Effects of long-term treatment with resveratrol and subcutaneous and oral estradiol administration on pituitary function in rats

Effects of long-term treatment with resveratrol and subcutaneous and oral estradiol administration on pituitary function in rats
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DOI:
10.1677/joe.1.06535
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发表时间:
2006-04-01
影响因子:
4
通讯作者:
Wuttke, W
Wuttke, W
中科院分区:
医学2区
文献类型:
--
作者:
Böttner, M;Christoffel, J;Wuttke, W

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Hormone replacement therapy (HRT) has been used for several decades to treat menopausal discomforts. However, in the light of recent studies that draw attention to the potential hazards of conventional HRT, various attempts have been undertaken to search for alternatives to classical HRT. Phytoestrogens are claimed to be capable of positively influencing menopausal symptoms, including hot flushes. We designed a long-term study of 3 months to assess the effects of subcutaneous and orally fed 17 beta-estradiol (E2), as well as the actions of resveratrol (RES) on pituitary function in female rats. Our results have demonstrated that RES binds with a 10-fold lower affinity to estrogen receptor (ER)-alpha than to ER beta. The data from the hi vivo study revealed that a dosage of 5 mu g and 50 mu g RES/kg bodyweight per day given to ovariectomized (OVX) rats achieved serum levels of 1.0 and 8.1 mu M respectively. Long-term treatment of OVX rats with RES revealed no estrogenic potential on pituitary function in vivo as assessed by LH and prolactin secretion and by regulation of mRNAs for LH alpha, LH beta, and GnRH receptor. Subcutaneous treatment with E2 in silastic capsules exerted stronger effects on LH and prolactin secretion, as well as on LH beta, LH alpha, GnRH receptor, and ER beta mRNA regulation compared with orally applied estradiol benzoate despite comparable serum levels. Levels of aryl hydrocarbon receptor (AhR) mRNA in the pituitary were increased following OVX and attenuated by longterm E2 treatment, whereas RES did not modulate AhR mRNA expression.