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大鼠心脏发育过程中α1 -肾上腺素能受体与Ca2+通道偶联的变化。

Changes in alpha 1-adrenoceptor coupling to Ca2+ channels during development in rat heart.

作者信息

Liu Q Y, Karpinski E, Pang P K

机构信息

Department of Physiology, University of Alberta, Edmonton, Canada.

出版信息

FEBS Lett. 1994 Jan 31;338(2):234-8. doi: 10.1016/0014-5793(94)80371-4.

Abstract

It has been reported in the literature that alpha 1-adrenoceptor activation in adult rat heart does not cause an increase in Ca2+ current but involves a decrease in I(t). This may explain in part the positive inotropic effect of alpha 1-adrenoceptor activation. In this study, the effect of phenylephrine, an alpha-adrenergic agonist, on L-type Ca2+ channel current was compared in young and neonatal rat myocytes. In the presence of propranolol, phenylephrine increased the Ca2+ current (reversed by prazosin) in neonatal but not in young rat myocytes suggesting that the coupling of the alpha 1-adrenoceptor to Ca2+ channels may switch during development.

摘要

文献报道,成年大鼠心脏中α1 -肾上腺素能受体激活不会导致Ca2+电流增加,而是涉及I(t)的降低。这可能部分解释了α1 -肾上腺素能受体激活的正性肌力作用。在本研究中,比较了α -肾上腺素能激动剂去氧肾上腺素对年轻和新生大鼠心肌细胞L型Ca2+通道电流的影响。在普萘洛尔存在的情况下,去氧肾上腺素增加了新生大鼠而非年轻大鼠心肌细胞的Ca2+电流(可被哌唑嗪逆转),这表明α1 -肾上腺素能受体与Ca2+通道的偶联在发育过程中可能会发生变化。

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