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穿孔膜片钳方法记录L型钙通道及脱氢紫堇碱对其影响的研究

孟红旭 王宝 刘建勋

中国药理学通报2011,Vol.27Issue(8):1051-1054,4.
中国药理学通报2011,Vol.27Issue(8):1051-1054,4.DOI:10.3969/j.issn.1001-1978.2011.08.005

穿孔膜片钳方法记录L型钙通道及脱氢紫堇碱对其影响的研究

Recording L-type calcium channel current by perforated patch clamp and effect of dehydrocorydaline on L-type calcium channel

孟红旭 1王宝 1刘建勋1

作者信息

  • 1. 中国中医科学院西苑医院实验研究中心,北京,100091
  • 折叠

摘要

Abstract

Aim To observe the difference of recording L-type calcium channel currents over time through by whole cell patch clamp and perforated patch clamp method and the effect of dehydrocorydaline on L-type calcium channel by perforated patch clamp method.Methods Whole cell patch clamp and perforated patch clamp were used to record L-type calcium channel current in acutely isolated rat ventricular myocytes.Results The L-type calcium channel current peak recorded by whole cell patch clamp decayed of the ( 34 ±23 )% ( n =10 ) within 15 minutes, while using perforated patch clamp, L-type calcium channel current peak attenuated ( 2. 7 ±3. 4 )% ( n =9 ) within 15 minutes; The inhibitory effect of ginsenoside Re( 100μmol · L-1 ) could be clearlv recorded by perforated patch clamp method. while the current decaying produced by whole cell patch clamp almost completely overshadowed the effects of ginsenoside Re. Dehydrocorydaline ( 10, 100 μmol · L-1 ) could inhibit L-type calcium channel current peak and the inhibitory rates were ( 9 ±7. 5 )%( n =5 )and ( 28. 6 ±8. 5 )%( n =5 )individually. Conclusions Perforated patch clamp method has more stability and accuracy than ordinary whole-cell patch clamp technique in recording L-type calcium channel current; dehydrocorydaline can suppress L-type calcium channel in a concentration-dependent manner.

关键词

穿孔膜片钳/全细胞膜片钳/心室肌细胞/L型钙通道/电流衰减/脱氢紫堇碱

Key words

perforated patch clamp/ whole cell patch clamp / ventricular myocytes / L-type calcium channel current decaying / dehydrocorydaline

分类

医药卫生

引用本文复制引用

孟红旭,王宝,刘建勋..穿孔膜片钳方法记录L型钙通道及脱氢紫堇碱对其影响的研究[J].中国药理学通报,2011,27(8):1051-1054,4.

基金项目

国家重大新药创新项目(No 2009ZX09301-005) (No 2009ZX09301-005)

国家自然科学基金重点项目(No 30830118) (No 30830118)

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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