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细菌内毒素对去精氨酸9-缓激肽心血管反应的选择性诱导。

Selective induction of cardiovascular responses to des-Arg9-bradykinin by bacterial endotoxin.

作者信息

Marceau F, Lussier A, St-Pierre S

出版信息

Pharmacology. 1984;29(2):70-4. doi: 10.1159/000137994.

Abstract

Bacterial lipopolysaccharide (LPS) induces in 5 h a hypotensive response mediated by the B1-receptor for kinins in the rabbit, an effect which is not observed in untreated animals. The present study is intended to evaluate the capacity of other acute toxic treatments to induce such a response and to analyze the mechanism of induction. Intravenous injections of inulin (20 mg), Naja venom (50 micrograms), compound 48/80 (1 mg), and etiocholanolone (6 mg) failed to induce hypotensive response to des-Arg9-bradykinin (the selective agonist of the B1-receptor) in 5 h. LPS from Salmonella (100 micrograms) and E. coli (10 micrograms) were highly effective, whereas trypsin (2 mg) gave doubtful responses. White blood cell counts revealed a profound and rapid neutropenic effect of the 2 LPS and a less marked one for trypsin. It is concluded that (1) LPS is a selective inducer of a new cardiovascular response to kinins mediated by the B1-receptor, and (2) that the mechanism of induction may include an intimate interaction between neutrophil leukocytes and blood vessel walls.

摘要

细菌脂多糖(LPS)在5小时内可诱导家兔产生一种由缓激肽B1受体介导的降压反应,未处理的动物未观察到这种效应。本研究旨在评估其他急性毒性处理诱导这种反应的能力,并分析诱导机制。静脉注射菊粉(20毫克)、眼镜蛇毒(50微克)、化合物48/80(1毫克)和表雄酮(6毫克)在5小时内未能诱导对去精氨酸9-缓激肽(B1受体的选择性激动剂)的降压反应。来自沙门氏菌(100微克)和大肠杆菌(10微克)的LPS非常有效,而胰蛋白酶(2毫克)的反应则不确定。白细胞计数显示,两种LPS均有显著且迅速的中性粒细胞减少作用,胰蛋白酶的作用则不太明显。结论是:(1)LPS是由B1受体介导的对缓激肽新的心血管反应的选择性诱导剂;(2)诱导机制可能包括中性粒细胞与血管壁之间的密切相互作用。

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