4.7 Review

Preclinical models of myocardial infarction: from mechanism to translation

期刊

BRITISH JOURNAL OF PHARMACOLOGY
卷 179, 期 5, 页码 770-791

出版社

WILEY
DOI: 10.1111/bph.15595

关键词

adverse cardiac remodelling; coronary artery ligation; heart failure; ischaemia; reperfusion; myocardial infarction

资金

  1. British Heart Foundation [RG/20/6/35095, PG/18/9/33548, TG/18/1/33408, PG/17/17/32877, RE/18/6/34217]
  2. Ministry of Higher Education of the Arab Republic of Egypt [NMM2/19]
  3. British Council in Egypt (Newton-Mosharafa Scholarship Fund)

向作者/读者索取更多资源

Approximately 7 million people are affected by acute myocardial infarction each year, and preclinical animal models have significantly advanced our understanding of the disease. While these models have limitations, careful selection is crucial for maximizing translational potential.
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.

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