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Curr Neuropharmacol. 2010 September; 8(3): 287–304.
PMCID: PMC3001221

A Systematic, Updated Review on the Antidepressant Agomelatine Focusing on its Melatonergic Modulation



To present an updated, comprehensive review on clinical and pre-clinical studies on agomelatine.


A MEDLINE, Psycinfo and Web of Science search (1966-May 2009) was performed using the following keywords: agomelatine, melatonin, S20098, efficacy, safety, adverse effect, pharmacokinetic, pharmacodynamic, major depressive disorder, bipolar disorder, Seasonal Affective Disorder (SAD), Alzheimer, ADHD, Generalized Anxiety Disorder (GAD), Panic Disorder (PD), Obsessive-Compulsive Disorder (OCD), anxiety disorders and mood disorder.

Study collection and data extraction:

All articles in English identified by the data sources were evaluated. Randomized, controlled clinical trials involving humans were prioritized in the review. The physiological bases of melatonergic transmission were also examined to deepen the clinical comprehension of agomelatine’ melatonergic modulation.

Data synthesis:

Agomelatine, a melatonergic analogue drug acting as MT1/MT2 agonist and 5-HT2C antagonist, has been reported to be an effective antidepressant therapy.


Although a bias in properly assessing the “sleep core” of depression may still exist with current screening instruments, therefore making difficult to compare agomelatine’ efficacy to other antidepressant ones, comparative studies showed agomelatine to be an intriguing option for depression and, potentially, for other therapeutic targets as well.

Keywords: Agomelatine, melatonin, depression, mood, cognition, Alzheimer, bipolar disorder.


The definition of depression essentially relies on depressed mood. Yet, depression represents a multi-dimensional condition. Among others, psychomotor symptoms, sleep disturbances, somatic, pain symptoms, anxiety, diurnal variation and seasonal patterns, could lead to very heterogeneous pictures, possibly underpined by different pathogenetic mechanism [1]. Hence, the associate burden may vary as well. Furthermore, Mood Disorders (MDs), particularly Major Depressive Disorder (MDD), are spread among general population, both with sub- and full-threshold manifestations: MDD has been estimated to be the fourth major cause of disability worldwide, and may become second only to cardiovascular diseases by around 2020 [2]. Although the social relevance of the phenomenon, less than 50% of all patients treated with the currently available antidepressants show full remission [3], with a large number of subjects showing residual and relapsing symptoms [4] and general poor antidepressant outcome still in a too high number of cases as demonstrated by the Sequenced Treatment Alternatives to Relive Depression (STAR*D), the largest antidepressant trial ever [5, 6]. A main reason for this is the still incomplete knowledge about the pathogenetic mechanisms of depression and about the inner actions of available antidepressants [3]. Also, a non-dimensional, categorical approach [7] may lead to the use of a single diagnosis to include heterogeneous clinical pictures, therefore leading to a non patient-tailored psychopharmacotherapy. Additionally, even when effectiveness is well-documented, current anti-depressants may be associated with impairing side-effects which may account for most of the discontinuation cases [8].

These considerations prompt for a better recognition and for an adequate clinical management of depression but also for the development of more selective and new-targeting drugs.

First Generation Antidepressants (FGAs) include Monoamine Oxidase Inhibitors (MAOIs) and Tricyclic Antidepressants (TCAs, 60s), while Second Generation Antidepressants (SGAs, 80s-90s) include Selective Serotonin Reuptake Inhibitors (SSRIs), Norepinephrine and Serotonin Reuptake Inhibitors (SNRIs), Norepinephrine Reuptake Inhibitors (NARIs), Norepinephrine and Specific Serotonergic Antidepressants (NASSAs) and Serotonin 5-HT2A Antagonists/Reuptake Inhibitors (SARIs) [3]. SSRIs still represent the most currently prescribed antidepressant class of drugs, nevertheless their efficacy has been questioned [9-16].

