Khan M M, Shibuya Y, Kambara T, Yamamoto T
Department of Neuroscience and Immunology, Graduate School of Medical Sciences, Kumamoto University, Japan.
Int J Exp Pathol. 1995 Feb;76(1):21-8.
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.
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。