Suppr超能文献

[维拉帕米对大鼠脑突触体中Ca2+及Ca(2+)Mg(2+)-ATP酶活性的影响]

[Effect of verapamil on Ca2+ and Ca(2+) Mg(2+)-ATPase activity in rat brain synaptosomes].

作者信息

Dong Z, Xue C S

机构信息

Department of Biochemical Pharmacology, Chongqing University of Medical Sciences, China.

出版信息

Zhongguo Yao Li Xue Bao. 1994 Sep;15(5):452-5.

PMID:7717074
Abstract

To elicit the correlation between the adrenergic transmitter release and calmodulin (CaM), the effect of verapamil on the free Ca2+ concentration was measured with fluorescence analysis and Ca(2+) Mg(2+)-ATPase activity in rat synaptosomes were studied. When stimulated with high-K+ or norepinephrine, the concentration of free Ca2+ in rat synaptosome was increased by verapamil 10, 50, and 100 mumol.L-1. But the free Ca2+ concentration in the resting synaptosome was reduced by verapamil. The activity of Ca(2+) Mg(2+)-ATPase in synaptosome was remarkably inhibited by verapamil in a dose-dependent manner. These results support our hypothesis that CaM not only acts directly on the vesicles to enhance the transmitter release, but also acts on the activity of Ca(2+) Mg(2+)-ATPase to reduce the free Ca2+ in the cytosol, and indirectly inhibited the transmitter release.

摘要

为了探究肾上腺素能递质释放与钙调蛋白(CaM)之间的相关性,采用荧光分析法测定了维拉帕米对游离Ca2+浓度的影响,并研究了大鼠突触体中Ca(2+) Mg(2+)-ATP酶活性。当用高钾或去甲肾上腺素刺激时,维拉帕米10、50和100 μmol·L-1可使大鼠突触体中游离Ca2+浓度升高。但维拉帕米可降低静息突触体中的游离Ca2+浓度。维拉帕米以剂量依赖性方式显著抑制突触体中Ca(2+) Mg(2+)-ATP酶的活性。这些结果支持了我们的假设,即CaM不仅直接作用于囊泡以增强递质释放,还作用于Ca(2+) Mg(2+)-ATP酶的活性以降低胞质溶胶中的游离Ca2+,并间接抑制递质释放。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验