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孕激素受体在排卵前促黄体生成素激增期间对下丘脑谷氨酸脱羧酶基因表达抑制中的作用。

Role of the progesterone receptor in restrained glutamic acid decarboxylase gene expression in the hypothalamus during the preovulatory luteinizing hormone surge.

作者信息

Brann Darrell W, Unda Richard, Mahesh Virendra B

机构信息

Institute of Molecular Medicine and Genetics, and Department of Neurology, Neurobiology Program, Medical College of Georgia, Augusta, GA 30912, USA.

出版信息

Neuroendocrinology. 2002 Nov;76(5):283-9. doi: 10.1159/000066628.

Abstract

Previous work by our laboratory demonstrated that activation of the progesterone receptor through exogenous administration of progesterone suppressed glutamic acid decarboxylase-67 (GAD(67)) mRNA in the hypothalamus of the estrogen-primed ovariectomized rat. Since GAD(67) is the major synthetic enzyme for the inhibitory transmitter, gamma-aminobutyric acid, the finding raised the possibility that the endogenous activation of the progesterone receptor may act to restrain GAD(67) expression during the natural preovulatory gonadotropin surge during proestrus in the rat, thereby allowing GnRH secretion and the resultant LH surge. To test this hypothesis, the progesterone receptor antagonist, RU486, was administered to regularly cycling proestrous rats and the effect on GAD(67) and GAD(65) mRNA levels in the preoptic area (POA) and medial basal hypothalamus (MBH) was examined. Serum luteinizing hormone (LH) levels were also examined in order to identify correlations between changes in POA and MBH GAD levels and production of the LH surge. GAD(67) mRNA levels in the POA were increased in the cycling rat during proestrus at 18.00 h at the peak and just preceding the termination of the LH surge. There was no change in GAD(67) mRNA levels in the MBH, and GAD(65) expression was also unchanged during proestrus in the POA and MBH. Treatment with the antiprogestin RU486 resulted in an increase in GAD(67) mRNA levels at 12.00 and 14.00 h in the POA, and in the MBH at 14.00, 16.00, and 18.00 h during proestrus, effects which preceded and correlated with the attenuated LH surge in RU486-treated rats at 18.00 h. GAD(65) mRNA levels were also elevated by RU486 at 14.00 and 16.00 h in the POA, and at 14.00 h in the MBH during proestrus. These findings suggest that the progesterone receptor plays a role in restraining GAD expression in the hypothalamus during proestrus, and that this effect may be important for the production of the GnRH and LH surge.

摘要

我们实验室之前的研究表明,通过外源给予孕酮激活孕酮受体可抑制雌激素预处理的去卵巢大鼠下丘脑谷氨酸脱羧酶67(GAD(67))的mRNA表达。由于GAD(67)是抑制性神经递质γ-氨基丁酸的主要合成酶,这一发现提示,在大鼠发情前期自然排卵前促性腺激素高峰期间,孕酮受体的内源性激活可能会抑制GAD(67)的表达,从而促使促性腺激素释放激素(GnRH)分泌及随后的促黄体生成素(LH)高峰。为验证这一假说,将孕酮受体拮抗剂RU486给予正常发情前期大鼠,并检测其对视前区(POA)和下丘脑内侧基底部(MBH)中GAD(67)和GAD(65) mRNA水平的影响。同时检测血清促黄体生成素(LH)水平,以确定POA和MBH中GAD水平变化与LH高峰产生之间的相关性。在发情前期18.00 h,即LH高峰峰值及即将结束时,正常发情大鼠POA中GAD(67) mRNA水平升高。MBH中GAD(67) mRNA水平无变化,发情前期POA和MBH中GAD(65)表达也未改变。抗孕激素RU486处理导致发情前期POA在12.00和14.00 h以及MBH在14.00、16.00和18.00 h时GAD(67) mRNA水平升高,这些影响先于并与RU486处理大鼠18.00 h时减弱的LH高峰相关。发情前期POA在14.00和16.00 h以及MBH在14.00 h时,RU486也使GAD(65) mRNA水平升高。这些发现表明,孕酮受体在发情前期抑制下丘脑GAD表达中起作用,且这一作用可能对GnRH和LH高峰的产生很重要。

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