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. 2015 Dec 1;38(12):1023–1028. doi: 10.14348/molcells.2015.0258

Peripheral Serotonin: a New Player in Systemic Energy Homeostasis

Jun Namkung 1, Hail Kim 1,*, Sangkyu Park 2,*
PMCID: PMC4696992  PMID: 26628041

Abstract

Whole body energy balance is achieved through the coordinated regulation of energy intake and energy expenditure in various tissues including liver, muscle and adipose tissues. A positive energy imbalance by excessive energy intake or insufficient energy expenditure results in obesity and related metabolic diseases. Although there have been many obesity treatment trials aimed at the reduction of energy intake, these strategies have achieved only limited success because of their associated adverse effects. An ancient neurotransmitter, serotonin is among those traditional pharmacological targets for anti-obesity treatment because it exhibits strong anorectic effect in the brain. However, recent studies suggest the new functions of peripheral serotonin in energy homeostasis ranging from the endocrine regulation by gut-derived serotonin to the autocrine/paracrine regulation by adipocyte-derived serotonin. Here, we discuss the role of serotonin in the regulation of energy homeostasis and introduce peripheral serotonin as a possible target for anti-obesity treatment.

Keywords: adipose tissue, energy homeostasis, obesity, tryptophan hydroxylase, serotonin

INTRODUCTION

Serotonin (5-hydroxytryptamine, 5-HT) is a neurotransmitter that is synthesized from the essential amino acid tryptophan by the sequential actions of tryptophan hydroxylase (TPH) and aromatic amino acid decarboxylase. Once serotonin is released, it exerts its biological action by binding to serotonin receptor (HTR). Its action is then terminated by uptake into cells through the serotonin transporter (SERT, Slc6a4) (Wade et al., 1996). Thus, serotonin is commonly thought to act locally in neural and paracrine circuits, and its functions vary depending on the tissues (Gershon and Tack, 2007).

The hydroxylation of tryptophan is the rate-limiting step in serotonin synthesis. Serotonin production is regulated by the activity of TPH and the availability of tryptophan. There are two isoforms of TPH; TPH1 is primarily expressed in peripheral tissues, whereas TPH2 is expressed in the central nervous system (CNS) (Walther and Bader, 2003; Zhang et al., 2004). Because serotonin cannot cross the blood-brain barrier, the central and peripheral serotonergic systems are functionally separated. In the CNS, serotonin is produced in the raphe nuclei of the brainstem and hypothalamus. By functioning as a neurotransmitter in CNS, serotonin regulates mood (Merens et al., 2007; Young and Leyton, 2002), sleep-wake behavior (Monti, 2011) and food intake (Lam et al., 2010). In the periphery, serotonin is mainly produced in the gut and pineal gland. Approximately 90% of serotonin in the body is produced by TPH1 in enterochromaffin cells in the gut, where it regulates intestinal motility (Keszthelyi et al., 2009). Gut-derived serotonin (GDS) is stored in platelets and controls hemodynamics upon activation of platelets (Keszthelyi et al., 2009). Serotonin is also present in other peripheral tissues (Gershon and Ross, 1966); it has been shown to play different roles in the mammary gland (Matsuda et al., 2004), liver (Lesurtel et al., 2006), and bone (Yadav et al., 2008) as well as in pancreatic β-cells (Kim et al., 2010; 2015; Ohara-Imaizumi et al., 2013).

Body energy homeostasis is a primitive and fundamental biological function that is regulated through complex physiological processes. As an ancient neurotransmitter that is conserved throughout the animal phyla, serotonin is a good candidate to play a fundamental role in the regulation of energy homeostasis. At least 14 HTRs, grouped into 7 families according to the signaling mechanisms, are widely expressed in mammalian tissues. This diversity of HTRs can provide diverse effects of serotonin on target cells (Hannon and Hoyer, 2008). Indeed, the functions of serotonin in energy homeostasis range from central control of food intake to direct regulation of adipose tissue activity in the periphery. In this review, we discuss the functional role of serotonin in systemic energy homeostasis.

