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Berberine elicits anti‐arrhythmic effects via IK1/Kir2.1 in the rat type 2 diabetic myocardial infarction model
Author(s) -
Wang Lihong,
Yu Changhua,
Fu Ying,
Li Qiang,
Sun Yuqian
Publication year - 2011
Publication title -
phytotherapy research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.019
H-Index - 129
eISSN - 1099-1573
pISSN - 0951-418X
DOI - 10.1002/ptr.3097
Subject(s) - berberine , myocardial infarction , medicine , infarction , cardiology , type 2 diabetes , diabetes mellitus , ligation , pharmacology , endocrinology
The purpose of this study was to explore the anti‐arrhythmic mechanisms of berberine in diabetic rats with myocardial infarction. Sixty rats were divided into four groups: (1) normal control; (2) myocardial infarction group (MI); (3) Type 2 diabetes with myocardial infarction group (T2DM+MI); and (4) Type 2 diabetic with myocardial infarction berberine‐treated group (BBR). Berberine (60 mg/kg/day) was administered after coronary artery ligation in the T2DM+MI group for 14 days. Currents were measured using whole‐cell patch‐clamp techniques. Western blot was performed for quantification of target proteins. The study showed that arrhythmias induced by myocardial infarction were aggravated in diabetic rats. Arrhythmia scores in the MI group were significantly higher than in the control group. Interestingly, the administration of berberine at a dose of 60 mg/kg/d recovered arrhythmia scores ( P > 0.05). RMP (Resting membrane potential) which could be recovered by berberine ( P < 0.05), was significantly reduced in both the infarction groups. I K1 current and current density markedly decreased in the MI and T2DM+MI groups ( P < 0.05) and could be reversed by berberine ( P < 0.05). The relative expression of Kir2.1 in rats in the MI and T2DM+MI group were both significantly decreased ( P < 0.05); berberine recovered depressed Kir2.1 to nearly normal levels. The results suggest that the effects of berberine on I K1 /Kir2.1 may be an important mechanism for producing anti‐arrhythmic effects. Copyright © 2010 John Wiley & Sons, Ltd.