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福司可林对心肌细胞中己糖转运的抑制作用。

Forskolin inhibition of hexose transport in cardiomyocytes.

作者信息

Geisbuhler T P, Sergeant S, Miramonti F L, Kim H D, Rovetto M J

出版信息

Pflugers Arch. 1987 Jun;409(1-2):158-62. doi: 10.1007/BF00584765.

Abstract

The effects of insulin, forskolin, isoproterenol, and epinephrine on 3-O-methylglucose (hexose) transport and cell cyclic AMP levels were determined in adult rat cardiomyocytes. Insulin stimulated hexose transport in these cells an average of 2.5-fold. Initial hexose transport rates at 1 mM hexose were 3.75 X 10(-2) nmol/mg cell protein/second in the absence of insulin, and 8.25 X 10(-2) nmol/mg cell protein/second in the presence of 12.3 microM insulin. Forskolin at 5 microM nearly abolished hexose transport within 3 s of exposure, but did not increase cell cyclic AMP concentrations within 9 s. The apparent Ki for hexose transport inhibition was about 0.3 microM forskolin. Epinephrine and isoproterenol at 50 microM increased cell cyclic AMP 4-fold during 9 s exposure, but did not affect hexose transport. Treatment of cells with these catecholamines of forskolin for up to 99 s increased cell cyclic AMP, but only forskolin inhibited hexose transport. We conclude from these results that forskolin acts on hexose transport independent of its action on adenyl cyclase, and that cyclic AMP does not inhibit or stimulate hexose transport.

摘要

在成年大鼠心肌细胞中测定了胰岛素、福斯高林、异丙肾上腺素和肾上腺素对3 - O - 甲基葡萄糖(己糖)转运及细胞环磷酸腺苷(cAMP)水平的影响。胰岛素刺激这些细胞中的己糖转运,平均增加2.5倍。在无胰岛素时,1 mM己糖的初始己糖转运速率为3.75×10⁻² nmol/mg细胞蛋白/秒,在存在12.3 μM胰岛素时为8.25×10⁻² nmol/mg细胞蛋白/秒。5 μM的福斯高林在暴露3秒内几乎完全抑制己糖转运,但在9秒内未增加细胞cAMP浓度。己糖转运抑制的表观半数抑制浓度(Ki)约为0.3 μM福斯高林。50 μM的肾上腺素和异丙肾上腺素在暴露9秒期间使细胞cAMP增加4倍,但不影响己糖转运。用这些儿茶酚胺或福斯高林处理细胞长达99秒可增加细胞cAMP,但只有福斯高林抑制己糖转运。我们从这些结果得出结论,福斯高林对己糖转运的作用独立于其对腺苷酸环化酶的作用,并且环磷酸腺苷不抑制或刺激己糖转运。

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