapeutic approach and may even aggravate the pathophysiology underpinning depression. Metab. Brain Dis. 2012;27(4):405–413. [http://dx.doi.org/10.1007/s11011-012-9326-6]. [PMID: 22773310]. [PubMed]
79. Köhler O., Petersen L., Mors O., Gasse C. Inflammation and depression: combined use of selective serotonin reuptake inhibitors and NSAIDs or paracetamol and psychiatric outcomes. Brain Behav. 2015;5(8):e00338. [http://dx.doi.org/10.1002/brb3.338]. [PMID: 26357585]. [PMC free article] [PubMed]
80. Berk M., Dean O., Drexhage H., McNeil J.J., Moylan S., O'Neil A., Davey C.G., Sanna L., Maes M. Aspirin: a review of its neurobiological properties and therapeutic potential for mental illness. BMC Med. 2013;18:11–74. [http://dx.doi.org/10.1186/ 1741-7015-11-74]. [PMC free article] [PubMed]
81. Perez-G M., Melo M., Keegan A.D., Zamorano J. Aspirin and salicylates inhibit the IL-4- and IL-13-induced activation of STAT6. J. Immunol. 2002;168(3):1428–1434. [http://dx.doi.org/
10.4049/jimmunol.168.3.1428]. [PMID: 11801685]. [PubMed]
82. Brunello N., Alboni S., Capone G., Benatti C., Blom J.M., Tascedda F., Kriwin P., Mendlewicz J. Acetylsalicylic acid accelerates the antidepressant effect of fluoxetine in the chronic escape deficit model of depression. Int. Clin. Psychopharmacol. 2006;21(4):219–225. [http://dx.doi.org/10.1097/00004850-200607000-00004]. [PMID: 16687993]. [PubMed]
83. Yang J.M., Rui B.B., Chen C., Chen H., Xu T.J., Xu W.P., Wei W. Acetylsalicylic acid enhances the anti-inflammatory effect of fluoxetine through inhibition of NF-κB, p38-MAPK and ERK1/2 activation in lipopolysaccharide-induced BV-2 microglia cells. Neuroscience. 2014;275(275):296–304. [http://dx.doi.org/
10.1016/j.neuroscience.2014.06.016]. [PMID: 24952332]. [PubMed]
84. Toussi S.S., Pan N., Walters H.M., Walsh T.J. Infections in children and adolescents with juvenile idiopathic arthritis and inflammatory bowel disease treated with tumor necrosis factor-α inhibitors: systematic review of the literature. Clin. Infect. Dis. 2013;57(9):1318–1330. [http://dx.doi.org/10.1093/cid/cit489]. [PMID: 23899685]. [PMC free article] [PubMed]
85. Tyring S., Gottlieb A., Papp K., Gordon K., Leonardi C., Wang A., Lalla D., Woolley M., Jahreis A., Zitnik R., Cella D., Krishnan R. Etanercept and clinical outcomes, fatigue, and depression in psoriasis: double-blind placebo-controlled randomised phase III trial. Lancet. 2006;367(9504):29–35. [http://dx.doi.org/
10.1016/S0140-6736(05)67763-X]. [PMID: 16399150]. [PubMed]
86. Krügel U., Fischer J., Radicke S., Sack U., Himmerich H. Antidepressant effects of TNF-α blockade in an animal model of depression. J. Psychiatr. Res. 2013;47(5):611–616. [http://dx.doi.
