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斑马鱼作为人类心血管疾病的可调控模型。

Zebrafish as a tractable model of human cardiovascular disease.

机构信息

Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.

Bateson Centre, University of Sheffield, Sheffield, UK.

出版信息

Br J Pharmacol. 2022 Mar;179(5):900-917. doi: 10.1111/bph.15473. Epub 2021 May 10.

Abstract

Mammalian models including non-human primates, pigs and rodents have been used extensively to study the mechanisms of cardiovascular disease. However, there is an increasing desire for alternative model systems that provide excellent scientific value while replacing or reducing the use of mammals. Here, we review the use of zebrafish, Danio rerio, to study cardiovascular development and disease. The anatomy and physiology of zebrafish and mammalian cardiovascular systems are compared, and we describe the use of zebrafish models in studying the mechanisms of cardiac (e.g. congenital heart defects, cardiomyopathy, conduction disorders and regeneration) and vascular (endothelial dysfunction and atherosclerosis, lipid metabolism, vascular ageing, neurovascular physiology and stroke) pathologies. We also review the use of zebrafish for studying pharmacological responses to cardiovascular drugs and describe several features of zebrafish that make them a compelling model for in vivo screening of compounds for the treatment cardiovascular disease. 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.

摘要

包括非人类灵长类动物、猪和啮齿动物在内的哺乳动物模型已被广泛用于研究心血管疾病的机制。然而,人们越来越希望使用替代模型系统,这些系统在替代或减少哺乳动物使用的同时,提供出色的科学价值。在这里,我们回顾了斑马鱼(Danio rerio)在研究心血管发育和疾病中的应用。比较了斑马鱼和哺乳动物心血管系统的解剖结构和生理学,并描述了使用斑马鱼模型研究心脏(例如先天性心脏病、心肌病、传导障碍和再生)和血管(血管内皮功能障碍和动脉粥样硬化、脂质代谢、血管老化、神经血管生理学和中风)病理学的机制。我们还回顾了使用斑马鱼研究心血管药物的药理反应,并描述了使它们成为治疗心血管疾病化合物体内筛选的有吸引力模型的几个斑马鱼特征。相关文章: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。要查看该部分中的其他文章,请访问 http://onlinelibrary.wiley.com/doi/10.1111/bph.v179.5/issuetoc.

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