羟色胺受体激动剂喹帕嗪对大鼠血清皮质酮浓度的影响。

R W Fuller, H D Snoddy, J A Clemens
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引用次数: 40

摘要

羟色胺受体激动剂喹帕嗪在大鼠腹腔注射后30分钟内(剂量为10 mg/kg)血清皮质酮升高;效果在1和2小时持续存在,但在4小时不存在。1.25 mg/kg剂量的喹帕嗪没有升高血清皮质酮,但在2.5-20 mg/kg剂量范围内与剂量相关。羟色胺受体拮抗剂甲基高林完全阻止了喹帕嗪的作用。在用5,7-二羟色胺预处理的大鼠中,喹帕嗪存在破坏血清素神经的作用,氟西汀预处理不增强(如l -5-羟色胺的作用)。这些数据与喹帕嗪增加血清皮质酮是直接刺激大脑中血清羟色胺受体的结果的观点是一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of quipazine, a serotonin receptor agonist, on serum corticosterone concentration in rats.

Quipazine, a serotonin receptor agonist, increased serum corticosterone within 30 min after its i.p. injection (at 10 mg/kg) into rats; the effect persisted at 1 and 2 hrs, but not at 4 hrs. Elevation of serum corticosterone did not occur with a 1.25 mg/kg dose of quipazine but was dose-related over a 2.5-20 mg/kg dose range. The effect of quipazine was completely prevented by methergoline, a serotonin receptor antagonist. The effect of quipazine was present in rats pretreated with 5,7-dihydroxytryptamine to destroy serotonin nerves and was not enhanced (as was the effect of L-5-hydroxytryptophan) by fluoxetine pretreatment. These data are compatible with the idea that quipazine increases serum corticosterone as a consequence of direct stimulation of serotonin receptors in brain.

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