Danger J M, Lamacz M, Mauviard F, Saint-Pierre S, Jenks B G, Tonon M C, Vaudry H
Groupe de Recherche en Endocrinologie Moléculaire, URA CNRS 650, Unité Affiliée INSERM, Université de Rouen, Mont-Saint-Aignan, France.
Gen Comp Endocrinol. 1990 Jan;77(1):143-9. doi: 10.1016/0016-6480(90)90215-8.
Previous studies have shown that the release of melanotropin from frog neurointermediate lobes is under the control of two neuropeptides: thyrotropin-releasing hormone (TRH) stimulates, while neuropeptide Y (NPY) inhibits alpha-melanocyte-stimulating hormone (alpha-MSH) secretion from intact neurointermediate lobes in vitro. The aim of the present study was to investigate possible interactions between the two regulatory peptides at the pituitary level. Whole neurointermediate lobes or acutely dispersed pars intermedia cells from Rana ridibunda were perifused in vitro for 2 to 7.5 hr and the concentrations of alpha-MSH released into the effluent perifusate were monitored by radioimmunoassay. Administration of TRH (10(-7) M) or NPY (10(-7) M) to dispersed cells induced, respectively, marked stimulation or inhibition of alpha-MSH release. The effects of the two neuropeptides were similar to those observed using intact neurointermediate lobes, suggesting that TRH and NPY act directly on melanotropic cells. Perifused whole neurointermediate lobes were exposed to NPY (10(-8) to 3 x 10(-7) M) for 120 min and a single dose of TRH (10(-8) M) was administered during the prolonged infusion of NPY. Using this procedure, we observed a dose-dependent inhibition of TRH-evoked alpha-MSH release. These data support the concept that TRH and NPY act through a common intracellular pathway to regulate alpha-MSH release.
以往的研究表明,青蛙神经中间叶促黑素的释放受两种神经肽的控制:促甲状腺激素释放激素(TRH)起刺激作用,而神经肽Y(NPY)则抑制体外完整神经中间叶中α-黑素细胞刺激素(α-MSH)的分泌。本研究的目的是探讨这两种调节肽在垂体水平上可能存在的相互作用。对来自食用蛙的整个神经中间叶或急性分散的垂体中间部细胞进行体外灌流2至7.5小时,并通过放射免疫测定法监测释放到流出灌流液中的α-MSH浓度。向分散细胞施用TRH(10^(-7) M)或NPY(10^(-7) M)分别诱导了α-MSH释放的显著刺激或抑制。这两种神经肽的作用与使用完整神经中间叶时观察到的作用相似,表明TRH和NPY直接作用于促黑素细胞。将灌流的整个神经中间叶暴露于NPY(10^(-8)至3×10^(-7) M)120分钟,并在NPY的长时间输注期间施用单剂量的TRH(10^(-8) M)。使用该程序,我们观察到TRH诱发的α-MSH释放受到剂量依赖性抑制。这些数据支持TRH和NPY通过共同的细胞内途径调节α-MSH释放的概念。