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Compelling data demonstrate that inflammation-associated anorexia directly results from the action of pro-inflammatory factors, primarily cytokines and prostaglandins E2, on the nervous system. For instance, the aforementioned pro-inflammatory factors can stimulate the activity of peripheral sensory neurons, and induce their own de novo synthesis and release into the brain parenchyma and cerebrospinal fluid. Ultimately, it results in the mobilization of a specific neural circuit that shuts down appetite. The present article describes the different cell groups and neurotransmitters involved in inflammation-associated anorexia and examines how they interact with neural systems regulating feeding such as the melanocortin system. A better understanding of the neurobiological mechanisms underlying inflammation-associated anorexia will help to develop appetite stimulants for cancer and AIDS patients.
Inflammation-associated anorexia refers to the reduction of food intake observed during acute and chronic inflammatory states in both men and animals. It is well established that laboratory animals reduce their food intake in response to the peripheral administration of pro-inflammatory cytokines such as interleukin-1β (IL-1β) or stimulants of the release of cytokines such as lipopolysaccharide (LPS). Notably, the administration of LPS reduces meals frequency, while that of IL-1β reduces both meals frequency and size (Langhans et al., 1993). LPS and IL-1β also induce an aversion for a novel food or a sucrose solution (Tazi et al., 1988; Langhans et al., 1990; Weingarten et al., 1993; Bauer et al., 1995; Goehler et al., 1995), inhibit food-motivated behavior (Bret-Dibat et al., 1995; Kent et al., 1996), render the consumption of sucrose less pleasurable (anhedonia) (Yirmiya, 1996; Borowski et al., 1998; Merali et al., 2003), and increase the preference for carbohydrates and avoidance for aversive substances (Aubert et al., 1995; Cross-Mellor et al., 2004; Aubert and Dantzer, 2005). Although appetite (and thus anorexia) cannot be directly evaluated in animals, most researchers have been using the term of “anorexia” in animals based on the assumption that reduced appetite accounts for the reduction of food intake that follows the administration of either cytokines or LPS (Konsman and Dantzer, 2001). Inflammation-associated anorexia is acknowledged to help maintaining body integrity in face of infections and physical injuries (Hart, 1988; Exton, 1997). In essence, it is part of a process of energy repartition involving reducing activities such as food seeking and digestion which would otherwise consume up the energy needed to develop immune responses. There is also some evidence that food deprivation per se prolongs the survival of mice infected with Listeria (Wing and Young, 1980), a phenomenon that possibly involves the reduction of the levels of micronutrients required for bacterial proliferation (Weinberg, 1984).
Patients with chronic inflammation commonly complain about early satiety and loss of appetite, which in the case of cancerous and HIV-positive individuals can accompany dramatic weight loss known as cachexia (Laviano et al., 2003; Tisdale, 2009). The microenvironment surrounding tumoral cells, as well as tumoral cells themselves, are thought to produce pro-inflammatory cytokines (Seruga et al., 2008), and tumor-bearing rodents frequently show anorexia (Bernstein and Fenner, 1983; Bernstein et al., 1985; Plata-Salaman et al., 1998; Meguid et al., 1999; Varma et al., 2001). It is important to mention that cachexia and anorexia are distinct phenomena which do not necessarily coexist (depending on tumor size and location, age); however, patients with both conditions show the worst prognosis (Laviano et al., 2003; Tisdale, 2009). Of note, the reduction of appetite observed in cancer patients does not solely result from inflammation but also from psychological distress and anticancer therapies (i.e., interferons) (Capuron et al., 2002). Unfortunately, efficient therapies to alleviate inflammation-associated anorexia are currently limited and, therefore, investigating their underlying mechanisms is truly relevant in the fight against cancer- and infection-related loss of appetite.
Communication from the periphery to the brain involves, in addition to endocrine mechanisms, cranial and spinal nerves innervations. Virtually all tissues are innervated by a dense network of cranial and/or spinal sensory terminals which are capable of detecting a wide range of physiological signals. It has been shown that peripheral sensory neurons can sense pro-inflammatory factors. Receptors and binding sites for IL-1β and prostaglandin E2 (PGE2), for instance, have been reported in vagal, spinal, and trigeminal sensory neurons (Matsumura et al., 1995; Goehler et al., 1997; Ek et al., 1998; Copray et al., 2001; Obreja et al., 2002; Patwardhan et al., 2008). Furthermore, electrophysiological studies demonstrated that both IL-1β and PGE2 rapidly depolarize vagal sensory neurons (Niijima, 1996; Gaige et al., 2004; Snitsarev et al., 2007), as well as trigeminal and spinal sensory neurons (Pitchford and Levine, 1991; England et al., 1996; Binshtok et al., 2008; Takeda et al., 2008).
