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血管紧张素II刺激成年兔心室肌细胞中的钠氢交换。

Angiotensin II stimulates sodium-hydrogen exchange in adult rabbit ventricular myocytes.

作者信息

Matsui H, Barry W H, Livsey C, Spitzer K W

机构信息

Nora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah School of Medicine, Salt Lake City, USA.

出版信息

Cardiovasc Res. 1995 Feb;29(2):215-21.

PMID:7736498
Abstract

OBJECTIVE

The aim was to characterise the effects of angiotensin II on Na+/H+ exchange in adult ventricular myocytes.

METHODS

Intracellular pH (pHi) was continuously measured with the fluorescent pH indicator, SNARF-1, in single resting myocytes obtained from adult rabbits by enzymatic dissociation. In some experiments cells were electrically paced to elicit contractions. All experiments were performed at 36 degrees C in HEPES buffered solution containing no added CO2 or HCO3- (pHo 7.4).

RESULTS

Rapid application of angiotensin II caused pHi to rise. The initial rate of rise and initial net H+ efflux responded to angiotensin II in a concentration dependent manner, EC50 = 7.8. Buffering of cytosolic calcium with the calcium chelator BAPTA did not affect the initial net H+ efflux elicited by 1 microM angiotensin II. The increase in steady state pHi was blocked by inhibitors of Na+/H+ exchange, amiloride (1 mM) and EIPA (10 microM). Angiotensin II also increased the rate of pHi recovery from intracellular acidosis at pHi values above approximately 6.9. During inhibition of Na+/H+ exchange the application of angiotensin II decreased steady state pHi. This acidosis was blocked by preincubation in dextrose-free solution containing 20.0 mM 2-deoxy-D-glucose and 10 microM EIPA. The positive inotropic effect of angiotensin II was markedly suppressed by amiloride.

CONCLUSIONS

Angiotensin II exerts a concentration dependent stimulatory effect on Na+/H+ exchange in adult rabbit ventricular myocytes. This effect does not appear to involve changes in cytosolic calcium. During inhibition of Na+/H+ exchange, angiotensin II causes pHi to fall, perhaps by stimulating metabolic acid production. The positive inotropic action of angiotensin II depends, in part, on stimulation of Na+/H+ exchange.

摘要

目的

本研究旨在描述血管紧张素II对成年心室肌细胞中Na⁺/H⁺交换的影响。

方法

采用荧光pH指示剂SNARF-1,在通过酶解从成年兔获取的单个静息心肌细胞中连续测量细胞内pH(pHi)。在一些实验中,对细胞进行电刺激以引发收缩。所有实验均在36℃的HEPES缓冲溶液中进行,该溶液不添加CO₂或HCO₃⁻(pHo 7.4)。

结果

快速应用血管紧张素II导致pHi升高。pHi的初始升高速率和初始净H⁺外流对血管紧张素II呈浓度依赖性反应,EC50 = 7.8。用钙螯合剂BAPTA缓冲胞质钙不影响1μM血管紧张素II引起的初始净H⁺外流。稳态pHi的升高被Na⁺/H⁺交换抑制剂氨氯地平(1 mM)和EIPA(10μM)阻断。血管紧张素II还增加了pHi在高于约6.9的pHi值时从细胞内酸中毒恢复的速率。在抑制Na⁺/H⁺交换期间,应用血管紧张素II降低了稳态pHi。这种酸中毒被预先在含有20.0 mM 2-脱氧-D-葡萄糖和10μM EIPA的无葡萄糖溶液中孵育所阻断。氨氯地平显著抑制了血管紧张素II的正性肌力作用。

结论

血管紧张素II对成年兔心室肌细胞中的Na⁺/H⁺交换具有浓度依赖性刺激作用。这种作用似乎不涉及胞质钙的变化。在抑制Na⁺/H⁺交换期间,血管紧张素II导致pHi下降,可能是通过刺激代谢性酸产生。血管紧张素II的正性肌力作用部分取决于对Na⁺/H⁺交换的刺激。

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