Edaravone inhibits apoptosis caused by ischemia/ reperfusion injury in a porcine hepatectomy model

AIM: TO investigate the effect of E3-methyl-l-phe- nyl-2-pyrazolin-5-one (Edr) on hepatic ischemia-reper- fusion (I/R) injury and liver regeneration in a porcine hepatectomy model. METHODS: One hour ischemia was induced by occlud- ing the vessels and the bile duct of the right and median lobes. A 40...

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Veröffentlicht in:World journal of gastroenterology : WJG 2012-07, Vol.18 (27), p.3520-3526
Hauptverfasser: Shimoda, Mitsugi, Iwasaki, Yoshimi, Okada, Toshie, Kubota, Keiichi
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Sprache:eng
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Zusammenfassung:AIM: TO investigate the effect of E3-methyl-l-phe- nyl-2-pyrazolin-5-one (Edr) on hepatic ischemia-reper- fusion (I/R) injury and liver regeneration in a porcine hepatectomy model. METHODS: One hour ischemia was induced by occlud- ing the vessels and the bile duct of the right and median lobes. A 40% left hepatectomy was performed after re- perfusion. Six animals received Edr (3 mg/kg per hour) intravenously and six control animals received saline just before reperfusion. Remnant liver volume, hemody- namics, aspartate aminotransferase (AST), alanine ami- notransferase, lactate dehydrogenase and lactic acid, were compared between the groups. The expression of transforming growth factor-β (TGF-β1) and toll-like receptor (TRL) mRNA in hepatic tissues was examined using reverse transcription polymerase chain reaction. Apoptosis was demonstrated by terminal deoxynucleo- tidyl transferase dUTP nick end labeling (TUNEL) stain- ing, respectively. RESULTS: Serum AS-I- (P = 0.029), and toll like recep- tor 4 level (P = 0.043) were significantly lower after 3 hin animals receiving Edr. In addition, TUNEL staining in Edr-treated pigs showed significantly fewer hepatocytes undergoing apoptosis compared with control pigs. After 1 mo, all factors were non-significantly different between the two groups. CONCLUSION: Edr is considered to reduce hepatic injury in the early stage of I/R injury in a porcine model.
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v18.i27.3520