Key result
Balloon injury and ApoE-deficient mouse models reliably reproduce distinct types of arterial stenosis.
Why the study?
Various in vivo rodent models for artery stenosis exist, but clear introduction and comparison of models for myointimal hyperplasia versus atherosclerosis are needed.
This paper provides a methodological guide for selecting appropriate mouse models to study artery stenosis driven by either myointimal hyperplasia or atherosclerosis.
Various in vivo laboratory rodent models for the induction of artery stenosis have been established to mimic diseases that include arterial plaque formation and stenosis, as observed for example in ischemic heart disease. Two highly reproducible mouse models - both resulting in artery stenosis but each underlying a different pathway of development - are introduced here. The models represent the two most common causes of artery stenosis; namely one mouse model for each myointimal hyperplasia, and atherosclerosis are shown. To induce myointimal hyperplasia, a balloon catheter injury of the abdominal aorta is performed. For the development of atherosclerotic plaque, the ApoE -/- mouse model in combination with western fatty diet is used. Different model-adapted options for the measurement and evaluation of the results are named and described in this manuscript. The introduction and comparison of these two models provides information for scientists to choose the appropriate artery stenosis model in accordance to the scientific question asked.
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Stubbendorff et al. (2014) studied Artery stenosis. Balloon catheter injury and ApoE -/- mouse model with western fatty diet was evaluated. Two reproducible mouse models for artery stenosis—balloon catheter injury for myointimal hyperplasia and the ApoE -/- model with western diet for atherosclerosis—are introduced and compared.
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