BHF Glasgow Cardiovascular Research Centre, Institute of Cardiovascular & Medical Sciences, University of Glasgow, Glasgow, UK.
Suez Canal University, Arab Republic of Egypt.
Br J Pharmacol. 2022 Mar;179(5):770-791. doi: 10.1111/bph.15595. Epub 2021 Aug 11.
Approximately 7 million people are affected by acute myocardial infarction (MI) each year, and despite significant therapeutic and diagnostic advancements, MI remains a leading cause of mortality worldwide. Preclinical animal models have significantly advanced our understanding of MI and have enabled the development of therapeutic strategies to combat this debilitating disease. Notably, some drugs currently used to treat MI and heart failure (HF) in patients had initially been studied in preclinical animal models. Despite this, preclinical models are limited in their ability to fully reproduce the complexity of MI in humans. The preclinical model must be carefully selected to maximise the translational potential of experimental findings. This review describes current experimental models of MI and considers how they have been used to understand drug mechanisms of action and support translational medicine development. 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.
每年约有 700 万人受到急性心肌梗死(MI)的影响,尽管在治疗和诊断方面取得了重大进展,但 MI 仍然是全球主要的死亡原因。临床前动物模型极大地促进了我们对 MI 的理解,并使对抗这种衰弱性疾病的治疗策略得以发展。值得注意的是,一些目前用于治疗 MI 和心力衰竭(HF)的药物最初是在临床前动物模型中进行研究的。尽管如此,临床前模型在其复制人类 MI 的复杂性的能力方面受到限制。必须仔细选择临床前模型,以最大限度地提高实验结果的转化潜力。本文描述了 MI 的当前实验模型,并探讨了它们如何用于了解药物作用机制和支持转化医学的发展。相关文章:本文是关于心血管疾病研究的临床前模型的专题的一部分(BJP 第 75 周年纪念)。要查看该部分的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.5/issuetoc.