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鸡和大鼠突触体中与氯化钾诱导的细胞内游离钙离子升高平台期相关的钙通道的药理学特性

Pharmacological characterisation of the calcium channels coupled to the plateau phase of KCl-induced intracellular free Ca2+ elevation in chicken and rat synaptosomes.

作者信息

Bowman D, Alexander S, Lodge D

机构信息

Lilly Research Centre, Windlesham, Surrey, U.K.

出版信息

Neuropharmacology. 1993 Nov;32(11):1195-202. doi: 10.1016/0028-3908(93)90013-s.

Abstract

The effect of various blockers of voltage operated calcium channels (VOCCs) was studied on the non-inactivating, plateau phase of KCl-induced intracellular free Ca2+ ([Ca2+]i) elevation in rat cortical and chicken forebrain synaptosomes. In chicken synaptosomes, omega-CgTx GVIA (0.1 nM to 1 microM) and omega-CgTx MVIIA (0.1 nM to 1 microM), both selective blockers of N-type Ca2+ channels, produced a concentration-dependent inhibition of the plateau phase of [Ca2+]i elevation. omega-CgTx GVIA (IC50 value 28 nM) was more potent than omega-CgTx MVIIA (IC50 value 78 nM), but at submaximal concentrations, took longer to reach its maximum effect (20 min for omega-CgTx GVIA; 10 min for omega-CgTx MVIIA). At 1 microM, the highest concentration tested, each toxin blocked > 85% of [Ca2+]i elevation. The effect of omega-CgTx GVIA on the extent and time-course of inhibition of [Ca2+]i elevation was maintained in a Na(+)-free, choline substituted, medium. omega-Aga IVA (300 nM), a selective blocker of P-type calcium channels, inhibited 28 +/- 5% of [Ca2+]i elevation. The effect of a combination of submaximal inhibitory concentrations of omega-CgTx GVIA (100 nM) and omega-Aga IVA (300 nM) was less than additive. In rat synaptosomes, omega-CgTx GVIA (1 microM) and omega-CgTx MVIIA (1 microM), blocked only 18 +/- 5% and 17 +/- 4% of the plateau phase of free Ca2+ elevation, respectively. omega-Aga IVA produced a concentration-dependent inhibition of [Ca2+]i elevation in this preparation. Threshold inhibition was observed at 1 nM, and maximum inhibition (64 +/- 8%) at 1 microM.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了多种电压门控钙通道(VOCCs)阻滞剂对大鼠皮层和鸡前脑突触体中氯化钾诱导的细胞内游离钙离子([Ca2+]i)升高的非失活平台期的影响。在鸡突触体中,ω-芋螺毒素GVIA(0.1 nM至1 μM)和ω-芋螺毒素MVIIA(0.1 nM至1 μM),这两种N型钙通道的选择性阻滞剂,对[Ca2+]i升高的平台期产生浓度依赖性抑制。ω-芋螺毒素GVIA(IC50值为28 nM)比ω-芋螺毒素MVIIA(IC50值为78 nM)更有效,但在亚最大浓度时,达到最大效应所需时间更长(ω-芋螺毒素GVIA为20分钟;ω-芋螺毒素MVIIA为10分钟)。在1 μM(测试的最高浓度)时,每种毒素阻断了>85%的[Ca2+]i升高。在无钠、胆碱替代的培养基中,ω-芋螺毒素GVIA对[Ca2+]i升高抑制程度和时间进程的影响得以维持。ω-阿加毒素IVA(300 nM),一种P型钙通道的选择性阻滞剂,抑制了28±5%的[Ca2+]i升高。亚最大抑制浓度的ω-芋螺毒素GVIA(100 nM)和ω-阿加毒素IVA(300 nM)联合使用的效果小于两者相加。在大鼠突触体中,ω-芋螺毒素GVIA(1 μM)和ω-芋螺毒素MVIIA(1 μM)分别仅阻断了游离钙离子升高平台期的18±5%和17±4%。ω-阿加毒素IVA在该制剂中对[Ca2+]i升高产生浓度依赖性抑制。在1 nM时观察到阈值抑制,在1 μM时达到最大抑制(64±8%)。(摘要截短于250字)

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