ANTIGLUCOCORTICOID ACTION OF DEHYDROEPIANDROSTERONE IN YOUNG OBESE ZUCKER RATS

被引:0
|
作者
WRIGHT, BE
PORTER, JR
BROWNE, ES
SVEC, F
机构
[1] LOUISIANA STATE UNIV,MED CTR,DEPT PHYSIOL,1100 FLORIDA AVE,NEW ORLEANS,LA 70119
[2] LOUISIANA STATE UNIV,MED CTR,DEPT MED,OBES RES PROGRAM,NEW ORLEANS,LA 70119
关键词
TYROSINE AMINOTRANSFERASE; ORNITHINE DECARBOXYLASE; LIVER; KIDNEY; DEXAMETHASONE; GLUCOCORTICOID ANTAGONIST;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Dehydroepiandrosterone (DHEA) reduces weight gain in the hypercorticosteronemic Zucker fatty rat, an animal model of genetic obesity. However, the mechanism of action of DHEA is still unclear. We propose that DHEA acts as an antiglucocorticoid in the Zucker fatty rat. To test this hypothesis we examined DHEA's ability to block the activation of the glucocorticoid-inducible enzymes tyrosine aminotransferase (TAT) and ornithine decarboxylase (ODC) by dexamethasone (i.p. 5-mu-g/100 g body weight) in hepatic tissue of 6-10 week old Zucker rats. Injections of DMSO, the vehicle, served as a control. DHEA alone did not affect TAT, but when DHEA (500-mu-g/100 g b.w.) was administered simultaneously with dexamethasone, activation did not occur. Similar results were seen using a second tissue (kidney). We conclude that DHEA can act acutely as an antiglucocorticoid in the young obese Zucker rat and hypothesize that its chronic anti-obesity effect may reflect, at least in part, a chronic antiglucocorticoid activity.
引用
收藏
页码:579 / 583
页数:5
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