Protective effect of N2-mercaptopropionylglycine on rats and dogs liver during ischemia/reperfusion process

Arq Gastroenterol. 2003 Jul-Sep;40(3):177-80. doi: 10.1590/s0004-28032003000300008. Epub 2004 Mar 15.

Abstract

Background: N2-mercaptopropionylglycine is a powerful super oxide synthesis inhibitor and has been tested as a preventive agent of metabolic and structural hepatic damage in the ischemia/reperfusion process.

Aim: To analyze some effects of N2-mercaptopropionylglycine administration to animals of two species submitted to normothermic liver ischemia/reperfusion.

Material and methods: Twenty-two rats and 22 dogs were divided into four groups: group I: rats that received intravenous saline 0.9%; group II: rats that received 100 mg/kg of N2-mercaptopropionylglycine; group III: dogs that received saline intravenous 0.9% and group IV: dogs that received 100 mg/kg N2-mercaptopropionylglycine.

Results: Ten minutes after the saline or drug administration, each group was submitted to left lobe liver ischemia for 25 minutes followed by reperfusion. Biochemical studies 24 hours after reperfusion revealed a significantly lower elevation of transaminases in animals of groups II (AST = 271 +/- 182; ALT = 261 +/- 161 ) and IV (AST = 101 +/- 45; ALT = 123 +/- 89) when compared to the controls group: I (AST = 2144 +/- 966; ALT = 1869 +/- 1040 00) and III (AST = 182 +/- 76.51; ALT = 277 +/- 219), respectively. Histology study demonstrated a significantly minor aggression to animals of groups II and IV when compared to groups I and III, respectively.

Conclusion: These results suggest a significant release of free radicals of oxygen in the process and that N2-mercaptopropionylglycine may have a significant protective effect on liver parenchyma when submitted to ischemia/reperfusion.

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antioxidants / pharmacology*
  • Aspartate Aminotransferases / blood
  • Cytoprotection / drug effects
  • Dogs
  • Ischemia / drug therapy*
  • Liver / blood supply*
  • Male
  • Rats
  • Rats, Wistar
  • Reperfusion Injury / prevention & control*
  • Tiopronin / pharmacology*

Substances

  • Antioxidants
  • Tiopronin
  • Aspartate Aminotransferases
  • Alanine Transaminase