Tyrosine phosphorylation of neuronal nitric oxide synthase (nNOS) during hypoxia in the cerebral cortex of newborn piglets: The role of nitric oxide

• Published in: Neuroscience letters 2009-10, Vol.462 (1), p.64-67
• Main Authors: Mishra, Om Prakash, Ashraf, Qazi M., Delivoria-Papadopoulos, Maria
• Format: Article
• Language: English
• Subjects: Adenosine Triphosphate - metabolism; Animals; Animals, Newborn; Biological and medical sciences; Blotting, Western; Cell Membrane - drug effects; Cell Membrane - metabolism; Cerebral Cortex - drug effects; Cerebral Cortex - metabolism; Densitometry; Electrophoresis, Polyacrylamide Gel; Fundamental and applied biological sciences. Psychology; Hypoxia; Hypoxia - drug therapy; Hypoxia - metabolism; Luminescence; Nitric Oxide - metabolism; Nitric Oxide Synthase Type I - antagonists & inhibitors; Nitric Oxide Synthase Type I - metabolism; nNOS; nNOSi; Phosphocreatine - metabolism; Phosphorylation - drug effects; Random Allocation; Swine; Tyrosine - metabolism; Tyrosine phosphorylation; Vertebrates: nervous system and sense organs
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2009.06.075

The present study aims to investigate the mechanism of activation of nNOS during hypoxia and tests the hypothesis that the hypoxia-induced increased tyrosine phosphorylation of nNOS in the cerebral cortical membranes of newborn piglets is mediated by nNOS-derived nitric oxide (NO). Fifteen newborn piglets were divided into normoxic (Nx, n = 5), hypoxic (Hx, n = 5) and hypoxic-pretreated with nNOS inhibitor I (Hx-nNOSi) groups. Hypoxia was induced by an FiO 2 of 0.07 for 60 min. nNOS inhibitor I (selectivity > 2500 vs endothelial NOS and >500 vs inducible NOS) was administered (0.4 mg/kg, i.v.) 30 min prior to hypoxia. Cortical membranes were isolated and tyrosine phosphorylation of nNOS determined by Western blot. Membrane protein was immunoprecipitated with nNOS antibody, separated on 12% SDS-PAGE and blotted with anti-phosphotyrosine antibody. Protein bands were detected by enhanced chemiluminescence, analyzed by densitometry and expressed as absorbance (OD × mm 2). Density (OD × mm 2) of tyrosine phosphorylated nNOS was 51.66 ± 14.11 in Nx, 118.39 ± 14.17 in Hx ( p < 0.05 vs Nx) and 45.56 ± 10.34 in Hx-nNOSi ( p < 0.05 vs Hx, p = NS vs Nx). The results demonstrate that pretreatment with nNOS inhibitor prevents the hypoxia-induced increased tyrosine phosphorylation of nNOS. We conclude that the mechanism of hypoxia-induced increased tyrosine phosphorylation of nNOS is mediated by nNOS-derived NO.