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浸水束缚应激大鼠结肠黏膜下 5-HT(3)受体介导的生长抑素依赖性分泌抑制途径被抑制。

Colonic submucosal 5-HT(3) receptor-mediated somatostatin-dependent secretoinhibitory pathway is suppressed in water-immersion restraint stressed rats.

机构信息

Department of Physiology, School of Basic Medical Sciences, Capital Medical University, Beijing (100069), PR China.

出版信息

Eur J Pharmacol. 2011 Apr 10;656(1-3):94-100. doi: 10.1016/j.ejphar.2011.01.026. Epub 2011 Feb 1.

Abstract

We have demonstrated that the activation of 5-hydroxytryptamine (5-HT) receptor 3 in the submucosal plexus suppresses 5-HT-induced colonic ion secretion by increasing submucosal somatostatin release. A number of psychological and physical stresses have impacts on the intestinal mucosal functions, including secretion and the epithelial barrier. Whether the 5-HT(3) receptor-mediated somatostatin-dependent secretoinhibitory pathway in the rat distal colon is involved in the stress process is still unknown. The present study aims to investigate the effect of the water-immersion restraint stress on this inhibitory pathway and its underlying mechanisms. Mucosa/submucosa preparations from the rat distal colon were mounted in the Ussing chambers for the measurement of short-circuit current (I(SC)). Real-time PCR and western blot were performed to study the expression of the 5-HT(3) receptor, 5-HT(4) receptor, and somatostatin receptor 2. Radioimmunoassay was used to measure somatostatin release. After 2h of water-immersion restraint stress, the membrane resistance (Rte) of rat mucosa/submucosa preparations was significantly decreased, but the baseline I(SC) and 5-HT-induced I(SC) responses were significantly increased. The protein expression of the submucosal 5-HT(3) receptors and mucosal somatostatin receptor 2 were down-regulated, and the 5-HT-induced somatostatin release from the mucosa/submucosa preparations was significantly reduced in the stress group. Taken together, these results suggest that the 5-HT(3) receptor-mediated somatostatin-dependent secretoinhibitory pathway is suppressed in the water-immersion restraint stressed rats, which may contribute to the acute stress-induced increase in colonic secretion.

摘要

我们已经证明,激活黏膜下神经丛中的 5-羟色胺(5-HT)受体 3 可以通过增加黏膜下生长抑素的释放来抑制 5-HT 诱导的结肠离子分泌。许多心理和身体应激都会对肠道黏膜功能产生影响,包括分泌和上皮屏障。5-HT(3)受体介导的生长抑素依赖性分泌抑制途径在大鼠远端结肠中是否参与应激过程尚不清楚。本研究旨在探讨水浸束缚应激对该抑制途径及其潜在机制的影响。大鼠远端结肠黏膜/黏膜下层标本置于 Ussing 室中,用于测量短路电流(I(SC))。实时 PCR 和 Western blot 用于研究 5-HT(3)受体、5-HT(4)受体和生长抑素受体 2 的表达。放射免疫测定用于测量生长抑素释放。水浸束缚应激 2 小时后,大鼠黏膜/黏膜下层标本的膜电阻(Rte)明显降低,但基础 I(SC)和 5-HT 诱导的 I(SC)反应明显增加。黏膜下层 5-HT(3)受体和黏膜生长抑素受体 2 的蛋白表达下调,应激组 5-HT 诱导的黏膜/黏膜下层标本中生长抑素释放明显减少。综上所述,这些结果表明,水浸束缚应激大鼠中 5-HT(3)受体介导的生长抑素依赖性分泌抑制途径被抑制,这可能导致急性应激引起的结肠分泌增加。

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