泸州医学院学报
瀘州醫學院學報
로주의학원학보
JOURNAL OF LUZHOU MEDICAL COLLEGE
2011年
1期
41-43
,共3页
李涛%李妙龄%雷明%谭晓秋%丁银元%杨艳%曾晓荣
李濤%李妙齡%雷明%譚曉鞦%丁銀元%楊豔%曾曉榮
리도%리묘령%뢰명%담효추%정은원%양염%증효영
小电导钙激活钾通道%心房细胞%膜片钳
小電導鈣激活鉀通道%心房細胞%膜片鉗
소전도개격활갑통도%심방세포%막편겸
SK2%Atrial myocyte%Patch clamp
目的:探讨一种有效的记录人心房肌细胞小电导钙激活钾通道(small conductance Ca2+-activated K+ channels,SK)电流的全细胞膜片钳方法.方法:以人心房肌细胞为研究对象,采用传统全细胞膜片钳技术,记录人心房肌细胞的小电导钙激活钾通道的宏观电流.传统全细胞模式形成后,分别记录在浴液中加入apamin(100nM)前后的电流,两者相减就得到了apamin敏感的SK2的电流.结果:采用传统全细胞膜片钳技术,能有效记录人心房肌细胞上apamin敏感的宏观电流.该电流是内向整流,去极化激活时,无明显失活现象,无尾电流出现,这些都符合SK2电流特性.结论:本实验提供了一种简单、有效的记录入心房肌细胞SK2宏观电流的方法,为今后深入的研究提供了实验基础.
目的:探討一種有效的記錄人心房肌細胞小電導鈣激活鉀通道(small conductance Ca2+-activated K+ channels,SK)電流的全細胞膜片鉗方法.方法:以人心房肌細胞為研究對象,採用傳統全細胞膜片鉗技術,記錄人心房肌細胞的小電導鈣激活鉀通道的宏觀電流.傳統全細胞模式形成後,分彆記錄在浴液中加入apamin(100nM)前後的電流,兩者相減就得到瞭apamin敏感的SK2的電流.結果:採用傳統全細胞膜片鉗技術,能有效記錄人心房肌細胞上apamin敏感的宏觀電流.該電流是內嚮整流,去極化激活時,無明顯失活現象,無尾電流齣現,這些都符閤SK2電流特性.結論:本實驗提供瞭一種簡單、有效的記錄入心房肌細胞SK2宏觀電流的方法,為今後深入的研究提供瞭實驗基礎.
목적:탐토일충유효적기록인심방기세포소전도개격활갑통도(small conductance Ca2+-activated K+ channels,SK)전류적전세포막편겸방법.방법:이인심방기세포위연구대상,채용전통전세포막편겸기술,기록인심방기세포적소전도개격활갑통도적굉관전류.전통전세포모식형성후,분별기록재욕액중가입apamin(100nM)전후적전류,량자상감취득도료apamin민감적SK2적전류.결과:채용전통전세포막편겸기술,능유효기록인심방기세포상apamin민감적굉관전류.해전류시내향정류,거겁화격활시,무명현실활현상,무미전류출현,저사도부합SK2전류특성.결론:본실험제공료일충간단、유효적기록입심방기세포SK2굉관전류적방법,위금후심입적연구제공료실험기출.
Objective: To establish an effective and stable method of recording small conductance Ca2+-activated K+ Channel (SK) currents in human atrial myocytes by conventional whole-cell patch clamp technique.Methods: Conventional whole-cell patch clamp technique was used to record apamin-sensitive currents in isolated right atrial myocytes from human right appendage. After conventional whole-cell configuration was made, apamin (100 nM)-a special blocker of SK2 current was added into extracellular solution. The apamin-sensitive current was obtained by using digital subtraction after apamin from control. Results: SK2 currents in human atrial myocytes were effectively recorded. SK2 current was inward rectification and not obvious effect of inactivation.Conclusion: Conventional whole-cell patch clamp technique can be used to record the SK2 currents. This method provides a basis for future research.