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没食子酸对大鼠化学诱导性心律失常后电生理特性及室性心律失常的影响。

Effect of gallic acid on electrophysiological properties and ventricular arrhythmia following chemical-induced arrhythmia in rat.

作者信息

Akbari Ghaidafeh, Dianat Mahin, Badavi Mohammad

机构信息

Department of Physiology, Persian Gulf Physiology Research Center, Faculty of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.

出版信息

Iran J Basic Med Sci. 2020 Feb;23(2):167-172. doi: 10.22038/IJBMS.2019.33296.7948.

Abstract

OBJECTIVES

Ventricular arrhythmias including ventricular tachycardia (VT) and ventricular fibrillation (VF) are the most important causes of mortality rate. Gallic acid (GA) has beneficial effects on cardiovascular diseases. The aim of this study was to evaluate the effects of GA on electrophysiological parameters such as QRS complex, heart rate (HR), PR interval parameters, and ventricular arrhythmia following chemical induction in rat.

MATERIALS AND METHODS

Seventy-two male rats were divided into 9 groups (n=8). Chronic groups pretreated by GA (10, 30, and 50 mg/kg, orally) and normal saline (N/S, 1 ml/kg, orally) for 10 days. At the start of the experiments (the first day) and on the final day of the experiments (tenth day), the electrocardiogram (lead II) was recorded. At acute group, GA (50 mg/kg), and anti-arrhythmic drugs such as propranolol, amiodarone, and verapamil injected via intravenous (IV). Then, arrhythmia induced by a CaCl 2.5% solution (140 mg/kg, IV). Afterward, percentage of premature ventricular beats (PVB), VF, and VT were recorded at 1, and 3 min.

RESULTS

These findings showed that chronic and acute doses of GA have positive inotropic and anti-dysrhythmic effects by significant reduction of PVB, VT and VF on comparison with the control group. These actions are comparable to anti-arrhythmic drugs such as quinidine, propranolol, amiodarone, and verapamil. GA has not significant effect on chronotropic and dromotropic properties.

CONCLUSION

Findings showed that GA has antiarrhythmic, and inotropic characteristics that suggested GA has effective for mild congestive heart failure, and cardiovascular disorders patients which susceptible to incidence of arrhythmias.

摘要

目的

室性心律失常,包括室性心动过速(VT)和室颤(VF)是死亡率的最重要原因。没食子酸(GA)对心血管疾病有有益作用。本研究的目的是评估GA对大鼠化学诱导后的电生理参数如QRS波群、心率(HR)、PR间期参数和室性心律失常的影响。

材料与方法

72只雄性大鼠分为9组(n = 8)。慢性组用GA(10、30和50mg/kg,口服)和生理盐水(N/S,1ml/kg,口服)预处理10天。在实验开始时(第一天)和实验最后一天(第十天)记录心电图(II导联)。在急性组,通过静脉注射(IV)给予GA(50mg/kg)以及抗心律失常药物如普萘洛尔、胺碘酮和维拉帕米。然后,用2.5%氯化钙溶液(静脉注射140mg/kg)诱导心律失常。之后,在1分钟和3分钟时记录室性早搏(PVB)、VF和VT的百分比。

结果

这些结果表明,与对照组相比,慢性和急性剂量的GA通过显著降低PVB、VT和VF具有正性肌力和抗心律失常作用。这些作用与抗心律失常药物如奎尼丁、普萘洛尔、胺碘酮和维拉帕米相当。GA对变时性和变传导性特性无显著影响。

结论

研究结果表明,GA具有抗心律失常和正性肌力特性,提示GA对轻度充血性心力衰竭以及易发生心律失常的心血管疾病患者有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebbf/7211353/6620530e8611/IJBMS-23-167-g001.jpg

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