NOS2 deficiency increases intestinal metabolism both in nonstimulated and endotoxemic mice

American Journal of Physiology - Gastrointestinal and Liver Physiology

Volumn 286, Issue 5 49-5, 2004, Pages

  Vissers, Yvonne L J ^a   Hallemeesch, Marcella M ^a   Soeters, Peter B ^a   Lamers, Wouter H ^a   Deutz, Nicolaas E P ^a  

^a MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

Knockout; Protein metabolism; Sepsis; Stable isotope

Indexed keywords

AMINO ACID; ARGININE DERIVATIVE; CELL PROTEIN; CITRULLINE; GLYCINE; INDUCIBLE NITRIC OXIDE SYNTHASE; ISOTOPE; N(G) NITROARGININE METHYL ESTER; PHENYLALANINE DERIVATIVE;

AMINO ACID METABOLISM; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ENDOTOXEMIA; ENZYME DEFICIENCY; INTESTINE CELL; INTESTINE FUNCTION; KNOCKOUT GENE; MALE; MORTALITY; MOUSE; NERVE CELL; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN METABOLISM; SURVIVAL; WILD TYPE;

ANIMALS; CITRULLINE; ENDOTOXEMIA; ENZYME INHIBITORS; GLUTAMINE; INTESTINES; LIPOPOLYSACCHARIDES; MALE; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NG-NITROARGININE METHYL ESTER; NITRIC OXIDE SYNTHASE; NITRIC OXIDE SYNTHASE TYPE I; NITRIC OXIDE SYNTHASE TYPE II; NITRIC OXIDE SYNTHASE TYPE III; PROTEINS;

EID: 1942455398     PISSN: 01931857     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpgi.00375.2003     Document Type: Article

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