Renal Handling of Uric Acid.

Autor: Andrade Sierra J, Flores Fonseca MM
Jazyk: angličtina
Zdroj: Contributions to nephrology [Contrib Nephrol] 2018; Vol. 192, pp. 1-7. Date of Electronic Publication: 2018 Jan 23.
DOI: 10.1159/000484271
Abstrakt: Hyperuricemia occurs in 21.4% of the adult population and is associated with several conditions that increase oxidative stress and contributes to the pathogenesis of inflammatory mechanisms for the development and progression of diseases. Serum blood or urine samples of uric acid levels were used to mainly identify clinical problems, depending on the uric acid pathway alterations, which include synthesis, reabsorption or its excretion. Several proteins that act particularly as transporters (URAT1, GLUT9, 1-NPT1, 1-NPT4, OAT4, 9-MCT9, hUAT1, etc.) have been identified in the recent past involving tubular transport and clearance leading to clinical benefits. Until now, the knowledge of uric acid homeostasis centers its primary investigation on understanding molecular and genetic mechanisms, including the genetic polymorphisms that induce genetic and acquire renal tubular disorder, which increases or diminishes urate excretion.
(© 2018 S. Karger AG, Basel.)
Databáze: MEDLINE