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首页> 外文期刊>American Journal of Physiology >Do beta 2-adrenergic receptors modulate Ca2+ in adult rat ventricular myocytes?
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Do beta 2-adrenergic receptors modulate Ca2+ in adult rat ventricular myocytes?

机译:β2-肾上腺素能受体调节成年大鼠心室肌细胞中的Ca2 +吗?

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摘要

We examined the role of beta 2-adrenergic receptors (ARs) in modulating calcium homeostasis in rat ventricular myocytes. Zinterol (10 microM), an agonist with a 25-fold greater affinity for beta 2-ARs over beta 1-ARs, modestly enhanced L-type calcium current (ICa) magnitude by approximately 30% and modestly accelerated the rate of Ca2+ concentration ([Ca2+]) decline (approximately 35%) but had little effect on the magnitude of the [Ca2+] transient (a nonsignificant 6% increase). However, 1 microM of the highly selective beta 1-AR antagonist CGP-20712A completely blocked the ICa increase induced by 10 microM zinterol. Pretreatment of cells with pertussis toxin (PTX) did not alter ICa enhancement by 10 microM zinterol, although it did abolish the ability of acetylcholine to block the forskolin-induced enhancement of ICa. Zinterol (10 microM) approximately doubled adenosine 3',5'-cyclic monophosphate (cAMP) accumulation, although one-half of this increase was blocked by CGP-20712A. In contrast, 1 microM of the nonselective beta-agonist isoproterenol increased cAMP production 15-fold. Thus we found no evidence that activation of beta 2-ARs modulates calcium homeostasis in rat ventricular myocytes, even after treatment with PTX.
机译:我们检查了β2肾上腺素受体(ARs)在调节大鼠心室肌细胞钙稳态中的作用。 Zinterol(10 microM)是对β2-AR的亲和力比β1-AR高25倍的激动剂,将L型钙电流(ICa)幅度适度提高了约30%,并适度地加快了Ca2 +浓度的速率( [Ca2 +])下降(大约35%),但对[Ca2 +]瞬变的幅度几乎没有影响(增加6%不明显)。但是,1 microM的高选择性β1-AR拮抗剂CGP-20712A完全阻断了10 microM的zinterol诱导的ICa升高。用百日咳毒素(PTX)预处理细胞并不会改变10 microM zinterol对ICa的增强作用,尽管它确实消除了乙酰胆碱阻止福司可林诱导的ICa增强作用的能力。 Zinterol(10 microM)大约使腺苷3',5'-环一磷酸(cAMP)积累增加了一倍,尽管这种增加的一半被CGP-20712A阻止。相反,1 microM的非选择性β激动剂异丙肾上腺素可使cAMP产生增加15倍。因此,我们发现没有证据表明即使使用PTX处理后,β2-ARs的活化也能调节大鼠心室肌细胞的钙稳态。

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