Saikosaponin D, a triterpene saponin from <i>Bupleurum falcatum</i> , restores circadian rhythm and attenuates hepatic fibrosis via Esr1-Per2 axis

Hepatic fibrosis, a precursor to chronic liver diseases, is linked to circadian rhythm disruptions. This study investigates the anti-fibrotic effects of saikosaponin D (SSd) from <i>Bupleurum falcatum L</i>. and its regulation of circadian genes. Transcriptomic and single-cell analyses revealed circadian gene dysregulation, particularly Period 2 (Per2), in liver fibrosis and hepatic stellate cells. SSd upregulated Per2 transcription via estrogen receptor 1 (Esr1), as confirmed by siRNA, real-time quantitative polymerase chain reaction, and Western blot analyses. <i>In vivo</i>, SSd alleviated fibrosis and hepatitis, increasing Esr1 but not Per2 protein levels. These findings suggest SSd exerts anti-fibrotic effects by modulating Esr1-mediated Per2 transcription.

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Publication Details

Journal
Journal of Asian Natural Products Research
Published
2025-04-09
DOI
https://doi.org/10.1080/10286020.2025.2482068
Citations
2
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
2.71
Controls
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article

Saikosaponin D, a triterpene saponin from Bupleurum falcatum , restores circadian rhythm and attenuates hepatic fibrosis via Esr1-Per2 axis

Yiyuan Zheng, Shanzhi Gu, Yanping Wang, Yong Li et al.
2 citations
Journal of Asian Natural Products Research
Liver Disease Diagnosis and Treatment
2.71
article

Saikosaponin D, a triterpene saponin from Bupleurum falcatum , restores circadian rhythm and attenuates hepatic fibrosis via Esr1-Per2 axis

Yiyuan Zheng, Shanzhi Gu, Yanping Wang, Yong Li, Chong Chen, Junmin Wang, Yiyi Fu
article en
2 citations

Abstract

Hepatic fibrosis, a precursor to chronic liver diseases, is linked to circadian rhythm disruptions. This study investigates the anti-fibrotic effects of saikosaponin D (SSd) from <i>Bupleurum falcatum L</i>. and its regulation of circadian genes. Transcriptomic and single-cell analyses revealed circadian gene dysregulation, particularly Period 2 (Per2), in liver fibrosis and hepatic stellate cells. SSd upregulated Per2 transcription via estrogen receptor 1 (Esr1), as confirmed by siRNA, real-time quantitative polymerase chain reaction, and Western blot analyses. <i>In vivo</i>, SSd alleviated fibrosis and hepatitis, increasing Esr1 but not Per2 protein levels. These findings suggest SSd exerts anti-fibrotic effects by modulating Esr1-mediated Per2 transcription.

Journal of Asian Natural Products ResearchVol. 28(1)
Shanghai University of Traditional Chinese Medicine (CN)
Zero hunger
Openalex Percentile: Top 11%
Liver Disease Diagnosis and Treatment
2.71
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