Why the study?
Coronary microvascular dysfunction causes the no-reflow phenomenon after cardiac ischemia, and early detection is crucial to track cardiovascular disease progression.
Pulse wave Doppler can be used in a mouse model to dynamically assess coronary flow reserve, demonstrating significant and persistent microvascular dysfunction following ischemia-reperfusion injury.
May guide preclinical microvascular therapy testing; leaves open translation of mouse Doppler CFR to clinical ischemia-reperfusion care.
After cardiac ischemia, there is often insufficient myocardial perfusion, even if flow has been successfully and completely restored in an upstream artery. This phenomenon, known as the "no-reflow phenomenon," is attributed to coronary microvascular dysfunction and has been associated with poor clinical outcomes. In clinical practice, a reduction in coronary flow reserve (CFR) is frequently used as an indicator of coronary artery disease. CFR is defined as the ratio of the peak flow velocity induced by pharmacologic or metabolic factors to the resting flow velocity. This protocol focused on assessing the dynamic changes in CFR before and after ischemia-reperfusion (IR) using pulse wave Doppler measurements. In this study, normal mice exhibited the ability to increase the peak velocity of coronary blood flow up to two times higher than the resting values under isoflurane stimulation. However, after ischemia-reperfusion, the CFR at 1 h significantly decreased compared to the pre-operation baseline. Over time, the CFR showed gradual recovery, but it remained below the normal level. Despite the preservation of systolic function, early detection of microvascular dysfunction is crucial, and establishing a practical guide could aid doctors in this task, while also facilitating the study of cardiovascular disease progression over time.
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Guo et al. (2023) studied this question.
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