Asymmetric Dimethylarginine Contributes to Airway Nitric Oxide Deficiency in Patients with Cystic Fibrosis

Autor: Jaques Belik, Suhail Al-Saleh, Jeremy A. Scott, Reshma Amin, Hartmut Grasemann, Mahroukh Rafii, Felix Ratjen, Darakhshanda Shehnaz, Paul B. Pencharz, Anne Mehl
Rok vydání: 2011
Předmět:
Zdroj: American Journal of Respiratory and Critical Care Medicine. 183:1363-1368
ISSN: 1535-4970
1073-449X
DOI: 10.1164/rccm.201012-1995oc
Popis: Rationale: Airway nitric oxide is reduced in cystic fibrosis airways. Asymmetric dimethylarginine is an endogenous nitric oxide synthase inhibitor that may contribute to nitric oxide deficiency in cystic fibrosis.Objectives: To test the hypothesis that asymmetric dimethylarginine is increased in cystic fibrosis and contributes to nitric oxide deficiency and airway obstruction.Methods: The concentrations of asymmetric dimethylarginine, symmetric dimethylarginine, and l-arginine were measured in sputum of clinically stable patients with cystic fibrosis, in patients with cystic fibrosis before and after treatment for a pulmonary exacerbation, and in healthy control subjects, using liquid chromatography-tandem mass spectrometry.Measurements and Main Results: Asymmetric dimethylarginine was increased in cystic fibrosis compared with control sputum, and the l-arginine/asymmetric dimethylarginine ratio was decreased. Symmetric dimethylarginine exceeded asymmetric dimethylarginine concentrations in control sputum...
Databáze: OpenAIRE