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长期应用咪达普利对陈旧性心肌梗死代偿区不应期和钠电流的影响 被引量:3

Effect of imidapril on the effective refractory period and sodium current of ventricular noninfarction zone in healed myocardial infarction
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摘要 目的探讨咪达普利(IMI)对家兔陈旧性心梗(HMI)后心脏有效不应期(ERP)及钠电流(I_(Na))的影响。方法选家兔制 HMI 模型,口服 IMI 0.625mg·kg^(-1)·d^(-1)(8周)。记录整体心脏 ERP 和单细胞 I_(NA)。结果 HMI 组ERP 显著延长,用 IMI 后则缩短。HMI 组代偿区细胞 I_(Na)降低,I_(Na)稳态失活曲线负移,恢复时间常数延长;应用 IMI,I_(Na)明显恢复。结论咪达普利可抑制 HMI 心脏 ERP 延长,并使降 I_(Na)得以恢复。这可能是该药减少陈旧性心梗后心律失常发生的机制之一。 Aim To investigate the effects of imidapril (IMI) on effective refractory period (ERP) and sodium current (I_(Na)) of myocytes in ventricular noninfarction zone of healed myocardial infarction (HMI) in rabbit models.Methods Rabbits with left coronary artery ligation were prepared and IMI (0.625 mg·kg^(-1)·d^(-1),8 weeks) was orally administered.The ERP and sodium current were recorded. Results The ERP in HMI heart was prolonged.The ERP in IMI group was lower significantly than that of HMI group.The I_(Na) density of myocyte in HMI ventricle decreased obviously.V_(1/2) of steady state inactivation of I_(Na) shifted to hyperpolarization,and time constant (τ) of recovery from inactivation in HMI ventricular myocyte was longer than that of sham ventricular myocyte.I_(Na) density in IMI group increased markedly as compared with that of HMI group.Conclusion IMI was shown to reverse the abnormal prolongation of ERP in rabbit heart with the HMI and increase I_(Na) density.It may be the mechanism of IMI preventing against antiarrhythmia in healed myocardical infarction.
出处 《药学学报》 CAS CSCD 北大核心 2005年第7期654-658,共5页 Acta Pharmaceutica Sinica
关键词 咪达普利 陈旧性心肌梗死 有效不应期 钠电流 imidapril healed myocardical infarction effective refractory period sodium current
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  • 1牛惠燕,刘念,李泱,卜军,周强,阮燕菲,张存泰,陆再英.早期口服卡维地洛对兔陈旧性心肌梗死边缘带不应期和钠电流的影响[J].中国心脏起搏与心电生理杂志,2005,19(3):218-221. 被引量:4
  • 2Wijffels MC, Kirchhof CJ, Dorland R, et al. Atrial fibrillation begets Atrial fibrillation, a study in awake chronically instrumented goats. Circulation, 1995,92 : 1954-1968. 被引量:1
  • 3Pandozi C, Bianconi L, Villani M, et al. Electrophysiological char- acteristics of the human atria after cardioversion of persistent atrial fibrillation. Circulation, 1998,98:2860-2865. 被引量:1
  • 4Finkielstein D, Schweitzer P. Role of angiotensin-converting enzyme inhibitors in the prevention of atrial fibrillation. Am J Cardiol,2004, 93:734-736. 被引量:1
  • 5Willems R, Sipido KR, Holemans P, et al. Different patterns of an- giotensin II and atrial natriuretic peptide secretion in a sheep model of atrial fibrillation. J Cardiovasc Electrophysiol, 2001,12: 1387- 1392. 被引量:1
  • 6Goette A, Staack T, Rocken C, et al. Increased expression of extracellular signal-regulated kinase and angiotensin-converting enzyme in human atria during atrial fibrillation. J Am Coll Cardiol,2000, 35 : 1669-1677. 被引量:1
  • 7Tsai CT, Lai LP, Lin JL, et al. Renin-angiotensin system gene poly- morphisms and atrial fibrillation. Circulation, 2004, 109 : 1640- 1646. 被引量:1
  • 8Nakashima H, Kumagai K, Urata H, et al. Angiotensin II antagonist prevents elactrical remodeling in atrial fibrillation. Circulation, 2000,101:2612-2617. 被引量:1
  • 9Touyz RM, Sventck P, Lariviere R, et al. Cytosolic calcium changes induced by angiotensin II in neonatal rat atrial and ventricular cardiomyocytes are mediated via angiotensin II subtype I receptors. Hypertension, 1996,27 : 1090-1096. 被引量:1
  • 10Liu E,Xu Z, Li J, et al. Enalapril, irbesartan, and angiotensin-( 1-7 ) prevent atrial taehycardia-induced ionic remodeling. Int J Cardiol, 2011,146:364-370. 被引量:1

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