Yuan Li , Yanxin Zhang , Guanqun Wan , Shaofei Song , Tingting Zhao , Renjie Cao , Weiwei Zeng , Min Huang , Yiming Jiang
{"title":"18β-glycyrrhetinic acid accelerates liver regeneration after partial hepatectomy in mice","authors":"Yuan Li , Yanxin Zhang , Guanqun Wan , Shaofei Song , Tingting Zhao , Renjie Cao , Weiwei Zeng , Min Huang , Yiming Jiang","doi":"10.1016/j.medidd.2025.100229","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>18β-Glycyrrhetinic acid (18β-GA), a key bioactive triterpenoid in <em>Glycyrrhiza uralensis</em> Fisch, is recognized for its hepatoprotective effects in liver injury. However, the effect of 18β-GA on liver regeneration after partial hepatectomy (PHx) remains unknown. This study aims to investigate the effects and underlying mechanisms of 18β-GA in facilitating liver regeneration after PHx.</div></div><div><h3>Methods</h3><div>PHx mice were orally gavaged with 18β-GA for 7 days. The promotion of 18β-GA on liver regeneration was evaluated by liver/body weight ratio, BrdU, Ki67 and PCNA. Cell cycle transition was performed to evaluate hepatocyte proliferation. The effects of 18β-GA on protein and mRNA expression levels within the MAPK/ERK signaling pathway were systematically evaluated.</div></div><div><h3>Results</h3><div>18β-GA significantly accelerated liver mass recovery and promoted hepatocyte proliferation after PHx. 18β-GA treatment facilitated the cellular G1/S phase transition and upregulated the expression of the proliferation-related protein CCND1, PCNA, and p-RB. Moreover, 18β-GA significantly increased the levels of growth factors including <em>Hgf</em>, <em>Egf</em>, <em>Tgf-α,</em> and <em>Hb-egf</em>. Furthermore, mechanistic investigations suggested that 18β-GA activated the MAPK/ERK signaling pathway, increasing the expression of p-ERK1/2, c-JUN, c-FOS, and c-MYC <em>in vitro</em> and <em>in vivo</em>. Application of ERK inhibitor U0126 effectively abolished 18β-GA-induced activation of MAPK/ERK signaling pathway.</div></div><div><h3>Conclusion</h3><div>18β-GA exhibited a significant promoting effect on liver recovery following PHx, potentially through modulation of the MAPK/ERK signaling pathway to accelerate liver regeneration.</div></div>","PeriodicalId":33528,"journal":{"name":"Medicine in Drug Discovery","volume":"28 ","pages":"Article 100229"},"PeriodicalIF":0.0000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine in Drug Discovery","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590098625000260","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/19 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
18β-Glycyrrhetinic acid (18β-GA), a key bioactive triterpenoid in Glycyrrhiza uralensis Fisch, is recognized for its hepatoprotective effects in liver injury. However, the effect of 18β-GA on liver regeneration after partial hepatectomy (PHx) remains unknown. This study aims to investigate the effects and underlying mechanisms of 18β-GA in facilitating liver regeneration after PHx.
Methods
PHx mice were orally gavaged with 18β-GA for 7 days. The promotion of 18β-GA on liver regeneration was evaluated by liver/body weight ratio, BrdU, Ki67 and PCNA. Cell cycle transition was performed to evaluate hepatocyte proliferation. The effects of 18β-GA on protein and mRNA expression levels within the MAPK/ERK signaling pathway were systematically evaluated.
Results
18β-GA significantly accelerated liver mass recovery and promoted hepatocyte proliferation after PHx. 18β-GA treatment facilitated the cellular G1/S phase transition and upregulated the expression of the proliferation-related protein CCND1, PCNA, and p-RB. Moreover, 18β-GA significantly increased the levels of growth factors including Hgf, Egf, Tgf-α, and Hb-egf. Furthermore, mechanistic investigations suggested that 18β-GA activated the MAPK/ERK signaling pathway, increasing the expression of p-ERK1/2, c-JUN, c-FOS, and c-MYC in vitro and in vivo. Application of ERK inhibitor U0126 effectively abolished 18β-GA-induced activation of MAPK/ERK signaling pathway.
Conclusion
18β-GA exhibited a significant promoting effect on liver recovery following PHx, potentially through modulation of the MAPK/ERK signaling pathway to accelerate liver regeneration.