Mitigation of methylglyoxal-induced hepatotoxicity by Boerhavia diffusa L. aerial extract: Insights from cellular and animal models

Debrupa Dutta , Nikita Khandelwal , Ashutosh Behera , Snehal Dongare , Bireswar Bhattacharya , Soumi Sukla
{"title":"Mitigation of methylglyoxal-induced hepatotoxicity by Boerhavia diffusa L. aerial extract: Insights from cellular and animal models","authors":"Debrupa Dutta ,&nbsp;Nikita Khandelwal ,&nbsp;Ashutosh Behera ,&nbsp;Snehal Dongare ,&nbsp;Bireswar Bhattacharya ,&nbsp;Soumi Sukla","doi":"10.1016/j.prenap.2024.100088","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p><em>Boerhavia diffusa</em> (Punarnava), is a perennial herb with a long-standing reputation for its antioxidative and anti-inflammatory properties, dating back to ancient times. Methylglyoxal is an advanced glycation end-product, known to be toxic in liver cell line as well as in mice model. Our objective is to illustrate the protective action of punarnava aerial extracts in methylglyoxal-induced hepatotoxicity in cell line and mice model.</p></div><div><h3>Methods</h3><p>Punarnava aerial parts were collected and different solvent extracts were prepared in methanol, dichloromethane and hexane by maceration followed by their LCMS/MS characterization, determination of total phenolic, total flavonoid contents and antioxidant activity by DPPH reagent. Cell viability of the extracts and methylglyoxal was assessed using different cell lines. <em>In vitro</em> protective effect of punarnava methanolic extract (PME) against methylglyoxal was evaluated by cell migration assay, NO and ROS production assays and Oil Red O staining in HepG2 cell line. BALB/c mice were pretreated with Punarnava methanolic extract (200 mg/kg and 400 mg/kg) for seven days followed by 290 mg/kg methylglyoxal administration for 6 hrs to induce hepatotoxicity. Serum glucose, AST, ALT, ALP and GSH level were checked and liver histopathological damages were identified.</p></div><div><h3>Results</h3><p>Among the three Punarnava extracts, PME possessed maximum antioxidant, total phenolic and flavonoid content as well as least cytotoxic to liver cell line. Methylglyoxal showed maximum toxicity in HepG2 cells with IC<sub>50</sub> (50 % inhibitory concentration) 3 µM. PME confers protection against methylglyoxal-induced cytotoxicity by decreasing ROS, promoting cell migration and preventing loss of cell viability. No significant change was observed in NO production and Oil Red O staining. PME-treated mice showed decrease in liver ALP levels and glucose with intact cellular morphology compared to hepatocyte steatosis and nuclear degeneration in methylglyoxal-treated group.</p></div><div><h3>Discussions</h3><p>Indigenous herb Punarnava is effective in protecting liver cells from damage induced by the glycolytic byproduct, methylglyoxal.</p></div>","PeriodicalId":101014,"journal":{"name":"Pharmacological Research - Natural Products","volume":"5 ","pages":"Article 100088"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacological Research - Natural Products","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950199724000764","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Boerhavia diffusa (Punarnava), is a perennial herb with a long-standing reputation for its antioxidative and anti-inflammatory properties, dating back to ancient times. Methylglyoxal is an advanced glycation end-product, known to be toxic in liver cell line as well as in mice model. Our objective is to illustrate the protective action of punarnava aerial extracts in methylglyoxal-induced hepatotoxicity in cell line and mice model.

Methods

Punarnava aerial parts were collected and different solvent extracts were prepared in methanol, dichloromethane and hexane by maceration followed by their LCMS/MS characterization, determination of total phenolic, total flavonoid contents and antioxidant activity by DPPH reagent. Cell viability of the extracts and methylglyoxal was assessed using different cell lines. In vitro protective effect of punarnava methanolic extract (PME) against methylglyoxal was evaluated by cell migration assay, NO and ROS production assays and Oil Red O staining in HepG2 cell line. BALB/c mice were pretreated with Punarnava methanolic extract (200 mg/kg and 400 mg/kg) for seven days followed by 290 mg/kg methylglyoxal administration for 6 hrs to induce hepatotoxicity. Serum glucose, AST, ALT, ALP and GSH level were checked and liver histopathological damages were identified.

Results

Among the three Punarnava extracts, PME possessed maximum antioxidant, total phenolic and flavonoid content as well as least cytotoxic to liver cell line. Methylglyoxal showed maximum toxicity in HepG2 cells with IC50 (50 % inhibitory concentration) 3 µM. PME confers protection against methylglyoxal-induced cytotoxicity by decreasing ROS, promoting cell migration and preventing loss of cell viability. No significant change was observed in NO production and Oil Red O staining. PME-treated mice showed decrease in liver ALP levels and glucose with intact cellular morphology compared to hepatocyte steatosis and nuclear degeneration in methylglyoxal-treated group.

Discussions

Indigenous herb Punarnava is effective in protecting liver cells from damage induced by the glycolytic byproduct, methylglyoxal.

白花蛇舌草叶提取物缓解甲基乙二醛诱导的肝毒性:细胞和动物模型的启示
背景Boerhavia diffusa(Punarnava)是一种多年生草本植物,因其抗氧化和抗炎特性而久负盛名,其历史可追溯到古代。甲基乙二醛是一种高级糖化终产物,在肝细胞系和小鼠模型中都具有毒性。我们的目的是说明 punarnava 植物萃取物对细胞系和小鼠模型中由甲基乙二醛诱导的肝毒性的保护作用。方法 收集 punarnava 植物部分,通过浸渍法在甲醇、二氯甲烷和正己烷中制备不同溶剂的萃取物,然后进行 LCMS/MS 表征,用 DPPH 试剂测定总酚、总黄酮含量和抗氧化活性。使用不同的细胞系对提取物和甲基乙二醛的细胞活力进行了评估。在 HepG2 细胞系中,通过细胞迁移试验、NO 和 ROS 生成试验以及油红 O 染色,评估了 punarnava 代谢提取物(PME)对甲基乙二醛的体外保护作用。用 Punarnava 代谢提取物(200 毫克/千克和 400 毫克/千克)对 BALB/c 小鼠进行为期七天的预处理,然后用 290 毫克/千克的甲基乙二醛诱导小鼠肝中毒 6 小时。结果在三种 Punarnava 提取物中,PME 的抗氧化剂、总酚和类黄酮含量最高,对肝细胞系的细胞毒性最小。甲基乙二酸对 HepG2 细胞的毒性最大,IC50(50% 抑制浓度)为 3 µM。PME 可通过减少 ROS、促进细胞迁移和防止细胞活力丧失来抵御甲基乙二醛诱导的细胞毒性。在 NO 生成和油红 O 染色方面未观察到明显变化。与甲基乙二醛处理组的肝细胞脂肪变性和核变性相比,PME 处理组的小鼠肝脏 ALP 水平和葡萄糖含量下降,细胞形态完好。
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
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信