org/10.1016/j.jpsychires.2013.01.007]. [PMID: 23394815]. [PubMed]
87. Schmidt F.M., Kirkby K.C., Himmerich H. The TNF-alpha inhibitor etanercept as monotherapy in treatment-resistant depression - report of two cases. Psychiatr. Danub. 2014;26(3):288–290. [PMID: 25191779]. [PubMed]
88. Raison C.L., Rutherford R.E., Woolwine B.J., Shuo C., Schettler P., Drake D.F., Haroon E., Miller A.H. A randomized controlled trial of the tumor necrosis factor antagonist infliximab for treatment-resistant depression: the role of baseline inflammatory biomarkers. JAMA Psychiatry. 2013;70(1):31–41. [http://dx.doi.org/10.1001/2013.jamapsychiatry.4]. [PMID: 22945416]. [PMC free article] [PubMed]
89. Weinberger J.F., Raison C.L., Rye D.B., Montague A.R., Woolwine B.J., Felger J.C., Haroon E., Miller A.H. Inhibition of tumor necrosis factor improves sleep continuity in patients with treatment resistant depression and high inflammation. Brain Behav. Immun. 2015;47:193–200. [http://dx.doi.org/10.1016/j.bbi.2014. 12.016]. [PMID: 25529904]. [PMC free article] [PubMed]
90. Schmidt F.M., Pschiebl A., Sander C., Kirkby K.C., Thormann J., Minkwitz J., Chittka T., Weschenfelder W., Holdt L.M., Teupser D., Hegerl U., Himmerich H. Impact of serum cytokine levels on EEG-measured arousal regulation in patients with major depressive disorder and healthy controls. Neuropsychobiology. 2015 [PMID: 26812192]. [PubMed]
91. Karson A., Demirtaş T., Bayramgürler D., Balci F., Utkan T. Chronic administration of infliximab (TNF-α inhibitor) decreases depression and anxiety-like behaviour in rat model of chronic mild stress. Basic Clin. Pharmacol. Toxicol. 2013;112(5):335–340. [http://dx.doi.org/10.1111/bcpt.12037]. [PMID: 23167806]. [PubMed]
92. Menter A., Augustin M., Signorovitch J., Yu A.P., Wu E.Q., Gupta S.R., Bao Y., Mulani P. The effect of adalimumab on reducing depression symptoms in patients with moderate to severe psoriasis: a randomized clinical trial. J. Am. Acad. Dermatol. 2010;62(5):812–818. [http://dx.doi.org/10.1016/j.jaad.2009.07.022]. [PMID: 20219265]. [PubMed]
93. Langley R.G., Feldman S.R., Han C., Schenkel B., Szapary P., Hsu M.C., Ortonne J.P., Gordon K.B., Kimball A.B. Ustekinumab significantly improves symptoms of anxiety, depression, and skin-related quality of life in patients with moderate-to-severe psoriasis: Results from a randomized, double-blind, placebo-controlled phase III trial. J. Am. Acad. Dermatol. 2010;63(3):457–465. [http://dx.doi.org/10.1016/j.jaad.2009.09. 014]. [PMID: 20462664]. [PubMed]
94. Murrough J.W., Iosifescu D.V., Chang L.C., Al Jurdi R.K., Green C.E., Perez A.M., Iqbal S., Pillemer S., Foulkes A., Shah A., Charney D.S., Mathew S.J. Antidepressant efficacy of ketamine in treatment-resistant major depression: a two-site randomized controlled trial. Am. J. Psychiatry. 2013;170(10):1134–1142. [http://
dx.doi.org/10.1176/appi.ajp.2013.13030392]. [PMID: 23982301]. [PMC free article] [PubMed]
95. Iadarola N.D., Niciu M.J., Richards E.M., Vande Voort J.L., Ballard E.D., Lundin N.B., Nugent A.C., Machado-Vieira R., Zarate C.A. Jr Ketamine and other N-methyl-D-aspartate receptor antagonists in the treatment of depression: a perspective review. Ther. Adv. Chronic Dis. 2015;6(3):97–114. [http://dx.doi.org/
10.1177/2040622315579059]. [PMID: 25954495]. [PMC free article] [PubMed]
96. Taniguchi T., Kanakura H., Takemoto Y., Yamamoto K. The antiinflammatory effects of ketamine in endotoxemic rats during moderate and mild hypothermia. Anesth. Analg. 2004;98(4):1114–1120. [http://dx.doi.org/10.1213/01.ANE.0000100740.07331.A2]. [PMID: 15041609]. [PubMed]
97. Helmer K.S., Cui Y., Chang L., Dewan A., Mercer D.W. Effects of ketamine/xylazine on expression of tumor necrosis factor-alpha, inducible nitric oxide synthase, and cyclo-oxygenase-2 in rat gastric mucosa during endotoxemia. Shock. 2003;20(1):63–69. [http://dx.doi.org/10.1097/01.shk.0000065766.72937.cf]. [PMID: 12813371]. [PubMed]
98. Wang N., Yu H.Y., Shen X.F., Gao Z.Q., Yang C., Yang J.J., Zhang G.F. The rapid antidepressant effect of ketamine in rats is associated with down-regulation of pro-inflammatory cytokines in the hippocampus. Ups. J. Med. Sci. 2015;120(4):241–248. [http://
dx.doi.org/10.3109/03009734.2015.1060281]. [PMID: 26220286]. [PMC free article] [PubMed]
99. Tan Y., Wang Q., She Y., Bi X., Zhao B. Ketamine reduces LPS-induced HMGB1 via activation of the Nrf2/HO-1 pathway and NF-κB suppression. J. Trauma Acute Care Surg. 2015;78(4):784–792. [http://dx.doi.org/10.1097/TA.0000000000000588]. [PMID: 25807407]. [PubMed]
100. Yang J.J., Wang N., Yang C., Shi J.Y., Yu H.Y., Hashimoto K. Serum interleukin-6 is a predictive biomarker for ketamine’s antidepressant effect in treatment-resistant patients with major depression. Biol. Psychiatry. 2015;77(3):e19–e20. [http://dx.doi.
