肾上腺素能抑制肾皮质腺苷酸环化酶。

E A Woodcock, C I Johnston, C A Olsson
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引用次数: 0

摘要

大鼠肾皮质匀浆中腺苷酸环化酶被α -肾上腺素能激动剂抑制。抑制作用需要钠离子和GTP。在0.2 M NaCl、10 μ M GTP和10 μ M普萘洛尔的作用下,l-肾上腺素最大抑制率为17.8 +/- 1.4% (S.E.M.)。l-去甲肾上腺素和α -甲基去甲肾上腺素也有类似的抑制作用。l-肾上腺素、l-去甲肾上腺素和α -去甲肾上腺素的EC50值分别为1.9 +/- 0.7、2.3 +/- 1.6和5.1 +/- 1.8微米。可乐定是一种局部激动剂,其抑制作用是肾上腺素的50%。苯肾上腺素和甲氧沙明在浓度达100微米时没有抑制作用。微摩尔浓度的酚妥拉明和育亨宾阻止了肾上腺素对腺苷酸环化酶的抑制作用。然而,哌唑嗪无效。因此腺苷酸环化酶偶联α -受体具有α -2特异性。在肾髓质匀浆中未观察到-肾上腺素能激动剂对腺苷酸环化酶的抑制作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alpha-adrenergic inhibition of renal cortical adenylate cyclase.

Adenylate cyclase in homogenates of rat renal cortex was inhibited by alpha-adrenergic agonists. Inhibition required sodium ion and GTP. A maximum inhibition of 17.8 +/- 1.4% (S.E.M.) was produced by l-epinephrine in the presence of 0.2 M NaCl, 10 microM GTP and 10 microM propranolol. Similar inhibition was produced by l-norepinephrine and alpha-methylnorepinephrine. The EC50 values for l-epinephrine, l-norepinephrine and alpha-methylnorepinephrine were respectively 1.9 +/- 0.7 microM, 2.3 +/- 1.6 microM and 5.1 +/- 1.8 microM. Clonidine was a partial agonist causing 50% as much inhibition as epinephrine. Phenylephrine and methoxamine did not inhibit at concentrations up to 100 microM. Micromolar concentrations of phentolamine and yohimbine prevented the inhibition of adenylate cyclase by epinephrine. However, prazosin was ineffective. Thus the adenylate cyclase coupled alpha-receptors have alpha-2 specificity. Inhibition of adenylate cyclase by alpha-adrenergic agonists was not observed in homogenates of renal medulla.

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