Suppr超能文献

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。

相似文献

1
Effects of atorvastatin on time-dependent change of fast sodium current in simulated acute ischaemic ventricular myocytes.
Cardiovasc J Afr. 2019;30(5):268-274. doi: 10.5830/CVJA-2019-021. Epub 2019 Jul 29.
3
Selective inhibition of physiological late Na current stabilizes ventricular repolarization.
Am J Physiol Heart Circ Physiol. 2018 Feb 1;314(2):H236-H245. doi: 10.1152/ajpheart.00071.2017. Epub 2017 Sep 29.
4
Bisoprolol inhibits sodium current in ventricular myocytes of rats with diastolic heart failure.
Clin Exp Pharmacol Physiol. 2007 Aug;34(8):714-9. doi: 10.1111/j.1440-1681.2007.04628.x.
6
Ranolazine improves abnormal repolarization and contraction in left ventricular myocytes of dogs with heart failure by inhibiting late sodium current.
J Cardiovasc Electrophysiol. 2006 May;17 Suppl 1(Suppl 1):S169-S177. doi: 10.1111/j.1540-8167.2006.00401.x.
7
Unique properties of the ATP-sensitive K⁺ channel in the mouse ventricular cardiac conduction system.
Circ Arrhythm Electrophysiol. 2011 Dec;4(6):926-35. doi: 10.1161/CIRCEP.111.964643. Epub 2011 Oct 9.
9
Tolterodine reduces veratridine-augmented late I, reverse-I and early afterdepolarizations in isolated rabbit ventricular myocytes.
Acta Pharmacol Sin. 2016 Nov;37(11):1432-1441. doi: 10.1038/aps.2016.76. Epub 2016 Aug 29.
10
Antiarrhythmic effect of crotonoside by regulating sodium and calcium channels in rabbit ventricular myocytes.
Life Sci. 2020 Mar 1;244:117333. doi: 10.1016/j.lfs.2020.117333. Epub 2020 Jan 18.

引用本文的文献

本文引用的文献

2
Moderate to high intensity statin in dialysis patients after acute myocardial infarction: A national cohort study in Asia.
Atherosclerosis. 2017 Dec;267:158-166. doi: 10.1016/j.atherosclerosis.2017.09.018. Epub 2017 Sep 27.
3
Statins and oxidative stress in the cardiovascular system.
Curr Pharm Des. 2017 Sep 26. doi: 10.2174/1381612823666170926130338.
4
The management of ventricular dysrhythmia in aconite poisoning.
Clin Toxicol (Phila). 2017 Jun;55(5):313-321. doi: 10.1080/15563650.2017.1291944. Epub 2017 Feb 20.
5
Pleiotropic Effects of Statins on the Cardiovascular System.
Circ Res. 2017 Jan 6;120(1):229-243. doi: 10.1161/CIRCRESAHA.116.308537.
6
Murine Electrophysiological Models of Cardiac Arrhythmogenesis.
Physiol Rev. 2017 Jan;97(1):283-409. doi: 10.1152/physrev.00007.2016.
7
Epidemiology and genetics of ventricular fibrillation during acute myocardial infarction.
J Geriatr Cardiol. 2016 Sep;13(9):789-797. doi: 10.11909/j.issn.1671-5411.2016.09.006.
8
Current statins show calcium channel blocking activity through voltage gated channels.
BMC Pharmacol Toxicol. 2016 Sep 21;17(1):43. doi: 10.1186/s40360-016-0086-5.
9
Global electrical heterogeneity: A review of the spatial ventricular gradient.
J Electrocardiol. 2016 Nov-Dec;49(6):824-830. doi: 10.1016/j.jelectrocard.2016.07.025. Epub 2016 Jul 28.

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