Kanyicska Béla, Sellix Michael T, Freeman Marc E
Department of Biological Science, Florida State University, Tallahassee, FL 32306-4340, USA.
Endocrine. 2003 Feb-Mar;20(1-2):53-8. doi: 10.1385/ENDO:20:1-2:53.
We have previously found that the ovarian steroid background determines the efficiency of the endothelin-mediated autocrine feedback regulation of prolactin (PRL) secretion. In this study, we investigated the role of endogenous endothelins in regulating PRL secretion during the estrous cycle. Adult female rats representing different stages of the 4-d cycle were sacrificed by decapitation, and the anterior pituitary cells were enzymatically dispersed using collagenase and hyaluronidase. PRL secretion of individual lactotrophs was measured in a PRL-specific reverse hemolytic plaque assay, and the influence of endogenous endothelins on PRL secretion was assessed by applying the selective ET(A) receptor antagonist peptide, BQ123. Blocking the endothelin-mediated autocrine feedback resulted in an increase in PRL secretion when cells were obtained at proestrus, estrus, and diestrus-1, whereas PRL secretion was decreased at diestrus-2 by ET(A) receptor blockade. These observations suggest that endogenous endothelins are predominantly inhibitory during proestrus, estrus, and diestrus-1, whereas at diestrus-2 their influence on PRL secretion is stimulatory. Whereas the bell-shaped concentration-response curves with BQ123 at proestrus and diestrus-1 may indicate a transition state in which endogenous endothelins can be both stimulatory and inhibitory, at estrus the influence of endogenous endothelins is unequivocally inhibitory in nature. We propose that intensification of the endogenous endothelin- mediated negative feedback at estrus may play a role in restraining PRL secretion following the estradiol- induced proestrous PRL surge.
我们之前发现,卵巢类固醇背景决定了内皮素介导的催乳素(PRL)分泌自分泌反馈调节的效率。在本研究中,我们调查了内源性内皮素在发情周期中调节PRL分泌的作用。通过断头处死代表4天周期不同阶段的成年雌性大鼠,并用胶原酶和透明质酸酶酶解分散垂体前叶细胞。在PRL特异性反向溶血空斑试验中测量单个催乳细胞的PRL分泌,并通过应用选择性ET(A)受体拮抗剂肽BQ123评估内源性内皮素对PRL分泌的影响。当在动情前期、发情期和间情期-1获取细胞时,阻断内皮素介导的自分泌反馈会导致PRL分泌增加,而在间情期-2,ET(A)受体阻断会使PRL分泌减少。这些观察结果表明,内源性内皮素在动情前期、发情期和间情期-1主要起抑制作用,而在间情期-2它们对PRL分泌的影响是刺激性的。虽然在动情前期和间情期-1使用BQ123时呈钟形浓度-反应曲线可能表明存在内源性内皮素既具有刺激性又具有抑制性的过渡状态,但在发情期,内源性内皮素的影响在本质上无疑是抑制性的。我们提出,发情期内源性内皮素介导的负反馈增强可能在抑制雌二醇诱导的动情前期PRL高峰后的PRL分泌中起作用。