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蛇毒神经毒素对递质释放的促进作用。

Facilitation of transmitter release by neurotoxins from snake venoms.

作者信息

Harvey A L, Anderson A J, Karlsson E

出版信息

J Physiol (Paris). 1984;79(4):222-7.

PMID:6152291
Abstract

Toxins C13S1C3 and C13S2C3 from green mamba venom (Dendroaspis angusticeps) acted like dendrotoxin to increase acetylcholine release in response to nerve stimulation in the chick biventer cervicis preparation. Proteins B and E from black mamba venom (Dendroaspis polylepis) had no prejunctional facilitatory activity. All four proteins are trypsin inhibitor homologues. Binding of a prejunctional facilitatory toxin (Polylepis toxin I) to motor nerves was rapid and did not require the presence of Ca2+ or nerve stimulation. Binding was not prevented by protease inhibitors that lacked facilitatory actions. Prejunctional facilitatory toxins also augmented transmitter release in the chick oesophagus and the mouse vas deferens preparations. The effects were rapid in onset and could wane spontaneously. 125I-labelled dendrotoxin bound specifically to rat brain synaptosomes with a KD of about 3 nM. Binding was prevented by native dendrotoxin but not by beta-bungarotoxin or atropine. It is concluded that prejunctional facilitatory toxins affect transmitter release at many types of nerve endings in addition to motor nerve terminals. From consideration of the structures of active and inactive molecules, it is thought that binding of the active toxins may involve several exposed lysine residues.

摘要

绿曼巴蛇毒(黑树眼镜蛇)中的毒素C13S1C3和C13S2C3的作用类似于树突毒素,在鸡双腹肌标本中,能增加神经刺激后乙酰胆碱的释放。黑曼巴蛇毒(黑树眼镜蛇)中的蛋白质B和E没有突触前促进活性。这四种蛋白质均为胰蛋白酶抑制剂同源物。突触前促进毒素(多鳞树眼镜蛇毒素I)与运动神经的结合迅速,且不需要Ca2+的存在或神经刺激。缺乏促进作用的蛋白酶抑制剂不能阻止其结合。突触前促进毒素还能增强鸡食管和小鼠输精管标本中的递质释放。其作用起效迅速,且可自发减弱。125I标记的树突毒素以约3 nM的解离常数特异性结合大鼠脑突触体。天然树突毒素可阻止其结合,但β-银环蛇毒素或阿托品则不能。结论是,除运动神经末梢外,突触前促进毒素还会影响多种类型神经末梢的递质释放。从活性和非活性分子的结构考虑,认为活性毒素的结合可能涉及几个暴露的赖氨酸残基。

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