Both the FGAs and SGAs are monoamine-based antidepressants. New monoamine-based antidepressants are currently in development or marketed, and they include 5-HT4 and 5-HT6 agonists as well as 5-HT7 antagonists [3]. According to the monoamine hypothesis of depression, monoamine-based antidepressants have been hypothesized to increase the synaptic availability of monoamines (which could be decreased in course of depression). Yet, this hypothesis of depression has been criticized since it was evident that increased availability of monoamines induced by antidepressants develops in a matter of hours with the therapeutic effect onset only after a mean lag-phase of several weeks [17]. Therefore, in the following decades, new non-monoamine-based antidepressants have been studied. They include the NK-1 receptors antagonists, CRF1 antagonists and the glutamatergic agents (NMDA blockers, AMPAkines, mGlu modulators, riluzole, lamotrigine) [3].


Recently, a novel approach to depression, focusing on circadian rhythms, has been the basis for the development of agomelatine (N-[2-(7-methoxy-1-naphthyl)ethyl]acetamide or S-20098), a melatonin (MT) analogue drug with a entirely new mechanism of action [18].

In mammals, changes in the sleep-wake cycle and in the periodicity of circadian rhythm profoundly influence the state of mood, which they have already been proposed as candidate markers [19, 20]. Likewise, it has been shown that manipulations of circadian rhythms, such as a total of REM sleep deprivation or phase advance in the sleep-wake cycle, may have antidepressant action. This has also been considered the rational for complementary or alternative strategies such as the “sleep deprivation therapy” and similar approaches [21]. Anyway, since studies demonstrated possible persistent sleep changes in the remission phase of depression, it is unclear whether it is a causative factor or part of the clinical picture [22]. Possibly, this may be also due to an incomplete action of antidepressant therapy, since currently available drugs may be unable to address the sleep depressive symptomatology. To date, agomelatine, represents the only available MT1/MT2 melatonergic receptors agonist and 5-HT2C antagonist (SAR), shown to induce resynchronization of circadian rhythms and antidepressant action in humans, [23, 24]. By avoiding 5-HT2A stimulation, agomelatine shows a more favorable side-effect profile compared SSRIs, concerning sexual functioning, weight-gain (drugs blocking the 5-HT2C and histamine receptors are usually associated with weight-gain although 5-HT2C per se shouldn’t be necessarily associated with this effect) and Gastro-Intestinal (GI) disturbances, without exhibiting discontinuation symptoms [11, 18, 25-27].


To identify relevant articles for this review, searches of the online databases MEDLINE and EMBASE were conducted using combinations of the search terms “agomelatine”, “melatonin”, “S20098”, “antidepressant”, “efficacy”, “safety”, “pharmacokinetic”, “pharmacodynamic”, “receptor binding”, “depression”, “Major Depressive Disorder” (MDD), “Bipolar Disorder” (BPD), “Seasonal Affective Disorder” (SAD), “Attention Deficit Hyperactivity Disorder” (ADHD) and “anxiety disorders”. Additional articles were identified scanning the reference lists of the retrieved articles. All English-language articles reporting original data related to agomelatine for major depression were included in this review while just RCT, non antidepressant-related agomelatine references were prioritized. Most relevant pre-clinical and clinical studies about agomelatine have been reported in Tables 11, 22 respectively.

Table 1
Agomelatine in Mood and Anxiety Conditions and More. Current Literature Evidences in Pre-Clinical and/or Animal Model Studies
Table 2
Agomelatine in Mood and Anxiety Conditions and More. Current Literature Evidences in Clinical Human Studies.


In humans, agomelatine is well absorbed following oral administration, but absolute bioavailability is relatively low (about 5-10%) due to its high first-pass metabolism [28], which may be considered in special populations such as the elderly or hepatic disordered patients. When given as a single 25- or 50mg amount, blood concentrations increased more than proportionately to the dose, possibly due to saturation of first-pass metabolism. Agomelatine has also moderate distribution in humans, with a volume of distribution of approximately 35 L., and is 85-95% bound to plasma proteins (again, this could taken in account prior prescription in special populations) [29]. Agomelatine appears to be extensively metabolized by the cytochrome P450 isoforms 1A1, 1A2 and 2C9 (majority of psychiatric medications undergo 2D6 or 3A4 or 1A2) to hydroxyl, desmethyl and epoxide metabolites with less activity than the parent drug. A major oxidative metabolite in humans, 3-hydroxy-7-desmethyl-agomelatine, has low affinity for MT1, MT2 and 5-HT2C receptors. The drug is eliminated mostly by urinary excretion of the metabolites (61-81% of dose in humans), with a small amount of the diol metabolite undergoing fecal excretion; the mean terminal elimination half-life is 2.3 hours [30].