org/10.1016/j.biopsych.2014.06.021]. [PMID: 25104172]. [PubMed]
101. Al Jurdi R.K., Swann A., Mathew S.J. Psychopharmacological Agents and Suicide Risk Reduction: Ketamine and Other Approaches. Curr. Psychiatry Rep. 2015;17(10):81. [http://dx.doi.org/10. 1007/s11920-015-0614-9]. [PMID: 26307033]. [PubMed]
102. Zhu X., Li P., Hao X., Wei K., Min S., Luo J., Xie F., Jin J. Ketamine-mediated alleviation of electroconvulsive shock-induced memory impairment is associated with the regulation of neuro- inflammation and soluble amyloid-beta peptide in depressive-like rats. Neurosci. Lett. 2015;599(599):32–37. [http://dx.doi.org/
10.1016/j.neulet.2015.05.022]. [PMID: 25980993]. [PubMed]
103. Schmidt F.M., Weschenfelder J., Sander C., Minkwitz J., Thormann J., Chittka T., Mergl R., Kirkby K.C., Faßhauer M., Stumvoll M., Holdt L.M., Teupser D., Hegerl U., Himmerich H. Inflammatory cytokines in general and central obesity and modulating effects of physical activity. PLoS One. 2015 [PMC free article] [PubMed]
104. Lin P.Y., Huang S.Y., Su K.P. A meta-analytic review of polyunsaturated fatty acid compositions in patients with depression. Biol. Psychiatry. 2010;68(2):140–147. [http://dx.doi.org/10.1016/ j.biopsych.2010.03.018]. [PMID: 20452573]. [PubMed]
105. Martins J.G., Bentsen H., Puri B.K. Eicosapentaenoic acid appears to be the key omega-3 fatty acid component associated with efficacy in major depressive disorder: a critique of Bloch and Hannestad and updated meta-analysis. Mol. Psychiatry. 2012;17(12):1144–1149. [http://dx.doi.org/10.1038/mp.2012.25]. [PMID: 22488258]. [PubMed]
106. Bloch M.H., Hannestad J. Omega-3 fatty acids for the treatment of depression: systematic review and meta-analysis. Mol. Psychiatry. 2012;17(12):1272–1282. [http://dx.doi.org/10.1038/ mp.2011.100]. [PMID: 21931319]. [PMC free article] [PubMed]
107. Lin P.Y., Mischoulon D., Freeman M.P., Matsuoka Y., Hibbeln J., Belmaker R.H., Su K.P. Are omega-3 fatty acids antidepressants or just mood-improving agents? The effect depends upon diagnosis, supplement preparation, and severity of depression. Mol. Psychiatry. 2012;17(12):1161–1163. [http://dx.doi.org/
10.1038/mp.2012.111]. [PMID: 22824812]. [PMC free article] [PubMed]
108. Fond G., Hamdani N., Kapczinski F., Boukouaci W., Drancourt N., Dargel A., Oliveira J., Le Guen E., Marlinge E., Tamouza R., Leboyer M. Effectiveness and tolerance of anti-inflammatory drugs’ add-on therapy in major mental disorders: a systematic qualitative review. Acta Psychiatr. Scand. 2014;129(3):163–179. [http://dx.doi.org/10.1111/acps.12211]. [PMID: 24215721]. [PubMed]
109. Sublette M.E., Ellis S.P., Geant A.L., Mann J.J. Meta-analysis of the effects of eicosapentaenoic acid (EPA) in clinical trials in depression. J. Clin. Psychiatry. 2011;72(12):1577–1584. [http://
dx.doi.org/10.4088/JCP.10m06634]. [PMID: 21939614]. [PMC free article] [PubMed]
110. Bhattacharya A., Sun D., Rahman M., Fernandes G. Different ratios of eicosapentaenoic and docosahexaenoic omega-3 fatty acids in commercial fish oils differentially alter pro-inflammatory cytokines in peritoneal macrophages from C57BL/6 female mice. J. Nutr. Biochem. 2007;18(1):23–30. [http://dx.doi.org/10.1016/j. jnutbio.2006.02.005]. [PMID: 16563716]. [PubMed]
111. Lu D.Y., Tsao Y.Y., Leung Y.M., Su K.P. Docosahexaenoic acid suppresses neuroinflammatory responses and induces heme oxygenase-1 expression in BV-2 microglia: implications of anti- depressant effects for ω-3 fatty acids. Neuropsychopharmacology. 2010;35(11):2238–2248. [http://dx.doi.org/10.1038/npp.2010.98]. [PMID: 20668435]. [PMC free article] [PubMed]
