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性腺类固醇在雌性生殖系统内以组织特异性方式调节前脑啡肽基因的表达。

Gonadal steroids regulate proenkephalin gene expression in a tissue-specific manner within the female reproductive system.

作者信息

Muffly K E, Jin D F, Okulicz W C, Kilpatrick D L

机构信息

Neurobiology Group, Worcester Foundation for Experimental Biology, Shrewsbury, Massachusetts 01545.

出版信息

Mol Endocrinol. 1988 Oct;2(10):979-85. doi: 10.1210/mend-2-10-979.

Abstract

Proenkephalin gene expression undergoes marked changes within the female reproductive system of rodents during the estrous cycle and in pregnancy. In order to define the factors responsible for this regulation, the effects of 17-beta-estradiol (E2) and progesterone (P4) have been examined in the ovary and uterus. In the ovary of the rat and hamster, E2 and P4 were without effect on proenkephalin RNA levels when injected individually. However, P4 increased ovarian transcript abundance 2- to 3-fold after pretreatment of animals with E2. In the uterus of either species, E2 had little effect but P4 alone stimulated both proenkephalin RNA abundance and total content severalfold. Glucocorticoids and androgen reproduced this stimulatory effect on proenkephalin transcript levels. The interaction between E2 and P4 on proenkephalin gene expression in the uterus varied with species. In the rat, E2 inhibited stimulation by P4, while in the hamster uterus the two hormones had a synergistic effect, producing a 15-fold elevation of proenkephalin RNA abundance and a 50-fold increase in total uterine content. These distinct steroid responses appear to account for tissue- and species-related differences in the variation of proenkephalin gene expression during the estrous cycle in the rodent ovary and uterus. The stimulatory effect of P4 was shown to involve direct steroid action on the uterus and to be inhibited both by the steroid antagonist RU-486 and the transcriptional inhibitor actinomycin D. These data are consistent with receptor-mediated activation of proenkephalin gene transcription in uterine cells.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在啮齿动物的发情周期和怀孕期间,前脑啡肽基因表达在雌性生殖系统内会发生显著变化。为了确定负责这种调节的因素,研究了17-β-雌二醇(E2)和孕酮(P4)对卵巢和子宫的影响。在大鼠和仓鼠的卵巢中,单独注射E2和P4对前脑啡肽RNA水平没有影响。然而,在用E2预处理动物后,P4使卵巢转录本丰度增加了2至3倍。在这两种动物的子宫中,E2影响不大,但单独的P4能刺激前脑啡肽RNA丰度和总含量增加几倍。糖皮质激素和雄激素对前脑啡肽转录水平产生了这种刺激作用。E2和P4在子宫中对前脑啡肽基因表达的相互作用因物种而异。在大鼠中,E2抑制P4的刺激作用,而在仓鼠子宫中,这两种激素具有协同作用,使前脑啡肽RNA丰度提高了15倍,子宫总含量增加了50倍。这些不同的类固醇反应似乎解释了啮齿动物卵巢和子宫在发情周期中前脑啡肽基因表达变化的组织和物种相关差异。P4的刺激作用表明涉及类固醇对子宫的直接作用,并且被类固醇拮抗剂RU - 486和转录抑制剂放线菌素D所抑制。这些数据与子宫细胞中前脑啡肽基因转录的受体介导激活一致。(摘要截短至250字)

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