Tijssen A M, Helder M N, Chu Z W, de Koning J
Division of Medical Pharmacology, Leiden/Amsterdam Center for Drug Research, Sylvius Laboratories, University of Leiden, The Netherlands.
J Reprod Fertil. 1997 Nov;111(2):235-42. doi: 10.1530/jrf.0.1110235.
The antagonistic control of LH concentrations by GnRH and the putative ovarian factor gonadotrophin surge-inhibiting or -attenuating factor (GnSIF/AF) was studied by perifusion of female rat pituitary glands in vitro. LH release and GnRH self-priming were measured in response to five (0.32-10 nmol l-1) or three (10 nmol l-1) 10 min pulses of GnRH. In the latter case, pulses were preceded by five 10 min pulses of either 1 mmol 8-bromo-cAMP l-1 plus 10 mmol theophylline l-1 or 1 mumol phorbol 12-myristate 13-acetate l-1. The stimulations were carried out in the presence or absence of steroid-free bovine follicular fluid, which possesses GnSIF/AF bioactivity, to study the effect of GnSIF/AF on the self-priming process during successive stimulations by GnRH. First, the effect of follicular fluid was studied on GnRH-induced LH release from pituitary glands collected during the ovarian cycle. Only when a clear self-priming effect was evident, as on day 2 of dioestrus and the day of pro-oestrus, follicular fluid antagonized the self-priming effect of GnRH. Second, when glands on day 2 of dioestrus were used, self-priming was displayed by various combinations of GnRH and follicular fluid. The pulses with the lowest concentrations of GnRH together with a high concentration of follicular fluid, however, led to stable low amplitude LH pulses. Finally, priming of the pituitary LH response to GnRH with 8-bromo-cAMP plus theophylline or phorbol 12-myristate 13-acetate was inhibited by follicular fluid. These results confirm the control of LH release by GnRH and GnSIF/AF bioactivity. The effect of GnSIF/AF in follicular fluid is most pronounced on the days before the LH surge, showing evidence of its important role in maintaining low LH concentrations during this period. GnSIF/AF neutralizes downstream actions of second messengers involved in GnRH self-priming.
通过体外灌流雌性大鼠垂体,研究了促性腺激素释放激素(GnRH)和假定的卵巢因子促性腺激素激增抑制或衰减因子(GnSIF/AF)对促黄体生成素(LH)浓度的拮抗控制作用。测量了对五个(0.32 - 10 nmol l-1)或三个(10 nmol l-1)10分钟GnRH脉冲的反应中LH释放和GnRH自增强情况。在后一种情况下,脉冲之前有五个10分钟的脉冲,分别为1 mmol 8-溴环磷酸腺苷l-1加10 mmol氨茶碱l-1或1 μmol佛波醇12-肉豆蔻酸酯13-乙酸酯l-1。刺激在有无具有GnSIF/AF生物活性的无类固醇牛卵泡液存在的情况下进行,以研究GnSIF/AF对GnRH连续刺激期间自增强过程的影响。首先,研究了卵泡液对卵巢周期不同阶段采集的垂体中GnRH诱导的LH释放的影响。仅在动情后期第2天和发情前期出现明显的自增强效应时,卵泡液才拮抗GnRH的自增强效应。其次,当使用动情后期第2天的垂体时,GnRH和卵泡液的不同组合表现出自增强作用。然而,最低浓度GnRH的脉冲与高浓度卵泡液一起导致稳定的低幅度LH脉冲。最后,卵泡液抑制了用8-溴环磷酸腺苷加氨茶碱或佛波醇12-肉豆蔻酸酯13-乙酸酯对垂体LH对GnRH反应的预激发作用。这些结果证实了GnRH和GnSIF/AF生物活性对LH释放的控制。卵泡液中GnSIF/AF的作用在LH激增前几天最为明显,表明其在此期间维持低LH浓度方面具有重要作用。GnSIF/AF中和参与GnRH自增强的第二信使的下游作用。