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蜘蛛毒素ω-Aga-IVA可阻断递质释放和突触前Ca2+电流。

Transmitter release and presynaptic Ca2+ currents blocked by the spider toxin omega-Aga-IVA.

作者信息

Protti D A, Uchitel O D

机构信息

Institute of Cell Biology, Faculty of Medicine, University of Buenos Aires, Argentina.

出版信息

Neuroreport. 1993 Dec 13;5(3):333-6. doi: 10.1097/00001756-199312000-00039.

DOI:10.1097/00001756-199312000-00039
PMID:7905295
Abstract

Mammalian neuromuscular transmission is resistant to L and N type calcium channel blockers but very sensitive to a low molecular weight funnel web spider venom toxin, FTX, which selectively blocks P type calcium channels. To further characterize the calcium channels involved in neuromuscular transmission we studied the effect of omega Agatoxin (omega-Aga-IVA) a polypeptide P type channel blocker from the same spider venom. We show that omega-Aga-IVA is a potent and irreversible inhibitor of the presynaptic Ca2+ currents and of acetylcholine release induced by electrical stimulation or by K+ depolarization. This provides further evidences that transmitter release at the mammalian neuromuscular junction is mediated by P type Ca2+ channels.

摘要

哺乳动物的神经肌肉传递对L型和N型钙通道阻滞剂具有抗性,但对一种低分子量漏斗网蜘蛛毒液毒素FTX非常敏感,FTX可选择性阻断P型钙通道。为了进一步表征参与神经肌肉传递的钙通道,我们研究了来自同一种蜘蛛毒液的多肽P型通道阻滞剂ω-阿加毒素(ω-Aga-IVA)的作用。我们发现ω-Aga-IVA是突触前Ca2+电流以及电刺激或K+去极化诱导的乙酰胆碱释放的强效且不可逆的抑制剂。这进一步证明,哺乳动物神经肌肉接头处的递质释放是由P型Ca2+通道介导的。

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