112. Calder P.C. n-3 fatty acids, inflammation and immunity: new mechanisms to explain old actions. Proc. Nutr. Soc. 2013;72(3):326–336. [http://dx.doi.org/10.1017/S0029665113001031]. [PMID: 23668691]. [PubMed]
113. Lee J.Y., Plakidas A., Lee W.H., Heikkinen A., Chanmugam P., Bray G., Hwang D.H. Differential modulation of Toll-like receptors by fatty acids: preferential inhibition by n-3 polyunsaturated fatty acids. J. Lipid Res. 2003;44(3):479–486. [http://dx.doi.org/10.1194/jlr.M200361-JLR200]. [PMID: 12562875]. [PubMed]
114. Gougol A., Zareh-Mohammadi N., Raheb S., Farokhnia M., Salimi S., Iranpour N., Yekehtaz H., Akhondzadeh S. Simvastatin as an adjuvant therapy to fluoxetine in patients with moderate to severe major depression: A double-blind placebo-controlled trial. J. Psychopharmacol. (Oxford) 2015;29(5):575–581. [http://dx.doi.org/10.1177/0269881115578160]. [PMID: 25827645]. [PubMed]
115. Ghanizadeh A., Hedayati A. Augmentation of fluoxetine with lovastatin for treating major depressive disorder, a randomized double-blind placebo controlled-clinical trial. Depress. Anxiety. 2013;30(11):1084–1088. [http://dx.doi.org/10.1002/da.22195]. [PMID: 24115188]. [PubMed]
116. Glaus J., Vandeleur C.L., Lasserre A.M., Strippoli M.P., Castelao E., Gholam-Rezaee M., Waeber G., Aubry J.M., Vollenweider P., Preisig M. Aspirin and statin use and the subsequent development of depression in men and women: Results from a longitudinal population-based study. J. Affect. Disord. 2015;182(182):126–131. [http://dx.doi.org/10.1016/j.jad.2015.03. 044]. [PMID: 25985382]. [PubMed]
117. You H., Lu W., Zhao S., Hu Z., Zhang J. The relationship between statins and depression: a review of the literature. Expert Opin. Pharmacother. 2013;14(11):1467–1476. [http://dx.doi.org/
10.1517/14656566.2013.803067]. [PMID: 23767773]. [PubMed]
118. Macedo A.F., Taylor F.C., Casas J.P., Adler A., Prieto-Merino D., Ebrahim S. Unintended effects of statins from observational studies in the general population: systematic review and meta-analysis. BMC Med. 2014;22:12–51. [http://dx.doi.org/10.1186/ 1741-7015-12-51]. [PMC free article] [PubMed]
119. Rosenson R.S., Tangney C.C., Casey L.C. Inhibition of proinflammatory cytokine production by pravastatin. Lancet. 1999;353(9157):983–984. [http://dx.doi.org/10.1016/S0140-6736(98) 05917-0]. [PMID: 10459915]. [PubMed]
120. Ferro D., Parrotto S., Basili S., Alessandri C., Violi F. Simvastatin inhibits the monocyte expression of proinflammatory cytokines in patients with hypercholesterolemia. J. Am. Coll. Cardiol. 2000;36(2):427–431. [http://dx.doi.org/10.1016/S0735-1097(00)00771-3]. [PMID: 10933353]. [PubMed]
121. Bustos C., Hernández-Presa M.A., Ortego M., Tuñón J., Ortega L., Pérez F., Díaz C., Hernández G., Egido J. HMG-CoA reductase inhibition by atorvastatin reduces neointimal inflammation in a rabbit model of atherosclerosis. J. Am. Coll. Cardiol. 1998;32(7):2057–2064. [http://dx.doi.org/10.1016/S0735-1097(98)00487-2]. [PMID: 9857893]. [PubMed]
122. Antonopoulos A.S., Margaritis M., Lee R., Channon K., Antoniades C. Statins as anti-inflammatory agents in atherogenesis: molecular mechanisms and lessons from the recent clinical trials. Curr. Pharm. Des. 2012;18(11):1519–1530. [http://dx.doi.org/10. 2174/138161212799504803]. [PMID: 22364136]. [PMC free article] [PubMed]
123. Kulkarni S.K., Bhutani M.K., Bishnoi M. Antidepressant activity of curcumin: involvement of serotonin and dopamine system. Psychopharmacology (Berl.) 2008;201(3):435–442. [http://dx. doi.org/10.1007/s00213-008-1300-y]. [PMID: 18766332]. [PubMed]
124. Menon V.P., Sudheer A.R. Antioxidant and anti-inflammatory properties of curcumin. Adv. Exp. Med. Biol. 2007;595:105–125. [http://dx.doi.org/10.1007/978-0-387-46401-5_3]. [PMID: 17569207]. [PubMed]