It is widely agreed that the action of pro-inflammatory factors on peripheral sensory terminals plays a prominent role when an inflammatory event is confined to a specific tissue. For example, trigeminal afferents that innervate the meninges are recruited upon inflammation limited to the intracranial cavity (i.e., meningitis, migraine), and the application of a mixture of pro-inflammatory agents on meninges sensory terminals induces profound feeding suppression in rats (Malick et al., 2001). More direct evidence of the involvement of the neural pathway in anorexia has been provided by experiments conducted in vagotomized animals. Rodents with bilateral subdiaphragmatic surgical vagotomy or chemical deafferentation (capsaicin) show attenuated anorexia and brain IL-1β expression in response to the intraperitoneal administration of LPS or IL-1β (Bret-Dibat et al., 1995; Laye et al., 1995; Sergeev and Akmaev, 2000) and are less sensitive to the aversive effects of peripheral IL-1β (Goehler et al., 1995). Likewise, vagotomy procedures attenuate anorexia in tumor-bearing rats (Bernstein, 1996).
The nucleus of the solitary tract (NTS) and the adjacent area postrema (AP) located in the dorso-caudal brainstem are the primary relays of vagal terminal fields in the central nervous system (Figure (Figure1).1). The NTS also receives indirect projections from some trigeminal and spinal sensory neurons (Gamboa-Esteves et al., 2001; Craig, 2002; Burstein and Jakubowski, 2005). Glutamate serves as the main neurotransmitter in vagal afferents terminals in the NTS, and it has been shown that LPS administration induces glutamate release in the NTS (Lin et al., 1999). In fact, one study has shown that the peripheral administration of metabotropic glutamate receptor antagonists attenuates inflammation-associated anorexia (Weiland et al., 2006), an effect that could possibly be explained by a reduction of vagal and/or spinal glutamatergic neurotransmission. The implication of the NTS in immune sensing is also demonstrated by neuroanatomical studies using the expression of c-fos as a marker of neuronal activation. Multiple investigators have reported robust c-fos expression in the NTS subsequently to an intraperitoneal inflammation (Wan et al., 1993; Rivest and Laflamme, 1995; Sagar et al., 1995; Konsman et al., 2000; Ge et al., 2001). Similarly, tumor-bearing rats show c-fos expression in the NTS (Konsman and Blomqvist, 2005; Ruud and Blomqvist, 2007).
In contrast with previously mentioned observations, several studies showed the intact anorectic effects of LPS and IL-1β in vagotomized animals (Schwartz et al., 1997; Porter et al., 1998; Wieczorek et al., 2005). The induction of c-fos in the NTS following either intravenous LPS or IL-1β is also preserved in vagotomized animals (Ericsson et al., 1997; Hermann et al., 2001), suggesting that an intact vagus nerve is not always required for the stimulation of NTS neurons in response to an immune challenge. Another mechanism by which pro-inflammatory factors trigger anorexia involves their direct action on the central nervous system. For instance, the intracerebroventricular administration of a small dose of LPS or IL-1β is sufficient to induce anorexia (Kent et al., 1992; Yao et al., 1999). Other cytokines such as tumor necrosis factor alpha and interleukin-6 similarly reduce feeding when centrally administered (Kapas and Krueger, 1992; Fantino and Wieteska, 1993; Plata-Salaman, 1996; Plata-Salaman et al., 1996; Sonti et al., 1996). IL-1β orchestrates the expression of other cytokines in the brain (Laye et al., 1994; Mingam et al., 2008a), and more importantly, the blockade of cerebral IL-1β receptor by its endogenous antagonist IL-1ra partially prevents LPS-induced anorexia (Laye et al., 2000). The action of pro-inflammatory cytokines directly on the central nervous system is referred in the literature to as “the humoral pathway” (Figure (Figure11).
