The 5-HT2C/2B Receptor Agonist m-Chlorophenylpiperazine (mCPP) Inhibits 2-Deoxy-D-glucose (2-DG)-Induced Hyperphagia in Rats.

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  • 5 HT2C 2B Receptor Agonist m Chlorophenylpiperazine mCPP Inhibits 2 Deoxy D glucose 2 DG Induced Hyperphagia in Rats

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Effects of the 5-HT2C/2B receptor agonist m-chlorophenylpiperazine (mCPP) on hyperphagia elicited by 2-deoxy-D-glucose (2-DG) were investigated in rats. mCPP apparently reduced 2-DG-induced hyperphagia. Suppressive effects of mCPP on hyperphagia induced by 2-DG were inhibited by the 5-HT2A/2B/2C receptor antagonist, ritanserin, although the 5-HT2A receptor antagonist ketanserin was without effect. Thus, inhibitory effects of mCPP on 2-DG-induced hyperphagia are mediated by the 5-HT2C/2B receptor. Our results demonstrate that mCPP can inhibit the bulimia model, 2-DG-induced hyperphagia.

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