TY - JOUR T1 - Vasopressin receptor antagonists: Mechanisms of action and potential effects in heart failure JF - Cleveland Clinic Journal of Medicine JO - Cleve Clin J Med SP - S20 LP - S23 VL - 73 IS - 6 suppl 2 AU - Gary Francis AU - Steven R. Goldsmith Y1 - 2006/06/01 UR - http://www.ccjm.org/content/73/6_suppl_2/S20.abstract N2 - Increased arginine vasopressin (AVP) secretion in heart failure may lead to vasoconstriction, left ventricular remodeling, and water retention—actions that promote afterload, preload, and hyponatremia and thereby cause disease progression. Interfering with AVP-mediated signaling pharmacologically may be beneficial in heart failure. Selective antagonism of the vasopressin 2 (V2) receptor may facilitate a safe diuresis and normalize low serum sodium levels, as demonstrated in preliminary clinical trials. Pure V2 antagonism, however, may stimulate AVP secretion and enhance V1a signaling, while pure V1a receptor antagonism may lead to unwanted V2 stimulation and secondary water retention and volume expansion. Combined V1a and V2 receptor antagonism could potentially prove advantageous as a therapy for heart failure by acting synergistically to facilitate diuresis and improve hemodynamics. ER -