Suzuki Fumitaka, Hashikura Yasuhiko, Ise Hirohiko, Ishida Akiko, Nakayama Jun, Takahashi Masafumi, Miyagawa Shin-Ichi, Ikeda Uichi
Department of Organ Regeneration, Shinshu University Graduate School of Medicine, Asahi, Matsumoto, Japan.
Transpl Int. 2005 Jul;18(7):844-53. doi: 10.1111/j.1432-2277.2005.00094.x.
Hepatic warm ischemia-reperfusion injury (IRI) during hepatectomy and liver transplantation is a major cause of liver dysfunction in which the pathologic role of free radicals is a major concern. To assess the effect of MCI-186 (edaravone) on hepatic IRI, male Wistar rats were subjected to partial hepatic ischemia for 60 min after pretreatment with vehicle (group C) or MCI-186 (group M), or after both MCI-186 pretreatment and additional administration of MCI-186 12 h after reperfusion (group MX). Groups M and MX showed significantly lower levels of serum alanine aminotransferase and hepatic lipid peroxidation than group C, and also significantly lower expression levels of mRNA for cytokines, chemokines and intercellular adhesion molecule-1. There were fewer tissue monocytes and neutrophils in groups M and MX than in group C. These effects were more marked in group MX than in group M. Our findings suggest that treatment with MCI-186 attenuates hepatic IRI in this rat in vivo model.
