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降钙素基因相关肽调节酸介导的大鼠胃窦生长抑素和胃泌素释放的调控。

Calcitonin gene-related peptide modulates acid-mediated regulation of somatostatin and gastrin release from rat antrum.

作者信息

Manela F D, Ren J, Gao J, McGuigan J E, Harty R F

机构信息

Department of Internal Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, USA.

出版信息

Gastroenterology. 1995 Sep;109(3):701-6. doi: 10.1016/0016-5085(95)90376-3.

Abstract

BACKGROUND & AIMS: Acid has been shown to stimulate calcitonin gene-related peptide (CGRP) release from peripheral sensory afferent nerve endings in the stomach. The aim of this study was to determine whether endogenous CGRP was involved, by a neurocrine mechanism, in acid-mediated stimulation of somatostatin and inhibition of gastrin release.

METHODS

A two-compartment sleeve of antral mucosal/submucosal tissue was perfused to determine sensory nerve and endocrine cell responses to luminal acid. CGRP receptor antagonist, CGRP8-37, was used to inhibit the actions of endogenously released CGRP.

RESULTS

Perfusion of the antral sleeve lumen with media of increasing hydrogen ion concentration caused pH-dependent increases in CGRP and somatostatin release and decrease in gastrin release. CGRP8-37 inhibited significantly basal somatostatin (-36%) and stimulated basal gastrin (+65%) release (P < 0.02). Furthermore, CGRP8-37 administration prevented luminal acid-mediated inhibition of gastrin release and stimulation of somatostatin release. These results indicate that CGRP8-37 prevented acid-mediated feedback inhibition of gastrin release and acid-induced feedforward somatostatin release.

CONCLUSION

These results suggest that CGRP plays an important role in the response of antral D and G cells to luminal acid and that local effector action of endogenous CGRP participates in regulation of antral regulatory peptide secretion.

摘要

背景与目的

酸已被证明可刺激胃外周感觉传入神经末梢释放降钙素基因相关肽(CGRP)。本研究的目的是确定内源性CGRP是否通过神经分泌机制参与酸介导的生长抑素刺激和胃泌素释放抑制。

方法

对胃窦黏膜/黏膜下组织的双室套管进行灌注,以确定感觉神经和内分泌细胞对腔内酸的反应。使用CGRP受体拮抗剂CGRP8 - 37抑制内源性释放的CGRP的作用。

结果

用氢离子浓度不断增加的培养基灌注胃窦套管腔,导致CGRP和生长抑素释放呈pH依赖性增加,胃泌素释放减少。CGRP8 - 37显著抑制基础生长抑素释放(-36%),并刺激基础胃泌素释放(+65%)(P < 0.02)。此外,给予CGRP8 - 37可防止腔内酸介导的胃泌素释放抑制和生长抑素释放刺激。这些结果表明,CGRP8 - 37可防止酸介导的胃泌素释放反馈抑制和酸诱导的生长抑素前馈释放。

结论

这些结果表明,CGRP在胃窦D细胞和G细胞对腔内酸的反应中起重要作用,内源性CGRP的局部效应作用参与胃窦调节肽分泌的调节。

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