Key result
This review provides an update on available mouse models of Type 1 and Type 2 diabetic vascular complications to aid in identifying mechanism-based targeted therapies.
Why the study?
Choosing appropriate animal models is important for understanding the multi-faceted pathogenesis of diabetes-driven vascular complications and identifying targeted therapies.
This review summarizes available mouse models for studying the pathogenesis of diabetes-associated macrovascular and microvascular complications to aid in identifying targeted therapies.
Animal model insights into diabetes vascular complications require human validation before clinical use; leaves open translation of pathways and therapies.
Diabetes is a chronic metabolic disorder associated with the accelerated development of macrovascular (atherosclerosis and coronary artery disease) and microvascular complications (nephropathy, retinopathy and neuropathy), which remain the principal cause of mortality and morbidity in this population. Current understanding of cellular and molecular pathways of diabetes-driven vascular complications, as well as therapeutic interventions has arisen from studying disease pathogenesis in animal models. Diabetes-associated vascular complications are multi-faceted, involving the interaction between various cellular and molecular pathways. Thus, the choice of an appropriate animal model to study vascular pathogenesis is important in our quest to identify innovative and mechanism-based targeted therapies to reduce the burden of diabetic complications. Herein, we provide up-to-date information on available mouse models of both Type 1 and Type 2 diabetic vascular complications as well as experimental analysis and research outputs. 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.
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Choi et al. (2021) conducted a review in Diabetes-associated vascular diseases. Animal models was evaluated. This review provides an update on available mouse models of Type 1 and Type 2 diabetic vascular complications to aid in identifying mechanism-based targeted therapies.
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