Inducible Nitric Oxide Synthase Inhibitors Reduce Urinary Markers of Systemic Oxidant Stress in Murine Proliferative Lupus Nephritis. (1st November 2005)

• Record Type: Journal Article
• Authors: Njoku, Chinedu J.; Patrick, Kennerly S.; Ruiz, Philip; Oates, Jim C.
• Is Part Of: Journal of investigative medicine. Volume 53:Number 7(2005)
• Page Start: 347
• Page End: 352
• Publication Date: 2005-11-01
• Subjects: nitric oxide synthase -- isoprostanes -- lupus nephritis; Clinical medicine -- Periodicals; Medicine -- Research -- Periodicals; Medicine; Research -- United States; Clinical medicine; Medicine -- Research; Periodicals; 616.075
• DOI: 10.2310/6650.2005.53705
• Languages: English
• ISSNs: 1081-5589

Abstract

Abstract : Background: Proliferative lupus nephritis (PLN) is characterized by increased expression of inducible nitric oxide (NO) synthase (iNOS). Inhibition of iNOS with N G -monomethyl L -arginine (L -NMMA) abrogates renal disease in two models of murine PLN, but the mechanism of this effect is unknown. Reactive oxygen species have both direct and indirect pathogenic effects in inflammatory lesions and are therefore potentially an important therapeutic target in PLN. We hypothesized that inhibition of iNOS activity would reduce ROS production in murine PLN. Methods: A dose escalation of L -NMMA (0, 20, 100, and 500 mg/kg/day) was performed in New Zealand Black × New Zealand White F1 (NZB/W) mice with active renal disease. Twenty-four-hour urine nitrate + nitrite (NOX) was measured with a chemiluminescence NO analyzer. Twenty-four-hour urine 8-isoprostane F2α (8-iso-PGF2α) was measured by gas chromatography-negative ion chemical ionization mass spectrometry. MRL-MpJFASlpr (MRL/lpr) and NZB/W mice were divided into three groups and given either L -NMMA, L -N6-iminoethyl-lysine (L -NIL), or distilled water for 2 weeks. Urine NOX and 8-iso-PGF2α were determined after 2 weeks. Results: L -NMMA reduced both urine NOX and 8-iso-PGF2α levels in a dose-dependent fashion in NZB/W and MRL/lpr mice. Urine NOX and 8-iso-PGF2α levels were highly correlated. Both specific (L -NIL) and nonspecific (L -NMMA) iNOS inhibition reduced urine NOX and 8-iso-PGF2α levels in both models of murine PLN. Conclusion: These findings suggest that iNOS activity is a major source of reactive oxidant stress in these models of murine PLN. Future studies will address the pathogenic role of reactive oxygen stress in PLN.