Suppr超能文献

药物性肝损伤的机制建模:探究固有免疫反应的作用

Mechanistic Modelling of Drug-Induced Liver Injury: Investigating the Role of Innate Immune Responses.

作者信息

Shoda Lisl Km, Battista Christina, Siler Scott Q, Pisetsky David S, Watkins Paul B, Howell Brett A

机构信息

DILIsym Services, Inc., Research Triangle Park, NC, USA.

UNC Institute for Drug Safety Sciences, University of North Carolina at Chapel Hill, Research Triangle Park, NC, USA.

出版信息

Gene Regul Syst Bio. 2017 May 30;11:1177625017696074. doi: 10.1177/1177625017696074. eCollection 2017.

Abstract

Drug-induced liver injury (DILI) remains an adverse event of significant concern for drug development and marketed drugs, and the field would benefit from better tools to identify liver liabilities early in development and/or to mitigate potential DILI risk in otherwise promising drugs. DILIsym software takes a quantitative systems toxicology approach to represent DILI in pre-clinical species and in humans for the mechanistic investigation of liver toxicity. In addition to multiple intrinsic mechanisms of hepatocyte toxicity (ie, oxidative stress, bile acid accumulation, mitochondrial dysfunction), DILIsym includes the interaction between hepatocytes and cells of the innate immune response in the amplification of liver injury and in liver regeneration. The representation of innate immune responses, detailed here, consolidates much of the available data on the innate immune response in DILI within a single framework and affords the opportunity to systematically investigate the contribution of the innate response to DILI.

摘要

药物性肝损伤(DILI)仍然是药物研发和上市药物中备受关注的不良事件,该领域将受益于更好的工具,以便在研发早期识别肝脏风险,并/或降低有潜力药物的潜在DILI风险。DILIsym软件采用定量系统毒理学方法,在临床前物种和人类中呈现DILI,用于肝脏毒性的机制研究。除了多种肝细胞毒性的内在机制(即氧化应激、胆汁酸积累、线粒体功能障碍)外,DILIsym还包括肝细胞与先天免疫反应细胞之间在肝损伤放大和肝再生中的相互作用。本文详细介绍的先天免疫反应的呈现,将DILI中关于先天免疫反应的大量现有数据整合在一个单一框架内,并有机会系统地研究先天反应对DILI的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9329/5459514/544ea3f8e624/10.1177_1177625017696074-fig1.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验