Evaluation of in vitro hepatotoxicity of perampanel in comparison with carbamazepine: old versus new

Gülnar Farmanlı, S. Ilgın, B. Ergun, Merve Baysal, A. Karaduman, Özlem Atlı Eklioğlu
{"title":"Evaluation of in vitro hepatotoxicity of perampanel in comparison with carbamazepine: old versus new","authors":"Gülnar Farmanlı, S. Ilgın, B. Ergun, Merve Baysal, A. Karaduman, Özlem Atlı Eklioğlu","doi":"10.55971/ejls.1324501","DOIUrl":null,"url":null,"abstract":"Since the liver metabolizes many drugs, including antiepileptics, this organ is the main target of drug-induced damage. There is very little data on hepatotoxicity due to carbamazepine and perampanel metabolized in the liver. The available data are based solely on published case reports. For this reason, this study aims to evaluate the hepatotoxicity of carbamazepine and perampanel, which are frequently used in treating epilepsy and which do not have a detailed investigation, although they are suspected of hepatotoxicity. Hepatotoxicity in the HepG2 cell line, IC50 values were calculated by MTT cytotoxicity test, followed by determination of apoptosis/necrosis, various biochemical analyzes (ALT, AST, urea), which is currently a biomarker for liver injury, and hepatotoxicity by ROS and GSH determination. Both drugs increased liver biomarkers, oxidative stress, and cytotoxicity in HepG2 cells. The investigation found that the drugs triggered liver apoptosis, not necrosis. In conclusion, Perampanel may have hepatotoxicity similar to carbamazepine.","PeriodicalId":176179,"journal":{"name":"European Journal of Life Sciences","volume":"67 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Life Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55971/ejls.1324501","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

Since the liver metabolizes many drugs, including antiepileptics, this organ is the main target of drug-induced damage. There is very little data on hepatotoxicity due to carbamazepine and perampanel metabolized in the liver. The available data are based solely on published case reports. For this reason, this study aims to evaluate the hepatotoxicity of carbamazepine and perampanel, which are frequently used in treating epilepsy and which do not have a detailed investigation, although they are suspected of hepatotoxicity. Hepatotoxicity in the HepG2 cell line, IC50 values were calculated by MTT cytotoxicity test, followed by determination of apoptosis/necrosis, various biochemical analyzes (ALT, AST, urea), which is currently a biomarker for liver injury, and hepatotoxicity by ROS and GSH determination. Both drugs increased liver biomarkers, oxidative stress, and cytotoxicity in HepG2 cells. The investigation found that the drugs triggered liver apoptosis, not necrosis. In conclusion, Perampanel may have hepatotoxicity similar to carbamazepine.
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
评价perampanel与卡马西平的体外肝毒性:新旧对比
由于肝脏代谢包括抗癫痫药在内的许多药物,因此肝脏是药物性损伤的主要目标。关于卡马西平和perampanel在肝脏代谢引起的肝毒性的数据很少。现有数据仅基于已发表的病例报告。因此,本研究旨在评估卡马西平和perampanel的肝毒性,这两种药物经常用于治疗癫痫,虽然怀疑有肝毒性,但没有详细的研究。对HepG2细胞系进行肝毒性试验,采用MTT细胞毒性试验计算IC50值,然后进行凋亡/坏死测定,进行各种生化分析(ALT、AST、尿素),这是目前肝损伤的生物标志物,并通过ROS和GSH测定肝毒性。这两种药物都增加了HepG2细胞的肝脏生物标志物、氧化应激和细胞毒性。研究发现,这些药物引发肝细胞凋亡,而不是肝坏死。总之,Perampanel可能具有与卡马西平相似的肝毒性。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Volatile components of Ferulago aucheri Boiss. (Apiaceae) Synthesis of thiazole derivatives as cholinesterase inhibitors with antioxidant activity Evaluation of volatile components of Achillea millefolium L. essential oil Determination of cytotoxic, antioxidant activities and LC/MS-MS profiles of three endemic Verbascum L. species HPLC method for simultaneous quantification of lumacaftor and ivacaftor bulk and pharmaceutical formulations
×
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