通过调节抗氧化酶和氧化应激对CCl4诱导的肝毒性的改善作用

IF 2.2 4区 医学 Q3 TOXICOLOGY Toxicology Research Pub Date : 2022-10-01 DOI:10.1093/toxres/tfac052
Arvind Kumar Shakya, Neetu Sharma, Monika Bhadauria, Satendra Kumar Nirala, Sadhana Shrivastava, Sangeeta Shukla
{"title":"通过调节抗氧化酶和氧化应激对CCl4诱导的肝毒性的改善作用","authors":"Arvind Kumar Shakya,&nbsp;Neetu Sharma,&nbsp;Monika Bhadauria,&nbsp;Satendra Kumar Nirala,&nbsp;Sadhana Shrivastava,&nbsp;Sangeeta Shukla","doi":"10.1093/toxres/tfac052","DOIUrl":null,"url":null,"abstract":"<p><p>Polyherbal Unani formulations have been used in the treatment of liver diseases for a long time. (Ibrahim M, Khaja MN, Aara A, Khan AA, Habeeb MA, Devi YP, Narasu ML, Habibullah CM. Hepatoprotective activity of <i>Sapindus mukorossi</i> and <i>Rheum emodi</i> extracts: <i>in vitro</i> and <i>in vivo</i> studies. <i>World J Gastroenterol</i>. 2008:<b>14</b>:2566-2571.) The aim of the present study was to investigate comparative hepatoprotective potential of Majoon-e-Dabeed-ul-ward (MD) and Sharbat-e-Deenar (SD) against CCl<sub>4</sub> induced subchronic hepatic toxicity. In vivo study, albino rats were divided into 5 groups. Group I was control; Group II was experimental control treated with CCl<sub>4</sub> (0.15 mL/kg, i.p. for 21 days); Groups III-IV treated with SD (2 mL/kg, p.o.) and MD (1,000 mg/kg, p.o.) for 5 days following CCl<sub>4</sub> intoxication as in group 2 respectively; and Group V was positive control treated with silymarin (50 mg/kg, p.o.). In vitro hepatoprotective activity of SD and MD (25, 50, and 100 μg/mL) was assessed by SRB assay and flow cytometry analysis. CCl<sub>4</sub> exposure significantly elevated the release of hepatic enzymes i.e. AST, ALT, LDH, and SALP in serum and lipid peroxidation in liver tissue which all these parameters were reversed after SD and MD administration. Therapy for 5 days also normalized the levels of antioxidant enzymes i.e. catalase, SOD, GPx, GR, tissue GSH, and aniline hydroxylase in CCl<sub>4</sub> treated group. DNA damage and histological alterations caused by CCl<sub>4</sub> were restored towards normal group. In vitro study showed protective effect of SD and MD against CCl<sub>4</sub> treated HepG2 cell lines and rat hepatocytes. The results suggested that MD has a significant hepatoprotective potential and regulatory effect on oxidative stress than SD against CCl<sub>4</sub> induced hepatotoxicity, and that this effect may be related to its antioxidant activity.</p>","PeriodicalId":105,"journal":{"name":"Toxicology Research","volume":"11 5","pages":"819-830"},"PeriodicalIF":2.2000,"publicationDate":"2022-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618100/pdf/tfac052.pdf","citationCount":"4","resultStr":"{\"title\":\"Ameliorative impact of herbal formulation -Majoon-Dabeed-ul-ward and Sharbat-e-Deenar against CCl<sub>4</sub> induced liver toxicity via regulation of antioxidant enzymes and oxidative stress.\",\"authors\":\"Arvind Kumar Shakya,&nbsp;Neetu Sharma,&nbsp;Monika Bhadauria,&nbsp;Satendra Kumar Nirala,&nbsp;Sadhana Shrivastava,&nbsp;Sangeeta Shukla\",\"doi\":\"10.1093/toxres/tfac052\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Polyherbal Unani formulations have been used in the treatment of liver diseases for a long time. (Ibrahim M, Khaja MN, Aara A, Khan AA, Habeeb MA, Devi YP, Narasu ML, Habibullah CM. Hepatoprotective activity of <i>Sapindus mukorossi</i> and <i>Rheum emodi</i> extracts: <i>in vitro</i> and <i>in vivo</i> studies. <i>World J Gastroenterol</i>. 2008:<b>14</b>:2566-2571.) The aim of the present study was to investigate comparative hepatoprotective potential of Majoon-e-Dabeed-ul-ward (MD) and Sharbat-e-Deenar (SD) against CCl<sub>4</sub> induced subchronic hepatic toxicity. In vivo study, albino rats were divided into 5 groups. Group I was control; Group II was experimental control treated with CCl<sub>4</sub> (0.15 mL/kg, i.p. for 21 days); Groups III-IV treated with SD (2 mL/kg, p.o.) and MD (1,000 mg/kg, p.o.) for 5 days following CCl<sub>4</sub> intoxication as in group 2 respectively; and Group V was positive control treated with silymarin (50 mg/kg, p.o.). In vitro hepatoprotective activity of SD and MD (25, 50, and 100 μg/mL) was assessed by SRB assay and flow cytometry analysis. CCl<sub>4</sub> exposure significantly elevated the release of hepatic enzymes i.e. AST, ALT, LDH, and SALP in serum and lipid peroxidation in liver tissue which all these parameters were reversed after SD and MD administration. Therapy for 5 days also normalized the levels of antioxidant enzymes i.e. catalase, SOD, GPx, GR, tissue GSH, and aniline hydroxylase in CCl<sub>4</sub> treated group. DNA damage and histological alterations caused by CCl<sub>4</sub> were restored towards normal group. In vitro study showed protective effect of SD and MD against CCl<sub>4</sub> treated HepG2 cell lines and rat hepatocytes. The results suggested that MD has a significant hepatoprotective potential and regulatory effect on oxidative stress than SD against CCl<sub>4</sub> induced hepatotoxicity, and that this effect may be related to its antioxidant activity.</p>\",\"PeriodicalId\":105,\"journal\":{\"name\":\"Toxicology Research\",\"volume\":\"11 5\",\"pages\":\"819-830\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2022-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618100/pdf/tfac052.pdf\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Toxicology Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/toxres/tfac052\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"TOXICOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Toxicology Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/toxres/tfac052","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 4