125. Abe Y., Hashimoto S., Horie T. Curcumin inhibition of inflammatory cytokine production by human peripheral blood monocytes and alveolar macrophages. Pharmacol. Res. 1999;39(1):41–47. [http://dx.doi.org/10.1006/phrs.1998.0404]. [PMID: 10051376]. [PubMed]
126. Buhrmann C., Mobasheri A., Busch F., Aldinger C., Stahlmann R., Montaseri A., Shakibaei M. Curcumin modulates nuclear factor kappaB (NF-kappaB)-mediated inflammation in human tenocytes in vitro: role of the phosphatidylinositol 3-kinase/Akt pathway. J. Biol. Chem. 2011;286(32):28556–28566. [http://dx. doi.org/10.1074/jbc.M111.256180]. [PMID: 21669872]. [PMC free article] [PubMed]
127. Yu J.J., Pei L.B., Zhang Y., Wen Z.Y., Yang J.L. Chronic Supplementation of Curcumin Enhances the Efficacy of Antidepressants in Major Depressive Disorder: A Randomized, Double-Blind, Placebo-Controlled Pilot Study. J. Clin. Psychopharmacol. 2015;35(4):406–410. [PMID: 26066335]. [PubMed]
128. Tizabi Y., Hurley L.L., Qualls Z., Akinfiresoye L. Relevance of the anti-inflammatory properties of curcumin in neurodegenerative diseases and depression. Molecules. 2014;19(12):20864–20879. [http://dx.doi.org/10.3390/molecules191220864]. [PMID: 25514226]. [PubMed]
129. Lopresti A.L., Maes M., Meddens M.J., Maker G.L., Arnoldussen E., Drummond P.D. Curcumin and major depression: a randomised, double-blind, placebo-controlled trial investigating the potential of peripheral biomarkers to predict treatment response and antidepressant mechanisms of change. Eur. Neuropsychopharmacol. 2015;25(1):38–50. [http://dx.doi.org/10.1016/j. euroneuro.2014.11.015]. [PMID: 25523883]. [PubMed]
130. Sanmukhani J., Satodia V., Trivedi J., Patel T., Tiwari D., Panchal B., Goel A., Tripathi C.B. Efficacy and safety of curcumin in major depressive disorder: a randomized controlled trial. Phytother. Res. 2014;28(4):579–585. [http://dx.doi.org/10.1002/ ptr.5025]. [PMID: 23832433]. [PubMed]
131. Efficacy and safety of electroconvulsive therapy in depressive disorders: a systematic review and meta-analysis. Lancet. 2003;361(9360):799–808. [http://dx.doi.org/10.1016/S0140-6736(03) 12705-5]. [PMID: 12642045]. [PubMed]
132. Lehtimäki K., Keränen T., Huuhka M., Palmio J., Hurme M., Leinonen E., Peltola J. Increase in plasma proinflammatory cytokines after electroconvulsive therapy in patients with depressive disorder. J. ECT. 2008;24(1):88–91. [http://dx.doi.org/
10.1097/YCT.0b013e3181571abb]. [PMID: 18379341]. [PubMed]
133. Stelzhammer V., Guest P.C., Rothermundt M., Sondermann C., Michael N., Schwarz E., Rahmoune H., Bahn S. Electroconvulsive therapy exerts mainly acute molecular changes in serum of major depressive disorder patients. Eur. Neuropsychopharmacol. 2013;23(10):1199–1207. [http://dx.doi.org/10.1016/ j.euroneuro.2012.10.012]. [PMID: 23183131]. [PubMed]
134. Fluitman S.B., Heijnen C.J., Denys D.A., Nolen W.A., Balk F.J., Westenberg H.G. Electroconvulsive therapy has acute immunological and neuroendocrine effects in patients with major depressive disorder. J. Affect. Disord. 2011;131(1-3):388–392. [http://dx.doi.org/10.1016/j.jad.2010.11.035]. [PMID: 21183225]. [PubMed]
135. Hestad K.A., Tønseth S., Støen C.D., Ueland T., Aukrust P. Raised plasma levels of tumor necrosis factor alpha in patients with depression: normalization during electroconvulsive therapy. J. ECT. 2003;19(4):183–188. [http://dx.doi.org/10.1097/00124509-200312000-00002]. [PMID: 14657769]. [PubMed]
136. Zhu X., Li P., Hao X., Wei K., Min S., Luo J., Xie F., Jin J. Ketamine-mediated alleviation of electroconvulsive shock-induced memory impairment is associated with the regulation of neuroinflammation and soluble amyloid-beta peptide in depressive-like rats. Neurosci. Lett. 2015;599(599):32–37. [http://dx.doi.
