首页> 美国卫生研究院文献>Reproductive Sciences >Interaction of Gonadal Steroids and Gonadotropin-Releasing Hormone on Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) and PACAP Receptor Expression in Cultured Rat Anterior Pituitary Cells
【2h】

Interaction of Gonadal Steroids and Gonadotropin-Releasing Hormone on Pituitary Adenylate Cyclase-Activating Polypeptide (PACAP) and PACAP Receptor Expression in Cultured Rat Anterior Pituitary Cells

机译:性腺激素和促性腺激素释放激素对大鼠垂体前叶垂体中垂体腺苷酸环化酶激活多肽(PACAP)和PACAP受体表达的相互作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Pituitary adenylate cyclase-activating polypeptide (PACAP) and its receptors are expressed in the hypothalamus, the gonadotrope cells of the anterior pituitary gland, and the gonads, forming an autocrine–paracrine system in these tissues. Within the pituitary, PACAP functions either alone or synergistically with gonadotropin-releasing hormone (GnRH) to stimulate gonadotropin gene expression and secretion. Our goal was to define the hormonal regulation of pituitary PACAP and PACAP receptor (PAC1) gene expression by dihydrotestosterone (DHT), estradiol, and progesterone alone or in conjunction with GnRH. Treatment of adult male rat pituitary cell cultures with DHT or progesterone augmented GnRH-mediated increase in PACAP messenger RNA (mRNA) levels, but neither had an effect when present alone. Conversely, estradiol treatment blunted PACAP gene expression but did not alter GnRH effects on PACAP expression. Expression of PACAP receptor mRNA was decreased by GnRH treatment, minimally increased by DHT treatment, but not altered by the addition of estradiol or progesterone. DHT and GnRH together blunted PACAP receptor gene expression. Taken together, these results suggest that the activity of the intrapituitary PACAP-PAC1 system is regulated via the complex interaction of gonadal steroids and hypothalamic GnRH.
机译:垂体腺苷酸环化酶激活多肽(PACAP)及其受体在下丘脑,垂体前叶的性腺细胞和性腺中表达,在这些组织中形成自分泌-旁分泌系统。在垂体内,PACAP单独起作用或与促性腺激素释放激素(GnRH)协同作用,以刺激促性腺激素基因的表达和分泌。我们的目标是通过单独使用二氢睾丸激素(DHT),雌二醇和孕酮或与GnRH结合来定义垂体PACAP和PACAP受体(PAC1)基因表达的激素调节。用DHT或孕激素处理成年雄性大鼠垂体细胞培养物可增强GnRH介导的PACAP信使RNA(mRNA)水平的升高,但单独使用时均无效。相反,雌二醇处理会使PACAP基因表达减弱,但不会改变GnRH对PACAP表达的影响。通过GnRH处理,PACAP受体mRNA的表达降低,通过DHT处理,PACAP受体mRNA的表达略有增加,但未因添加雌二醇或孕酮而改变。 DHT和GnRH共同削弱了PACAP受体基因的表达。两者合计,这些结果表明,通过性腺类固醇和下丘脑GnRH的复杂相互作用,调节了垂体PACAP-PAC1系统的活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号