Agomelatine acts as a MT1 and MT2 agonist (reported to act as a partial agonist on the MT receptors in the pars tuberalis of the rat) [31] and as a 5-HT2C and 5-HT2B serotonin (5-hydroxytryptamine, 5-HT) antagonist [32]. Blockade of 5-HT2C receptor, a subtype of 5-HT that binds the endogenous 5-HT neurotransmitter being a Gq/G11 protein-coupled receptor (GPCR) mediating excitatory neurotransmission [33], causes release of both Norepinephrine (NE) and Dopamine (DA) at the frontocortical dopaminergica and adrenergic pathways [32] by different classes of drugs including the SSRI fluoxetine and norquetiapine, the principal metabolite of the atypical antipsychotic quetiapine [34, 35].This is why these agents could be called Norepinephrine and Dopamine Disinhibitors (NDDIs) as coined by Millan (2003) [36], acting across the peripheral and brain Central Nervous System (CNS) including the striatum, prefrontal cortex, nucleus accumbens, hippocampus, hypothalamus, amygdala, and many other areas [37]. The profile of pharmacological actions predicts not only antidepressant actions due to the NDDI mechanism of 5-HT2C antagonism [38] (interestingly, studies on 5-HT agonists as potential antidepressant drugs were discontinued within the recent years [39]),but also sleep-enhancing properties due to MT1 and MT2 potent agonist actions [32]. The expression of MT1 receptors has been shown to have diurnal rhythmicity, regulated by light and the internal clock, whereas the expression for mRNA of 5-HT2C, but not 5-HT1A or 5-HT2A receptors, has a circadian rhythm pattern in mammals [40].

While functional desensitization of 5-HT1A auto-receptors in the Dorsal Raphe nucleus (DRn) occurs after chronic administration of several classes of antidepressants and it is considered as a core mechanism implicated in the mood restoration, neither the acute or chronic treatment with agomelatine changed the density of 5-HT1A receptors and their coupling with G proteins in the DRn and the hippocampus in rats nor in the Frontal Cortex (FC) [41]. These data indicate that the antidepressant action of agomelatine is not mediated by the same mechanisms of SSRIs and TCAs [41, 42].

Also, the DA-ergic transmission may be indirectly modulated by the melatonergic one; starting with light-stimulation at the Pigmented Epithelium (PE) of the retina, hosting D2-like receptors. A balance between GABA, DA and MT exists all over the CNS [43-47] as demonstrated by Electroretinographic (ERG) studies both in health volunteers [48] and in course of SAD [49]. Agomelatine’ “emotional blunting”, due to DA direct antagonism, should therefore be hypothesized. However, microdialysis studies reported dopamine levels in the nucleus Accumbens (ACn), a structure proven to be involved in course of depression in rats [50] and the striatum to be unaffected by agomelatine [51] whereas it remarkably rises at the prefrontal cortex of rats [52, 53]. The 5-HT2C blockade also enhances the activity of FC’s DA-ergic and adrenergic activity, while a stimulatory and entraining effect of melatonin (and agomelatine) on Tubero-Infundibular DA-ergic neurons (TIDA) activity and inhibition of Prolactin (PRL) secretion, seems to be independent on 5-HT2C blockade [32, 54].

On a solely chronobiological basis, agomelatine should not behave differently from an agent like ramelteon (another MT1/MT2 agonist unaffecting 5-HT2C neurotransmission). Agomelatine, on contrast, has a dual phased action: at night, its sleep-promoting melatonergic effects prevail over its potentially anti-hypnotic 5-HT2C blockade, whereas during the day, its antidepressant action via 5-HT2C inhibition is uncoupled from melatonin’s nocturnal actions (this may also be considered as an advantage of agomelatine vs. other classes of antidepressants) [19].


