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突触前活性神经毒素α-拉托毒素与ω-芋螺毒素GVIA之间的相互作用:对大鼠和鸡突触体中钙通量及结合参数的研究

Interactions between the presynaptically active neurotoxins alpha-latrotoxin and omega-conotoxin GVIA: studies on calcium fluxes and binding parameters in rat and chicken synaptosomes.

作者信息

Scheer H W

机构信息

Department of Pharmacology, University of Montréal, Qué., Canada.

出版信息

Can J Physiol Pharmacol. 1990 Aug;68(8):1049-54. doi: 10.1139/y90-158.

Abstract

Possible interactions between alpha-latrotoxin, an activator of synaptosomal calcium uptake, and omega-conotoxin GVIA, an inhibitor of voltage-sensitive calcium channels of the N-type, were investigated in rat and chicken synaptosomal preparations. While omega-conotoxin GVIA potently and effectively inhibited calcium uptake induced by elevated potassium in chick synaptosomes, little or no effect of omega-conotoxin GVIA was observed either in potassium-treated rat synaptosomes or in alpha-latrotoxin-exposed synaptosomes of either spaces. In contrast to the lack of effect of omega-conotoxin on stimulated calcium uptake in rat synaptosomes, cadmium effectively inhibited calcium uptake induced by either potassium or alpha-latrotoxin. Synaptosomal calcium transport induced by alpha-latrotoxin can be bidirectional, since alpha-latrotoxin also induced efflux of preaccumulated calcium. Competition experiments revealed that binding of 125I-labelled omega-conotoxin and 125I-labelled alpha-latrotoxin was similar in either chicken or rat synaptosomes. Neither alpha-latrotoxin nor omega-conotoxin competed with the binding of the other ligand in either species. The results reported here show that (1) elevated potassium evokes calcium uptake principally through N-channels in avian but not in rat synaptosomes; (2) alpha-latrotoxin-activated calcium fluxes are omega-conotoxin insensitive but cadmium sensitive; (3) the molecular acceptors for the two ligands are likely to be unrelated synaptic membrane constituents.

摘要

在大鼠和鸡的突触体标本中,研究了突触体钙摄取激活剂α-拉毒素与N型电压敏感性钙通道抑制剂ω-芋螺毒素GVIA之间可能的相互作用。虽然ω-芋螺毒素GVIA能有效且有力地抑制鸡突触体中高钾诱导的钙摄取,但在经钾处理的大鼠突触体或任一部位经α-拉毒素处理的突触体中,未观察到ω-芋螺毒素GVIA有明显作用。与ω-芋螺毒素对大鼠突触体中刺激的钙摄取缺乏作用相反,镉能有效抑制钾或α-拉毒素诱导的钙摄取。α-拉毒素诱导的突触体钙转运可以是双向的,因为α-拉毒素也能诱导预积累钙的外流。竞争实验表明,在鸡或大鼠突触体中,125I标记的ω-芋螺毒素和125I标记的α-拉毒素的结合情况相似。在这两个物种中,α-拉毒素和ω-芋螺毒素都不会与另一种配体的结合相互竞争。此处报道的结果表明:(1)高钾主要通过禽类而非大鼠突触体中的N通道引发钙摄取;(2)α-拉毒素激活的钙通量对ω-芋螺毒素不敏感,但对镉敏感;(3)这两种配体的分子受体可能是不相关的突触膜成分。

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