Indirect dexamethasone down-regulation of the liver fatty acid-binding protein expression in rat liver

被引:31
|
作者
Foucaud, L [1 ]
Niot, I [1 ]
Kanda, T [1 ]
Besnard, P [1 ]
机构
[1] Univ Bourgogne 1, Ecole Natl Super Biol Appl Nutr & Alimentat, UPRES 2422, Lab Physiol Nutr, F-21000 Dijon, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM | 1998年 / 1391卷 / 02期
关键词
liver fatty acid-binding protein; liver; endocrine gene regulation; lipid metabolism;
D O I
10.1016/S0005-2760(97)00213-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 pretended when 320 mu M 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. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:204 / 212
页数:9
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