Abstract

SummaryDrugs activating 5-hydroxytryptamine 2C receptors (5-HT2CRs) potently suppress appetite, but the underlying mechanisms for these effects are not fully understood. To tackle this issue, we generated mice with global 5-HT2CR deficiency (2C null) and mice with 5-HT2CRs re-expression only in pro-opiomelanocortin (POMC) neurons (2C/POMC mice). We show that 2C null mice predictably developed hyperphagia, hyperactivity, and obesity and showed attenuated responses to anorexigenic 5-HT drugs. Remarkably, all these deficiencies were normalized in 2C/POMC mice. These results demonstrate that 5-HT2CR expression solely in POMC neurons is sufficient to mediate effects of serotoninergic compounds on food intake. The findings also highlight the physiological relevance of the 5-HT2CR-melanocortin circuitry in the long-term regulation of energy balance.

Highlights

  • The central 5-hydroxytryptamine (5-HT) system, including the 5-HT2C receptors (5-HT2CRs) plays critical roles in the regulation of energy homeostasis

  • Using PCR primers specific for 5-HT2CR mRNA, we found that expression of 5-HT2CR mRNA was disrupted in the cerebral cortex, whole hypothalamus, arcuate nucleus of hypothalamus (ARC), and brainstem of 2C null mice

  • POMC mRNA is expressed in the anterior pituitary gland, we found no endogenous 5-HT2CR mRNA expressed in the pituitary of wild-type (WT) mice

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Summary

SUMMARY

Drugs activating 5-hydroxytryptamine 2C receptors (5-HT2CRs) potently suppress appetite, but the underlying mechanisms for these effects are not fully understood. To tackle this issue, we generated mice with global 5-HT2CR deficiency (2C null) and mice with 5-HT2CRs re-expression only in pro-opiomelanocortin (POMC) neurons (2C/POMC mice). We show that 2C null mice predictably developed hyperphagia, hyperactivity, and obesity and showed attenuated responses to anorexigenic 5-HT drugs. All these deficiencies were normalized in 2C/POMC mice. These results demonstrate that 5-HT2CR expression solely in POMC neurons is sufficient to mediate effects of serotoninergic compounds on food intake. The findings highlight the physiological relevance of the 5-HT2CR-melanocortin circuitry in the long-term regulation of energy balance

INTRODUCTION
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EXPERIMENTAL PROCEDURES

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