CENTRAL REGULATION OF ENERGY HOMEOSTASIS BY SEROTONIN

Central serotonin has been considered a target for anti-obesity treatment since an inverse relationship between central serotonin level and food intake was established. Fenfluramine, which increases serotonin release, is the prototypical agent for serotonergic suppression of feeding (Lam and Heisler, 2007). Inhibiting serotonin synthesis in the brain via intraventricular injection of p-chlorophenylalanine (PCPA), an irreversible TPH inhibitor, induces hyperphagia and weight gain in rats (Breisch et al., 1976). Serotonin reuptake inhibitors, such as sibutramine and fluoxetine, and monoamine oxidase inhibitors, such as clorgyline and pargyline, reduce food intake (Feldman, 1988; Heal et al., 1998; Heisler et al., 1997). Thus, central serotonin functions as an anorexigenic neurotransmitter.

Studies using receptor-specific drugs and knock-out (KO) mice have provided insight into the role of specific HTRs in regulating appetite. The involvement of HTR2C and HTR1B was initially suggested by the anorectic effect of m-chlorophenylpiperazine (mCPP) (Kennett and Curzon, 1988). Anorectic effect of fenfluramine was attenuated by HTR2C antagonist (Vickers et al., 1999). HTR2C agonist induced hypophagia (Lam et al., 2008) and improved glucose tolerance and insulin sensitivity in obese mouse model (Zhou et al., 2007). A major contribution of HTR2C to feeding control was confirmed by a study of Htr2c KO mice (Tecott et al., 1995). Htr2c KO mice are hyperphagic and obese, and the anorectic effect of mCPP disappears in Htr2c KO mice (Nonogaki et al., 1998). However, the anorectic effect of leptin is not related to Htr2c KO. In addition, Htr1b KO mice exhibited hyperphagia (Bouwknecht et al., 2001) and a selective HTR1B agonist induced hypophagia in mice (Halford and Blundell, 1996). Recently, lorcaserin ([1R]-8-Chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine), a selective HTR2C agonist, was approved for obesity treatment (Colman et al., 2012). Lorcaserin decreased body weight without influencing energy expenditure (Martin et al., 2010).

Appetite is regulated by the hypothalamic feeding circuits (Sohn et al., 2013). Briefly, anorexigenic proopiomelanocortin (POMC) neurons release α-melanocyte-stimulating hormone (α-MSH), the endogenous ligand of the melanocortin 4 receptor (MC4R), to reduce appetite and food intake. Orexigenic neuro-peptide Y/agouti-related peptide (NPY/AgRP) neurons increase appetite and food intake by releasing the endogenous MC4R antagonist AgRP, and they suppress POMC neurons by releasing GABA. Studies of the effects of serotonin on the hypothalamic feeding circuits revealed that serotonin reciprocally activates POMC neurons through HTR2C while inhibiting NPY/AgRP neurons via HTR1B (Heisler et al., 2002). Taken together, central serotonin inhibits food intake by modulating hypothalamic feeding circuits (Fig. 1).

Fig. 1.

Fig. 1.

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Appetite is regulated by central serotonin. Serotonin acts via HTR1B and HTR2C on downstream melanocortin pathways to suppress appetite in the brain. Serotonin suppresses the production and release of AgRP, an endogenous melanocortin receptor antagonist, through HTR1B and increases the production and release of α-MSH, an endogenous melanocortin receptor agonist, through HTR2C. Overall, central serotonin suppresses food intake.

Since TPH2 is responsible for the serotonin production in the brain, Tph2 KO mice were expected to be hyperphagic and obese. Although central serotonin levels were selectively decreased, the body weights of Tph2 KO mice were lower than littermate control (Alenina et al., 2009; Gutknecht et al., 2012; Savelieva et al., 2008). In addition, Htr1b KO mice did not develop obesity, despite having hyperphagia (Bouwknecht et al., 2001). These findings suggest that central serotonin may upregulate energy expenditure in the body. Indeed, intraventricular injection of serotonin increases resting oxygen consumption without obvious behavioral effects (Le Feuvre et al., 1991). The injection of serotonin into the paraventricular nucleus and ventromedial nucleus of the hypothalamus increases sympathetic tone, resulting in the upregulation of the activity of brown adipose tissue (BAT) (Sakaguchi and Bray, 1989). Fenfluramine also increases sympathetic tone and activates BAT that is reversed by BAT sympathectomy (Arase et al., 1988; Rothwell and Stock, 1987). Taken together, these findings indicate that central serotonin decreases energy intake by reducing appetite and increases energy expenditure by activating BAT through the sympathetic nervous system.

