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有证据表明,氨氯吡咪通过抑制蛋白激酶活性来拮抗胰岛素刺激的蛋白磷酸化。

Evidence that amiloride antagonises insulin-stimulated protein phosphorylation by inhibiting protein kinase activity.

作者信息

Holland R, Woodgett J R, Hardie D G

出版信息

FEBS Lett. 1983 Apr 18;154(2):269-73. doi: 10.1016/0014-5793(83)80163-x.

Abstract

The diuretic drug amiloride antagonises the insulin-dependent increase in phosphorylation of ATP-citrate lyase in hepatocytes isolated from rats that had been starved and refed a fat-free diet. Studies with a range of protein kinases and protein phosphatases that have been shown to phosphorylate or dephosphorylate purified ATP-citrate lyase in vitro revealed that amiloride was a non-specific inhibitor of all protein kinases tested, but did not significantly affect any of the protein phosphatases. These results cast doubt on previous claims that growth factors stimulate phosphorylation of ribosomal protein S6 by activating an amiloride-sensitive Na+/H+ exchange system, and that insulin inhibits a protein phosphatase that is activated by amiloride.

摘要

利尿药氨氯吡咪可拮抗从饥饿后再喂无脂饮食的大鼠分离出的肝细胞中,ATP-柠檬酸裂解酶磷酸化的胰岛素依赖性增加。对一系列已证实在体外可使纯化的ATP-柠檬酸裂解酶磷酸化或去磷酸化的蛋白激酶和蛋白磷酸酶进行的研究表明,氨氯吡咪是所测试的所有蛋白激酶的非特异性抑制剂,但对任何一种蛋白磷酸酶均无显著影响。这些结果对先前的说法提出了质疑,即生长因子通过激活氨氯吡咪敏感的Na+/H+交换系统刺激核糖体蛋白S6的磷酸化,以及胰岛素抑制由氨氯吡咪激活的一种蛋白磷酸酶。

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