Vasopressin Antagonists: Role in the Management of Hyponatremia
Author(s) -
Karen Yeates,
A. Ross Morton
Publication year - 2006
Publication title -
american journal of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 85
eISSN - 1421-9670
pISSN - 0250-8095
DOI - 10.1159/000094539
Subject(s) - hyponatremia , vasopressin , medicine , endocrinology , electrolyte disorder , arginine vasopressin receptor 2 , antidiuretic , urine osmolality , free water clearance , plasma osmolality , thirst , aquaporin 2 , heart failure , syndrome of inappropriate antidiuretic hormone secretion , receptor , antagonist , engineering , water channel , mechanical engineering , inlet
Hyponatremia is a common electrolyte disorder associated with potentially serious or life-threatening consequences. Serum osmolality and sodium concentration [Na+] are regulated by thirst, the hormone arginine vasopressin (AVP), and renal water and sodium handling. Hyponatremia is frequently caused by dysregulation of AVP, which accompanies disorders of water retention, such as congestive heart failure (CHF) and the syndrome of inappropriate secretion of antidiuretic hormone (SIADH). Clinical trials with AVP receptor antagonists have confirmed the important role of AVP in the pathophysiology of hyponatremia and suggest these agents are efficacious in treating hyponatremia associated with SIADH, cirrhosis, and CHF. Acting directly at AVP receptors in the renal tubules, these agents promote aquaresis - the electrolyte-sparing excretion of free water - in patients with hyponatremia. In clinical trials, AVP receptor antagonists have been shown to increase the serum [Na+] and urine output while decreasing urine osmolality.
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