Ferruz J, Ahmed C E, Ojeda S R, Lara H E
Department of Biochemistry and Molecular Biology, Faculty of Chemistry and Pharmaceutical Sciences, Universidad de Chile, Santiago.
Endocrinology. 1992 Mar;130(3):1345-51. doi: 10.1210/endo.130.3.1537296.
Experiments were undertaken to study the role that neuropeptide-Y (NPY) and adrenergic autoreceptors may play in the regulation of norepinephrine (NE) release from the rat ovary. Ovaries from 28- to 32-day-old rats were preincubated with [3H]NE, and the release of the recently taken up catecholamine in response to electric field stimulation was assessed. The release was strictly dependent on the presence of extracellular calcium and decreased when the frequency of stimulation was increased. This drop in [3H]NE release was significantly reversed by exposure of the ovaries during stimulation to yohimbine, a selective alpha 2-adrenoreceptor blocker. The existence of prejunctional alpha 2-adrenergic autoreceptors in ovarian nerves was further suggested by the ability of exogenous NE to mimic the inhibitory effect of high frequency stimulation. NPY inhibited by 40% the release of [3H]NE induced by electrical stimulation. The specificity of this effect and its prejunctional nature were demonstrated by the finding that avian pancreatic polypeptide, a structural homolog of NPY that is not recognized by prejunctional NPY receptors of the Y2 subtype, failed to alter the induced release of [3H]NE. Neither NPY, avian pancreatic polypeptide, nor peptide-YY, another member of the pancreatic polypeptide fold family, altered progesterone or estradiol secretion from whole ovaries or granulosa cells in culture, suggesting that NPY (and its structural homologs) does not directly affect ovarian steroidogenesis. The results suggest that 1) the release of NE from ovarian sympathetic nerves is subjected to a dual modulatory influence provided by NE itself and NPY; and 2) this regulatory effect is exerted via specific prejunctional receptors. Such NE/NPY actions are likely to regulate the availability of NE to its postsynaptic receptors during ovarian development and adult function. The fact that NPY is mostly released during high frequency stimulation raises the possibility of NPY involvement in ovarian dysfunctions associated with situations of enhanced sympathetic discharge, such as strenuous exercise and psychogenic amenorrhea.
开展实验以研究神经肽Y(NPY)和肾上腺素能自受体在调节大鼠卵巢去甲肾上腺素(NE)释放中可能发挥的作用。将28至32日龄大鼠的卵巢用[3H]NE进行预孵育,并评估电场刺激后最近摄取的儿茶酚胺的释放情况。释放严格依赖于细胞外钙的存在,并且当刺激频率增加时释放减少。在刺激期间将卵巢暴露于育亨宾(一种选择性α2-肾上腺素能受体阻滞剂)可显著逆转[3H]NE释放的这种下降。外源性NE模拟高频刺激的抑制作用的能力进一步提示卵巢神经中存在节前α2-肾上腺素能自受体。NPY抑制电刺激诱导的[3H]NE释放的40%。该作用的特异性及其节前性质通过以下发现得以证明:禽胰多肽是NPY的结构同源物,不被Y2亚型的节前NPY受体识别,它未能改变诱导的[3H]NE释放。NPY、禽胰多肽或胰多肽折叠家族的另一个成员肽YY均未改变整个卵巢或培养的颗粒细胞中孕酮或雌二醇的分泌,这表明NPY(及其结构同源物)不直接影响卵巢类固醇生成。结果表明:1)卵巢交感神经释放NE受到NE自身和NPY提供的双重调节影响;2)这种调节作用通过特定的节前受体发挥。这种NE/NPY作用可能在卵巢发育和成年功能期间调节NE对其突触后受体的可用性。NPY大多在高频刺激期间释放这一事实增加了NPY参与与交感神经放电增强情况相关的卵巢功能障碍的可能性,如剧烈运动和精神性闭经。