Regulation of leptin gene expression and secretion by steroid hormones

被引:53
作者
Brann, DW [1 ]
De Sevilla, L [1 ]
Zamorano, PL [1 ]
Mahesh, VB [1 ]
机构
[1] Med Coll Georgia, Dept Physiol & Endocrinol, Augusta, GA 30912 USA
关键词
steroid; leptin; ovariectomy; rat;
D O I
10.1016/S0039-128X(99)00049-5
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
Previous work has shown that 17 beta-estradiol is the primary ovarian signal regulating body weight and adiposity, although its mechanisms of action remain unclear. We hypothesized that 17 beta-estradiol could enhance leptin levels as a mechanism of its anorectic effects. Administration of 5 mu g 17 beta-estradiol subcutaneously (s.c.) for 2 days significantly elevated leptin mRNA levels in adipose tissue as compared to vehicle controls (P < 0.003). A time-course administration of estrogen showed increased mRNA levels in adipose tissue between 6 and 12 h after estrogen injection as compared to vehicle controls (P < 0.03). Corresponding to the increased leptin mRNA levels at 6 and 12 h, elevated plasma leptin levels were observed at 12 h after estrogen administration as compared to controls (P < 0.05). Administration of progesterone (1 mg/rat) after estradiol injection did not enhance the elevated leptin mRNA levels in adipose tissue. Serum leptin levels from cycling rats did not differ significantly between metestrous and proestrous animals. In conclusion, the present studies demonstrate that 17 beta-estradiol can regulate leptin gene expression and secretion in the female rat, thus providing a better understanding of the possible anorectic effect of estrogens. (C) 1999 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:659 / 663
页数:5
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