Agomelatine and melatonin are not synonymous neither the supposed antidepressant MT1 and MT2 agonism should be considered in the strict sense of hormone substitutive modulation. On the other hand, agomelatine, next to the exogenous hormone, is the most melatonin-mimic agent developed for antidepressant therapy [55].

There are three types of receptors for melatonin: 1 and 2, which are both involved in sleep, and 3, which is actually the enzyme NRH: quinine oxidoreductase 2 and not thought to be involved in sleep physiology. There are several different agents acting at melatonin receptor sites. Melatonin itself, available over the counter, acts at melatonin 1 and 2 receptors as well as at the melatonin 3 side. Ramelteon seems to provide sleep onset though not necessarily sleep maintenance, being ineffective for jet lag treating [56-58], in contrast to the MT1/MT2 agonist tasimelteon [59], without modulation of the 5-HT-ergic transmission.

In order to assess the clinical actions of agomelatine, the melatonergic modulation and serotonergic one should considered separately, briefly recalling the physiologic mechanisms of the hormone melatonin and, when comparative study have been performed, reporting a side-by-side profile of both.

Synthesis of Melatonin

The indoleamine melatonin (N-acetyl-5-methoxytrypt-amine) is synthesized from the amino acid tryptophan via 5-HT synthesis. Production of melatonin by the pineal gland is under the influence of the Suprachiasmatic Nucleus (SCN) of the hypothalamus, which receives information from the retina about the daily pattern of light and darkness. Both SCN rhythmicity and melatonin production are affected by non-image-forming light information traveling through the retino-hypothalamic tract (RHT). The melatonin signal forms part of the system that regulates the circadian cycle by chemically causing drowsiness and lowering the body temperature, but is the SCN that controls the daily cycle in most components of the paracrine and the endocrine system rather than the melatonin signal. The responsiveness of the SCN to melatonin is therefore strongly regulated by the circadian clock, while chronic melatonin (or agomelatine) agonism of the SCN melatonin receptors didn’t result in their desensitization in animal models [60]. Also, both melatonin and agomelatine activities on circadian rhythms depends on the SCN integrity but not the pineal gland as demonstrated in animal studies [61-63] in a dose-dependent fashion [64].

Aging and Melatonin

Under the age of 3 months, little melatonin is secreted, and there is no variation with light exposure. The production peak is reached at the age of 3 years and then this declines, especially during puberty, to a level which is maintained until around age of 40 before it fall further [65, 66]. This may also account for a variety of depression-related patterns and outcomes among different aged populations. MT and its receptor agonists, including agomelatine, correct age-related changes in circadian response to environmental stimuli in rodents, and could prove to be useful in treating/preventing or delaying disturbances of circadian rhythmicity and/or sleep in older people [67, 68].

Light and Circadian “Rhythms”

Production of melatonin by the pineal gland is inhibited by light and permitted by darkness. Hence melatonin has been called "the hormone of darkness" and its onset each evening is called the Dim-Light Melatonin Onset (DLMO). Secretion of melatonin, as well as its level in blood, peaks in the middle of the night, and gradually falls during the second half of the night, with normal variations in timing according to an individual's chronotype [69-71]. This justifies the use of melatonin, and its analogue agomelatine, to promote sleep in those with delayed sleep onset or to reset the internal clock that occurs with jet lag, shift working, or due to other causes [56, 72-74], possibly recovering from the Delayed Sleep-Phase Syndrome (DSPS) too [75]. Light-time exposure (“photoperiod”) is a pivotal element in regulating circadian rhythms, thus it is unsurprising that bright “light therapy” stimulation has already been proposed as an antidepressant and SAD treatment option [19, 76, 77].

SCN and the Anxiolytic Effect

Melatonin appears to have two effects on the SCN which are mediated either by a direct effect on the circadian rhythm generating cells or by activation by the GABA-ergic neurons within the SCN which inhibits its activity [78-80]. A GABA-ergic modulating action, along with a 5-HT2C one, may also account for the reported anxiolytic effects of agomelatine [81-83]. While melatonin-like drugs have been reported to overlap the GABA agonists activity (such as diazepam), neither agomelatine nor melatonin substituted benzodiazepines in anxiety-stressed rats trained to discriminate the different drugs, suggesting that agomelatine anti-anxiety effect may be not as addictive as the diazepam’ one (therefore being a core feature when it comes to choice the proper drug in abusers and other addictive-behavior populations) [83-86]. On the other hand, agomelatine’ anxiolytic effect strictly resembles those of selective 5-HT2C antagonists, thus the melatonergic-agonism may be not entirely account for [25]. Efficacy of agomelatine in GAD has been reported by an RCT investigation by Stein et al. (2008) but further investigations in PD, OCD, and other Anxiety Spectrum disorders are needed [87].

