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糖类对(前)胰岛素生物合成的影响。

The effect of sugars on (pro)insulin biosynthesis.

作者信息

Ashcroft S J, Bunce J, Lowry M, Hansen S E, Hedeskov C J

出版信息

Biochem J. 1978 Aug 15;174(2):517-26. doi: 10.1042/bj1740517.

Abstract

Rates of incorporation of [4,5-(3)H]leucine into insulin plus proinsulin, designated ;(pro)insulin', and total protein in rat pancreatic islets were measured. Glucose stimulates rates of total protein and (pro)insulin biosynthesis, but (pro)insulin biosynthesis is stimulated preferentially. Mannose and N-acetylglucosamine also stimulate (pro)insulin and total protein biosynthesis; inosine and dihydroxyacetone stimulate (pro)insulin biosynthesis specifically. Fructose does not stimulate (pro)insulin biosynthesis when tested alone, but does so in the presence of low concentrations of glucose, mannose or N-acetylglucosamine. Many glucose analogues do not stimulate (pro)insulin biosynthesis. Mannoheptulose inhibits synthesis of (pro)insulin and total protein stimulated by glucose or mannose but not by dihydroxyacetone, inosine or N-acetylglucosamine; phloretin (9mum) inhibits N-acetylglucosamine-stimulated (pro)insulin biosynthesis preferentially. The data are in agreement with the view that the same glucose-sensor mechanism may control both insulin release and biosynthesis, and ;substrate-site' model is suggested. The threshold for stimulation of biosynthesis of (pro)insulin and total protein is lower than that found for glucose-stimulated insulin release; moreover the biosynthetic response to an elevation of glucose concentration is slower than that found for insulin release. The physiological implication of these findings is discussed. Caffeine and isobutylmethylxanthine, at concentrations known to increase islet 3':5'-cyclic AMP and potentiate glucose-induced insulin release, were without effect on rates of glucose-stimulated (pro)insulin biosynthesis.

摘要

测定了[4,5-(³H)]亮氨酸掺入大鼠胰岛中胰岛素加胰岛素原(称为“(前体)胰岛素”)和总蛋白的速率。葡萄糖刺激总蛋白和(前体)胰岛素的生物合成速率,但(前体)胰岛素的生物合成受到优先刺激。甘露糖和N-乙酰葡糖胺也刺激(前体)胰岛素和总蛋白的生物合成;肌苷和二羟基丙酮特异性地刺激(前体)胰岛素的生物合成。单独测试时,果糖不刺激(前体)胰岛素的生物合成,但在低浓度葡萄糖、甘露糖或N-乙酰葡糖胺存在时会刺激。许多葡萄糖类似物不刺激(前体)胰岛素的生物合成。甘露庚酮糖抑制由葡萄糖或甘露糖刺激的(前体)胰岛素和总蛋白的合成,但不抑制由二羟基丙酮、肌苷或N-乙酰葡糖胺刺激的合成;根皮素(9μM)优先抑制N-乙酰葡糖胺刺激的(前体)胰岛素生物合成。这些数据与相同的葡萄糖传感机制可能控制胰岛素释放和生物合成的观点一致,并提出了“底物位点”模型。刺激(前体)胰岛素和总蛋白生物合成的阈值低于葡萄糖刺激胰岛素释放的阈值;此外,对葡萄糖浓度升高的生物合成反应比对胰岛素释放的反应慢。讨论了这些发现的生理意义。已知浓度的咖啡因和异丁基甲基黄嘌呤可增加胰岛3':5'-环磷酸腺苷并增强葡萄糖诱导的胰岛素释放,但对葡萄糖刺激的(前体)胰岛素生物合成速率没有影响。

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