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首页> 外文期刊>Biochimica et biophysica acta: international journal of biochemistry and biophysics >Indirect dexamethasone down-regulation of the liver fatty acid-binding protein expression in rat liver.
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Indirect dexamethasone down-regulation of the liver fatty acid-binding protein expression in rat liver.

机译:间接地塞米松下调大鼠肝脏中肝脏脂肪酸结合蛋白的表达。

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摘要

The effects of glucocorticoids on the regulation of the liver fatty acid-binding protein (L-FABP) were studied in vivo and in primary culture of hepatocytes in rats. No change in L-FABP cytosolic content and mRNA levels occurred after adrenalectomy. By contrast, a twofold decrease in L-FABP expression was found in dexamethasone (Dex) treated rats. In primary culture of rat hepatocytes, insulin did not modify the L-FABP mRNA levels, whereas Dex produced a significant decrease. This down-regulation was independent of specific glucocorticoid receptors, of alteration in the turnover of L-FABP mRNA and did not require a de novo protein synthesis. However, it was totally prevented when 320 microM oleic acid was added in the culture medium. These findings show that the dex-mediated down-regulation of the L-FABP expression found in vivo is not due to a direct endocrine effect, but is likely secondary to changes in cellular lipid metabolism. Copyright 1998 Elsevier Science B.V.
机译:在大鼠体内以及在肝细胞的原代培养中,研究了糖皮质激素对肝脏脂肪酸结合蛋白(L-FABP)调节的影响。肾上腺切除术后L-FABP胞质含量和mRNA水平无变化。相比之下,在地塞米松(Dex)处理的大鼠中发现L-FABP表达降低了两倍。在大鼠肝细胞的原代培养中,胰岛素并未改变L-FABP mRNA的水平,而Dex则产生了明显的降低。这种下调独立于特定的糖皮质激素受体,不依赖于L-FABP mRNA的更新,并且不需要从头合成蛋白质。但是,在培养基中添加320μM的油酸是完全可以避免的。这些发现表明,在体内发现的右旋介导的L-FABP表达下调不是由于直接的内分泌作用,而是可能继发于细胞脂质代谢的改变。版权所有1998 Elsevier Science B.V.

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