Vanecek J, Klein D C
Section on Neuroendocrinology, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Endocrinology. 1992 Feb;130(2):701-7. doi: 10.1210/endo.130.2.1733718.
GnRH stimulates LH release by increasing intracellular Ca2+ ([Ca2+]i). Melatonin is known to inhibit GnRH-stimulated LH release from neonatal rat pituitary cells. In the present report, the issue of whether melatonin acts through [Ca2+]i was addressed. [Ca2+]i was studied in cells in suspension, using Fluo-3 as a fluorescent indicator. In neonatal rat pituitary cells, melatonin inhibited the GnRH-induced [Ca2+]i increase in a dose-dependent manner; the GnRH-induced increase in [Ca2+]i was inhibited 40% by 100 nM melatonin. The relative potencies of several indoles as inhibitors of the GnRH stimulation of [Ca2+]i in neonatal pituitary cells (2-iodo-melatonin greater than melatonin greater than 6-hydroxymelatonin) correlate with their known potencies to inhibit LH release and with their binding affinity to high affinity melatonin receptors, which indicates that these receptors probably mediate the effects of melatonin. Further support for this interpretation comes from the observation that melatonin does not inhibit the GnRH effect on [Ca2+]i in cells obtained from adolescent rat pituitary glands, which lack melatonin receptors and are insensitive to melatonin as an inhibitor of GnRH-stimulated LH release. The possible involvement of an inhibitory G-protein was also investigated by studying the effects of pertussis toxin. Pretreatment with pertussis toxin antagonized the effects of melatonin on [Ca2+]i and LH release. This indicates that melatonin may inhibit the GnRH-induced increase in [Ca2+]i through a mechanism involving a pertussis toxin-sensitive G-protein. To examine the role of extracellular Ca2+ in this effect, the effects of melatonin were examined in a low Ca2+ medium. Under these conditions, the effect of melatonin was markedly reduced, which indicates that melatonin may act by inhibiting Ca2+ influx. These observations indicate that melatonin inhibits GnRH stimulation of [Ca2+]i in neonatal rat gonadotrophs, and this probably explains the inhibitory action of melatonin on GnRH stimulation of LH release.
促性腺激素释放激素(GnRH)通过增加细胞内钙离子浓度([Ca2+]i)来刺激促黄体生成素(LH)的释放。已知褪黑素可抑制新生大鼠垂体细胞中GnRH刺激的LH释放。在本报告中,探讨了褪黑素是否通过[Ca2+]i发挥作用这一问题。使用Fluo-3作为荧光指示剂,对悬浮细胞中的[Ca2+]i进行了研究。在新生大鼠垂体细胞中,褪黑素以剂量依赖的方式抑制GnRH诱导的[Ca2+]i升高;100 nM褪黑素可使GnRH诱导的[Ca2+]i升高受到40%的抑制。几种吲哚作为新生垂体细胞中GnRH刺激的[Ca2+]i抑制剂的相对效力(2-碘褪黑素大于褪黑素大于6-羟基褪黑素)与其已知的抑制LH释放的效力以及它们与高亲和力褪黑素受体的结合亲和力相关,这表明这些受体可能介导了褪黑素的作用。对这一解释的进一步支持来自以下观察结果:褪黑素对青春期大鼠垂体腺细胞中GnRH对[Ca2+]i的作用没有抑制作用,这些细胞缺乏褪黑素受体,并且对褪黑素作为GnRH刺激的LH释放抑制剂不敏感。还通过研究百日咳毒素的作用来探讨抑制性G蛋白的可能参与情况。用百日咳毒素预处理可拮抗褪黑素对[Ca2+]i和LH释放的作用。这表明褪黑素可能通过涉及百日咳毒素敏感G蛋白的机制来抑制GnRH诱导的[Ca2+]i升高。为了研究细胞外钙离子在这种作用中的作用,在低钙培养基中检测了褪黑素的作用。在这些条件下,褪黑素的作用明显减弱,这表明褪黑素可能通过抑制钙离子内流来发挥作用。这些观察结果表明,褪黑素抑制新生大鼠促性腺细胞中GnRH对[Ca2+]i的刺激,这可能解释了褪黑素对GnRH刺激的LH释放的抑制作用。