Disruption of NO-cGMP signaling by neonatal hyperoxia impairs relaxation of lung parenchyma

American Journal of Physiology - Lung Cellular and Molecular Physiology

Volumn 293, Issue 4, 2007, Pages

  Sopi, Ramadan B ^a   Haxhiu, Musa A ^a   Martin, Richard J ^a   Dreshaj, Ismail A ^a   Kamath, Suneel ^a   Zaidi, Syed I A ^a  

^a CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

Arginase; L arginine; Lung strips; N nitro L arginine methyl ester; Nitric oxide synthase

Indexed keywords

ARGININE; BETHANECHOL; CYCLIC GMP; N(G) NITROARGININE METHYL ESTER; NITRIC OXIDE; NITRIC OXIDE SYNTHASE;

AMBIENT AIR; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIOAVAILABILITY; BRONCHUS HYPERREACTIVITY; CONTROLLED STUDY; ELECTRIC FIELD; ENZYME INHIBITION; HYPEROXIA; LUNG INJURY; LUNG PARENCHYMA; NONHUMAN; OXYGEN BREATHING; PRIORITY JOURNAL; RAT; RISK FACTOR; SIGNAL TRANSDUCTION; SPRAGUE DAWLEY RAT;

AGING; ANIMALS; ANIMALS, NEWBORN; ARGINASE; ARGININE; CYCLIC GMP; ELECTRIC STIMULATION; ENZYME INHIBITORS; HYPEROXIA; LUNG; NG-NITROARGININE METHYL ESTER; NITRIC OXIDE; NITRIC OXIDE SYNTHASE; RATS; RATS, SPRAGUE-DAWLEY; SIGNAL TRANSDUCTION;

EID: 35348831783     PISSN: 10400605     EISSN: 15221504     Source Type: Journal    
DOI: 10.1152/ajplung.00182.2007     Document Type: Article

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