org/10.1016/j.neulet.2015.05.022]. [PMID: 25980993]. [PubMed]
137. van Buel E.M., Patas K., Peters M., Bosker F.J., Eisel U.L., Klein H.C. Immune and neurotrophin stimulation by electro- convulsive therapy: is some inflammation needed after all? Transl. Psychiatry. 2015;5:e609. [http://dx.doi.org/10.1038/tp.2015.100]. [PMID: 26218851]. [PMC free article] [PubMed]
138. Dougherty D.D., Rezai A.R., Carpenter L.L., Howland R.H., Bhati M.T., O’Reardon J.P., Eskandar E.N., Baltuch G.H., Machado A.D., Kondziolka D., Cusin C., Evans K.C., Price L.H., Jacobs K., Pandya M., Denko T., Tyrka A.R., Brelje T., Deckersbach T., Kubu C., Malone D.A., Jr A. Randomized Sham-Controlled Trial of Deep Brain Stimulation of the Ventral Capsule/Ventral Striatum for Chronic Treatment-Resistant Depression. Biol. Psychiatry. 2015;78(4):240–248. [http://dx.doi.
org/10.1016/j.biopsych.2014.11.023]. [PMID: 25726497]. [PubMed]
139. Mosley P.E., Marsh R., Carter A. Deep brain stimulation for depression: Scientific issues and future directions. Aust. N. Z. J. Psychiatry. 2015;49(11):967–978. [Epub ahead of print]. [http://dx.doi.org/10.1177/0004867415599845]. [PMID: 26276049]. [PubMed]
140. Calleja-Castillo J.M., De La Cruz-Aguilera D.L., Manjarrez J., Velasco-Velázquez M.A., Morales-Espinoza G., Moreno-Aguilar J., Hernández M.E., Aguirre-Cruz L., Pavón L. Chronic deep brain stimulation of the hypothalamic nucleus in wistar rats alters circulatory levels of corticosterone and proinflammatory cytokines. 2013. [PMC free article] [PubMed]
141. Perez-Caballero L., Pérez-Egea R., Romero-Grimaldi C., Puigdemont D., Molet J., Caso J.R., Mico J.A., Pérez V., Leza J.C., Berrocoso E. Early responses to deep brain stimulation in depression are modulated by anti-inflammatory drugs. Mol. Psychiatry. 2014;19(5):607–614. [http://dx.doi.org/10.1038/ mp.2013.63]. [PMID: 23711979]. [PubMed]
142. Dunn A.L., Trivedi M.H., Kampert J.B., Clark C.G., Chambliss H.O. Exercise treatment for depression: efficacy and dose response. Am. J. Prev. Med. 2005;28(1):1–8. [http://dx.doi.org/10.1016/ j.amepre.2004.09.003]. [PMID: 15626549]. [PubMed]
143. Rethorst C.D., Wipfli B.M., Landers D.M. The antidepressive effects of exercise: a meta-analysis of randomized trials. Sports Med. 2009;39(6):491–511. [http://dx.doi.org/10.2165/00007256-200939060-00004]. [PMID: 19453207]. [PubMed]
144. Trivedi M.H., Greer T.L., Church T.S., Carmody T.J., Grannemann B.D., Galper D.I., Dunn A.L., Earnest C.P., Sunderajan P., Henley S.S., Blair S.N. Exercise as an augmentation treatment for nonremitted major depressive disorder: a randomized, parallel dose comparison. J. Clin. Psychiatry. 2011;72(5):677–684. [http://dx.doi.org/10.4088/JCP.10m06743]. [PMID: 21658349]. [PubMed]
145. Bergman D. The endocrinology of exercise. Intern. Emerg. Med. 2013;8(Suppl. 1):S17–S21. [http://dx.doi.org/10.1007/s11739-013-0921-2]. [PMID: 23475807]. [PubMed]
146. Rethorst C.D., Toups M.S., Greer T.L., Nakonezny P.A., Carmody T.J., Grannemann B.D., Huebinger R.M., Barber R.C., Trivedi M.H. Pro-inflammatory cytokines as predictors of antidepressant effects of exercise in major depressive disorder. Mol. Psychiatry. 2013;18(10):1119–1124. [http://dx.doi.org/
10.1038/mp.2012.125]. [PMID: 22925832]. [PMC free article] [PubMed]
147. Kapsimalis F., Basta M., Varouchakis G., Gourgoulianis K., Vgontzas A., Kryger M. Cytokines and pathological sleep. Sleep Med. 2008;9(6):603–614. [http://dx.doi.org/10.1016/j.sleep.2007. 08.019]. [PMID: 18024171]. [PubMed]
148. Lange T., Dimitrov S., Born J. Effects of sleep and circadian rhythm on the human immune system. Ann. N. Y. Acad. Sci. 2010;1193:48–59. [http://dx.doi.org/10.1111/j.1749-6632.2009.05300.x]. [PMID: 20398008]. [PubMed]
