Network Pharmacology-Based Prediction and Verification of the Potential Mechanisms of He's Yangchao Formula against Diminished Ovarian Reserve

Liuqing Yang; Ying Zhao; Hongbin Xu; Yang Ma; Lin Wang; Jing Ma; Qin Zhang

doi:10.1155/2022/8361808

Network Pharmacology-Based Prediction and Verification of the Potential Mechanisms of He's Yangchao Formula against Diminished Ovarian Reserve

Evid Based Complement Alternat Med. 2022 Jun 6:2022:8361808. doi: 10.1155/2022/8361808. eCollection 2022.

Authors

Liuqing Yang¹, Ying Zhao², Hongbin Xu³, Yang Ma², Lin Wang², Jing Ma¹, Qin Zhang¹

Affiliations

¹ Department of TCM Gynecology, Hangzhou TCM Hospital, Zhejiang Chinese Medical University, Hangzhou 310007, China.
² Zhejiang Chinese Medical University, Hangzhou 310053, China.
³ Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

Abstract

Background: He's Yangchao formula (HSYC) has been clinically proven to be effective in treating diminished ovarian reserve (DOR). However, the underlying molecular mechanisms of HSYC in DOR are unclear.

Objective: This study aims to predict the underlying mechanisms of He's Yangchao formula (HSYC) against DOR through network pharmacology strategies and verify in vivo.

Methods: Systematic network pharmacology was used to speculate the bioactive components, potential targets, and the underlying mechanism of HSYC in the treatment of DOR. Then, the CTX-induced DOR mouse model was established to verify the effect of HSYC against DOR and the possible molecular mechanisms as predicted in the network pharmacology approach.

Results: A total of 44 active components and 423 potential targets were obtained in HSYC. In addition, 91 targets of DOR were also screened. The identified hub genes were AKT1, ESR1, IL6, and P53. Further molecular docking showed that the four hub targets were well-bound with their corresponding compounds. In vivo experiments showed that HSYC could promote the recovery of the estrous cycle and increase the number of primordial, growing follicles and corpora lutea. Besides, The results of qRT-PCR showed HSYC could regulate the expression of AKT1, ESR1, P53, and IL6 in DOR mice.

Conclusion: It was demonstrated that HSYC could increase ovarian reserves, and AKT1, ESR1, IL6, and P53 may play an essential role in this effect, which provided a new reference for the current lack of active interventions of DOR.