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血管紧张素 II 在衰竭心脏完整心室中的自分泌作用:血管紧张素 II 从内部改变心脏的兴奋性。

Intracrine action of angiotensin II in the intact ventricle of the failing heart: angiotensin II changes cardiac excitability from within.

机构信息

School of Medicine, Medical Sciences Campus, UPR, San Juan, PR 00936-5067, USA.

出版信息

Mol Cell Biochem. 2011 Dec;358(1-2):309-15. doi: 10.1007/s11010-011-0981-4. Epub 2011 Jul 9.

Abstract

The influence of intracellular injection of angiotensin II (Ang II) on electrical properties of single right ventricular fibers from the failing heart of cardiomyopathic hamsters (TO2) was investigated in the intact ventricle of 8-month-old animals. Intracellular injection was performed using pressure pulses (40-70 psi) for short periods of time (20 ms) while recoding the action potential simultaneously from the same fiber. The results indicated that intracellular Ang II caused a hyperpolarization of 7.7 mV ± 4.3 mV (n = 39) (4 animals) (P < 0.05) followed by a small fall in membrane potential. The action potential duration was significantly increased at 50% and at 90% repolarization, and the refractoriness was significantly enhanced. The effect of intracellular Ang II on action potential duration was related to the inhibition of potassium conductance through PKC activation because Bis-1 (360 nM), a selective PKC inhibitor, abolished the effect of the peptide. Injections performed in different fibers of the same ventricle showed a variable effect of Ang II on action potential duration and generated spontaneous rhythmicity. The effect of intracellular Ang II on action potential duration and cardiac refractoriness remains for more than 1 h after interruption of the intracellular injection of the peptide.

摘要

在 8 月龄动物的完整心室中,研究了细胞内注射血管紧张素 II(Ang II)对心肌病仓鼠(TO2)衰竭心脏的单个右心室纤维电生理特性的影响。通过短时间(20 毫秒)的压力脉冲(40-70 psi)进行细胞内注射,同时从同一纤维上同步记录动作电位。结果表明,细胞内 Ang II 引起 7.7 mV ± 4.3 mV 的超极化(n = 39)(4 只动物)(P <0.05),随后膜电位略有下降。动作电位时程在 50%和 90%复极时显著延长,不应期显著增强。细胞内 Ang II 对动作电位时程的影响与通过 PKC 激活抑制钾电流有关,因为 PKC 选择性抑制剂 Bis-1(360 nM)可消除肽的作用。在同一心室的不同纤维中进行的注射显示出 Ang II 对动作电位时程的可变作用,并产生自发性节律性。中断肽的细胞内注射后,细胞内 Ang II 对动作电位时程和心脏不应期的影响持续超过 1 小时。

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