Title of article :
Hepatic Ischemia/Reperfusion Injury Is Diminished by Atorvastatin in Wistar Rats
Author/Authors :
Cلmara-Lemarroy، نويسنده , , Carlos Rodrigo and Guzmلn-de la Garza، نويسنده , , Francisco Javier and Alarcَn-Galvلn، نويسنده , , Gabriela and Cordero-Pérez، نويسنده , , Paula and Muٌoz-Espinosa، نويسنده , , Linda and Torres-Gonzلlez، نويسنده , , Liliana and Fernلndez-Garza، نويسنده , , Nancy Esthela، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Abstract :
Background and Aims
al occlusion of the hepatoduodenal ligament (HDL) is often used during liver surgeries in order to reduce blood loss, resulting in ischemia/reperfusion injury (I/R). The aim of the study was to investigate the effects of atorvastatin (ATOR) on hepatic I/R injury and on serum levels of tumor necrosis factor-alpha (TNF-α), endothelin-1 (ET-1), antithrombin III (ATIII) and intracellular adhesion molecule-1 (ICAM-1).
s
ischemia was induced in Wistar rats by clamping the HDL for 60 min, followed by either 60 or 180 min reperfusion. Rats received either vehicle or 10 mg/kg ATOR before hepatic I/R. Control group received sham surgery. Livers were examined for histological damage and serum AST, ALT, TNF-α, ET-1, ATIII and ICAM-1 concentrations were measured.
s
I/R, AST and ALT were significantly elevated, ATIII levels were significantly depleted, both TNF-α and ICAM-1 levels increased and ET-1 was significantly elevated (at 180 min). ATOR pretreatment attenuated these alterations and diminished histological injury scores.
sions
sults show that ATOR protects the liver from I/R injury.
Keywords :
Ischemia/reperfusion , Liver , Atorvastatin , pro-inflammatory cytokines , Rat , Endothelial adhesion molecules
Journal title :
Archives of Medical Research
Journal title :
Archives of Medical Research