Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis

BACKGROUND: L-arginine is the common substrate for nitric oxide synthases and arginases. Increased arginase levels in the blood of patients with cystic fibrosis may result in L-arginine deficiency and thereby contribute to low airway nitric oxide formation and impaired pulmonary function. METHODS: P...

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Detalles Bibliográficos
Autores principales: Grasemann, Hartmut, Schwiertz, Raphael, Grasemann, Corinna, Vester, Udo, Racké, Kurt, Ratjen, Felix
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526723/
https://www.ncbi.nlm.nih.gov/pubmed/16764721
http://dx.doi.org/10.1186/1465-9921-7-87

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526723/
https://www.ncbi.nlm.nih.gov/pubmed/16764721
http://dx.doi.org/10.1186/1465-9921-7-87

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