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Insulin inhibition of α-adrenergic actions in liver

机译:胰岛素抑制肝脏中α-肾上腺素的作用

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pThe effects of insulin on alpha-agonist (phenylephrine)- and [Arg8]vasopressin-induced Ca2+ and glucose release and mitochondrial Ca2+ fluxes in isolated perfused rat livers were examined. Insulin (6 nM) inhibited the ability of phenylephrine (1 and 0.5 microM) to elicit Ca2+ and glucose release, whereas it was without effect on vasopressin (10 and 2.5 nM) actions. Correspondingly, insulin inhibited the action of phenylephrine to induce a stable increase in mitochondrial Ca2+ uptake, but it did not affect the alteration caused by vasopressin. Phenylephrine and vasopressin caused transient increases in hepatocyte respiration. Insulin inhibited the effect of phenylephrine on this parameter, but not that of vasopressin. Insulin added alone did not alter any of the above parameters. It is concluded from these data that insulin does not alter cellular Ca2+ fluxes and respiration themselves, but selectively inhibits alpha-adrenergic stimulation of these processes. It is proposed that insulin acts either to inhibit binding of alpha-agonists to their specific plasma-membrane receptors or to alter generation and/or degradation of the putative alpha-adrenergic ‘second messenger’. If this latter possibility is the case, then the alpha-adrenergic ‘second messenger’ must be different from the ‘second messenger’ of vasopressin./p
机译:>检查了胰岛素对分离的灌注大鼠肝脏中α-激动剂(去氧肾上腺素)和[Arg8]加压素诱导的Ca2 +,葡萄糖释放和线粒体Ca2 +通量的影响。胰岛素(6 nM)抑制了去氧肾上腺素(1和0.5 microM)引起Ca2 +和葡萄糖释放的能力,而对血管加压素(10和2.5 nM)的作用没有影响。相应地,胰岛素抑制了去氧肾上腺素的作用,从而诱导线粒体Ca2 +吸收的稳定增加,但它不影响由加压素引起的改变。苯肾上腺素和加压素引起肝细胞呼吸的短暂增加。胰岛素抑制去氧肾上腺素对该参数的作用,但不抑制加压素的作用。单独添加胰岛素不会改变任何上述参数。从这些数据可以得出结论,胰岛素不会改变细胞内Ca2 +流量和自身呼吸作用,而是选择性抑制这些过程的α-肾上腺素能刺激。有人建议胰岛素起抑制α-激动剂与其特异的血浆膜受体结合的作用,或改变推定的α-肾上腺素“第二信使”的产生和/或降解。如果是后一种情况,则α-肾上腺素的“第二信使”必须不同于加压素的“第二信使”。

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