Zanisi M, Messi E, Motta M, Martini L
Department of Endocrinology, University of Milan, Italy.
Endocrinology. 1987 Dec;121(6):2199-204. doi: 10.1210/endo-121-6-2199.
The present experiments were performed to clarify whether LHRH might inhibit its own secretion via an ultrashort feedback mechanism acting directly on the hypothalamus. Using an in vitro system, mediobasal hypothalami (MBHs) of adult male rats were perifused in either the presence or absence of a LHRH agonistic analog [D-Ser(TBU)6,Des-Gly10] LHRH ethylamide shown not to cross-react in the LHRH RIA. In the first series of experiments, six MBHs per chamber were initially perifused with control medium and submitted to two K+ stimulations (110 mM) for 5 min every 30 min; the control medium was then replaced by medium containing the LHRH analog (5 microM), and three additional K+ pulses were applied. In the second series of experiments, a single MBH per chamber was exposed for the duration of the experiments to either control medium or medium containing the LHRH analog (5 microM). In both cases, pulses of K+ were applied to the tissue. The amounts of endogenous LHRH released both under basal conditions and after K+ stimulation were measured in the effluent (1 ml every 5 min) with a specific RIA. The results show that the LHRH analog inhibits basal secretion of endogenous LHRH from the MBH, and diminishes or abolishes the response to K+ stimulations. The specificity of the inhibitory effect exerted by the LHRH analog on LHRH secretion was shown by the inability of TRH to mimic the effect of the LHRH analog. The data are consistent with the hypothesis that LHRH, acting at a hypothalamic level, might participate in the control of its own release via an ultrashort feedback mechanism.
进行本实验是为了阐明促性腺激素释放激素(LHRH)是否可能通过直接作用于下丘脑的超短反馈机制来抑制其自身分泌。利用体外系统,在成年雄性大鼠的内侧基底部下丘脑(MBH)存在或不存在LHRH激动剂类似物[D - Ser(TBU)6,Des - Gly10]LHRH乙酰胺的情况下进行灌流,该类似物在LHRH放射免疫分析(RIA)中显示无交叉反应。在第一系列实验中,每个腔室中的六个MBH最初用对照培养基灌流,并每30分钟接受两次5分钟的K⁺刺激(110 mM);然后将对照培养基替换为含有LHRH类似物(5 μM)的培养基,并施加另外三个K⁺脉冲。在第二系列实验中,每个腔室中的单个MBH在实验期间暴露于对照培养基或含有LHRH类似物(5 μM)的培养基中。在这两种情况下,均对组织施加K⁺脉冲。用特异性RIA测量流出物(每5分钟1 ml)中基础条件下和K⁺刺激后释放的内源性LHRH量。结果表明,LHRH类似物抑制MBH中内源性LHRH的基础分泌,并减弱或消除对K⁺刺激的反应。促甲状腺激素释放激素(TRH)无法模拟LHRH类似物的作用,这表明LHRH类似物对LHRH分泌的抑制作用具有特异性。这些数据与以下假设一致,即LHRH在下丘脑水平起作用,可能通过超短反馈机制参与其自身释放的控制。