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Activation of 5-HT1C-receptors suppresses excessive wheel running induced by semi-starvation in the rat.

作者信息

Wilckens T, Schweiger U, Pirke K M

机构信息

Max Planck Institut für Psychiatrie, München, Federal Republic of Germany.

出版信息

Psychopharmacology (Berl). 1992;109(1-2):77-84. doi: 10.1007/BF02245483.

DOI:10.1007/BF02245483
PMID:1365675
Abstract

Male Wistar rats were housed in cages linked to running wheels and fed on a schedule designed to reduce their body weight by 20-30%. During this period of semi-starvation the rats increased their daily running wheel activity (RWA) by up to 30 km/day. RWA could be kept at this level provided that body weight was kept constant. Different serotonin receptor (5-HT) agonists and antagonists were tested for their effects on RWA and it was found that RWA could be suppressed only by agonists with high affinity for the 5-HT1C receptor (TFMPP, mCPP, DOI and quipazine). Serotonin receptor agonists, which do not pass the blood-brain barrier, and 5-HT itself had no effect on RWA. The inhibitory effect of the agonists on RWA was prevented by pretreatment with antagonists that also had high affinity for 5-HT1C receptors (mianserin, metergoline and mesulergine). From these results we conclude that semi-starvation-induced hyperactivity can be blocked by 5-HT1C agonists. Furthermore we suggest that the animal model presented in this study might be a useful tool for in vivo studies on selective 5-HT1C receptor activation.

摘要

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Evidence that mCPP may have behavioural effects mediated by central 5-HT1C receptors.有证据表明,mCPP可能具有由中枢5-羟色胺1C受体介导的行为效应。
Br J Pharmacol. 1988 May;94(1):137-47. doi: 10.1111/j.1476-5381.1988.tb11508.x.
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Molecular pharmacology and biology of 5-HT1C receptors.5-羟色胺1C受体的分子药理学与生物学
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Relative efficacies of piperazines at the phosphoinositide hydrolysis-linked serotonergic (5-HT-2 and 5-HT-1c) receptors.哌嗪类药物在磷酸肌醇水解相关的5-羟色胺能(5-HT-2和5-HT-1c)受体上的相对效能
J Pharmacol Exp Ther. 1987 Aug;242(2):552-7.