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速激肽:对胃部的局部作用及脑干反应。

Tachykinins: local gastric effects and brain stem responses.

作者信息

Barber W D, Stevenson G D, Burks T F

出版信息

Am J Physiol. 1987 Mar;252(3 Pt 1):G365-73. doi: 10.1152/ajpgi.1987.252.3.G365.

Abstract

The gastric motor or mechanical effects of a group of peptides, the tachykinins, were evaluated in anesthetized cats to determine the relationship between local motor events and brain stem neurons that regulate gastric activity. The peptides evaluated were substance P, physalaemin, and eledoisin. The tachykinin-induced gastric changes were dose related and were characterized by initial distention-sustained contraction-late distention phases. At lower doses distention was the dominant effect with a sustained contraction-late distention response appearing as the dose increased. The sustained contraction-late distention phases were frequently accompanied by phasic contractions with a frequency of 2-4/min. Atropine had a significant effect on the sustained contraction phase but no effect on the phasic contractions or distention phases. Bilateral cervical vagotomy had a significant effect on the early distention phase, suggesting a link with brain stem mechanisms. The activity of brain stem units that responded to phasic distention of the stomach reflected the tachykinin-induced changes in gastric distention. Although the gastric effects of these tachykinins shared distinct similarities, certain differences in the time sequence of the distention-contraction interactions suggests the possibility that dissimilar receptor types may be involved in the mechanisms of action. Their mechanisms of action may also involve a direct effect on the effector organ.

摘要

为了确定局部运动事件与调节胃活动的脑干神经元之间的关系,研究人员在麻醉猫身上评估了一组肽类(速激肽)对胃运动或机械作用的影响。所评估的肽类包括P物质、雨蛙肽和eledoisin。速激肽引起的胃部变化与剂量相关,其特征为初始扩张-持续收缩-后期扩张阶段。在较低剂量时,扩张是主要效应,随着剂量增加,会出现持续收缩-后期扩张反应。持续收缩-后期扩张阶段常伴有频率为2-4次/分钟的节律性收缩。阿托品对持续收缩阶段有显著影响,但对节律性收缩或扩张阶段无影响。双侧颈迷走神经切断术对早期扩张阶段有显著影响,表明与脑干机制存在联系。对胃的节律性扩张有反应的脑干神经元的活动反映了速激肽引起的胃部扩张变化。尽管这些速激肽的胃效应有明显相似之处,但扩张-收缩相互作用的时间顺序存在某些差异,这表明可能涉及不同类型的受体参与作用机制。它们的作用机制也可能涉及对效应器官的直接影响。

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