Cardiovascular Disease Program, Monash Biomedicine Discovery Institute and Department of Pharmacology, Monash University, Clayton, Victoria, Australia.
State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Br J Pharmacol. 2022 Mar;179(5):882-899. doi: 10.1111/bph.15450. Epub 2021 May 10.
Cardiac fibrosis (scarring), characterised by an increased deposition of extracellular matrix (ECM) proteins, is a hallmark of most types of cardiovascular disease and plays an essential role in heart failure progression. Inhibition of cardiac fibrosis could improve outcomes in patients with cardiovascular diseases and particularly heart failure. However, pharmacological treatment of the ECM build-up is still lacking. In this context, preclinical models of heart disease are important tools for understanding the complex pathogenesis involved in the development of cardiac fibrosis which in turn could identify new therapeutic targets and the facilitation of antifibrotic drug discovery. Many preclinical models have been used to study cardiac fibrosis and each model provides mechanistic insights into the many factors that contribute to cardiac fibrosis. This review discusses the most frequently used rodent models of cardiac fibrosis and also provides context for the use of particular models of heart failure. LINKED ARTICLES: This article is part of a themed issue on Preclinical Models for Cardiovascular disease research (BJP 75th Anniversary). To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.5/issuetoc.
心肌纤维化(瘢痕形成)的特征是细胞外基质(ECM)蛋白的过度沉积,是大多数类型心血管疾病的标志,在心力衰竭的进展中起着至关重要的作用。抑制心肌纤维化可能改善心血管疾病患者的预后,尤其是心力衰竭患者的预后。然而,针对 ECM 堆积的药理学治疗仍然缺乏。在这种情况下,心脏病的临床前模型是理解心脏纤维化发展中涉及的复杂发病机制的重要工具,这反过来又可以确定新的治疗靶点和促进抗纤维化药物的发现。已经使用了许多临床前模型来研究心肌纤维化,每个模型都为导致心肌纤维化的许多因素提供了机制上的见解。本文讨论了最常用于研究心肌纤维化的啮齿动物模型,并为特定心力衰竭模型的使用提供了背景信息。
本文是心血管疾病研究的临床前模型专题(BJP 75 周年纪念)的一部分。要查看本节中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.5/issuetoc.