Cognitive Functions, Alzheimer’s Disease and Delirium

Melatonin receptors appear to be important in mechanisms of learning and memory in mice [88] and the hormone can alter electrophysiological processes associated with memory, such as Long-Term Potentiation (LTP). Spatial visual memory, as well as the ventral hippocampal expression of the synaptic Neural Cell Adhesion Molecule (NCAM), were reported to improve in animal model treated with agomelatine [89].

The first published evidence that melatonin may be useful in Alzheimer's disease was the demonstration that this neurohormone prevents neuronal death caused by exposure to the amyloid beta protein, a neurotoxic substance that accumulates in the brains of affected patients [90, 91]. Melatonin also inhibits the aggregation of the amyloid beta protein into neurotoxic micro-aggregates which seem to underlie the neurotoxicity of this protein, causing neuronal death and formation of neurofibrillary tangles, which are the other neuropathological landmark of Alzheimer's disease [90]. Melatonin has been shown to prevent the hyperphosphorylation of the tau protein in rats [92]. Hyper-phosphorylation of tau protein can also result in the formation of neurofibrillary tangles [92]. Studies in rats suggest that melatonin may be effective for treating Alzheimer's disease [92]. These same neurofibrillary tangles can be found in the hypothalamus in patients with Alzheimer's disease, adversely affecting their bodies' production of melatonin. Patients with this specific affliction often show heightened afternoon agitation, called “sundowning”, mainly due to cholinergic transmission. This phenomenon, has been shown in many studies to be effectively treated with melatonin supplements taken at bedtime [92]. The sundowning syndrome (possibly also related to progressive light-decrease) often characterizes many delirium cases and mood and/or cognitive disorders (especially when essentially due to cholinergic hypo-functioning). Indeed, melatonergic agonism could indirectly reduce the DA-ergic central activity and may promote the GABA-ergic activity (therefore complicating the delirium and other cognitive impairments pictures). While melatonergic drugs could be considered in recovering a better profile light-rhythm, they could carefully considered prior being administered to cognitive-impaired patients both in course of neurodegenerative diseases or when cognitive symptoms occur in course of depression as part of the illness or as potential consequences of some antidepressant therapies, as it may occur with long-term treatments with SSRIs drugs.

Melatonin and Dopamine-Related Motor Disorders

Inhibition of DA release by melatonin has been demonstrated in specific areas of the mammalian CNS (especially, the hypothalamus, hippocampus, medulla-pons and retina) [93]. Anti-DA-ergic activities of MT, mediated by BDZ/GABAA receptors, has also been demonstrated in the striatum [94]. DA-ergic transmission has a pivotal role in the circadian entrainment of the fetus, in coordination of body movement and reproduction; MT may also modulate DA-ergic pathways involved in movement disorders in humans. In Parkinson patients, MT may exacerbate symptoms (because of its putative interference with DA release) and, on the other side, protect against neurodegeneration (by virtue of its antioxidant properties and its effects on mitochondrial activity). MT appears to be effective in the treatment of Tardive Dyskinesia (TD), a severe movement disorder associated with long-term blockade of the postsynaptic D2 receptors induced by antipsychotic drugs (especially by first generation ones). The interaction of MT with the DA-ergic system may play a significant role in the non-photic and photic entrainment of the biological clock [95] as well as in the fine-tuning of motor coordination in the striatum [93]. These interactions and the antioxidant nature of melatonin, including degenerative and possibly primary cases of rethinopathies due to antipsychotic treatment [96], may also suggest agomelatine and other melatonergic-drugs to be considered as potentially helpful in the treatment of DA-related disorders, which could also be taken into account in case of motor side effects eventually due to some antidepressant therapies as it is the case of potential extrapyramidal effects of SSRIs antidepressants [97].


