TY - JOUR
T1 - Beneficial effect of MCI-186 on hepatic warm ischemia-reperfusion in the rat
AU - Ninomiya, Mizuki
AU - Shimada, Mitsuo
AU - Harada, Noboru
AU - Shiotani, Satoko
AU - Hiroshige, Shoji
AU - Soejima, Yuji
AU - Suehiro, Taketoshi
AU - Sugimachi, Keizo
PY - 2002/11/1
Y1 - 2002/11/1
N2 - Despite growing evidence that reactive oxygen species are responsible for deleterious effects of ischemia-reperfusion (I/R) injury of the liver, there exists, until now, no reliable antioxidant therapeutics applicable in the clinical setting. We investigated the effects of free radical scavenger, 3-methyl-1-phenyl-2-pyrazolin-5-one (MCI-186), using an isolated liver perfusion model to elucidate its possible therapeutic effects on hepatic warm I/R injury. Isolated livers from Wistar rats were reperfused for 120 min with an oxygenated KrebsHenseleit bicarbonate buffer after 1 hr of warm ischemia. Addition of MCI-186 (1 mg/L) into the perfusate significantly improved portal flow, hepatic enzyme release into the perfusate, total bile production, histologic alteration, and malondialdehyde concentration but not sinusoidal endothelial cell function as assessed by the clearance of hyaluronic acid. MCI-186 seems to have protective effects against hepatic warm I/R injury by attenuating the damage of the hepatocyte, which is the major target of oxidative damage in this model.
AB - Despite growing evidence that reactive oxygen species are responsible for deleterious effects of ischemia-reperfusion (I/R) injury of the liver, there exists, until now, no reliable antioxidant therapeutics applicable in the clinical setting. We investigated the effects of free radical scavenger, 3-methyl-1-phenyl-2-pyrazolin-5-one (MCI-186), using an isolated liver perfusion model to elucidate its possible therapeutic effects on hepatic warm I/R injury. Isolated livers from Wistar rats were reperfused for 120 min with an oxygenated KrebsHenseleit bicarbonate buffer after 1 hr of warm ischemia. Addition of MCI-186 (1 mg/L) into the perfusate significantly improved portal flow, hepatic enzyme release into the perfusate, total bile production, histologic alteration, and malondialdehyde concentration but not sinusoidal endothelial cell function as assessed by the clearance of hyaluronic acid. MCI-186 seems to have protective effects against hepatic warm I/R injury by attenuating the damage of the hepatocyte, which is the major target of oxidative damage in this model.
UR - http://www.scopus.com/inward/record.url?scp=0036853007&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0036853007&partnerID=8YFLogxK
U2 - 10.1097/00007890-200211270-00021
DO - 10.1097/00007890-200211270-00021
M3 - Article
C2 - 12451250
AN - SCOPUS:0036853007
SN - 0041-1337
VL - 74
SP - 1470
EP - 1472
JO - Transplantation
JF - Transplantation
IS - 10
ER -