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DOI 10.1080/09513590.2023.2244600

Медицинская библиотека · Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology · 2023

CangFu Daotan decoction improves polycystic ovarian syndrome by downregulating FOXK1.

Wang Chenye, Yu Jia, Ding Caifei, Chen Chunyue

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Аннотация

Objective

Polycystic ovarian syndrome (PCOS) is a prevalent gynecologic disorder, often associated with abnormal follicular development. Cangfu Daotan decoction (CFD) is a traditional Chinese medicine formula that is effective in alleviating PCOS clinically, but the specific mechanism remains unclear. Forkhead box K1 (FOXK1) is associated with cellular function. This study aimed to explore the effects of CFD and FOXK1 on PCOS.

Methods

High-fat diet and letrozole were combined to establish PCOS rat models. Next, primary GCs were extracted from those PCOS rats. Then, GC cells were transfected with si-FOXK1 or oe-FOXK1. CFD-contain serum was prepared, and experiments were conducted to investigate the regulation of FOXK1 by CFD.

Results

FOXK1 was highly expressed in GCs of PCOS rats. Further investigation revealed that FOXK1 overexpression resulted in inhibition of proliferation and DNA synthesis, along with promotion of apoptosis and autophagy in GCs. Additionally, it was found that FOXK1 promoted the expressions of the AMP-activated protein kinase (AMPK)/mammalian target of rapamycin (mTOR) pathway-related proteins. Interestingly, treatment with CFD reversed all the effects of FOXK1 overexpression in GCs.

Conclusion

This study demonstrated that CFD exerted a protective role in PCOS by inhibiting FOXK1, which provided a research basis for the application of CFD in PCOS, and suggested that FOXK1 is a novel therapeutic target in PCOS treatment.

Для цитирования: Wang Chenye, Yu Jia, Ding Caifei, Chen Chunyue. CangFu Daotan decoction improves polycystic ovarian syndrome by downregulating FOXK1.. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology. 2023. DOI: 10.1080/09513590.2023.2244600.

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