Among the biological bases of depression, an impairment of neuroplasticity and cellular resilience has been proposed [98] with antidepressant medication reported contributing in its normalization [99-101]. Chronic stress, excess of concentrations of glutamate, biogenic amines and glucocorticoids affect the morphology of hippocampal CA3 pyramidal neurons, resulting in a pronounced debranching of apical dendrites. This affect can be blocked or counteracted by different compounds including antidepressant drugs.

A 2008 study by Gressens and colleagues demonstrated the efficacy of agomelatine in neuroprotection and neuroplasticity of newborn rats. White matter cysts (mimic human periventricular leukomalacia), previously induced by intraperitoneal injection of glutamatergic-like agents (ibotenate), partially recovered with melatonin (administered 2h within acute lesion) and agomelatine (up to 8h after) [102]. Neurocognitive and antidepressant actions have also been demonstrated in “depressed” rodents (using the Forced Swimming Test (FST)) comparing agomelatine vs. imipramine or vs. melatonin or vs. fluoxetine [103], while mice circadian system was also proved to improve with agomelatine therapy (using the Phase Response Curve (PRC) record) as long as motor activity initiative (using the daily wheel revolution Chronobiology Kit®) [20, 104]. Agomelatine treatment also resulted in prolonged overstimulation of melatonin receptors, thus attenuating the effect of light on the circadian timing system [105].


Profound disturbances in sleep architecture often occur in MDD and Bipolar Disorders (BPDs) [19]. MDD with Melancholic features is associated with sleep-awake phases advance, often showing up with praecox final awake and reduced REM latency. MDD with seasonal patterns (MDDSP) is clinically characterized by depressed mood occurring at almost the same time every year since the disorder is first experienced [106]. US prevalence has been estimated to be at least 5% among general population with F:M ratio of about 5:1 [107]. Since most of the world population is located further from the equator, more people could be affected, prompting for a better comprehension of the phenomenon. The pathophysiology of MDDSP is not fully understood, although it is assumed to be associated with altered circadian rhythms. Basic circadian rhythms are regulated by several endogenous or exogenous pacemakers, which major endogenous one is probably located in the hypothalamus. One of the major exogenous pacemakers is the light–dark cycle, in which different durations of light or dark hours affect the timing of sleep induction, hormone secretion, and many other biological rhythms. In health, euthymic subjects, the ratio of light to dark hours triggers the SCN to induce certain activities, including sleep, hormone secretion, and the secretion of melatonin (which may only serve as a marker associated with changes related to MDDSP) via stimulating the pineal gland. MDDSP is characterized, among other things, by a basic state of “phase-delay” circadian rhythm. This means that the same triggered activities (by the SCN) are induced at a later time in the day (24-hour clock) than in non-MDDSP patients. Empirical data suggest that when a person is exposed to bright light during the light hours, the SCN is stimulated to induce its activities at an early time in the 24-hour cycle. This is termed ‘phase-advance’ circadian rhythm. If it is administered to a MDDSP patient, the ‘phase-advance’ is superimposed on a “phase-delay” status, which may bring the system to an equilibrium, normalizing circadian rhythms, and at the same time ameliorating the depressive symptoms of MDDSP [108-110], Fig. (11).

Fig. (1)
MDDSP and sleep phases switches.

Melatonin, Agomelatine and Bipolar Spectrum Disorders

Melatonin has been considered for BPD, SAD, and other clinical pictures where circadian disturbances are involved [111, 112] as well other stress-related conditions. About 20 years ago Ehlers et al. articulated the hypothesis concerning the way in which stressful life events that disrupt an individual’s normal routines (“social zeitgebers”) could initiate a cascade that – in vulnerable subjects – might lead to an episode of depression or mania [113]. Among psychiatric illnesses, BPD is second only to unipolar depression as a cause of global disability [114] and may largely go under-diagnosed [115]. Symptomatic patients with BP-I disorder experience depressive symptoms three to four times more than manic symptoms [116, 117] and symptomatic patients with BP-II disorder experience depressive symptoms approximately 39 times more than hypomanic ones [118]. These considerations prompt for a better recognition and management of depressive states associated with BPD and their clinical features. It has been observed that BPD might have a "trait marker" of hypersensitivity of the melatonin receptors [119]. Anyway, this could be contrasted with drug-free recovered bipolar individuals not showing light hypersensitivity [120]. A comprehensive review by Gao et al. (2005) focused on RCT studies of newly introduced drugs (including agomelatine) for the acute and long-term treatment of bipolar depression. Preliminary open-label observations of agomelatine addiction to lithium or valproate in the treatment of bipolar depression showed the efficacy of the melatonergic drug at doses of 25mg/day after 6 weeks of augmentation treatment. Anyway these results need RCT confirmations [121].

