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The role of 5‐HT2c receptor on corticosterone‐mediated food intake
Authors:Tongtong Ge  Zhuo Zhang  Jiayin Lv  Yunong Song  Jie Fan  Wei Liu  Xuefeng Wang  F. Scott Hall  Bingjin Li  Ranji Cui
Affiliation:1. Jilin Provincial Key Laboratory on Molecular and Chemical Genetics, The Second Hospital of Jilin University, Changchun, Jilin, People's Republic of China;2. Department of Orthopedics, China‐Japan Union Hospital of Jilin University 126 Xiantai Street, Nanguan District, Changchun, People's Republic of China;3. Department of Pharmacology and Experimental Therapeutics, University of Toledo College of Pharmacy and Pharmaceutical Sciences, Toledo, OH, USA
Abstract:Corticosterone plays an important role in feeding behavior. However, its mechanism remains unclear. Therefore, the present study aimed to investigate the effect of corticosterone on feeding behavior. In this study, cumulative food intake was increased by acute corticosterone administration in a dose‐dependent manner. Administration of the 5‐HT2c receptor agonist m‐chlorophenylpiperazin (mCPP) reversed the effect of corticosterone on food intake. The anorectic effects of mCPP were also blocked by the 5‐HT2c receptor antagonist RS102221 in corticosterone‐treated mice. Both corticosterone and mCPP increased c‐Fos expression in hypothalamic nuclei, but not the nucleus of the solitary tract. RS102221 inhibited c‐Fos expression induced by mCPP, but not corticosterone. In addition, mCPP had little effect on TH and POMC levels in the hypothalamus. Furthermore, mCPP antagonized decreasing effect of the leptin produced by corticosterone. Taken together, our findings suggest that 5‐HT2c receptors and leptin may be involved in the effects of corticosterone‐induced hyperphagia.
Keywords:5‐HT  c‐fos  corticosterone  feeding behavior  receptor
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