Experimental liver fibrosis research: update on animal models, legal issues and translational aspects.

Christian Liedtke, Tom Luedde, Tilman Sauerbruch, David Scholten, Konrad Streetz, Frank Tacke, René Tolba, Christian Trautwein, Jonel Trebicka, Ralf Weiskirchen
{"title":"Experimental liver fibrosis research: update on animal models, legal issues and translational aspects.","authors":"Christian Liedtke,&nbsp;Tom Luedde,&nbsp;Tilman Sauerbruch,&nbsp;David Scholten,&nbsp;Konrad Streetz,&nbsp;Frank Tacke,&nbsp;René Tolba,&nbsp;Christian Trautwein,&nbsp;Jonel Trebicka,&nbsp;Ralf Weiskirchen","doi":"10.1186/1755-1536-6-19","DOIUrl":null,"url":null,"abstract":"<p><p>Liver fibrosis is defined as excessive extracellular matrix deposition and is based on complex interactions between matrix-producing hepatic stellate cells and an abundance of liver-resident and infiltrating cells. Investigation of these processes requires in vitro and in vivo experimental work in animals. However, the use of animals in translational research will be increasingly challenged, at least in countries of the European Union, because of the adoption of new animal welfare rules in 2013. These rules will create an urgent need for optimized standard operating procedures regarding animal experimentation and improved international communication in the liver fibrosis community. This review gives an update on current animal models, techniques and underlying pathomechanisms with the aim of fostering a critical discussion of the limitations and potential of up-to-date animal experimentation. We discuss potential complications in experimental liver fibrosis and provide examples of how the findings of studies in which these models are used can be translated to human disease and therapy. In this review, we want to motivate the international community to design more standardized animal models which might help to address the legally requested replacement, refinement and reduction of animals in fibrosis research. </p>","PeriodicalId":12264,"journal":{"name":"Fibrogenesis & Tissue Repair","volume":"6 1","pages":"19"},"PeriodicalIF":0.0000,"publicationDate":"2013-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/1755-1536-6-19","citationCount":"308","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fibrogenesis & Tissue Repair","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/1755-1536-6-19","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 308

Abstract

Liver fibrosis is defined as excessive extracellular matrix deposition and is based on complex interactions between matrix-producing hepatic stellate cells and an abundance of liver-resident and infiltrating cells. Investigation of these processes requires in vitro and in vivo experimental work in animals. However, the use of animals in translational research will be increasingly challenged, at least in countries of the European Union, because of the adoption of new animal welfare rules in 2013. These rules will create an urgent need for optimized standard operating procedures regarding animal experimentation and improved international communication in the liver fibrosis community. This review gives an update on current animal models, techniques and underlying pathomechanisms with the aim of fostering a critical discussion of the limitations and potential of up-to-date animal experimentation. We discuss potential complications in experimental liver fibrosis and provide examples of how the findings of studies in which these models are used can be translated to human disease and therapy. In this review, we want to motivate the international community to design more standardized animal models which might help to address the legally requested replacement, refinement and reduction of animals in fibrosis research.

实验性肝纤维化研究:动物模型、法律问题和翻译方面的最新进展。
肝纤维化被定义为过度的细胞外基质沉积,是基于产生基质的肝星状细胞与大量肝驻留和浸润细胞之间复杂的相互作用。对这些过程的研究需要在动物体内和体外进行实验。然而,在转化研究中使用动物将面临越来越多的挑战,至少在欧盟国家是这样,因为2013年通过了新的动物福利规则。这些规则将迫切需要优化有关动物实验的标准操作程序,并改善肝纤维化界的国际交流。这篇综述更新了当前的动物模型、技术和潜在的病理机制,目的是促进对最新动物实验的局限性和潜力的批判性讨论。我们讨论了实验性肝纤维化的潜在并发症,并提供了如何将这些模型的研究结果转化为人类疾病和治疗的例子。在这篇综述中,我们希望激励国际社会设计更标准化的动物模型,这可能有助于解决法律要求的纤维化研究中动物的替代、改进和减少。
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