Suppr超能文献

某些自主神经药物对十二指肠平滑肌的作用。

Effects of some autonomic drugs on duodenal smooth muscle.

作者信息

Anuras S, Faulk D L, Christensen J

出版信息

Am J Physiol. 1979 Jan;236(1):E33-8. doi: 10.1152/ajpendo.1979.236.1.E33.

Abstract

Longitudinal muscle strips (LMS) and circular muscle strips (CMS), 2 mm wide and 1.5--2 cm long, from opossum duodenum were exposed to some autonomic agonists. The cholinergic agonists, acetylcholine, carbachol, methacholine, and bethanechol stimulated only tonic contractions in LMS and tonic followed by phasic contractions in CMS. These effects were abolished by atropine 10(-6) M. The ED50S of all cholinergic agonists for LMS were significantly lower than for CMS. Norepinephrine caused initial contraction (abolished by phenoxybenzamine, 10(-4) M), followed by relaxation (abolished by propranolol, 10(-5) M), and isopropylnorepinephrine caused relaxation (abolished by propranolol, 10(-5) M) in both layers. There were no differences in relative potencies for adrenergic agonists between the layers. Tetrodotoxin did not affect the response to adrenergic agonists. Thus, the potency of cholinergic agonists is greater in longitudinal than in circular muscle, and the layers respond differently to cholinergic agonists. The alpha-adrenergic receptors mediate contraction and beta-adrenergic receptors mediate relaxation on the duodenal smooth muscle.

摘要

从负鼠十二指肠获取宽2毫米、长1.5 - 2厘米的纵行肌条(LMS)和环行肌条(CMS),将其暴露于一些自主神经激动剂。胆碱能激动剂乙酰胆碱、卡巴胆碱、醋甲胆碱和氨甲酰甲胆碱仅刺激纵行肌条产生强直性收缩,而刺激环行肌条时则先产生强直性收缩,随后产生相性收缩。这些效应可被10^(-6) M的阿托品消除。所有胆碱能激动剂对纵行肌条的半数有效剂量(ED50)均显著低于对环行肌条的ED50。去甲肾上腺素引起初始收缩(可被10^(-4) M的酚苄明消除),随后松弛(可被10^(-5) M的普萘洛尔消除),而异丙肾上腺素在两层肌肉中均引起松弛(可被10^(-5) M的普萘洛尔消除)。两层肌肉对肾上腺素能激动剂的相对效价没有差异。河豚毒素不影响对肾上腺素能激动剂的反应。因此,胆碱能激动剂在纵行肌中的效力大于环行肌,且两层肌肉对胆碱能激动剂的反应不同。α - 肾上腺素能受体介导十二指肠平滑肌收缩,β - 肾上腺素能受体介导其松弛。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验