PERIPHERAL REGULATION OF ENERGY HOMEOSTASIS BY SEROTONIN

In contrast to the anorectic effect of central serotonin, several lines of evidences suggest different functions of serotonin in the periphery. Slc6a4 (SERT) KO mice were expected to be slim due to the increased serotonin activity in the brain; however, they exhibited an obese phenotype (Murphy and Lesch, 2008). Body weight is reduced in Tph1 and Tph2 double KO mice as well as in Tph1 KO mice (Alenina et al., 2009; Gutknecht et al., 2012; Savelieva et al., 2008). In addition, the enhancement of serotonin activity using a selective SERT inhibitor (SSRI) is associated with transient weight loss (Serretti and Mandelli, 2010). These discordant results suggest that peripheral serotonin and central serotonin play opposite roles in the regulation of energy homeostasis.

Peripheral serotonin is produced in the gut and stored in platelets. There is also a small amount of free serotonin in plasma. The level of serotonin in the blood is determined by the production of serotonin from enterochromaffin cells in the gut. Several studies have reported increased serotonin production and blood serotonin levels in various animal models of obesity and diabetes. Kim et al. (2011) reported that the serum serotonin level was elevated in C57BL/6 mice fed a high fat diet (HFD) compared to mice fed a low fat diet (LFD). Bertrand et al. reported that rats fed a Western diet showed increased expression of Tph1 and increased serotonin secretion from the gut (Bertrand et al., 2011). Haub et al. also reported that duodenal serotonin content was increased in ob/ob mice, a mouse model of obesity (Haub et al., 2011). In contrast, Sumara et al. (2012) documented that fasting induced serotonin production in the gut, modestly increasing the plasma serotonin level. Difficulties in measuring blood serotonin levels are responsible for these discrepant blood serotonin levels (Brand and Anderson, 2011). Although Kim et al. (2011) identified serotonin as the most highly upregulated metabolite in the serum of mice fed an HFD, this data needs to be interpreted carefully. They used an LFD as a control instead of a standard chow diet. An LFD contains more carbohydrate than an HFD. This difference can substantially change the availability of tryptophan and affect serotonin production in the periphery and brain. Bertrand et al. (2011) and Haub et al. (2011) reported increased serotonin production in the gut, but they did not measure blood serotonin levels directly. Sumara et al. (2012) reported a modest increase in plasma serotonin levels, which reached 24 μM after 48 h of fasting. However, 24 μM plasma serotonin is a much higher concentration than that usually observed. Earlier reports of serotonin concentration in platelet-poor plasma have ranged from 0.6 to 179 nM, with a mean of 31.6 nM and a median of 14.8 nM (Brand and Anderson, 2011). Thus, whether feeding or fasting changes blood serotonin concentrations remains an open question.

Since the 1960s, the biological functions of peripheral serotonin in the regulation of energy homeostasis have been extensively studied using chemical agonists and antagonists. However, most of data are controversial because of off-target effects. Recently, tissue-specific gene KO technology has allowed us to dissect the complex functions of HTRs in different tissues. In conjunction with recent studies using tissue-specific gene KO of serotonergic systems, reinterpreting the data that have been published over the last several decades provides better understanding on the functions of peripheral serotonin in the regulation of energy metabolism.

In the liver, hepatocytes do not produce serotonin. It is released from platelets upon activation and induces hepatic regeneration through HTR2B (Lesurtel et al., 2006). Recently, using gut-specific Tph1 KO mice, Sumara et al. provided clear insight into the important role of GDS in the liver (Sumara et al., 2012). The gut-specific Tph1 KO mice showed improved glucose disposal and reduced hepatic gluconeogenesis, and these effects were diminished by the administration of serotonin. Liver-specific Htr2b KO mice exhibited a similar phenotype (Sumara et al., 2012), indicating that GDS regulates hepatic glucose metabolism through HTR2B. Similar data have indicated that in fasted mice, plasma glucose concentrations are elevated after the injection of serotonin (Watanabe et al., 2010). In contrast to the increased hepatic glucose production that is triggered by serotonin, plasma triglyceride, cholesterol, and nonesterified fatty acid concentrations are decreased after the injection of serotonin (Watanabe et al., 2010). Portal infusion of serotonin also increases hepatic glucose uptake (Moore et al., 2004). These data suggest that serotonin may induce lipogenesis or triacylglycerol synthesis in the liver and/or white adipose tissue (WAT). Indeed, Haub et al. indirectly showed that serotonin increases the fat content in the liver (Haub et al., 2011). Duodenal serotonin content was increased in ob/ob mice, and HTR3 antagonist treatment reduced the elevated serotonin levels and increased SERT in the duodenum. In these mice, treatment with an HTR3 antagonist also reduced fat content, inflammation, and necrosis in the liver (Haub et al., 2011). Thus, GDS seems to induce hepatic steatosis.