It initially seemed surprising that cytokines are capable of acting on the central nervous system when considering that the blood-brain barrier prevents most blood-borne pro-inflammatory factors and immune cells to access the brain. In fact, the central nervous system does contain immunocompetent cells which are fully capable of detecting pathogen-associated molecular patterns and of producing pro-inflammatory factors in response to injury and inflammatory challenges (Rivest, 2003). Furthermore, specialized areas of the brain known as circumventricular organs are devoid of a blood-brain barrier, and as such are readily accessible to systemic pathogen-associated molecular patterns such as LPS (Rivest, 2003). The mammalian brain contains four known circumventricular organs which are the AP, the median eminence, the subfornical organ, and the organum vasculosum of the lamina terminalis. Brain cells capable of producing IL-1β have been identified as perivascular macrophages, microglial cells and macrophages in the choroid plexus and meninges (van Dam et al., 1992, 1995; Buttini and Boddeke, 1995; Konsman et al., 1999; Goehler et al., 2006). Numerous studies have reported the presence of IL-1 binding sites and receptors (IL-1R) prominently in brain endothelial cells (Farrar et al., 1987; Takao et al., 1990; Ban et al., 1991; Cunningham et al., 1992; Ericsson et al., 1995; French et al., 1999; Konsman et al., 2004), choroid plexus, and to a lesser extent in some neurons of the hippocampus, arcuate nucleus and amygdala. Recently, Ching et al. (2007) elegantly demonstrated using a genetic approach that the selective deletion of IL-1R in brain endothelial cells prevents intravenous IL-1-induced fever and hypothalamo–pituitary–adrenal axis stimulation (this study, however, did not survey food intake). Another study showed that the pharmacological inhibition of nuclear factor kappa B (NF-kB), a transcription factor downstream of IL-1 signaling pathway in endothelial cells, attenuates IL-1-induced anorexia (Nadjar et al., 2005). Similarly, LPS-induced anorexia is blunted in mice lacking MyD88 (Myeloid differentiation primary response gene 88) (Wisse et al., 2007), which is a critical molecular component of both IL-1 and LPS signaling in perivascular and endothelial cells (Gosselin and Rivest, 2008).
All the aforementioned data demonstrate that LPS and IL-1β signaling in brain endothelial cells (and possibly perivascular cells) plays a critical role in inflammation-associated anorexia. However, these data do not explain how LPS or IL-1β ultimately change the activity of neurons involved in feeding. The production and release of PGE2 within the intracranial cavity is promoted by the stimulation of IL-1R and LPS receptor positioned in cells forming the blood-brain barrier including endothelial cells, choroid plexus and meninges (Rivest, 1999; Ek et al., 2001; Konsman et al., 2004). In turn, PGE2 are thought to directly act on neurons important in feeding. In agreement with such a view, the central administration of PGE2 induces c-fos expression in brain sites directly comparable to that recruited by IL-1β (Lacroix et al., 1996). Additionally, it has been consistently shown that the pharmacological inhibition and the genetic deletion of enzymes synthesizing PGE2 reduce anorexia following peripheral LPS or IL-1β (Johnson et al., 2002; Lugarini et al., 2002; Pecchi et al., 2006; Elander et al., 2007). According to the literature, PGE2 bind four known G proteins-coupled receptors (EP1-4) which are abundantly expressed in the preoptic area, hypothalamus and hindbrain including the NTS (Zhang and Rivest, 1999; Oka et al., 2000; Engblom et al., 2001) (Figure (Figure1).1). Also, EP3 has been recently implicated in the regulation of feeding since mice lacking this receptor develop hyperphagia (Sanchez-Alavez et al., 2007). Finally, there is direct evidence that PGE2 can modulate the electrophysiological activity of PGE2-sensitive neurons in brain regions important in feeding such as the NTS. For example, the application of PGE2 in NTS preparation rapidly enhances glutamatergic transmission, while it reduces presynaptic vagal neurotransmission (Marty et al., 2008).
The regulation of appetite involves multiple internal and environmental factors which are integrated in specific neuronal groups distributed across the neuraxis. The brainstem contributes to the short-term regulation of appetite in response to signals arising from the gut. Notably, early studies in decerebrate animals demonstrated that the brainstem is sufficient to produce post-prandial satiety (Grill and Smith, 1988). Within the brainstem, the NTS plays an important role in the control of satiety and aversion by acting as viscero-sensory relays for gastrointestinal signals predominantly conveyed through the vagus nerve (Adachi et al., 1991; Schwartz, 2000). As mentioned earlier, NTS neurons integrate signals originating from both the neural and humoral pathways (Figure (Figure1),1), making this brain structure one of the most important site in mediating inflammation-associated anorexia. The administration of IL-1 into the fourth ventricle, which provides cerebrospinal fluid to the brainstem, is sufficient to induce c-fos in NTS and, more importantly, a profound anorexia (DeBoer et al., 2009). Among NTS neurons known to be activated in response to LPS are neurons producing glucagon-like peptide 1 (GLP-1) (Rinaman, 1999), a well-known anorectic peptide (Kinzig et al., 2002). Specifically, the pharmacological inhibition of GLP-1 receptor in the brainstem attenuates LPS-induced anorexia, suggesting that GLP-1-producing neurons directly contribute to anorexia (Grill et al., 2004).
