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从冬绿树中分离出的倍半萜多香木萜在豚鼠回肠和气管中的“体外”作用

Action of polygodial, a sesquiterpene isolated from Drymis winteri, in the guinea-pig ileum and trachea 'in vitro'.

作者信息

El Sayah M, Cechinel Filho V, Yunes R A, Pinheiro T R, Calixto J B

机构信息

Department of Pharmacology, Universidade Federal de Santa Catarina, Florianópolis, Brazil.

出版信息

Eur J Pharmacol. 1998 Mar 5;344(2-3):215-21. doi: 10.1016/s0014-2999(97)01570-7.

Abstract

This study describes the action of the sesquiterpene polygodial, the major constituent isolated from the bark of Drymis winteri in the guinea pig ileum and trachea in vitro. Polygodial (5 to 128 microM), added for 20 min, did not affect the resting tone of the preparations, but caused graded inhibition, associated in some cases with rightward displacement of the acetylcholine, histamine (1 nM to 10 microM), bradykinin (0.1 nM to 1 microM) and KCl (1 to 100 mM)-contraction response curves. When assessed in the guinea-pig trachea, polygodial (5 to 342 microM) caused significant inhibition of bradykinin (10 pM to 1 microM), 9,11-dideoxy-9alpha,11alpha-methano-epoxy prostaglandin F2alpha (0.1 to 1000 nM) and KCl (1 to 100 mM)-induced contractions, although the action against bradykinin was not concentration-dependent. Polygodial (5 to 80 microM) caused a small but significant shift to the right of substance P and also the selective agonist of tachykinin NK2 receptor [beta-Ala8]neurokinin A-(4-10)-induced contractions in guinea pig trachea. This action of polygodial seems to be quite selective towards tachykinin NK2 receptors since up to 432 microM, polygodial had no effect against contraction caused by tachykinin NK1 receptor agonist, substance P methyl ester. When tested in the guinea-pig trachea from animals which had been actively sensitised to ovalbumin, polygodial (30 to 40 microM) caused time and concentration-dependent inhibition of ovalbumin-mediated contraction. In addition, polygodial (85 to 342 microM) inhibited contraction induced by compound 48/80 (1 to 1000 microg/ml), in the guinea-pig trachea from non-sensitised animals. These findings and those from our previous study are consistent with the notion that the main sesquiterpene polygodial isolated from the bark of D. winteri is responsible for most, if not all, of the relevant pharmacological action reported previously for the extract of this plant. Thus, polygodial could be of potential value in the development of a new drug for the treatment of asthma, allergy and other inflammatory processes.

摘要

本研究描述了从智利铁木树皮中分离出的主要成分倍半萜多香木萜在豚鼠回肠和气管中的体外作用。添加20分钟的多香木萜(5至128微摩尔)不影响标本的静息张力,但会引起分级抑制,在某些情况下与乙酰胆碱、组胺(1纳摩尔至10微摩尔)、缓激肽(0.1纳摩尔至1微摩尔)和氯化钾(1至100毫摩尔)收缩反应曲线的右移相关。在豚鼠气管中评估时,多香木萜(5至342微摩尔)可显著抑制缓激肽(10皮摩尔至1微摩尔)、9,11 - 二脱氧 - 9α,11α - 亚甲基 - 环氧前列腺素F2α(0.1至1000纳摩尔)和氯化钾(1至100毫摩尔)诱导的收缩,尽管对缓激肽的作用不具有浓度依赖性。多香木萜(5至80微摩尔)可使P物质以及速激肽NK2受体的选择性激动剂[β - 丙氨酸8]神经激肽A -(4 - 10)诱导的豚鼠气管收缩轻微但显著右移。多香木萜的这种作用似乎对速激肽NK2受体具有相当的选择性,因为高达4

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