Kacsóh B, Tóth B E, Avery L M, Grosvenor C E
Pennsylvania State University, Department of Molecular and Cell Biology, University Park 16802.
Life Sci. 1993;52(3):259-69. doi: 10.1016/0024-3205(93)90217-q.
Bromocryptine potently decreased prolactin (PRL) secretion of pituitary glands of 2-day-old rats in vitro (up to 85% inhibition; ED50 between 0.1 and 1.0 nM) without altering the bioactivity to immunoreactivity (B/I) ratio. Bromocryptine tended to suppress growth hormone (GH) secretion although the effect did not reach statistical significance. Angiotensin-II (A-II; 1-1000 nM) stimulated PRL secretion in a dose-dependent manner without affecting secretion of GH. The B/I ratio of PRL secreted in response to A-II was increased. Somatostatin (SRIF) had no effect on PRL secretion but inhibited GH secretion in a dose-dependent manner; significant inhibition (50%) was observed at 100 nM. A 6-h exposure to ovine PRL (oPRL) in concentrations equipotent with 1.2-120 ng/ml rat PRL (rPRL) in the Nb2 bioassay had no effect on immunoreactive rPRL secretion. Salmon calcitonin (sCT) and endothelin-3 (ET-3; 0.1-100 nM) failed to inhibit secretion of PRL or GH. PRL secretion was slightly stimulated by sCT with no apparent dose-response relationship. The present findings suggest that neonatal pituitary glands do not display autoregulation of PRL secretion, and sCT and ET-3 (either endogenous or milk-derived) may not function as PRL inhibiting factors in 2-day-old pups. Thus, the receptors of PRL, sCT and ET-3 on lactotropes, or their functional coupling with inhibition of basal PRL secretion, occur at a later stage of development. The specificity of the PRL releasing factor (PRF) activity of A-II at this age is unique for established PRFs and might reflect a physiological function of PRL in osmoregulation. The increased B/I ratio of PRL secreted in response to A-II may be due to the release of specific PRL variants, and might be a sign of functional heterogeneity among lactotropes. The differential sensitivity of PRL and GH to the applied secretagogues suggests that the intracellular regulation of PRL and GH are compartmentalized in the mammosomatotrope cell.
溴隐亭在体外能显著降低2日龄大鼠垂体的催乳素(PRL)分泌(抑制率高达85%;半数有效量在0.1至1.0 nM之间),且不改变生物活性与免疫反应性(B/I)的比值。溴隐亭虽有抑制生长激素(GH)分泌的趋势,但该效应未达到统计学显著水平。血管紧张素-II(A-II;1 - 1000 nM)以剂量依赖方式刺激PRL分泌,而不影响GH分泌。A-II刺激分泌的PRL的B/I比值升高。生长抑素(SRIF)对PRL分泌无影响,但以剂量依赖方式抑制GH分泌;在100 nM时观察到显著抑制(50%)。在Nb2生物测定中,以与1.2 - 120 ng/ml大鼠PRL(rPRL)等效的浓度,使大鼠暴露于绵羊PRL(oPRL)6小时,对免疫反应性rPRL分泌无影响。鲑鱼降钙素(sCT)和内皮素-3(ET-3;0.1 - 100 nM)未能抑制PRL或GH的分泌。sCT对PRL分泌有轻微刺激作用,但无明显剂量反应关系。目前的研究结果表明,新生大鼠垂体不显示PRL分泌的自动调节,并且sCT和ET-3(无论是内源性还是源自乳汁)在2日龄幼崽中可能不作为PRL抑制因子发挥作用。因此,催乳素细胞上PRL、sCT和ET-3的受体,或它们与基础PRL分泌抑制的功能偶联,在发育后期才出现。A-II在这个年龄段的PRL释放因子(PRF)活性的特异性对于已确定 的PRF来说是独特的,可能反映了PRL在渗透压调节中的生理功能。A-II刺激分泌的PRL的B/I比值升高可能是由于特定PRL变体的释放,可能是催乳素细胞功能异质性的一个标志。PRL和GH对所应用的促分泌素的不同敏感性表明,PRL和GH的细胞内调节在乳腺生长激素细胞中是分隔的。