NTS neurons activated in response to inflammation send projections to the lateral parabrachial nucleus (lPB), bed nucleus of the stria terminalis (BST), central amygdala (CeA) and paraventricular nucleus of the hypothalamus (PVN) (Ericsson et al., 1994; Tkacs and Li, 1999; Buller and Day, 2002; Crane et al., 2003; Gaykema et al., 2007) (Figure (Figure1).1). The exact role of the aforementioned structures in feeding behavior remains understudied, however, it is known that these structures all receive visceral- and gustatory-related information and are, individually or collectively, implicated in hypophagic behaviors such as stress-induced anorexia (Koob, 1999), satiety/aversion (Reilly and Trifunovic, 2000; Sclafani et al., 2001; Ferreira et al., 2006; Becskei et al., 2007), food avoidance and preference (Kelley et al., 2003; Ferreira et al., 2006). Yet the direct implication of these structures in anorexia will require further testing.
The PVN deserves a special mention. Indeed, lesions of the PVN increase food intake (Gold, 1970; Choi and Dallman, 1999), indicating the pivotal role of this structure in reducing feeding. In addition, we previously showed that the expression of c-fos in the PVN positively correlates with the intensity of anorexia after LPS administration (Gautron et al., 2005). While it is admitted that corticotropin-releasing hormone (CRH)-producing neurons of the PVN control the hypothalamo–pituitary–adrenal axis, they are also good candidates to contribute to the anorectic effect of inflammation in view of the facts that CRH exerts anorectic effects (Dunn and Berridge, 1990) and the immunoneutralization of CRH attenuates IL-1-induced anorexia (Uehara et al., 1989). However, CRH is produced in widespread brain sites and the contribution of PVN CRH-expressing neurons in anorexia relative to other sites has not been verified. Cocaine- and amphetamine-regulated transcript (CART) is another anorectic peptide produced in the PVN (Kristensen et al., 1998). Interestingly enough, CART-expressing neurons of the PVN are activated in response to LPS (Fuzesi et al., 2008), number of which also innervate the NTS. Together, it indicates that inflammation-associated anorexia presumably engages reciprocally connected neuronal groups in the NTS and PVN (Figure (Figure11).
The melanocortin system tightly regulates appetite downstream of hormonal indicators of energy status such as leptin, insulin and ghrelin. The arcuate nucleus of the hypothalamus (Arc) contains pro-opiomelanocortin neurons (POMC) which produce the anorectic peptides alpha-melanocyte stimulating hormone (α-MSH) and CART. Importantly, α-MSH is an endogenous agonist of the melanocortin-4 receptor (MC4R) which is a major regulator of food intake (Seeley et al., 2004; Cone, 2006). Uniquely, the Arc also contains neurons which produce the orexigenic peptides agouti-related protein (AgRP) and neuropeptide Y (NPY). AgRP is an endogenous MC4R antagonist. Persuasive evidence has established that the activity of both populations of neurons is oppositely regulated by the humoral signals leptin and ghrelin (Seeley et al., 2004). In fact, whereas leptin signaling in POMC neurons mediates its anorectic effects (Hill et al., 2008), ghrelin signaling in AgRP neurons promotes its stimulatory effects on appetite (Luquet et al., 2007). Ultimately, these neurons project to a number of brain sites involved in feeding including the NTS, PVN, lateral hypothalamus and lPB to modulate their activity in face of changes in energy status (Figure (Figure11).
