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N-Acetylcysteine ameliorates the late phase of liver ischaemia/reperfusion injury in the rabbit with hepatic steatosis.

Abstract
Steatotic livers are highly susceptible to I/R (ischaemia/reperfusion) injury and, therefore, the aim of the present study was to evaluate the in vivo effect of NAC (N-acetylcysteine) on hepatic function in the early and initial late phase of warm liver I/R injury in steatotic rabbits. Twelve New Zealand White rabbits were fed a high-cholesterol (2%) diet. The control group (n=6) underwent lobar liver ischaemia for 1 h, followed by 6 h of reperfusion. In the treated group receiving NAC (n=6), an intravenous infusion of NAC was administered prior to and during the 6 h reperfusion period. Systemic and hepatic haemodynamics were monitored continuously. ALT (alanine aminotransferase) activity and bile production were measured. NMR spectroscopy was used to analyse bile composition. Oxidation of DHR (dihydrorhodamine) to RH (rhodamine) was used as a marker of production of reactive oxygen and nitrogen species. Moderate centrilobular hepatic steatosis was demonstrated by histology. The results showed that NAC administration significantly improved portal flow, hepatic microcirculation, bile composition and bile flow after 5 h of reperfusion. NAC administration was also associated with less hepatocellular injury, as indicated by ALT serum activity, and decreased the oxidation of DHR to RH. In conclusion, NAC administration decreased the extent of I/R injury in the steatotic liver, particularly during the late phase of reperfusion.
AuthorsGiuseppe Fusai, George K Glantzounis, Tarek Hafez, Wenxuan Yang, Alberto Quaglia, Hemant Sheth, Sanjeev Kanoria, Harry Parkes, Alexander Seifalian, Brian R Davidson
JournalClinical science (London, England : 1979) (Clin Sci (Lond)) Vol. 109 Issue 5 Pg. 465-73 (Nov 2005) ISSN: 0143-5221 [Print] England
PMID15982189 (Publication Type: Journal Article)
Chemical References
  • Cholesterol, Dietary
  • Alanine Transaminase
  • Acetylcysteine
Topics
  • Acetylcysteine (therapeutic use)
  • Alanine Transaminase (metabolism)
  • Animals
  • Bile (metabolism)
  • Cholesterol, Dietary (administration & dosage)
  • Fatty Liver (complications, etiology, pathology)
  • Hemodynamics (drug effects)
  • Liver (physiopathology)
  • Liver Circulation (drug effects)
  • Magnetic Resonance Spectroscopy
  • Microcirculation (drug effects)
  • Oxidation-Reduction (drug effects)
  • Oxidative Stress (drug effects)
  • Rabbits
  • Reperfusion Injury (etiology, prevention & control)

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