Key result
Insulin stimulates the release of endothelial nitric oxide to regulate blood flow and enhance glucose uptake in skeletal muscle.
The vascular endothelium plays an active role in regulating blood flow and insulin action via the release of nitric oxide, which is impaired in conditions like obesity, type 2 diabetes, and hypertension.
Shared endothelial impairment across insulin-resistant states merits mechanistic exploration; leaves open any therapeutic implications pending interventional trials.
Insulin resistance is the primary abnormality associ-ated with obesity, type 2 diabetes, and hypertension(1,2). Interestingly, these disease processes alsoshare a common underlying impairment of vascular endothelial function. For many years the endothelium was thought of as nothing more than a benign barrier between blood and extracellular space. But intensive investigations demonstrate a myriad of actions by the endothelium, in-cluding regulation of blood flow (3,4), vascular tone (5), vascular permeability (6), and the immune response (7). The capillary endothelium regulates blood flow via the release of several vasoactive agents, in particular nitric oxide (NO) (8). Baron (4) first demonstrated that insulin can stimulate the release of endothelial NO, thereby reg-ulating blood flow and its own delivery. Insulin has mul-tiple hemodynamic actions to enhance its ability to increase glucose uptake in skeletal muscle (4, 9–11). The three major methods include: 1) increasing blood flow to
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Joyce M. Richey (2013) conducted a review in Insulin resistance, obesity, type 2 diabetes, hypertension. Nitric oxide was evaluated. Insulin stimulates the release of endothelial nitric oxide to regulate blood flow and enhance glucose uptake in skeletal muscle.
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