Although Slc6a4 KO mice are obese and the body weights of Tph1 KO mice are reduced (Alenina et al., 2009; Gutknecht et al., 2012; Murphy and Lesch, 2008; Savelieva et al., 2008), the body weights of gut-specific Tph1 KO mice are comparable to those of wild type control mice (Sumara et al., 2012). Furthermore, GDS-induced lipolysis through HTR2B was confirmed in gut-specific Tph1 KO mice and fat-specific Htr2b KO mice (Sumara et al., 2012). These discordant data suggest that serotonin other than GDS may play a different role in the regulation of systemic energy homeostasis. Because lipid accumulation in adipose tissue is a key feature of obesity, adipose tissue is the most likely candidate. Recently, two independent studies have highlighted the role of adipocyte-derived serotonin in energy storage in WAT and in energy expenditure in BAT (Crane et al., 2015; Oh et al., 2015). In a diet-induced obesity mouse model, Tph1 expression and tissue serotonin concentrations were increased in epididymal and subcutaneous WAT (Oh et al., 2015) as well as in BAT (Crane et al., 2015). Crane et al. (2015) showed that Tph1 KO mice were protected from obesity and related metabolic dysfunctions. Tph1 KO mice gained significantly less weight and had lower adiposity and less hepatic lipid accumulation when fed an HFD. Glycemic control was improved in Tph1 KO mice as well, although glucose uptake was similar in the muscle, liver and heart, indicating the contribution of BAT to the increased basal metabolic rate (Crane et al., 2015). Indeed, Tph1 KO mice showed similar food intake, but their energy expenditure was enhanced. BAT activity increased in a UCP1-dependent manner in Tph1 KO mice. The obesogenic action of peripheral serotonin was confirmed again using a peripheral TPH inhibitor LP-533401 (Crane et al., 2015).

Oh et al. (2015) independently demonstrated similar functions of peripheral serotonin using the systemic TPH inhibitor PCPA and the peripheral TPH inhibitor LP-533401. Intraperitoneal injection of PCPA resulted in decreased weight gain and lower adiposity after an HFD, although intraventricular injection of PCPA reduced serotonin production in the brain and induced hyperphagia and obesity (Breisch et al., 1976; Oh et al., 2015). Systemic PCPA injection reduced lipogenesis in WAT and induced beige adipogenesis in inguinal WAT as well as increased BAT activity, thereby decreasing adiposity and improving glucose homeostasis and insulin sensitivity. In particular, both PCPA and LP-533401 induced the expression of UCP1 and DIO2 in BAT and inguinal WAT (Oh et al., 2015). Furthermore, a cell-autonomous effect of serotonin in adipose tissue has been shown in adipocyte-specific Tph1 KO mice (Oh et al., 2015). In BAT, β-adrenergic signaling turns on the thermogenic gene program through an intracellular increase in cyclic AMP (cAMP). cAMP then activates protein kinase A (PKA) and downstream targets of PKA, thereby inducing UCP1 expression (Collins et al., 2010). Adipocyte-specific Tph1 KO induced UCP1 and DIO2 expression in BAT (Oh et al., 2015). Basal cAMP levels and PKA activity were higher in the BAT of the adipocyte-specific Tph1 KO mice, and serotonin attenuated the isoproterenol-mediated increase in intracellular cAMP in BAT (Crane et al., 2015). In addition, HFD robustly induced beige adipogenesis in inguinal WAT of the adipocyte-specific Tph1 KO mice (Oh et al., 2015). Taken together, these recent studies suggest that serotonin negatively regulates the sensitivity of adipose tissues to β-adrenergic stimulation.

