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• W2064697632 abstract "The 5-HT1A agonist, 8-hydroxy-2-(di-n-propylamino) tetralin (8-OH-DPAT) at dose of 1 mg/kg s.c. increased food intake in free feeding rats. 8-OH-DPAT-induced feeding was blocked by metergoline which has comparable affinity for 5-HT1A, 5-HT1B, 5-HT1C and 5-HT2 receptors. This is consistent with the hyperphagia being mediated by an action at 5-HT receptors. Evidence against the involvement of 5-HT2 or 5-HT3 receptors was provided by the lack of effect of methysergide, ketanserin, MDL 72222 and ICS 205930 on the feeding response. Blockade of the hyperphagia by (−)- but not (+)pendolol which stereoselectively interacts with 5-HT1 receptors indicated an involvement of this receptor type. The lack of effect of ketanserin suggest that the 5-HT1C site is not involved as it has high affinity for both 5-HT2 and 5-HT1C receptors. Blockade of the hyperphagia by spiperone suggest mediation by 5-HT1A rather than 5-HT1B receptors. Although spiperone also blocks dopamine and α2-adrenoreceptors, involvement of these sites is unlikely as neither the DA antagonist haloperidol nor the α2-adrenoceptor antagonist idazoxan blocked 8-OH-DPAT-included feeding. These results indicate that 8-OH-DPAT-induced feeding is mediated by 5-HT1A receptors." @default.
• W2064697632 created "2016-06-24" @default.
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• W2064697632 date "1988-06-01" @default.
• W2064697632 modified "2023-10-18" @default.
• W2064697632 title "Evidence that the hyperphagic response to 8-OH-DPAT is mediated by 5-HT1A receptors" @default.
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• W2064697632 doi "https://doi.org/10.1016/0014-2999(88)90019-2" @default.
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