Héry M, François-Bellan A M, Héry F, Deprez P, Becquet D
Laboratoire de Neuroendocrinologie Expérimentale, INSERM U297, Faculté de Médecine Nord, Institut Fédératif Jean Roche, Marseille, France.
Endocrine. 1997 Oct;7(2):261-5. doi: 10.1007/BF02778149.
Luteinizing hormone-releasing hormone (LHRH release, which serves as the primary drive to the hypothalamic-pituitary gonadal axis, is controlled by many neuromediators. Serotonin has been implicated in this regulation. However, it is unclear whether the central effect of serotonin on LHRH secretion is exerted directly on LHRH neurosecretory neurons or indirectly via multisynaptic pathways. The present studies were undertaken in order to examine whether LHRH secretion from immortalized LHRH cell lines is directly regulated by serotonin and, if so, to identify the receptor subtype involved. 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT), a 5-HT1A/7 receptor agonist, stimulated LHRH release from GT1-1 cells. This effect was blocked by ritanserin, a 5-HT2/7 receptor antagonist, but not by SDZ-216-525, a 5-HT1A antagonist. Basal LHRH release was not affected by the 5-HT2 agonist DOI. Reverse transcription and polymerase chain reaction technique (RT-PCR) was used in order to identify 5-HT1A and 5-HT7 receptor mRNA in immortalized LHRH cell lines. GT1-1 cells express mRNA for the 5-HT7, but not the 5-HT1A receptor subtypes. These results demonstrate a direct stimulatory effect of serotonin on LHRH release via 5-HT7 receptor.
促黄体生成素释放激素(LHRH释放,它是下丘脑 - 垂体 - 性腺轴的主要驱动力,受多种神经介质控制。血清素与这种调节有关。然而,血清素对LHRH分泌的中枢作用是直接作用于LHRH神经分泌神经元还是通过多突触途径间接作用尚不清楚。进行本研究是为了检查永生化LHRH细胞系中LHRH的分泌是否直接受血清素调节,如果是,确定所涉及的受体亚型。8 - 羟基 - 2 - (二正丙基氨基)四氢萘(8 - OH - DPAT),一种5 - HT1A / 7受体激动剂,刺激GT1 - 1细胞释放LHRH。这种作用被5 - HT2 / 7受体拮抗剂利坦色林阻断,但未被5 - HT1A拮抗剂SDZ - 216 - 525阻断。5 - HT2激动剂DOI对基础LHRH释放无影响。采用逆转录聚合酶链反应技术(RT - PCR)来鉴定永生化LHRH细胞系中的5 - HT1A和5 - HT7受体mRNA。GT1 - 1细胞表达5 - HT7受体亚型的mRNA,但不表达5 - HT1A受体亚型的mRNA。这些结果表明血清素通过5 - HT7受体对LHRH释放有直接刺激作用。