Ethanol preconditioning reduces hepatic i/r injury by inhibiting the complement system activation

Journal of Surgical Research

Volumn 166, Issue 2, 2011, Pages 314-323

  Ma, Zheng Wei ^a   Feng, Xiao Bin ^a   Zheng, Shu Guo ^a   Bie, Ping ^a   Wang, Shu Guang ^a   Li, Kun ^a   Zhang, Yu Jun ^a   Dong, Jia Hong ^a  

^a THIRD MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

complement system; ethanol preconditioning; liver ischemia reperfusion

Indexed keywords

ALANINE AMINOTRANSFERASE; ALCOHOL; ASPARTATE AMINOTRANSFERASE; COMPLEMENT COMPONENT C3; INTERLEUKIN 1BETA; MALONALDEHYDE;

ALANINE AMINOTRANSFERASE BLOOD LEVEL; ALCOHOL BLOOD LEVEL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ASPARTATE AMINOTRANSFERASE BLOOD LEVEL; COMPLEMENT ACTIVATION; COMPLEMENT BLOOD LEVEL; COMPLEMENT DEPOSITION; CONTROLLED STUDY; CYTOKINE PRODUCTION; DOWN REGULATION; HEMOLYSIS; HISTOPATHOLOGY; ISCHEMIC PRECONDITIONING; LIPID PEROXIDATION; LIVER ISCHEMIA; LIVER LEVEL; LIVER PROTECTION; MALE; NONHUMAN; PRIORITY JOURNAL; RAT; REPERFUSION INJURY; SURVIVAL TIME;

ANIMALS; CENTRAL NERVOUS SYSTEM DEPRESSANTS; COMPLEMENT ACTIVATION; COMPLEMENT C3; ETHANOL; GENE EXPRESSION; HEMOLYSIS; INTERLEUKIN-1BETA; ISCHEMIC PRECONDITIONING; LIPID PEROXIDATION; LIVER DISEASES; MALE; MALONDIALDEHYDE; RATS; RATS, SPRAGUE-DAWLEY; REPERFUSION INJURY; RNA, MESSENGER;

EID: 79952488372     PISSN: 00224804     EISSN: 10958673     Source Type: Journal    
DOI: 10.1016/j.jss.2009.05.037     Document Type: Article

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