Key result
Exercise and ischemia activate key signaling pathways in skeletal muscle, including nuclear receptors, kinases, and hypoxia-inducible factors, which drive paracrine regenerative angiogenesis.
Why the study?
Peripheral artery disease benefits from exercise via vascular remodeling, but the underlying skeletal muscle molecular signaling pathways driving paracrine regenerative angiogenesis required synthesis.
This review highlights the molecular mechanisms by which exercise induces limb muscle angiogenesis, suggesting potential targets for 'exercise-mimicking' therapeutics in peripheral artery disease.
May inform exercise-mimicking drug development for PAD; leaves open whether targeting these pathways improves clinical outcomes.
Exercise has a profound effect on cardiovascular disease, particularly through vascular remodeling and regeneration. Peripheral artery disease (PAD) is one such cardiovascular condition that benefits from regular exercise or rehabilitative physical therapy in terms of slowing the progression of disease and delaying amputations. Various rodent pre-clinical studies using models of PAD and exercise have shed light on molecular pathways of vascular regeneration. Here, I review key exercise-activated signaling pathways (nuclear receptors, kinases, and hypoxia inducible factors) in the skeletal muscle that drive paracrine regenerative angiogenesis. The rationale for highlighting the skeletal muscle is that it is the largest organ recruited during exercise. During exercise, skeletal muscle releases several myokines, including angiogenic factors and cytokines that drive tissue vascular regeneration via activation of endothelial cells, as well as by recruiting immune and endothelial progenitor cells. Some of these core exercise-activated pathways can be extrapolated to vascular regeneration in other organs. I also highlight future areas of exercise research (including metabolomics, single cell transcriptomics, and extracellular vesicle biology) to advance our understanding of how exercise induces vascular regeneration at the molecular level, and propose the idea of "exercise-mimicking" therapeutics for vascular recovery.
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Vihang A. Narkar (2023) conducted a review in Peripheral artery disease and limb ischemia. Exercise was evaluated. Exercise and ischemia activate key signaling pathways in skeletal muscle, including nuclear receptors, kinases, and hypoxia-inducible factors, which drive paracrine regenerative angiogenesis.
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