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蛋白激酶C在人生长激素对大鼠脂肪细胞的胰岛素样作用中的作用

Role of kinase C in the insulin-like effects of human growth hormone in rat adipocytes.

作者信息

Smal J, De Meyts P

机构信息

Department of Diabetes, Endocrinology and Metabolism, City of Hope National Medical Center, Duarte, CA 91010.

出版信息

Biochem Biophys Res Commun. 1987 Sep 30;147(3):1232-40. doi: 10.1016/s0006-291x(87)80202-4.

Abstract

Insulin and to a smaller extent, human growth hormone (hGH), both stimulate lipogenesis in isolated rat adipocytes preincubated 4 hours in the absence of hormone. The non-additivity of maximal doses suggested that hGH may share a subset of the metabolic pathways stimulated by insulin. We explored whether kinase C may be involved in the common lipogenic effect of both hormones. The stimulation of lipogenesis by phorbol ester 12-myristate 13-acetate (PMA) (an activator of kinase C) was not additive to the stimulation by either insulin or hGH. Downregulation of kinase C resulted in a marked decrease of the maximal insulin effect (44 +/- 9%) and even more of the hGH effect (64 +/- 14%). These data suggest that kinase C either mediates part of, or modulates, the effect of insulin and hGH on lipogenesis.

摘要

胰岛素以及在较小程度上的人生长激素(hGH),均能刺激在无激素条件下预孵育4小时的离体大鼠脂肪细胞的脂肪生成。最大剂量的非相加性表明,hGH可能共享胰岛素所刺激的一部分代谢途径。我们探究了蛋白激酶C是否可能参与这两种激素的共同脂肪生成作用。佛波酯12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)(一种蛋白激酶C激活剂)对脂肪生成的刺激作用,与胰岛素或hGH的刺激作用并非相加。蛋白激酶C的下调导致胰岛素最大效应显著降低(44±9%),hGH效应降低得更多(64±14%)。这些数据表明,蛋白激酶C要么介导胰岛素和hGH对脂肪生成作用的一部分,要么对其起调节作用。

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