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切断迷走神经可增强外周给予5-羟色胺的食欲抑制作用。

The anorectic action of peripherally administered 5-HT is enhanced by vagotomy.

作者信息

Fletcher P J, Burton M J

出版信息

Physiol Behav. 1985 Jun;34(6):861-6. doi: 10.1016/0031-9384(85)90004-6.

Abstract

Peripherally administered 5-HT produced a greater suppression of food intake in rats with subdiaphragmatic vagotomy than in sham-operated controls. The enhanced anorexia to 5-HT in vagotomised rats and the anorexia in sham-operated controls were reversed by methysergide, indicating the involvement of 5-HT receptors in the observed anorexia in both groups of animals. Thus the increased suppression of food intake in vagotomised rats cannot be explained in terms of non-specific effects of 5-HT. Both vagotomised and sham-operated rats showed an equivalent degree of anorexia when treated with fenfluramine suggesting that the receptor mechanism responsible for the anorectic action of 5-HT plays little or no part in the action of fenfluramine. Systemic administration of 5-HT was found to slow the rate of gastric clearance. Unlike the anorexia induced by 5-HT this effect was not reversed by methysergide. Thus it appears that peripherally administered 5-HT interacts with the vagus nerve but the mechanism responsible for 5-HT anorexia is independent of any action on gastric clearance.

摘要

与假手术对照组相比,外周给予5-羟色胺(5-HT)对膈下迷走神经切断术大鼠的食物摄入量产生了更大的抑制作用。麦角新碱可逆转迷走神经切断术大鼠对5-HT增强的厌食反应以及假手术对照组的厌食反应,这表明5-HT受体参与了两组动物所观察到的厌食反应。因此,迷走神经切断术大鼠食物摄入量抑制作用的增强不能用5-HT的非特异性作用来解释。用芬氟拉明治疗时,迷走神经切断术大鼠和假手术对照组均表现出同等程度的厌食,这表明负责5-HT厌食作用的受体机制在芬氟拉明的作用中几乎不起作用或不起作用。发现全身给予5-HT可减慢胃排空速率。与5-HT诱导的厌食不同,这种作用不能被麦角新碱逆转。因此,似乎外周给予的5-HT与迷走神经相互作用,但5-HT厌食的机制独立于对胃排空的任何作用。

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