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α-2-巨球蛋白和细菌弹性蛋白酶在豚鼠铜绿假单胞菌败血症性休克中的作用。

Role of alpha-2-macroglobulin and bacterial elastase in guinea-pig pseudomonal septic shock.

作者信息

Khan M M, Shibuya Y, Kambara T, Yamamoto T

机构信息

Department of Neuroscience and Immunology, Graduate School of Medical Sciences, Kumamoto University, Japan.

出版信息

Int J Exp Pathol. 1995 Feb;76(1):21-8.

Abstract

An essential role of alpha-2-macroglobulin (alpha 2M) was revealed in the prevention of septic shock induced in guinea-pigs by an elastase producing strain (IFO-3455) of Pseudomonas aeruginosa. When bacterial peritonitis was induced by inoculating fibrin-thrombin clot containing viable bacteria at a dose of 10(9) c.f.u./kg body weight, the guinea-pigs (n = 6) died within 7-8 hours due to septic shock. Prior to the shock, consumption of two-thirds of the circulating alpha 2M was observed. When circulating alpha 2M was depleted 4 hours after the bacterial inoculation, the guinea-pigs immediately developed shock and died within one hour. This shock was prevented either with a specific elastase inhibitor, HONHCOCH(CH2C6H5)CO-Ala-Gly-NH2, zincov (6 microM), or with human alpha 2M. Simultaneous depletion of circulating Hageman factor also prevented shock in the alpha 2M-depleted animals. These results indicate that septic shock was induced through activation of the Hageman factor dependent system by the bacteria-produced elastase which survived alpha 2M in the circulation.

摘要

α-2-巨球蛋白(α2M)在预防由铜绿假单胞菌产弹性蛋白酶菌株(IFO-3455)诱导的豚鼠败血症休克中发挥了重要作用。当以10(9) c.f.u./kg体重的剂量接种含有活菌的纤维蛋白-凝血酶凝块诱导细菌性腹膜炎时,豚鼠(n = 6)在7-8小时内死于败血症休克。在休克之前,观察到循环中的α2M消耗了三分之二。在细菌接种4小时后循环中的α2M被耗尽时,豚鼠立即发生休克并在1小时内死亡。用特异性弹性蛋白酶抑制剂HONHCOCH(CH2C6H5)CO-Ala-Gly-NH2(锌伏,6 microM)或人α2M可预防这种休克。同时消耗循环中的Hageman因子也可预防α2M耗尽动物的休克。这些结果表明,败血症休克是由细菌产生的弹性蛋白酶激活Hageman因子依赖性系统诱导的,该弹性蛋白酶在循环中可抵抗αM。

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