Experimental data suggesting that inflammation mediated rat liver mitochondrial dysfunction results from secondary hypoxia rather than from direct effects of inflammatory mediators

Frontiers in Physiology

Volumn 4 JUN, Issue , 2013, Pages

  Weidinger, Adelheid ^a   Dungel, Peter ^a   Perlinger, Martin ^a   Singer, Katharina ^a   Ghebes, Corina ^a   Duvigneau, J Catharina ^b   Müllebner, Andrea ^b   Schäfer, Ute ^c   Redl, Heinz ^a   Kozlov, Andrey V ^a  

^a LUDWIG BOLTZMANN INSTITUTE FOR EXPERIMENTAL AND CLINICAL TRAUMATOLOGY   (Austria)

^b UNIVERSITY OF VETERINARY MEDICINE   (Austria)

^c MEDICAL UNIVERSITY OF GRAZ   (Austria)

Author keywords

Cytokine; Free iron; Ho 1; Il 6; Inos; Lipopolysaccharide; Liver; Reoxygenation

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; HEME OXYGENASE; INTERLEUKIN 6; IRON CHELATE; NITRIC OXIDE SYNTHASE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL DAMAGE; CELL FUNCTION; CELL MEMBRANE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENE EXPRESSION; HYPOXEMIA; IN VIVO STUDY; INFLAMMATION; ISCHEMIA; LIVER CELL; LIVER MITOCHONDRION; MALE; MEDIATOR RELEASE; MULTIPLE ORGAN FAILURE; NONHUMAN; PRECISION CUT LIVER SLICE; RAT; REGULATORY MECHANISM; REOXYGENATION; SYSTEMIC INFLAMMATORY RESPONSE SYNDROME;

EID: 84882695464     PISSN: None     EISSN: 1664042X     Source Type: Journal    
DOI: 10.3389/fphys.2013.00138     Document Type: Article

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