The nature of disruption of melatonin secretion in MDD has been under intensive study ever since it has been proposed as “low melatonin syndrome” [122] and replicated by a number of studies [19], whereas there is no evidence of agomelatine increasing the levels of melatonin. However, increases in melatonin secretion in depressive symptomatology has also been reported [123]. The differences could be due to changes in depressive symptomatology or to the pattern of melatonin secretion, inasmuch as there are studies showing that daytime melatonin secretion in depressives is increased [19, 124]. Interestingly, lower levels of illumination in post-menopausal women have been reported to be associated with more complaints of sleep and depressive symptoms [125] whereas post-partum depression was already suggested as a possible marker/predictor of bipolar depression [126]. Bright light treatment of women suffering from ante-partum depression advanced the rhythm of melatonin secretion and also mitigated depressive symptoms [19]. Also, a marked reduction in sleep during the night immediately before switching from depression to mania was noted in bipolar depressed patients [127].

Yet, measurement of melatonin levels has shown significantly lower levels in unipolar and bipolar depressed patients [128]. The significance of the association of sleep disturbances and melatonin levels in bipolar depressed patients is still far away from a satisfactory knowledge.

Melatonin, Agomelatine and Major Depression

Both animal and human studies demonstrated agomelatine to be an effective treatment for MDD [38, 81, 129-132]. The efficacy of agomelatine in severe depression [133, 134] has been investigated by Montgomery and Kasper (2007) by a pooled analysis of 3 positive placebo-controlled studies (doses were 25 to 50mg/die) proving it to be an effective treatment [135]. Sleep abnormalities in depression are mainly characterized by increased Rapid Eye Movements (REM) sleep and reduced Slow-Wave Sleep (SWS) [40] with most of available antidepressants (including TCAs and SSRIs) causing REM sleep suppression and increasing in REM sleep onset latency [136, 137]. Decreased cholinergic activity and increased 5-HT-ergic one are the two main factors affecting REM sleep suppression [40]; the decrease in amount of REM sleep appears to be greatest during the early phases of treatment, gradually diminishing during long-term treatment, except after Monoamine Oxidase Inhibitors (MAO-I) administration when REM sleep is often absent for many months. Many antidepressant medications, including SSRIs, have repeatedly been reported to worse sleep, mainly due to 5-HT2 stimulation; on the other hand, excessive sleep, daytime sleepiness and sedation may be experienced by patients tacking antidepressant medications [40]. 5-HT2 blocking antidepressants, as mirtazapine, have been shown to improve sleep continuity and may therefore represent a good option for depressed patients with marked insomnia. Agomelatine (25mg/day for 6 weeks) contributes to restore sleep architecture in depressed patients as shown by polysomnography records, improving sleep quality and continuity: SWS’s duration increases without modifying REM sleep time [138]. An RCT investigation by Lemoine et al. (2007) compared venlafaxine to agomelatine for subjective sleep in course of MDD showing a greater improvement with the melatonergic drug [139]. A RCT study by Kennedy et al. (2008), also investigated the sexual side effect profile of agomelatine in comparison with venlafaxine [140].


