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大鼠主动脉对各种激动剂的收缩机制。

The mechanism of contraction of rat aorta to various agonists.

作者信息

Krishnamurty V S, Grollman A

出版信息

Arch Int Pharmacodyn Ther. 1976 Apr;220(2):180-8.

PMID:952579
Abstract

To elucidate the mechanism of contraction of the smooth muscle of the rat's aorta, its response to norepinephrine (NE), 5-hydroxytrypatamine (5-HT) and potassium chloride (KCI) was determined before and after pretreatment with reserpine and beta-diethylamionethyl 2-2-diphenylpropyl acetate (SKF 525-A). Unlike the rabbit's aorta, contraction of the rat's aorta induced by NE was inhibited by SKF 525-A. After the induction of maximal contraction, SKF 525-A induced a graded rapid relaxation after KCl, less so after 5-HT, and least after NE. Pretreatment with reserpine failed to induce supersensitivity to NE. After incubation in a Ca++-free or Na+ and Ca++-free Krebs solution, the rat's aorta failed to contract even on the addition of Ca++ or NE.

摘要

为阐明大鼠主动脉平滑肌的收缩机制,在利血平和β - 二乙胺基乙基2,2 - 二苯基丙酸乙酯(SKF 525 - A)预处理前后,测定了其对去甲肾上腺素(NE)、5 - 羟色胺(5 - HT)和氯化钾(KCl)的反应。与兔主动脉不同,SKF 525 - A可抑制NE诱导的大鼠主动脉收缩。在诱导最大收缩后,SKF 525 - A可使KCl后出现分级快速舒张,5 - HT后舒张程度较小,NE后舒张程度最小。利血平预处理未能诱导对NE的超敏反应。在无钙或无钠和钙的 Krebs 溶液中孵育后,即使加入钙或NE,大鼠主动脉也无法收缩。

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