...
首页> 外文期刊>Journal of neuroendocrinology >Alteration in hypothalamic neuropeptide Y (NPY) secretion may underlie female reproductive ageing: induction of steroid-induced luteinising hormone surge by NPY in ovariectomised aged rats.
【24h】

Alteration in hypothalamic neuropeptide Y (NPY) secretion may underlie female reproductive ageing: induction of steroid-induced luteinising hormone surge by NPY in ovariectomised aged rats.

机译:下丘脑神经肽Y(NPY)分泌的改变可能是女性生殖老化的基础:NPY在去卵巢的老年大鼠中诱导类固醇诱导的黄体生成激素激增。

获取原文
获取原文并翻译 | 示例
           

摘要

A large body of evidence suggests that a defect in the hypothalamic function may be the primary cause of reproductive ageing in female rats. We have previously shown that luteinising hormone (LH)-surge associated changes in hypothalamic neuropeptide Y (NPY) gene expression and median eminence (ME) NPY levels seen in young rats do not occur in middle-aged (MA) rats. The present study examined whether hypothalamic NPY release is altered during the steroid-induced LH surge in ovariectomised (OVX) MA rats, and whether exogenous NPY initiates steroid-induced LH surge in OVX old rats. In the first study, NPY release from the ME-arcuate nucleus, as assessed by the push-pull cannula technique, was significantly increased before and during the progesterone-induced LH surge in oestrogen (E(2))-primed ovariectomised young rats (2-3 months old). This antecedent increase in NPY release seen in young rats was not apparent in MA rats (11-13 months old) in association with a delayed and attenuated LH surge. In the second study, whereas progesterone failed to induce LH surges in E(2)-primed ovariectomised old rats (23-25 months old), intracerebroventricular NPY (0.1-0.5 microg) injections at 1100, 1200 and 13.00 h resulted in LH surge induction in E(2) + progesterone-primed ovariectomised old rats. Because increased hypothalamic NPY synthesis and release is obligatory for the preovulatory LH discharge in young rats, the present findings suggest that alteration in NPY release from the ME-arcuate nucleus contributes to the delayed and reduced LH surges in MA rats and may be involved in the subsequent loss of the LH surges in old rats.
机译:大量证据表明,下丘脑功能缺陷可能是雌性大鼠生殖衰老的主要原因。我们以前已经证明,在年轻大鼠中发现的黄体生成激素(LH)浪涌相关的下丘脑神经肽Y(NPY)基因表达和中位突出(ME)NPY水平变化在中年(MA)大鼠中不发生。本研究检查了在卵巢切除的(OVX)MA大鼠中类固醇诱导的LH激增期间下丘脑NPY释放是否改变,以及在OVX老大鼠中外源性NPY是否引发了类固醇诱导的LH激增。在第一项研究中,经推挽套管技术评估,在孕激素诱导的雌激素(E(2))促排卵的年轻大鼠中,LH激增之前和期间,ME弧状核从NPY释放显着增加( 2-3个月大)。与延迟和减弱的LH激增有关,在MA大鼠(11-13个月大)中,在幼鼠中观察到的这种NPY释放的增加并不明显。在第二项研究中,孕酮未能在E(2)致卵巢切除的老大鼠(23-25个月大)中诱导LH激增,而在1100、1200和13.00 h时脑室内NPY(0.1-0.5微克)注射导致LH激增E(2)+孕激素引发的去卵巢老大鼠中的诱导。由于下丘脑NPY合成和释放的增加对于幼鼠排卵前LH的释放是必须的,因此本研究结果表明,ME弧状核中NPY释放的改变会导致MA大鼠LH波动的延迟和减少,并且可能参与了随后老年大鼠的LH激增丧失。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

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