Key result
Diminished bioavailability of nitric oxide is a key mechanism responsible for endothelial dysfunction and impaired endothelium-dependent vascular relaxation in patients with essential hypertension.
This review highlights that diminished nitric oxide bioavailability is a key mechanism underlying endothelial dysfunction in patients with essential hypertension.
Supports NO bioavailability as hypertension research target; leaves open clinical outcome benefits.
The discovery of the endothelium as a major regulator of vascular tone triggered intense research among basic and clinical investigators to unravel the physiologic and pathophysiologic significance of this phenomenon. Importantly, endothelial modulation of the contractile state of vascular smooth muscle has been shown to be impaired in atherosclerosis and in several conditions known to be associated with the premature development of atherosclerosis. Studies in several different animal models of arterial hypertension, and in patients with both essential and secondary hypertension, have demonstrated an association between elevated systemic blood pressure and impaired endothelium-dependent vascular relaxation. More recently, a diminished bioavailability of nitric oxide (NO) has been identified as a mechanism responsible for endothelial dysfunction in hypertensive patients. Different processes may, in turn, explain this decreased vascular activity of NO. The present review focuses on those clinical studies that are aimed at identifying the precise abnormality responsible for reduced NO-dependent vasodilation in patients with essential hypertension. Understanding of the basic mechanisms of this process may prove to be beneficial for the development of more specific therapies and ultimately for the outcome of hypertensive patients.
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Cardillo et al. (1998) conducted a review in systemic arterial hypertension. Diminished bioavailability of nitric oxide was evaluated. Diminished bioavailability of nitric oxide is a key mechanism responsible for endothelial dysfunction and impaired endothelium-dependent vascular relaxation in patients with essential hypertension.
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