Angiotensin receptor blockers (ARBs) selectively inhibit the binding of angiotensin II (ANG II) to angiotensin II type 1 (AT1) receptors.1-5
The renin-angiotensin system (RAS) regulates blood pressure and fluid electrolyte balance.2,6-8 Uncontrolled RAS leads to the development of hypertension and congestive heart failure.2,6-9 Angiotensin II (ANG II) is the primary hormone that mediates increased vasoconstriction, cardiac contractility, and cardiac, renal, and vascular hypertrophy, stimulates adrenal aldosterone secretion, and increases renal tubular sodium absorption.6-8 Increased aldosterone can increase reabsorption of sodium and the excretion of potassium by the kidney, which can result in increased salt and water retention, increased blood volume and potassium loss. This combined with the vasoconstrictive effects of ANG II increases blood pressure.2,6-8,10
ANG II actions are mediated by AT1 and AT2 receptors.2,5-8 Most pathological cardiovascular actions of ANG II come from its interaction with the AT1 receptor.1-3,11 The negative effects of ANG II may be partially offset by AT2 receptor stimulation, which has favorable effects on vasodilation, tissue growth and repair, and cardioprotective effects.11-13
Angiotensin receptor blockers (ARBs) antagonize the actions of the RAS by blocking ANG II from binding with AT1 receptors, while preserving the positive effects mediated by AT2 receptor stimulation.1-3 ARBs lower blood pressure, modestly decrease aldosterone production, and can reverse vascular hypertrophy.1-3,9,11-13
References
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