Mouse models of atherosclerosis: a historical perspective and recent advances

被引:0
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作者
Yee Ting Lee
Hiu Yu Lin
Yin Wah Fiona Chan
Ka Hou Christien Li
Olivia Tsz Ling To
Bryan P Yan
Tong Liu
Guangping Li
Wing Tak Wong
Wendy Keung
Gary Tse
机构
[1] University of Hong Kong,School of Biomedical Sciences, Li Ka Shing Faculty of Medicine
[2] University of Cambridge,School of Biological Sciences
[3] Newcastle University,Faculty of Medicine
[4] Chinese University of Hong Kong,Department of Medicine and Therapeutics
[5] Monash University,Department of Epidemiology and Preventive Medicine
[6] Tianjin Institute of Cardiology,Tianjin Key Laboratory of Ionic
[7] Second Hospital of Tianjin Medical University,Molecular Function of Cardiovascular disease, Department of Cardiology
[8] Chinese University of Hong Kong,School of Life Sciences
[9] The University of Hong Kong,Stem Cell & Regenerative Medicine Consortium, Li Ka Shing Faculty of Medicine
[10] Pokfulam,undefined
[11] Li Ka Shing Institute of Health Sciences,undefined
[12] Chinese University of Hong Kong,undefined
来源
Lipids in Health and Disease | / 16卷
关键词
Mouse models; Atherosclerosis; ApoE; LDL receptor; Reactive oxygen species; ER stress; Mitochondrial dysfunction;
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摘要
Atherosclerosis represents a significant cause of morbidity and mortality in both the developed and developing countries. Animal models of atherosclerosis have served as valuable tools for providing insights on its aetiology, pathophysiology and complications. They can be used for invasive interrogation of physiological function and provide a platform for testing the efficacy and safety of different pharmacological therapies. Compared to studies using human subjects, animal models have the advantages of being easier to manage, with controllable diet and environmental risk factors. Moreover, pathophysiological changes can be induced either genetically or pharmacologically to study the harmful effects of these interventions. There is no single ideal animal model, as different systems are suitable for different research objectives. A good understanding of the similarities and differences to humans enables effective extrapolation of data for translational application. In this article, we will examine the different mouse models for the study and elucidation of the pathophysiological mechanisms underlying atherosclerosis. We also review recent advances in the field, such as the role of oxidative stress in promoting endoplasmic reticulum stress, mitochondrial dysfunction and mitochondrial DNA damage, which can result in vascular inflammation and atherosclerosis. Finally, novel therapeutic approaches to reduce vascular damage caused by chronic inflammation using microRNA and nano-medicine technology, are discussed.
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