Myotoxicity and physiological effects of three Trimeresurus flavoviridis phospholipases A2.

Biochemistry international Pub Date : 1992-12-01
H Kihara, R Uchikawa, S Hattori, M Ohno
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Abstract

When basic proteins I and II from Trimeresurus flavoviridis (Habu snake) venom, which are Lys-49-phospholipase A2 (PLA2) with low activity, were injected intramuscularly into mice, myonecrosis was induced accompanied by a rapid increase of plasma creatine kinase level. This increase was about 2 times greater than that raised by highly active T. flavoviridis Asp-49-PLA2 which has been regarded as a myotoxic factor. Calcium-dependent depolarization of frog muscle fibers was observed with basic proteins I and II but not with Asp-49-PLA2. Indirect hemolysis of rat erythrocytes was induced by Asp-49-PLA2 but not by basic proteins I and II. Myotoxicity and depolarization effects appear to be not necessarily related to lipolytic activity of proteins although hemolytic effects is in parallel to lipolytic potency. Light microscopic observations of muscle preparations treated with three PLA2s showed similar histological changes, i.e., myolytic necrosis without hemorrhage and infiltration of polymorphonuclear cells. The structural and functional elements of PLA2s for eliciting myotoxicity are discussed.

三种黄病毒Trimeresurus磷脂酶A2的肌毒性和生理作用。
将黄毒Trimeresurus flavviridis (Habu)蛇毒碱性蛋白I和II,即低活性的lys -49-磷脂酶A2 (PLA2)注入小鼠肌肉后,引起小鼠肌坏死,血浆肌酸激酶水平迅速升高。这种增加是高度活跃的黄病毒T. Asp-49-PLA2所增加的2倍,后者被认为是一种肌毒因子。青蛙肌纤维的钙依赖性去极化与碱性蛋白I和II有关,而与Asp-49-PLA2无关。Asp-49-PLA2能诱导大鼠红细胞间接溶血,而碱性蛋白I和II不能。肌毒性和去极化效应似乎不一定与蛋白质的溶脂活性有关,尽管溶血作用与溶脂效力是平行的。光镜下观察三种PLA2s处理后的肌肉组织的组织学变化相似,即肌溶性坏死,无出血和多形核细胞浸润。本文讨论了PLA2s引发肌毒性的结构和功能因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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