摘要

复方乌纳尼制剂长期以来一直用于治疗肝脏疾病。Ibrahim M, Khaja MN, Aara A, Khan AA, Habeeb MA, Devi YP, Narasu ML, Habibullah CM。无子和大黄提取物的肝保护作用:体外和体内研究。世界胃肠病杂志,2008,14:2566-2571。本研究的目的是比较majon -e- dabeed -ul-ward (MD)和sharbate -e- deenar (SD)对CCl4诱导的亚慢性肝毒性的肝保护潜力。体内实验将白化大鼠分为5组。第一组为对照组;II组为CCl4治疗的实验对照(0.15 mL/kg, ig, 21 d);第三、四组与第二组一样,在氯化氯化中毒后分别给予SD (2 mL/kg, p.o)和MD (1000 mg/kg, p.o) 5天;V组为水飞蓟素(50 mg/kg, p.o.)处理的阳性对照。采用SRB法和流式细胞术检测SD和MD(25、50、100 μg/mL)的体外保肝活性。CCl4暴露显著提高了血清中AST、ALT、LDH和SALP等肝酶的释放和肝组织脂质过氧化,而SD和MD给药后这些参数均被逆转。治疗5天后,CCl4治疗组抗氧化酶(过氧化氢酶、超氧化物歧化酶、GPx、GR、组织GSH和苯胺羟化酶)水平也恢复正常。CCl4引起的DNA损伤和组织学改变向正常组恢复。体外研究表明,SD和MD对CCl4处理的HepG2细胞系和大鼠肝细胞具有保护作用。结果提示,MD对CCl4诱导的肝毒性具有显著的肝保护作用和对氧化应激的调节作用,这种作用可能与其抗氧化活性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Ameliorative impact of herbal formulation -Majoon-Dabeed-ul-ward and Sharbat-e-Deenar against CCl4 induced liver toxicity via regulation of antioxidant enzymes and oxidative stress.

Polyherbal Unani formulations have been used in the treatment of liver diseases for a long time. (Ibrahim M, Khaja MN, Aara A, Khan AA, Habeeb MA, Devi YP, Narasu ML, Habibullah CM. Hepatoprotective activity of Sapindus mukorossi and Rheum emodi extracts: in vitro and in vivo studies. World J Gastroenterol. 2008:14:2566-2571.) The aim of the present study was to investigate comparative hepatoprotective potential of Majoon-e-Dabeed-ul-ward (MD) and Sharbat-e-Deenar (SD) against CCl4 induced subchronic hepatic toxicity. In vivo study, albino rats were divided into 5 groups. Group I was control; Group II was experimental control treated with CCl4 (0.15 mL/kg, i.p. for 21 days); Groups III-IV treated with SD (2 mL/kg, p.o.) and MD (1,000 mg/kg, p.o.) for 5 days following CCl4 intoxication as in group 2 respectively; and Group V was positive control treated with silymarin (50 mg/kg, p.o.). In vitro hepatoprotective activity of SD and MD (25, 50, and 100 μg/mL) was assessed by SRB assay and flow cytometry analysis. CCl4 exposure significantly elevated the release of hepatic enzymes i.e. AST, ALT, LDH, and SALP in serum and lipid peroxidation in liver tissue which all these parameters were reversed after SD and MD administration. Therapy for 5 days also normalized the levels of antioxidant enzymes i.e. catalase, SOD, GPx, GR, tissue GSH, and aniline hydroxylase in CCl4 treated group. DNA damage and histological alterations caused by CCl4 were restored towards normal group. In vitro study showed protective effect of SD and MD against CCl4 treated HepG2 cell lines and rat hepatocytes. The results suggested that MD has a significant hepatoprotective potential and regulatory effect on oxidative stress than SD against CCl4 induced hepatotoxicity, and that this effect may be related to its antioxidant activity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Toxicology Research
Toxicology Research TOXICOLOGY-
CiteScore
3.60
自引率
0.00%
发文量
82
期刊介绍: A multi-disciplinary journal covering the best research in both fundamental and applied aspects of toxicology
期刊最新文献
Unveiling the interspecies correlation and sensitivity factor analysis of rat and mouse acute oral toxicity of antimicrobial agents: first QSTR and QTTR Modeling report. Stress survival and longevity of Caenorhabditis elegans lacking NCS-1. Lipid-core nanocapsules containing simvastatin do not affect the biochemical and hematological indicators of toxicity in rats. Proteomics reveals that nanoplastics with different sizes induce hepatocyte apoptosis in mice through distinct mechanisms involving mitophagy dysregulation and cell cycle arrest. Antibiotic contaminants and their impact in Gingee River, Puducherry: insights from SPE-UPLC-MS/MS and zebrafish study.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1