Earlier studies reported increased plasma leptin levels in response to LPS in mice and rats (Sarraf et al., 1997; Faggioni et al., 1999; Finck and Johnson, 1999; Mastronardi et al., 2000), making leptin a potential candidate involved in inflammation-associated anorexia. Moreover, the melanocortin system has been shown to be involved in acute and chronic inflammatory-associated anorexia based on neuroanatomical (Sergeyev et al., 2001; Reyes and Sawchenko, 2002; Borges et al., 2007; Scarlett et al., 2007), pharmacological (Huang et al., 1999; Wisse et al., 2001), electrophysiological (Scarlett et al., 2007), and transgenic mice studies (Marks et al., 2001). However, parallel studies have challenged the role played by leptin and the melanocortin system in anorexia by showing that intraperitoneal LPS does not elevate plasma leptin levels in rats (Giovambattista et al., 2000; Gautron et al., 2005; Spencer et al., 2007). In addition, leptin- and leptin receptor-deficient animals are still fully responsive to the anorectic effects of LPS (Faggioni et al., 1997; Lugarini et al., 2005). One of our studies also failed to observe increased c-fos expression in POMC neurons in response to LPS (Gautron et al., 2005). Likewise, no significant variation of expression for NPY, AgRP or POMC mRNA in the Arc of LPS-treated rodents using RNase protection assay or in situ hybridization were found (Turrin et al., 2001; Johnson et al., 2002; Gautron et al., 2005). Finally, Reyes and Sawchenko (Reyes and Sawchenko, 2002) demonstrated that IL-1-induced anorexia was not prevented by chemical lesion of the Arc or the physical disruption of its projections.
If previous studies have not firmly established the role played by the melanocortin system in triggering anorexia during inflammation, nevertheless they have suggested its modulatory role. For example, a recent study has evidenced that the immunoneutralization of leptin attenuates LPS-induced anorexia in rats at 8 and 24h after LPS (Sachot et al., 2004). This observation agrees with studies showing that inflammatory anorexia due to LPS or turpentine is lowered whenever leptin falls, i.e., after food restriction (Lennie, 1998; Gautron et al., 2005).
The regulation of the hedonic aspects of food intake (i.e., palatability, reward) primarily involves the lateral hypothalamus and connected brain sites such as the nucleus accumbens and ventral tegmental area. The lateral hypothalamus uniquely contains a population of neurons expressing the neuropeptides orexins (Sakurai et al., 1998) which are well established to control arousal and stimulate feeding (Mieda et al., 2004). As expected, fasting is associated with increased c-fos in orexins neurons as well as up-regulated prepro-orexin mRNA expression (Sakurai et al., 1998). One early study demonstrated that peripheral LPS reduces lateral hypothalamus auto-stimulation in rats (Borowski et al., 1998), suggesting that inflammation results in the inhibition of this brain site. In agreement with such a view, we demonstrated that LPS suppressed c-fos expression in the lateral hypothalamus of fasted rats (Gautron et al., 2005). The previous study was followed by other works showing that LPS specifically reduces c-fos expression in orexins neurons (Becskei et al., 2008; Park et al., 2008; Gaykema and Goehler, 2009). The inhibition of orexins neurons in response to LPS is concomitant to the activation of nucleus accumbens neurons (Park et al., 2008), and it has been previously proposed that gabaergic neurons located in the rostral nucleus accumbens produces anhedonia and reduction in motivated feeding by inhibiting orexins neurons (Kelley, 1999). It is therefore likely that the aforementioned circuitry is involved in LPS-induced anhedonia.
Many promising pharmacological agents have been clinically tested but, unfortunately, failed to demonstrate therapeutic efficacy against anorexia or cachexia. Among other examples, endocannabinoids showed limited effects in AIDS patients (Beal and Flynn, 1995) and no greater effect over placebo in advanced cancer patients (Strasser et al., 2006). Pharmacological agents currently in use to combat anorexia are thalidomide, eicosapentaenoic acid (a long chain ω-3 polyunsaturated fatty acid), corticosteroids and progestrogens derivates (Mattox, 2005; Tisdale, 2006). Despite the fact they exert well documented anti-inflammatory actions, these agents show only temporary benefits on appetite, numerous side effects and their mechanism of actions on feeding remain unclear.
Nutritional approaches are not only necessary to prevent deficiencies and reduce gastrointestinal upsets, but also to increase the survival time of cancer patients by reducing whole body inflammation. For instance, a low fat and high fibers diet has been shown to prolong the survival of women with breast cancer (Zhang et al., 1995; Pierce et al., 2007). Some studies also suggested that rats fed on fish oil (rich in long chain ω-3 polyunsaturated fatty acid) show reduced anorexia in response to IL-1 and tumor growth (Hellerstein et al., 1989; Goncalves et al., 2006). In addition, the use of non-steroidal anti-inflammatory drugs combined with a diet enriched in ω-3 can modestly improve appetite in cancer patients (Lundholm et al., 1994; Wigmore et al., 2000; Cerchietti et al., 2004; Jatoi et al., 2004). By contrast, other studies have failed to demonstrate any beneficial effects of ω-3-enriched diets in LPS-treated mice and cancerous patients (Mingam et al., 2008b; Mazzotta and Jeney, 2009). Despite these contradictory results, considering the key role played by PGE2 in immune-to-brain communication, therapeutic trials involving the manipulation of eicosanoids metabolism by pharmacological and nutritional means is considered a useful strategy to lower anorexia (Figure (Figure11).
