孔健强, 吴秀荣. 金环蛇(Bungarus fasciatus)蛇毒的分离及其毒性组分的药理研究J. 药学学报, 1983, 18(2): 97-103.
引用本文: 孔健强, 吴秀荣. 金环蛇(Bungarus fasciatus)蛇毒的分离及其毒性组分的药理研究J. 药学学报, 1983, 18(2): 97-103.
KONG Jian-qiang, WU Xiu-rong. SEPARATION OF BUNGARUS FASCIATUS VENOM AND PRELIMINARY PHARMACOLOGICAL STUDIES OF ITS TOXIC COMPONENTSJ. Acta Pharmaceutica Sinica, 1983, 18(2): 97-103.
Citation: KONG Jian-qiang, WU Xiu-rong. SEPARATION OF BUNGARUS FASCIATUS VENOM AND PRELIMINARY PHARMACOLOGICAL STUDIES OF ITS TOXIC COMPONENTSJ. Acta Pharmaceutica Sinica, 1983, 18(2): 97-103.

金环蛇(Bungarus fasciatus)蛇毒的分离及其毒性组分的药理研究

SEPARATION OF BUNGARUS FASCIATUS VENOM AND PRELIMINARY PHARMACOLOGICAL STUDIES OF ITS TOXIC COMPONENTS

  • 摘要: 金环蛇毒用羧甲基纤维素柱层析分离出17个蛋白组分,其中5个组分是毒性较大的致死成分。在这5个组分中,Ⅺ、Ⅻ、ⅩⅤ是心脏毒,ⅩⅢ、ⅩⅣ是神经毒。心脏毒组分Ⅺ、ⅫⅩⅤ使离体大鼠心脏挛缩,心跳停止于收缩期;使小鸡离体颈二腹肌挛缩,最后致痉挛性麻痹;对兔眼结合膜有局部刺激作用,使结合膜充血水肿。组分ⅩⅤ还具有直接溶血作用。神经毒组分ⅩⅢ阻断大鼠、小鸡、青蛙神经肌肉标本的突触传递,标本对乙酰胆碱的反应消失,对直接刺激以及对高浓度氯化钾的反应无减少,神经末梢乙酰胆碱的释放最无显著改变;使蛙腹直肌乙酰胆碱量效曲线平行右移,新斯的明可以对抗这个作用。组分ⅩⅣ的作用与组分ⅩⅢ相似。实验提示,组分ⅩⅢ、ⅩⅣ是作用于终板后膜的神经毒。

     

    Abstract: The venom of Bungarus fasciatus was separated into seventeen fractions in a CM-cellulose column with ammonium acetate buffer by linear pH and ionic strength gradient elution. Fractions Ⅺ, Ⅻ and ⅩⅤ were shown to be cardiotoxic principles similar :to cobra card iotoxinand fraction ⅩⅢ and ⅩⅣ were neurotoxic principles which acted on the p ostsynaptics N-cholinergic receptors of the motor endplate.The cardiotoxic fractions were shown to produce systolic standstill ofthe isolated rat heart, to induce contracture of the baby chick biventer cervicis muscle and to produce local irritation on rabbit eyes. Fraction ⅩⅤ exhibited direct hemolytic activity on washed guinea pig erythrocytes.Fraction ⅩⅢ was shown, to be a neurotoxin on neuromuscular preparations. The twitch response of the skeletal muscle to indirect stimulation were progressively abolished in the baby chick biventer ceryicis muscle, the rat phrenic nerve diaphragm and the frog sartorium, muscle, while the responses to direct stimulation or to high K+ were not appreciably affected. The Ach release of the rat phrenic nerve ending was also unaffected. The response to Ach (even 10 times the initial) was completely abolished inthe chick biventer cervicis muscle. The Ach dose-response curve was shifted to the right and was antagonized by neostigmine. The blocking actions were partially reversible in frog sartorium muscle and rat phrenic nerve diaphragm after repeated washings with physiological solution. It is concluded that fraction ⅩⅢ is a neurotoxin which acts on postsynaptic cholinergic receptors of motor endplate to produce nondepolarization type neuromuscular block.

     

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