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阿托伐他汀对模拟急性缺血性心室肌细胞快速钠电流时间依赖性变化的影响。

Effects of atorvastatin on time-dependent change of fast sodium current in simulated acute ischaemic ventricular myocytes.

作者信息

Li Hongshi, Wan Zheng, Li Xiaolong, Teng Tianming, Du Xin, Nie Jing

机构信息

Department of Cardiology, Tianjin Medical University General Hospital, Tianjin Medical University, Tianjin 300070, PR China.

Department of Cardiology, Tianjin Medical University General Hospital, Tianjin Medical University, Tianjin 300070, PR China . Email:

出版信息

Cardiovasc J Afr. 2019;30(5):268-274. doi: 10.5830/CVJA-2019-021. Epub 2019 Jul 29.

Abstract

INTRODUCTION

Our previous experiments showed that the transient sodium current (I) was abnormally increased in early ischaemia and atorvastatin could inhibit I. The aim of this study was to observe the time-dependent effects of simulated ischaemia on I and characterise the direct effects of atorvastatin on ischaemic I.

METHODS

Left ventricular myocytes were isolated from Wistar rats and randomly divided into two groups: a control group (normal to simulated ischaemia) and a statin group (normal to simulated ischaemia with 5 µmol/l atorvastatin). The I was recorded under normal conditions (as baseline) by whole-cell patch clamp and recorded from three to 21 minutes in the next phase of simulated ischaemic conditions.

RESULTS

In the control group, normalised I (at -40 mV) was increased to the peak (1.15 ± 0.08 mA) at three minutes of ischaemia compared with baseline (0.95 ± 0.04 mA, p < 0.01), it subsequently returned to baseline levels at nine and 11 minutes of ischaemia (0.98 ± 0.12 and 0.92 ± 0.12 mA, respectively), and persistently decreased with prolonged ischaemic time. In the statin group, there were no differences between baseline and the early stages of ischaemia (0.97 ± 0.04 mA at baseline vs 0.92 ± 0.12 mA in ischaemia for three minutes, p > 0.05).

CONCLUSION

Our results suggest that, in the early stages of ischaemia, changes in I in ventricular myocytes are time-dependent, showing an initial increase followed by a decrease, while atorvastatin inhibited the transient increase in I and made the change more gradual.

摘要

引言

我们之前的实验表明,短暂性钠电流(I)在早期缺血时异常增加,阿托伐他汀可抑制该电流。本研究旨在观察模拟缺血对I的时间依赖性影响,并明确阿托伐他汀对缺血性I的直接作用。

方法

从Wistar大鼠分离左心室肌细胞,随机分为两组:对照组(从正常到模拟缺血)和他汀组(从正常到模拟缺血并加入5μmol/L阿托伐他汀)。通过全细胞膜片钳在正常条件下(作为基线)记录I,并在模拟缺血条件的下一阶段3至21分钟记录。

结果

在对照组中,缺血3分钟时标准化I(在-40mV时)相较于基线(0.95±0.04mA,p<0.01)增加至峰值(1.15±0.08mA),随后在缺血9分钟和11分钟时恢复至基线水平(分别为0.98±0.12mA和0.92±0.12mA),并随着缺血时间延长持续下降。在他汀组中,基线与缺血早期无差异(基线时为0.97±0.04mA,缺血3分钟时为0.92±0.12mA,p>0.05)。

结论

我们的结果表明,在缺血早期,心室肌细胞中I的变化具有时间依赖性,呈现先增加后降低的趋势,而阿托伐他汀抑制了I的短暂增加,使变化更为平缓。

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