| Literature DB >> 31740428 |
Anne T Reutens1, Karin Jandeleit-Dahm2, Merlin Thomas3, Agus Salim4, Alysha M De Livera5, Leon A Bach6, Peter G Colman7, Timothy M E Davis8, Elif I Ekinci9, Greg Fulcher10, Peter Shane Hamblin11, Mark A Kotowicz12, Richard J MacIsaac13, Claire Morbey14, David Simmons15, Georgia Soldatos16, Gary Wittert17, Ted Wu18, Mark E Cooper19, Jonathan E Shaw20.
Abstract
PURPOSE: Kidney disease caused by type 1 diabetes can progress to end stage renal disease and can increase mortality risk. Nicotinamide adenine dinucleotide phosphate (NADPH) oxidase (Nox) plays a major role in producing oxidative stress in the kidney in diabetes, and its activity is attenuated by GKT137831, an oral Nox inhibitor with predominant inhibitory action on Nox-1 and Nox - 4. Previous studies have demonstrated renoprotective effects with GKT137831 in various experimental models of type 1 diabetes-related kidney disease. This study will evaluate the effect of GKT137831 in treating clinical diabetic kidney disease.Entities:
Keywords: Albuminuria; Diabetic nephropathy; NADPH oxidase; Type 1 diabetes
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Year: 2019 PMID: 31740428 DOI: 10.1016/j.cct.2019.105892
Source DB: PubMed Journal: Contemp Clin Trials ISSN: 1551-7144 Impact factor: 2.226