18β-glycyrrhetinic acid accelerates liver regeneration after partial hepatectomy in mice

Q2 Medicine
Medicine in Drug Discovery Pub Date : 2025-12-01 Epub Date: 2025-09-19 DOI:10.1016/j.medidd.2025.100229
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 ,&nbsp;Yanxin Zhang ,&nbsp;Guanqun Wan ,&nbsp;Shaofei Song ,&nbsp;Tingting Zhao ,&nbsp;Renjie Cao ,&nbsp;Weiwei Zeng ,&nbsp;Min Huang ,&nbsp;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.
18β-甘草次酸促进小鼠肝部分切除后肝脏再生
目的18β-甘草次酸(glycyrrhetinic acid, 18β-GA)是甘草中具有重要生物活性的三萜,对肝损伤具有保护作用。然而,18β-GA对部分肝切除术(PHx)后肝脏再生的影响尚不清楚。本研究旨在探讨18β-GA促进PHx后肝脏再生的作用及其机制。方法用18β-GA灌胃sphx小鼠7 d。采用肝重比、BrdU、Ki67和PCNA评价18β-GA对肝再生的促进作用。细胞周期转换评价肝细胞增殖。系统评估18β-GA对MAPK/ERK信号通路蛋白和mRNA表达水平的影响。结果18β- ga显著加速PHx后肝脏质量恢复,促进肝细胞增殖。18β-GA处理促进了细胞G1/S期转变,并上调了增殖相关蛋白CCND1、PCNA和p-RB的表达。此外,18β-GA显著提高Hgf、Egf、Tgf-α、Hb-egf等生长因子水平。此外,机制研究表明,18β-GA激活了MAPK/ERK信号通路,增加了p-ERK1/2、c-JUN、c-FOS和c-MYC在体外和体内的表达。ERK抑制剂U0126的应用有效地消除了18β- ga诱导的MAPK/ERK信号通路的激活。结论18β- ga对PHx后肝脏恢复具有显著促进作用,可能通过调节MAPK/ERK信号通路加速肝脏再生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Medicine in Drug Discovery
Medicine in Drug Discovery Medicine-Pharmacology (medical)
CiteScore
8.30
自引率
0.00%
发文量
30
审稿时长
21 days
期刊介绍:
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书