149. Lange T., Dimitrov S., Fehm H.L., Westermann J., Born J. Shift of monocyte function toward cellular immunity during sleep. Arch. Intern. Med. 2006;166(16):1695–1700. [http://dx.doi.org/10.1001/ archinte.166.16.1695]. [PMID: 16983046]. [PubMed]
150. Himmerich H., Beitinger P.A., Fulda S., Wehrle R., Linseisen J., Wolfram G., Himmerich S., Gedrich K., Wetter T.C., Pollmächer T. Plasma levels of tumor necrosis factor alpha and soluble tumor necrosis factor receptors in patients with narcolepsy. Arch. Intern. Med. 2006;166(16):1739–1743. [http://dx.doi.org/
10.1001/archinte.166.16.1739]. [PMID: 16983052]. [PubMed]
151. Axelsson J., Rehman J.U., Akerstedt T., Ekman R., Miller G.E., Höglund C.O., Lekander M. Effects of sustained sleep restriction on mitogen-stimulated cytokines, chemokines and T helper 1/ T helper 2 balance in humans. PLoS One. 2013;8(12):e82291. [http://
dx.doi.org/10.1371/journal.pone.0082291]. [PMID: 24349251]. [PMC free article] [PubMed]
152. Chennaoui M., Drogou C., Sauvet F., Gomez-Merino D., Scofield D.E., Nindl B.C. Effect of acute sleep deprivation and recovery on Insulin-like Growth Factor-I responses and inflammatory gene expression in healthy men. Eur. Cytokine Netw. 2014;25(3):52–57. [PMID: 25373853]. [PubMed]
153. Voderholzer U., Fiebich B.L., Dersch R., Feige B., Piosczyk H., Kopasz M., Riemann D., Lieb K. Effects of sleep deprivation on nocturnal cytokine concentrations in depressed patients and healthy control subjects. J. Neuropsychiatry Clin. Neurosci. 2012;24(3):354–366. [http://dx.doi.org/10.1176/appi.neuropsych.11060142]. [PMID: 23037650]. [PubMed]
154. Benedetti F., Lucca A., Brambilla F., Colombo C., Smeraldi E. Interleukine-6 serum levels correlate with response to antidepressant sleep deprivation and sleep phase advance. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2002;26(6):1167–1170. [http://dx.doi.org/10.1016/S0278-5846(02)00255-5]. [PMID: 12452541]. [PubMed]
155. Pandey G.N., Rizavi H.S., Ren X., Bhaumik R., Dwivedi Y. Toll-like receptors in the depressed and suicide brain. J. Psychiatr. Res. 2014;53:62–68. [http://dx.doi.org/10.1016/j.jpsychires. 2014.01.021]. [PMID: 24565447]. [PMC free article] [PubMed]
156. Strekalova T., Evans M., Costa-Nunes J., Bachurin S., Yeritsyan N., Couch Y., Steinbusch H.M., Eleonore Köhler S., Lesch K.P., Anthony D.C. Tlr4 upregulation in the brain accompanies depression- and anxiety-like behaviors induced by a high-cholesterol diet. Brain Behav. Immun. 2015;48:42–47. [http://dx.doi.org/10.1016/j.bbi.2015.02.015]. [PMID: 25712260]. [PubMed]
157. Gárate I., García-Bueno B., Madrigal J.L., Caso J.R., Alou L., Gómez-Lus M.L., Leza J.C. Toll-like 4 receptor inhibitor TAK-242 decreases neuroinflammation in rat brain frontal cortex after stress. J. Neuroinflammation. 2014;11:8. [http://dx.doi.org/
10.1186/1742-2094-11-8]. [PMID: 24410883]. [PMC free article] [PubMed]
158. Li J., Csakai A., Jin J., Zhang F., Yin H. Therapeutic Developments Targeting Toll-like Receptor-4-Mediated Neuro- inflammation. ChemMedChem. 2015 [Epub ahead of print]. [http://dx.doi.org/10.1002/cmdc.201500188]. [PMC free article] [PubMed]
159. Li X., Jope R.S. Is glycogen synthase kinase-3 a central modulator in mood regulation? Neuropsychopharmacology. 2010;35(11):2143–2154. [http://dx.doi.org/10.1038/npp.2010.105]. [PMID: 20668436]. [PMC free article] [PubMed]
160. Martin M., Rehani K., Jope R.S., Michalek S.M. Toll-like receptor-mediated cytokine production is differentially regulated by glycogen synthase kinase 3. Nat. Immunol. 2005;6(8):777–784. [http://dx.doi.org/10.1038/ni1221]. [PMID: 16007092]. [PMC free article] [PubMed]
161. Yuskaitis C.J., Jope R.S. Glycogen synthase kinase-3 regulates microglial migration, inflammation, and inflammation-induced neurotoxicity. Cell. Signal. 2009;21(2):264–273. [http://dx.doi.
