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组胺在补体肽C3a和C5a-去精氨酸(经典过敏毒素)致痉挛作用中的作用

Role of histamine in the spasmogenic effect of the complement peptides C3a and C5a-desArg (classical anaphylatoxin).

作者信息

Sorgenfrei J, Damerau B, Vogt W

出版信息

Agents Actions. 1982 Apr;12(1-2):118-21. doi: 10.1007/BF01965121.

Abstract

The role of endogenous histamine in the spasmogenic effect of the complement-derived peptides C3a and C5a-desArg (isolated from yeast-activated hog serum) was studied in strips of terminal guinea-pig ileum. The effect of C3a is apparently histamine-independent; it neither induces histamine release from the test organ nor is its spasmogenic action inhibited by the H1-antihistaminics pheniramine and triprolidine, used in concentrations effective against histamine. However, endogenous histamine may be involved in the spasmogenic effect of C5a-desArg; when applied repeatedly C5a-desArg induces histamine release during its first and second application. Furthermore, both H1-antihistaminics inhibited C5a-desArg-induced contractions considerably, though less efficiently than those of added histamine.

摘要

在内源性组胺在补体衍生肽C3a和C5a-去精氨酸(从酵母激活的猪血清中分离)的致痉挛作用中的作用研究中,使用豚鼠回肠末端条带进行了实验。C3a的作用显然不依赖组胺;它既不诱导受试器官释放组胺,其致痉挛作用也不受H1抗组胺药非尼拉敏和曲普利啶的抑制,这两种药物使用的浓度对组胺有效。然而,内源性组胺可能参与C5a-去精氨酸的致痉挛作用;当重复应用时,C5a-去精氨酸在首次和第二次应用时诱导组胺释放。此外,两种H1抗组胺药都能显著抑制C5a-去精氨酸诱导的收缩,尽管效果不如添加组胺的情况。

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