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胰岛素介导肝脏白蛋白和苹果酸酶信使核糖核酸的异步积累。

Insulin mediates the asynchronous accumulation of hepatic albumin and malic enzyme messenger RNAs.

作者信息

Drake R L, Mucenski C G

出版信息

Biochem Biophys Res Commun. 1985 Jul 16;130(1):317-24. doi: 10.1016/0006-291x(85)90420-6.

Abstract

We have compared the rate of accumulation of hepatic albumin and malic enzyme mRNAs following insulin treatment of diabetic rats to determine whether insulin coordinately increases mRNA levels or specifically induces the accumulation of individuals mRNAs. Initially, the quantities of both albumin and malic enzyme mRNAs are reduced in diabetic rats compared to normal rats as determined by RNA blot analysis using complementary DNA probes. Following insulin administration for 12 h, albumin and malic enzyme mRNA levels increase at similar rates. However, after 12 h the rate of malic enzyme mRNA accumulation increases dramatically while albumin mRNA continues to increase at its initial rate. This accelerated rate of accumulation of malic enzyme mRNA continued through 60 h of hormone treatment and was associated with the onset of hepatic lipogenesis. Thus, our results suggest that insulin regulates the accumulation of mRNAs encoding these two inducible proteins in an asynchronous manner directly related to the metabolic requirements of the animal.

摘要

我们比较了胰岛素治疗糖尿病大鼠后肝脏白蛋白和苹果酸酶mRNA的积累速率,以确定胰岛素是协同增加mRNA水平还是特异性诱导单个mRNA的积累。最初,通过使用互补DNA探针的RNA印迹分析确定,与正常大鼠相比,糖尿病大鼠中白蛋白和苹果酸酶mRNA的量均减少。给予胰岛素12小时后,白蛋白和苹果酸酶mRNA水平以相似的速率增加。然而,12小时后,苹果酸酶mRNA的积累速率急剧增加,而白蛋白mRNA继续以其初始速率增加。这种苹果酸酶mRNA积累的加速速率在激素治疗的60小时内持续存在,并与肝脏脂肪生成的开始相关。因此,我们的结果表明,胰岛素以与动物代谢需求直接相关的异步方式调节编码这两种诱导性蛋白质的mRNA的积累。

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