Reduced Renal Methylarginine Metabolism Protects against Progressive Kidney Damage.


Tomlinson, JA; Caplin, B; Boruc, O; Bruce-Cobbold, C; Cutillas, P; Dormann, D; Faull, P; Grossman, RC; Khadayate, S; Mas, VR; Nitsch, DD; Wang, Z; Norman, JT; Wilcox, CS; Wheeler, DC; Leiper, J; (2015) Reduced Renal Methylarginine Metabolism Protects against Progressive Kidney Damage. Journal of the American Society of Nephrology, 26 (12). pp. 3045-59. ISSN 1046-6673 DOI: https://doi.org/10.1681/ASN.2014030280

Full text not available from this repository.

Abstract

: Nitric oxide (NO) production is diminished in many patients with cardiovascular and renal disease. Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of NO synthesis, and elevated plasma levels of ADMA are associated with poor outcomes. Dimethylarginine dimethylaminohydrolase-1 (DDAH1) is a methylarginine-metabolizing enzyme that reduces ADMA levels. We reported previously that a DDAH1 gene variant associated with increased renal DDAH1 mRNA transcription and lower plasma ADMA levels, but counterintuitively, a steeper rate of renal function decline. Here, we test the hypothesis that reduced renal-specific ADMA metabolism protects against progressive renal damage. Renal DDAH1 is expressed predominately within the proximal tubule. A novel proximal tubule-specific Ddah1 knockout (Ddah1(PT-/-)) mouse demonstrated tubular cell accumulation of ADMA and lower NO concentrations, but unaltered plasma ADMA concentrations. Ddah1(PT-/-) mice were protected from reduced kidney tissue mass, collagen deposition, and profibrotic cytokine expression in two independent renal injury models: folate nephropathy and unilateral ureteric obstruction. Furthermore, a study of two independent kidney transplant cohorts revealed higher levels of human renal allograft methylarginine-metabolizing enzyme gene expression associated with steeper function decline. We also report an association among DDAH1 expression, NO activity, and uromodulin expression supported by data from both animal and human studies, raising the possibility that kidney DDAH1 expression exacerbates renal injury through uromodulin-related mechanisms. Together, these data demonstrate that reduced renal tubular ADMA metabolism protects against progressive kidney function decline. Thus, circulating ADMA may be an imprecise marker of renal methylarginine metabolism, and therapeutic ADMA reduction may even be deleterious to kidney function.<br/>

Item Type: Article
Faculty and Department: Faculty of Epidemiology and Population Health > Dept of Non-Communicable Disease Epidemiology
Research Centre: EHR Research Group
PubMed ID: 25855779
Web of Science ID: 365466000019
URI: http://researchonline.lshtm.ac.uk/id/eprint/2145742

Statistics


Download activity - last 12 months
Downloads since deposit
0Downloads
248Hits
Accesses by country - last 12 months
Accesses by referrer - last 12 months
Impact and interest
Additional statistics for this record are available via IRStats2

Actions (login required)

Edit Item Edit Item