org/10.1016/j.cellsig.2008.10.014]. [PMID: 19007880]. [PMC free article] [PubMed]
162. Maes M., Fišar Z., Medina M., Scapagnini G., Nowak G., Berk M. New drug targets in depression: inflammatory, cell-mediated immune, oxidative and nitrosative stress, mitochondrial, antioxidant, and neuroprogressive pathways. And new drug candidates--Nrf2 activators and GSK-3 inhibitors. Inflammopharmacology. 2012;20(3):127–150. [http://dx.doi.org/10.1007/s10787-011-0111-7]. [PMID: 22271002]. [PubMed]
163. Fajemiroye J.O., Polepally P.R., Chaurasiya N.D., Tekwani B.L., Zjawiony J.K., Costa E.A. Oleanolic acid acrylate elicits antidepressant-like effect mediated by 5-HT1A receptor. Sci. Rep. 2015;5:11582. [http://dx.doi.org/10.1038/srep11582]. [PMID: 26199018]. [PMC free article] [PubMed]
164. Yi L.T., Li J., Liu Q., Geng D., Zhou Y.F., Ke X.Q., Chen H., Weng L.J. Antidepressant-like effect of oleanolic acid in mice exposed to the repeated forced swimming test. J. Psycho- pharmacol. (Oxford) 2013;27(5):459–468. [http://dx.doi.org/10.1177/ 0269881112467090]. [PMID: 23151611]. [PubMed]
165. Lee S., Kim D.H., Lee C.H., Jung J.W., Seo Y.T., Jang Y.P., Ryu J.H. Antidepressant-like activity of the aqueous extract of Allium macrostemon in mice. J. Ethnopharmacol. 2010;131(2):386–395. [http://dx.doi.org/10.1016/j.jep.2010.07.015]. [PMID: 20637276]. [PubMed]
166. O’Connor J.C., Lawson M.A., André C., Moreau M., Lestage J., Castanon N., Kelley K.W., Dantzer R. Lipopolysaccharide-induced depressive-like behavior is mediated by indoleamine 2,3-dioxygenase activation in mice. Mol. Psychiatry. 2009;14(5):511–522. [http://dx.doi.org/10.1038/sj.mp.4002148]. [PMID: 18195714]. [PMC free article] [PubMed]
167. Liu Y.N., Peng Y.L., Liu L., Wu T.Y., Zhang Y., Lian Y.J., Yang Y.Y., Kelley K.W., Jiang C.L., Wang Y.X. TNFα mediates stress-induced depression by upregulating indoleamine 2,3-dioxygenase in a mouse model of unpredictable chronic mild stress. Eur. Cytokine Netw. 2015;26(1):15–25. [PMID: 26083579]. [PMC free article] [PubMed]
168. Miyaoka T., Wake R., Furuya M., Liaury K., Ieda M., Kawakami K., Tsuchie K., Taki M., Ishihara K., Araki T., Horiguchi J. Minocycline as adjunctive therapy for patients with unipolar psychotic depression: an open-label study. Prog. Neuropsychopharmacol. Biol. Psychiatry. 2012;37(2):222–226. [http://dx.doi.org/10.1016/j.pnpbp.2012.02.002]. [PMID: 22349578]. [PubMed]
169. Dean O.M., Maes M., Ashton M., Berk L., Kanchanatawan B., Sughondhabirom A., Tangwongchai S., Ng C., Dowling N., Malhi G.S., Berk M. Protocol and rationale-the efficacy of minocycline as an adjunctive treatment for major depressive disorder: a double blind, randomised, placebo controlled trial. Clin. Psychopharmacol. Neurosci. 2014;12(3):180–188. [http://dx.doi.
org/10.9758/cpn.2014.12.3.180]. [PMID: 25598820]. [PMC free article] [PubMed]
170. Lichtblau N., Schmidt F.M., Schumann R., Kirkby K.C., Himmerich H. Cytokines as biomarkers in depressive disorder: current standing and prospects. Int. Rev. Psychiatry. 2013;25(5):592–603. [http://dx.doi.org/10.3109/09540261.2013.813442]. [PMID: 24151804]. [PubMed]
171. Abbasi S.H., Hosseini F., Modabbernia A., Ashrafi M., Akhondzadeh S. Effect of celecoxib add-on treatment on symptoms and serum IL-6 concentrations in patients with major depressive disorder: randomized double-blind placebo-controlled study. J. Affect. Disord. 2012;141(2-3):308–314. [http://dx.doi.
org/10.1016/j.jad.2012.03.033]. [PMID: 22516310]. [PubMed]

Articles from Current Neuropharmacology are provided here courtesy of Bentham Science Publishers