A review by Ghosh and Hellewell, (2007) evidenced the effect and tolerability of agomelatine in MDD [141] which resulted better tolerated than SSRIs and SNRIs in MDD patients treated for 4-8 weeks on doses ranging from 5 to 100mg/day [142], including a favorable sexual functioning profile which is an important cause of SSRIs non-compliance [143], Table 11. As reported by Loo et al. in a 2003 RCT investigation, agomelatine did not modify cardiovascular parameters, including ECG recordings, neither provoked biological abnormalities, weight or vital signs changes; slightly more adverse effects and severe treatment-related adverse events occurred, however, in the 100mg/day group (i.e. nausea was generally more frequent in the paroxetine comparison group) [142]. RCT studies by Kennedy and Emsley (2006) and Olié and Kasper (2007) also confirmed good tolerability (similar to placebo) of 25-50mg/day of agomelatine [18, 144]. Montgomery et al. (2004) focused on discontinuation symptoms: patients abruptly switched from agomelatine 25mg/day (12 weeks) to placebo were compared to those continuing on the same regimen, to placebo-placebo and also compared to paroxetine-to placebo (20mg/day for 12 weeks) vs. paroxetine-paroxetine subjects. After one week, paroxetine discontinued patients experienced significantly more discontinuation symptoms (P<0.001), compared to paroxetine-continuing ones. On the other side, 2 weeks after agomelatine cessation, patients discontinuation symptoms were comparable to those of the placebo group [15, 81]. Better acceptability of agomelatine (25 and 50 mg/day) compared with paroxetine (20mg/day) in healthy male volunteers was also assessed by an 8-week, placebo-controlled study by Montejo et al. (2008) [145]. A large sampled (subjects=339) 24-week, double-blind, placebo-controlled RCT study by Goodwin et al. (2009) demonstrated agomelatine to prevent relapse in patients treated for MDD with no appreciable withdrawal syndrome in comparison to placebo (confirming efficacy seen in short-term studies) [146]. Yet, despite a general good tolerability profile, prescribers should note the requirement to conduct liver function tests (LFTs) in accordance with the recent guidance by the European Agency of Medicines (EMEA) since recent literature evidences prompt for a risk for elevation of liver enzymes with agomelatine (although underpinning mechanism is still under investigation) [147-149]. Finally, a lack of literature data of agomelatine safety and tolerability in older, pregnant or adolescent patients still exists, whereas pharmacokinetic issues suggest prudence in these populations.


At writing time, a paucity of investigations about agomelatine antidepressant efficacy and tolerability in human samples still exists, although most of available data suggest its efficacy and safety at doses of 25-50mg/kg. In comparison to other antidepressants, the tolerability profile of this agent makes it a treatment option for patients who cannot tolerate currently available antidepressants [150].

Preliminary observations on agomelatine use in depressed subjects are available although its peculiar pharmacodynamic profile suggests to explore also other conditions. The MT1 and MT2 agonism, as well the 5-HT2C (and 5-HT2B) antagonism, involve more complex neuronal firing mechanisms (involving DA-ergic and GABA-ergic modulations), further complicating the comprehension of agomelatine’ biological and clinical actions. Additionally, the Hamilton Rating Scale for Depression (HAM-D) and Anxiety (HAM-A), Clinical Global Impression (CGI) and Montgomery-Asberg Depression Rating Scale (MADRS) showed significant improvement with agomelatine vs. placebo [151, 152]. Possibly, the rating instruments may be inappropriate to adequately assess the sleep and circadian symptoms of depression, leading to a bias in comparative studies involving agomelatine and other classes of antidepressant.


Expectations from new antidepressant therapies go beyond efficacy alone, to include advantages in tolerability and safety. Although current diagnostic instruments and rating scales may be unable to cover the sleep disturbances of depression in a proper and comprehensive manner, agomelatine efficacy on MDD symptoms has been pointed out by preliminary observations both on pre-clinical and clinical samples. Due to its pharmacological profile, agomelatine does not induce the side effects related to common antidepressant prescriptions (i.e. gastrointestinal disorders, weight gain, sexual dysfunction, serotonin syndrome, insomnia, discontinuation syndrome, and others) [153], making the drug an intriguing option in the antidepressants scenario.


The authors read and approved the final version of the manuscript, having no conflicts of interests nor financial support to state.

Table 3
Comparison of SSRIs Efficacy and Tolerability vs. Agomelatine


The authors sincerely acknowledge Mrs. Rita Santi Amantini for her secretary assistance and Maria Giovanna Colicchio, MD for her support.


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