通过使用两种钙调素拮抗剂N-(氨基己基)-5-氯-1-萘磺酰胺和N-(6-氨基己基)-1-萘磺酰胺的不同作用,更清楚地证明了突触体中钙/钙调素依赖事件。

S Imai, M Onozuka
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引用次数: 0

摘要

1. 为了更清楚地证明钙/钙调素依赖事件,我们在大鼠大脑皮质突触体中使用32Pi研究了两种钙调素拮抗剂W-7和W-5对与钙内流相关的突触素I磷酸化和去甲肾上腺素释放的不同影响。2. 钙离子载体(A23187)对突触素I磷酸化和去甲肾上腺素释放的刺激作用被W-7显著降低,被W-5轻微降低;而强钙调素拮抗剂和弱钙调素拮抗剂对a23187刺激的突触体钙摄取均无影响。3.H-8预孵化能降低W-5和w -7对a23187刺激的突触素I磷酸化的抑制量,但不影响它们的抑制作用,也不影响离子载体刺激的去甲肾上腺素释放,从而表明W-5可能是两种钙调素拮抗剂非钙调素介导作用的适当对照。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clearer demonstration of calcium/calmodulin-dependent events in synaptosomes by use of the differential effects of two calmodulin antagonists, N-(aminohexyl)-5-chloro-1-naphthalenesulfonamide and N-(6-aminohexyl)-1-naphthalenesulfonamide.

1. In order to demonstrate more clearly calcium/calmodulin-dependent events, the differential effects of two calmodulin antagonists, W-7 and W-5, on synapsin I phosphorylation and norepinephrine release associated with calcium influx, were investigated using 32Pi in synaptosomes derived from rat cerebral cortex. 2. The calcium ionophore (A23187)-stimulatory effect on synapsin I phosphorylation and norepinephrine release was markedly reduced by W-7 and slightly reduced by W-5; whereas neither the strong nor the weak calmodulin antagonist had an effect on A23187-stimulated synaptosomal uptake of calcium. 3. Preincubation with H-8 reduced both W-5- and W-7-inhibited A23187-stimulated synapsin I phosphorylation by the same amount but did not affect their inhibitory effect nor the ionophore-stimulated norepinephrine release, thereby suggesting that W-5 may serve as an appropriate control for non-calmodulin-mediated effect of both calmodulin antagonists.

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