Once again, appetite is regulated both by internal and environmental factors. Cancer patients are submitted to intense stress, and efforts to attenuate anorexia using anti-inflammatory agents and nutrition may be in vain if their psychological distress is not addressed. In this regard, attention to the patient's psychological well-being has been shown to help patients regaining interest for food (Holland et al., 1977). Presumably, one mechanism by which stress reduces appetite is by directly interfering with neural systems involved in feeding including POMC and CRH neurons (Koob, 1999; Liu et al., 2007); another mechanism is by aggravating peripheral inflammation (Gibb et al., 2008).
Agents that reduce the activity of vagal and/or spinal nerves such as anti-emetics and analgesics can also be used to treat cancer patients (Davis et al., 2006). While it is unclear whether sensory afferents can directly detect tumors, it has been proposed that reducing the activity of peripheral sensory afferents may result in augmented appetite in cancer. For example, the blockade of type 3 serotonergic receptors (5-HT3R) improves the ability of cancer patients to enjoy food (Edelman et al., 1999). Binding sites for 5-HT3R are abundant in the NTS/AP (Marazziti et al., 2001), but the receptor mRNA itself is found in the nodose ganglion and not the NTS/AP (Tecott et al., 1993; Morales and Wang, 2002). Thus, 5-HT3R ligands act on receptors produced by vagal neurons and transported to their terminals located within the NTS and AP. These treatments in combination with adequate nutrition are useful to alleviate nausea, pain and gastrointestinal tract discomfort but they do not directly address the problem of loss of appetite. Perhaps, utilizing drugs that target NTS neurotransmitters could be useful. For example, exendin-(9-39) which is an antagonist of GLP-1 receptor has been shown to attenuate LPS-induced anorexia in rats (Grill et al., 2004).
A neurobiological roadmap of the mechanisms underlying anorexia is now available and, to effectively alleviate anorexia, it would be preferable to target neural circuits well known to be involved in the control of feeding. Thus far, the most promising strategy to attenuate anorexia consists in modulating the melanocortin system by adjusting the circulating levels of endogenous or exogenous factors which are known to act on Arc neurons (Figure (Figure1).1). We previously mentioned that the immunoneutralization of leptin, for instance, efficiently attenuates LPS-induced anorexia in rats (Sachot et al., 2004). Conversely, the administration of ghrelin, which stimulates NPY neurons, has given encouraging results in cancer patients (Neary et al., 2004; Wynne et al., 2005). The melanocortin system is not only regulated by hormones but also regulated by endogenous neurotransmitters. The stimulation of the serotonin receptor 2C (5-HT2CR) in POMC neurons reduces feeding (Xu et al., 2008). While increased serotonergic neurotransmission is observed in LPS-treated animals (Dunn, 1992; MohanKumar et al., 1999; Nolan et al., 2000), interestingly, 5-HT2CR antagonists administration attenuates peripheral and central LPS-induced anorexia (von Meyenburg et al., 2003a,b; Asarian et al., 2007). Together, it suggests that modulating the signaling pathways of various hormones and neurotransmitters acting on Arc neurons can reduce anorexia.
Recent studies have shown that orexins neurons are inhibited in response to peripheral inflammation (Gaykema and Goehler, 2009), which is a remarkable observation given the role of the lateral hypothalamus in regulating hedonic processes and the fact that cancer and AIDS patients often show anhedonia. Modafinil, a psychostimulant which stimulates orexin neurons (Scammell et al., 2000), has already been shown to diminish fatigue and improve quality of life in cancer patients (Blackhall et al., 2009; Spathis et al., 2009). It would be interesting to further test the ability of this drug along with compounds that target specifically the orexinergic system to reduce anorexia and anhedonia.
In conclusion, multiple factors and neural systems contribute to inflammation-associated anorexia and no single intervention will suffice in order to reverse the neurochemical changes responsible for anorexia in cancer and AIDS patients. Moreover, targeting the central nervous system is always complicated because of the blood-brain barrier and the lack of specificity of many available pharmacological agents. Nevertheless, the research on feeding behavior is permanently evolving, and new neural mechanisms are being regularly discovered, giving researchers opportunities to evaluate new therapeutics.
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.