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大鼠α2巨球蛋白是大鼠离体肺中抗原诱导白三烯的选择性抑制剂。

Rat alpha 2 macroglobulin is a selective inhibitor of antigen-induced leucotrienes in rat isolated lungs.

作者信息

Ufkes J G, Ottenhof M, van Rooij H H, van Gool J

机构信息

Department of Pharmacology, University of Amsterdam, The Netherlands.

出版信息

Br J Exp Pathol. 1988 Aug;69(4):457-64.

Abstract

Exogenously administered, purified rat alpha 2 macroglobulin (alpha 2M, recognized as an acute phase reactant with anti-inflammatory properties) greatly inhibits the increase of the pulmonary resistance during the antigen-induced bronchoconstriction in rats in vivo, whereas a BaSO4 pretreatment (a method to induce a broad spectrum of serum acute phase reactants, including alpha 2M) covers a broader bronchoprotection: suppression of the decrease of the dynamic lung compliance as well. To explain these differences we studied the influence of both alpha 2M and BaSO4 on the antigen-induced bronchoconstriction in rat isolated lungs in relation to the mediator release in lung-effluents. We report here that in this model alpha 2M only inhibits the antigen-induced SRS-A release, whereas the concomitant release of histamine and 5-HT was unaffected. As distinct from alpha 2M the BaSO4 pretreatment suppressed both the antigen-induced bronchoconstriction and the histamine, 5-HT and SRS-A release to a high extent. These data suggest that alpha 2M can be considered as a selective inhibitor of leucotrienes, which offers an explanation for several anti-inflammatory properties of alpha 2M, including protection against the antigen-induced increase of the pulmonary resistance in vivo.

摘要

外源性给予纯化的大鼠α2巨球蛋白(α2M,被认为是一种具有抗炎特性的急性期反应物)能显著抑制大鼠体内抗原诱导的支气管收缩过程中肺阻力的增加,而硫酸钡预处理(一种诱导包括α2M在内的多种血清急性期反应物的方法)具有更广泛的支气管保护作用:还能抑制动态肺顺应性的降低。为了解释这些差异,我们研究了α2M和硫酸钡对大鼠离体肺中抗原诱导的支气管收缩的影响,并将其与肺灌流液中的介质释放相关联。我们在此报告,在该模型中,α2M仅抑制抗原诱导的慢反应物质A(SRS - A)释放,而组胺和5 - 羟色胺(5 - HT)的伴随释放未受影响。与α2M不同,硫酸钡预处理在很大程度上抑制了抗原诱导的支气管收缩以及组胺、5 - HT和SRS - A的释放。这些数据表明,α2M可被视为白三烯的选择性抑制剂,这为α2M的多种抗炎特性提供了解释,包括对体内抗原诱导的肺阻力增加的保护作用。

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