Purification engineering technology research center of Sichuan Province Natural Medicine
四川省天然药物分离纯化工程技术研究中心

文献

跳过导航链接首页 > 关于普思 > 新闻资讯 > 详细内容

Xi-yang Tang, Qing-chang Wu, Lv-qi Xie, Yao Li, Miao Chen, Cai-lian Fan, Yi Dai,Transcriptomic, artificial neural network and Chou-Talalay analysis based investigation of potential mechanism and active components of Qi-Lin pill in treating diminished ovarian reserve,Journal of Ethnopharmacology,Volume 357,2026,120935,ISSN 0378-8741.

本文来自:    发布时间:2026-08-18

发表期刊:Journal of Ethnopharmacology

发表时间:2026

Abstract:

Ethnopharmacological relevance

Qi-Lin pill (QLP), which is derived from the renowned Wu-Zi-Yan-Zong formulation of the Tang Dynasty, has been used for tonifying the kidneys, replenishing vital essence, and treating infertility and menstrual disorders. However, its mechanisms and active components for treating diminished ovarian reserve (DOR) remain unclear.

Aim of the study

Herein, we integrated transcriptomics, artificial neural network (ANN), and Chou-Talalay analysis to elucidate the potential mechanisms and active components responsible for the effects of QLP.

Materials and methods

First, QLP was orally administered to a cisplatin (CDDP)-induced mouse model of DOR; ovarian index, estrous cycle, ovarian tissue morphology, and biochemical parameters were observed to assess efficacy. Second, transcriptomics analysis was performed to reveal the possible mechanisms of QLP, and qRT-PCR and western blotting were used to validate the expressions of key signaling molecules in vivo. Third, the aforementioned mechanisms of QLP were further investigated in CDDP-induced functional impairment of estradiol (E2) synthesis in ovarian granulosa-like KGN cells via using siRNA-mediated depletion and specific inhibition. Subsequently, UPLC-QQQ-MS was used to quantify 33 compounds in 13 batches of QLP. Then, the ANN with feature importance analysis was used to correlate the chemical constituents in the content assay with pharmacological indicators to screen for potential active ingredients. Finally, the synergistic effect of the selected components was investigated using the Chou-Talalay index method in the CDDP-induced functional damage model of human ovarian granulosa-like tumor cells (KGN).

Results

QLP restored estrous cyclicity, ovarian index, serum hormones (follicle-stimulating hormone, anti-Müllerian hormone, E2), and follicular development (antral follicles and corpora lutea). Mechanistically, QLP ameliorated CDDP-induced functional damage of the ovaries in vivo and in vitro by upregulating follicle-stimulating hormone receptor (FSHR) expression and activating the ADCY1/cAMP/PKA/CREB signaling pathway, which resulted in upregulated aromatase expression and increased E2 synthesis. Subsequently, ten potentially active compounds, including paeoniflorin, albiflorin, danshensu, gallic acid, betaine, 2,3,5,4′-tetrahydroxystilbene-2-O-β-D-glucoside, salvianolic acid A, hesperidin, nobiletin, and epimedin C, were selected by ANN combined with feature importance analysis. Finally, these ten components were divided into two mixture forms, one of which comprised monoterpenoids (paeoniflorin and albiflorin) in a mixture. Two optimized mixtures synergistically amplified FSHR expression and cAMP/PKA/CREB signaling via Chou-Talalay analysis, thus boosting E2 and aromatase in KGN cells.

Conclusion

These findings reveal that QLP could exert its effects through a multicomponent synergistic interaction involving cAMP-mediated steroidogenesis, thus providing new insights into the mechanism by which this traditional Chinese medicine prescription treats ovarian dysfunction.

https://doi.org/10.1016/j.jep.2025.120935






上一篇:Jiaxin Li, Xiangxin Feng, Hongjun Jiang, Xinhui Mo, Chang Liu, Xiong

下一篇:没有了

联系我们

4000-369-963  028-85370565

18080489829@163.com

四川省 成都市 武侯区 武科西二路8号

关于普思

 新闻资讯

研发机构

 服务平台

产品

中药化学对照品

化合物库

热销原料

技术服务

高分辨质谱分析

药物单体纯化

中药创新药

普思生物为您提供中药化学对照品、高纯化学试剂、天然产物化合物库等优质产品,
仅用于科学研究、工业应用等非医疗用途范畴,不可用于人的临床治疗或试验,非药用,非食用。

友情链接:全球化学品供应商搜索   盖德化工网    成都普思生物科技股份有限公司版权所有   蜀ICP备08100078号

在线
咨询

在线咨询服务时间:8:30-17:30

选择客服在线沟通:

咨询
热线

4000-369-963  
7*24小时客服服务热线


028-85370565 / 18080489829 (何女士)

关注
微信

关注官方微信
顶部