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Nephrol Dial Transplant (2002) 17: 1999-2002
© 2002 European Renal Association-European Dialysis and Transplant Association


Brief Reports

Net renal extraction of asymmetrical (ADMA) and symmetrical (SDMA) dimethylarginine in fasting humans

Robert J. Nijveldt1,*, Paul A. M. van Leeuwen1,, Coen van Guldener2,4, Coen D. A. Stehouwer2, Jan A. Rauwerda1 and Tom Teerlink3

1 Departments of Surgery, 2 Internal Medicine and 3 Clinical Chemistry, VU University Medical Center, Amsterdam and 4 Department of Internal Medicine, Amphia Hospital (Langendijk), Breda, The Netherlands

Background. Recently, the potential importance of dimethylarginines as endogenously produced inhibitors of nitric oxide synthase has become clearer. Interestingly, elevated levels have been reported in patients with vascular disease, but especially in patients suffering end-stage renal disease. Although the kidney obviously seems to play a key role in the elimination of dimethylarginines, clear insight into the renal handling of these compounds is lacking. Thus, our aim was to investigate the renal extraction of dimethylarginines.

Methods. Plasma concentrations of dimethylarginines were determined in both arterial and renal venous blood in 20 fasting patients with normal renal function. Renal extraction was calculated as the arteriovenous concentration difference divided by the arterial concentration times 100%.

Results. A significant renal extraction was found for both dimethylarginines. Renal extraction was significantly higher for asymmetrical dimethylarginine (ADMA) when compared with symmetrical dimethylarginine (SDMA) (16.2 vs 10.5% respectively, P=0.001). In addition, arterial SDMA concentration, but not ADMA concentration, significantly correlated with arterial creatinine concentration.

Conclusions. In healthy humans, the kidney contributes to the regulation of plasma levels of dimethylarginines, since both ADMA and SDMA were significantly extracted from the arterial supply. Interestingly, a higher renal extraction of ADMA was found when compared to SDMA extraction, which strongly suggests the presence of an additional catabolic pathway for ADMA in the kidney.

Keywords: L-arginine; nitric oxide; nitric oxide synthase; renal failure

Correspondence and offprint requests to: P. A. M. van Leeuwen, PhD, MD, Department of Surgery, PO Box 7057, 1007 MB Amsterdam, The Netherlands. Email: pam.vleeuwen{at}vumc.nl

*R. J. Nijveldt, MD, is a recipient of a fellowship from the Council for Medical Research of the Netherlands Organisation for Scientific Research.


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