The BDNF/TrkB/CREB signaling improves chronic stress-induced decreased ovarian reserve by inhibiting pyroptosis of granulosa cells and disorders of sex hormone secretion.

IF 5.3 3区 医学 Q1 REPRODUCTIVE BIOLOGY
Yuanyuan Chen, Jun Tang, Yi Wen, Zhaohua Liu, Yi Zhang, Man Luo
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Abstract

Background: Decreased ovarian reserve (DOR) seriously affects female reproductive health. However, the mechanism of DOR remains unknown. This study aimed to explore the mechanism of BDNF/TrkB/CREB signaling in granulosa cell pyroptosis and sex hormone secretion in DOR.

Methods: Recombinant BDNF (rBDNF) and TrkB antagonist ANA-12 were used to investigate the effects of the BDNF-TrkB signaling pathway on chronic unpredictable stress (CUS)-induced DOR in vivo. The mechanism of the BDNF-TrkB signaling pathway in NE-induced pyroptosis and sex hormone secretion was further investigated in vitro by the combined application of the CREB antagonist KG-501.

Results: The CUS model reduced BDNF expression in brain tissue, peripheral blood, and ovarian tissues and inhibited p-TrkB/TrkB, p-PI3K/PI3K, and p-AKT/AKT expression. rBDNF enhanced the ovarian index and improved histological structure in CUS mice, restored the disordered estrus cycle, reduced the serum corticosterone level, and increased the pregnancy rate and embryo number. rBDNF inhibited serum FSH, LH, and NE levels and apoptosis in CUS mice while increasing AMH, E2, P, and T levels, accompanied by downregulated NLRP3, ASC, GSDMD-N, Cleaved Caspase-1, IL-18, and IL-1β levels. However, the ANA-12 effect on the above factors was opposite to that of rBDNF. Mechanistically, the BDNF-TrkB signaling pathway inhibited NE-induced pyroptosis of granulosa cells and sex hormone secretion disorders by promoting CREB phosphorylation.

Conclusion: Our findings indicate that the BDNF-TrkB signaling pathway inhibits pyroptosis of granulosa cells and sex hormone secretion disorders by promoting CREB phosphorylation, thereby improving DOR. These results provide a new theoretical basis in DOR for targeting the BDNF-TrkB-CREB axis.

BDNF/TrkB/CREB信号通过抑制颗粒细胞焦亡和性激素分泌紊乱,改善慢性应激诱导的卵巢储备下降。
背景:卵巢储备功能下降严重影响女性生殖健康。然而,DOR的机制尚不清楚。本研究旨在探讨BDNF/TrkB/CREB信号在DOR中颗粒细胞焦亡和性激素分泌中的作用机制。方法:采用重组BDNF (rBDNF)和TrkB拮抗剂ANA-12研究BDNF-TrkB信号通路对体内慢性不可预知应激(CUS)诱导的DOR的影响。在体外联合应用CREB拮抗剂KG-501进一步研究BDNF-TrkB信号通路在ne诱导的凋亡和性激素分泌中的作用机制。结果:CUS模型降低脑组织、外周血、卵巢组织BDNF表达,抑制p-TrkB/TrkB、p-PI3K/PI3K、p-AKT/AKT表达。rBDNF提高CUS小鼠卵巢指数,改善组织学结构,恢复紊乱的发情周期,降低血清皮质酮水平,增加妊娠率和胚胎数。rBDNF抑制CUS小鼠血清FSH、LH、NE水平和细胞凋亡,提高AMH、E2、P和T水平,下调NLRP3、ASC、GSDMD-N、Cleaved Caspase-1、IL-18和IL-1β水平。而ANA-12对上述因子的作用与rBDNF相反。机制上,BDNF-TrkB信号通路通过促进CREB磷酸化抑制ne诱导的颗粒细胞焦亡和性激素分泌紊乱。结论:BDNF-TrkB信号通路通过促进CREB磷酸化抑制颗粒细胞焦亡和性激素分泌紊乱,从而改善DOR。这些结果为DOR靶向BDNF-TrkB-CREB轴提供了新的理论依据。
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来源期刊
Journal of Ovarian Research
Journal of Ovarian Research REPRODUCTIVE BIOLOGY-
CiteScore
6.20
自引率
2.50%
发文量
125
审稿时长
>12 weeks
期刊介绍: Journal of Ovarian Research is an open access, peer reviewed, online journal that aims to provide a forum for high-quality basic and clinical research on ovarian function, abnormalities, and cancer. The journal focuses on research that provides new insights into ovarian functions as well as prevention and treatment of diseases afflicting the organ. Topical areas include, but are not restricted to: Ovary development, hormone secretion and regulation Follicle growth and ovulation Infertility and Polycystic ovarian syndrome Regulation of pituitary and other biological functions by ovarian hormones Ovarian cancer, its prevention, diagnosis and treatment Drug development and screening Role of stem cells in ovary development and function.
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