Oride Aki, Kanasaki Haruhiko, Tumurbaatar Tuvshintugs, Zolzaya Tumurgan, Okada Hiroe, Hara Tomomi, Kyo Satoru
Department of Obstetrics and Gynecology, Shimane University School of Medicine, 89-1 Enya Cho, Izumo, Shimane, 693-8501, Japan.
Reprod Sci. 2020 Mar;27(3):806-814. doi: 10.1007/s43032-020-00154-1. Epub 2020 Jan 31.
Clomiphene citrate (CC) and letrozole stimulate the hypothalamic-pituitary-ovarian axis and are used widely as oral fertility drugs to induce folliculogenesis. We examined whether these drugs increase Kiss-1 expression in hypothalamic cell models. We utilized two hypothalamic cell models, mHypoA-50 and mHypoA-55, which originated from Kiss-1 neurons in the anteroventral periventricular (AVPV) nucleus and arcuate (ARC) nucleus of the mouse hypothalamus, respectively. The cells were stimulated with CC or letrozole, after which Kiss-1 mRNA expression was determined. CC stimulated Kiss-1 gene expression in mHypoA-50 and mHypoA-55 cells. The basal expression of Kiss-1 was significantly increased in the presence of estradiol (E2) in mHypoA-50 cells, and the CC-induced increase in Kiss-1 expression was not observed in the presence of E2 in these cells. In contrast, E2 did not modify the basal expression of Kiss-1 in mHypoA-55 cells, and CC-induced Kiss-1 expression was still observed in the presence of E2. The significant increase in Kiss-1 gene expression in mHypoA-50 and mHypoA-55 cells was blunted in the presence of estrogen receptor antagonists. Aromatase was expressed in mHypoA-50 and mHypoA-55 cells. Letrozole, an aromatase inhibitor, increased Kiss-1 expression in mHypoA-55 ARC cells but not in mHypoA-50 AVPV cells. Although the basal expression of Kiss-1 was increased by E2, letrozole did not modulate Kiss-1 expression in mHypoA-50 cells. Letrozole-induced Kiss-1 gene expression in mHypoA-55 cells was not modulated in the presence of E2. The fertility drugs CC and letrozole modulated Kiss-1 expression in hypothalamic cell models.
枸橼酸氯米芬(CC)和来曲唑可刺激下丘脑 - 垂体 - 卵巢轴,被广泛用作口服促生育药物以诱导卵泡生成。我们研究了这些药物是否会增加下丘脑细胞模型中Kiss - 1的表达。我们使用了两种下丘脑细胞模型,mHypoA - 50和mHypoA - 55,它们分别源自小鼠下丘脑腹内侧视前区(AVPV)核和弓状核(ARC)的Kiss - 1神经元。用CC或来曲唑刺激这些细胞,之后测定Kiss - 1 mRNA的表达。CC刺激了mHypoA - 50和mHypoA - 55细胞中Kiss - 1基因的表达。在mHypoA - 50细胞中,雌二醇(E2)存在时Kiss - 1的基础表达显著增加,并且在这些细胞中E2存在时未观察到CC诱导的Kiss - 1表达增加。相反,E2并未改变mHypoA - 55细胞中Kiss - 1的基础表达,并且在E2存在时仍观察到CC诱导的Kiss - 1表达。在雌激素受体拮抗剂存在的情况下,mHypoA - 50和mHypoA - 55细胞中Kiss - 1基因表达的显著增加受到抑制。mHypoA - 50和mHypoA - 55细胞中表达芳香化酶。来曲唑,一种芳香化酶抑制剂,增加了mHypoA - 55 ARC细胞中Kiss - 1的表达,但在mHypoA - 50 AVPV细胞中未增加。尽管E2增加了Kiss - 1的基础表达,但来曲唑并未调节mHypoA - 50细胞中Kiss - 1的表达。在E2存在的情况下,来曲唑诱导的mHypoA - 55细胞中Kiss - 1基因表达未受到调节。促生育药物CC和来曲唑调节了下丘脑细胞模型中Kiss - 1的表达。