HTR2A and HTR3 have been identified as receptors mediating the obesogenic effects of serotonin in adipose tissues. Diet-induced thermogenesis was robustly increased in the BAT of Htr3a KO mice (Oh et al., 2015). In immortalized brown adipocytes, HTR3 antagonist activated the PKA pathway by increasing cAMP production and increased mitochondrial respiration (Oh et al., 2015). Thus, Htr3a KO mice were resistant to HFD-induced obesity and showed the improved insulin sensitivity upon an HFD. In contrast to Tph1 KO mice, Htr3a KO mice maintained WAT mass and did not show histological differences compared with littermate control mice, suggesting that another HTR plays a different role in WAT (Oh et al., 2015). In vitro experiments using 3T3-L1 adipocytes have provided a hint of the role of serotonin in adipogenesis (Kinoshita et al., 2010; Oh et al., 2015). Serotonin is produced in mature adipocytes and TPH1 expression is required for the differentiation of 3T3-L1 preadipocytes (Kinoshita et al., 2010). Treatment with a TPH inhibitor or disruption of Tph1 gene in 3T3-L1 preadipocytes resulted in reduced adipogenesis (Kinoshita et al., 2010), and serotonin increased lipid accumulation in human and mouse fat cells (Gres et al., 2013). HTR2A expression increased in the hypertrophied 3T3-L1 adipocytes and WAT of db/db mice, and HTR2A activation reduced adiponectin expression in hypertrophied 3T3-L1 adipocytes (Uchida-Kitajima et al., 2008). HTR2A antagonist inhibited adipogenesis (Kinoshita et al., 2010), and HTR2A agonist increased lipid accumulation (Oh et al., 2015). HTR2A antagonists increased circulating adiponectin levels in diabetic patients (Nomura et al., 2005; Yamakawa et al., 2003). Thus, serotonin increases energy storage in WAT through HTR2A and inhibits energy expenditure in BAT through HTR3.

CONCLUSION

Based on the newly identified roles of peripheral serotonin in energy homeostasis, serotonin can be considered as an energy-saving hormone. Modulating the peripheral serotonergic system may be a good strategy for anti-obesity treatment because it can decrease obesity and increase insulin sensitivity. In general, receptor-specific activation or inhibition is thought to be a better strategy for drug development. However, serotonin plays different roles in different tissues by acting through different receptors. Thus, inhibition of serotonin synthesis in adipose tissue is a potentially beneficial strategy for anti-obesity treatment. This strategy increases insulin sensitivity by simultaneously decreasing lipogenesis and increasing adaptive thermogenesis.

There are still several questions remained to be solved. Mitochondrial biogenesis was enhanced in BAT by Htr3 or Tph1 KO, but the mechanism how serotonin regulates mitochondrial biogenesis and function is largely unknown. How the inhibition of serotonin synthesis induces beige adipogenesis and which HTR is responsible for the beige adipogenesis are also unknown, as is the mechanism that underlies GDS-mediated regulation of hepatic steatosis. It is also of interest to know how serotonin plays opposite functions in WAT by acting through HTR2A and HTR2B, which increases lipogenesis and lipolysis, respectively.

The evidences in support of serotonin as a metabolic regulator in the development of obesity are increasing. Nonetheless, the majority of the data are derived from animal studies, and the clinical relevance of serotonin in humans remains undetermined. More accurate information regarding blood serotonin levels in different clinical settings also needs to be obtained.

Fig. 2.

Fig. 2.

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Energy homeostasis is regulated by peripheral serotonin. TPH1 expression and the production of serotonin in the periphery are increased by an HFD. Adipocyte-derived serotonin may increase energy storage and adipogenesis in WAT through HTR2A and inhibit adaptive thermogenesis in BAT through HTR3. Gut-derived serotonin promotes gluconeogenesis and suppresses hepatic glucose uptake through HTR2B, indicating that GDS regulates hepatic glucose metabolism.

Acknowledgments

This research was supported by the Bio & Medical Technology Development Program of the National Research Foundation of Korea (NRF), which is funded by the Korean government, MSIP (NRF-2014M3A9D5A01073546 to H.K.), and by the Basic Science Research Program of the NRF, which is funded by the Ministry of Education (NRF-2015R1D1A3A03015699 to S.P.)

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