内分泌学
内科学
兴奋剂
基因敲除
MAPK/ERK通路
促性腺激素减退症
PI3K/AKT/mTOR通路
生物
蛋白激酶B
促性腺激素释放激素
受体
信号转导
激素
医学
促黄体激素
细胞生物学
基因
生物化学
作者
Menglong Xiong,Yuting Li,Shan Tan,Chunlin Yang,Lin Liu,Chen Zhi-heng
标识
DOI:10.1096/fj.202403365r
摘要
Isolated hypogonadotropic hypogonadism (IHH) is caused by defective gonadotropin-releasing hormone (GnRH) secretion or action, resulting in absent or incomplete pubertal development and infertility. However, the pathogenesis mechanism of IHH is not fully understood. This study utilized PROK2/PROKR2 knockdown mice and GT1-7 cells to investigate the effects and potential mechanismsof the NK3R agonist senktide on GnRH deficiency and related syndromes. In this investigation, PROK2/PROKR2 knockdown resulted in a deficiency of GnRH neurons, reduced levels of LSH, FSH, and E2, and the inhibition of the MAPK/ERK and PI3K/AKT pathways in mice. However, this effect was reversed by senktide. Furthermore, the inhibition of MAPK/ERK or PI3K/AKT signaling pathways counteracted the remission of the GnRH insufficiency and associated syndrome by senktide in mice with PROK2/PROKR2 knockdown. In summary, NK3R agonist senktide alleviated the GnRH insufficiency and related syndromes caused by PROK2/PROKR2 knockdown via the MAPK/ERK pathway and the PI3K/AKT pathway.
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