Polyenylphosphatidylcholine pretreatment protects rat liver from ischemia/reperfusion injury


Demirbilek S., Karaman A., GÜRÜNLÜOĞLU K., Taş E., Akin M., Aksoy R. T., ...Daha Fazla

Hepatology Research, cilt.34, sa.2, ss.84-91, 2006 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 34 Sayı: 2
  • Basım Tarihi: 2006
  • Doi Numarası: 10.1016/j.hepres.2005.09.040
  • Dergi Adı: Hepatology Research
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.84-91
  • Anahtar Kelimeler: Hepatic ischemia/reperfusion, Lecithin, Liver ischemia/reperfusion, Oxidative stress, Polyenylphosphatidylcholine
  • Gazi Üniversitesi Adresli: Hayır

Özet

Background: Hepatic injury induced by ischemia/reperfusion following surgery, transplantation, or circulatory shock combined with resuscitation is a major clinical problem. Polyenylphosphatidylcholine (PPC) has strong antioxidant, cytoprotective and anti-inflammatory effects. Aim: In this study, the influence of PPC pretreatment on ischemia-reperfusion (I/R) injury of the liver was examined in rats. Methods: The animals were divided into three groups: control (n = 10), I/R (n = 15) and I/R + PPC (n = 15). PPC was given 100 mg/day for 7 days before experiment. Several parameters of hepatic damage, oxidative stress, neutrophil infiltration and nuclear factor kappa beta (NF-κB) expression were measured as well as microscopic examination. Results: We observed that a significant reduction in AST and ALT values in the PPC treated group when compared with the ischemic group. The increases in hepatic total NO2 + NO3 and MDA, and decreases in SOD and GSH levels after reperfusion were partially, but significantly, inhibited by PPC pretreatment. I/R induced increase in hepatic myeloperoxidase content and NF-κB expression were also lowered by PPC pretreatment. Animals pretreated with PPC presented minimal hemorrhage and reduced signs of liver injury. Conclusion: PPC pretretament provided significant protection againts I/R injury to the liver. This treatment could be therapeutic in liver transplantation and other conditions associated with I/R injury. © 2005 Elsevier Ireland Ltd. All rights reserved.