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矛头蝮(睫角棕榈蝮)肌毒素III(一种碱性磷脂酶A2)对脂质体和小鼠腓肠肌的影响。

Effects of Bothrops asper (terciopelo) myotoxin III, a basic phospholipase A2, on liposomes and mouse gastrocnemius muscle.

作者信息

Bultrón E, Gutiérrez J M, Thelestam M

机构信息

Departamento de Bioquímica, Facultad de Medicina, Universidad de Panamá.

出版信息

Toxicon. 1993 Feb;31(2):217-22. doi: 10.1016/0041-0101(93)90289-u.

Abstract

The action of Bothrops asper myotoxin III, a basic phospholipase A2 which induces acute muscle damage, was studied in mouse gastrocnemius muscle in vivo and in vitro and in multilamellar liposomes. Myonecrosis occurred rapidly after myotoxin injection, as indicated by histological alterations and by a drastic increment in plasma creatine kinase levels. A dose-dependent release of creatine kinase from mouse gastrocnemius muscle incubated in vitro with the toxin was observed. Myotoxin III affected negatively charged multilamellar liposomes, as evidenced by the release of peroxidase trapped in the vesicles. In contrast, very little effect was observed on positively charged vesicles. When gastrocnemius muscle or liposomes were incubated at 4 degrees C there was no membrane-disruptive effect. Inhibition of phospholipase A2 activity, by elimination of calcium and addition of EDTA, resulted in a significant, but not total, reduction in both muscle-damaging and liposomal disrupting effects. It is proposed that B. asper myotoxin III affects cellular and artificial membranes inducing prominent alterations in membrane permeability to ions and macromolecules. Membrane-disrupting activity is probably related to a molecular region different from the catalytic site, although enzymatic activity greatly enhances myotoxin action.

摘要

矛头蝮蛇肌毒素III是一种碱性磷脂酶A2,可导致急性肌肉损伤。本文对其在小鼠腓肠肌的体内、体外以及多层脂质体中的作用进行了研究。注射肌毒素后,组织学改变以及血浆肌酸激酶水平急剧升高表明,肌坏死迅速发生。在体外将毒素与小鼠腓肠肌一起孵育时,观察到肌酸激酶呈剂量依赖性释放。肌毒素III对带负电荷的多层脂质体有影响,囊泡中捕获的过氧化物酶释放证明了这一点。相比之下,对带正电荷的囊泡几乎没有影响。当腓肠肌或脂质体在4℃孵育时,没有膜破坏作用。通过去除钙并添加乙二胺四乙酸(EDTA)抑制磷脂酶A2活性,可使肌肉损伤和脂质体破坏作用显著但不完全降低。有人提出,矛头蝮蛇肌毒素III会影响细胞膜和人工膜,导致膜对离子和大分子的通透性发生显著改变。膜破坏活性可能与不同于催化位点的分子区域有关,尽管酶活性会大大增强肌毒素的作用。

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