Guidelines on models of diabetic heart disease

Author:

Heather Lisa C.1,Hafstad Anne D.2ORCID,Halade Ganesh V.3ORCID,Harmancey Romain4ORCID,Mellor Kimberley M.5ORCID,Mishra Paras K.6ORCID,Mulvihill Erin E.78ORCID,Nabben Miranda910ORCID,Nakamura Michinari11ORCID,Rider Oliver J.12,Ruiz Matthieu1314,Wende Adam R.15ORCID,Ussher John R.161718ORCID

Affiliation:

1. Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford, United Kingdom

2. Department of Medical Biology, Faculty of Health Sciences, UiT—The Arctic University of Norway, Tromso, Norway

3. Department of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama

4. Division of Cardiology, Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas

5. Department of Physiology, University of Auckland, Auckland, New Zealand

6. Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska

7. Energy Substrate Laboratory, University of Ottawa Heart Institute, Ottawa, Ontario, Canada

8. Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario, Canada

9. Department of Genetics and Cell Biology, Maastricht University Medical Center, CARIM School of Cardiovascular Diseases, Maastricht, The Netherlands

10. Department of Clinical Genetics, Maastricht University Medical Center, CARIM School of Cardiovascular Diseases, Maastricht, The Netherlands

11. Department of Cell Biology and Molecular Medicine, Cardiovascular Research Institute, Rutgers New Jersey Medical School, Newark, New Jersey

12. Radcliffe Department of Medicine, University of Oxford Centre for Clinical Magnetic Resonance Research, University of Oxford, Oxford, United Kingdom

13. Montreal Heart Institute, Montreal, Quebec, Canada

14. Department of Nutrition, Université de Montréal, Montreal, Quebec, Canada

15. Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama

16. Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Alberta, Canada

17. Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada

18. Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, Alberta, Canada

Abstract

Diabetes is a major risk factor for cardiovascular diseases, including diabetic cardiomyopathy, atherosclerosis, myocardial infarction, and heart failure. As cardiovascular disease represents the number one cause of death in people with diabetes, there has been a major emphasis on understanding the mechanisms by which diabetes promotes cardiovascular disease, and how antidiabetic therapies impact diabetic heart disease. With a wide array of models to study diabetes (both type 1 and type 2), the field has made major progress in answering these questions. However, each model has its own inherent limitations. Therefore, the purpose of this guidelines document is to provide the field with information on which aspects of cardiovascular disease in the human diabetic population are most accurately reproduced by the available models. This review aims to emphasize the advantages and disadvantages of each model, and to highlight the practical challenges and technical considerations involved. We will review the preclinical animal models of diabetes (based on their method of induction), appraise models of diabetes-related atherosclerosis and heart failure, and discuss in vitro models of diabetic heart disease. These guidelines will allow researchers to select the appropriate model of diabetic heart disease, depending on the specific research question being addressed.

Funder

British Heart Foundation

Gouvernement du Canada | Canadian Institutes of Health Research

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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