Abstract

The incidence and mortality of sepsis and the associated development of acute kidney injury (AKI) remain high, despite intense research into potential treatments. Targeting the inflammatory response and/or sepsis-induced alterations in the (micro)circulation are two therapeutic strategies. Another approach could involve modulating the downstream mechanisms that are responsible for organ system dysfunction. Activation of inducible nitric oxide (NO) synthase (iNOS) during sepsis leads to elevated NO levels that influence renal hemodynamics and cause peroxynitrite-related tubular injury through the local generation of reactive nitrogen species. In many organs iNOS is not constitutively expressed; however, it is constitutively expressed in the kidney and, in humans, a relationship between the upregulation of renal iNOS and proximal tubular injury during systemic inflammation has been demonstrated. For these reasons, the selective inhibition of renal iNOS might have important implications for the treatment of sepsis-induced AKI. Various animal studies have demonstrated that selective iNOS inhibition—in contrast to nonselective NOS inhibition—attenuates sepsis-induced renal dysfunction and improves survival, a finding that warrants investigation in clinical trials. In this Review, the selective inhibition of iNOS as a potential novel treatment for sepsis-induced AKI is discussed.

Author affiliations

Department of Intensive Care Medicine and the Department of Pharmacology and Toxicology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands. (S Heemskerk). Department of Pharmacology and Toxicology, Center for Molecular Life Sciences, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands. (R Masereeuw). (F G M Russel). Department of Intensive Care Medicine, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands. (P Pickkers).

Correspondence to: S Heemskerk Email: s.heemskerk@ic.umcn.nl

Published online 29 September 2009