Nitrite, a novel method to decrease ischemia/reperfusion injury in the rat liver

World J Gastroenterol. 2015 Feb 14;21(6):1775-83. doi: 10.3748/wjg.v21.i6.1775.

Abstract

Aim: To investigate whether nitrite administered prior to ischemia/reperfusion (I/R) reduces liver injury.

Methods: Thirty-six male Sprague-Dawley rats were randomized to 3 groups, including sham operated (n = 8), 45-min segmental ischemia of the left liver lobe (IR, n = 14) and ischemia/reperfusion (I/R) preceded by the administration of 480 nmol of nitrite (n = 14). Serum transaminases were measured after 4 h of reperfusion. Liver microdialysate (MD) was sampled in 30-min intervals and analyzed for glucose, lactate, pyruvate and glycerol as well as the total nitrite and nitrate (NOx). The NOx was measured in serum.

Results: Aspartate aminotransferase (AST) at the end of reperfusion was higher in the IR group than in the nitrite group (40 ± 6.8 μkat/L vs 22 ± 2.6 μkat/L, P = 0.022). Similarly, alanine aminotransferase (ALT) was also higher in the I/R group than in the nitrite group (34 ± 6 μkat vs 14 ± 1.5 μkat, P = 0.0045). The NOx in MD was significantly higher in the nitrite group than in the I/R group (10.1 ± 2.9 μmol/L vs 3.2 ± 0.9 μmol/L, P = 0.031) after the administration of nitrite. During ischemia, the levels decreased in both groups and then increased again during reperfusion. At the end of reperfusion, there was a tendency towards a higher NOx in the I/R group than in the nitrite group (11.6 ± 0.7 μmol/L vs 9.2 ± 1.1 μmol/L, P = 0.067). Lactate in MD was significantly higher in the IR group than in the nitrite group (3.37 ± 0.18 mmol/L vs 2.8 ± 0.12 mmol/L, P = 0.01) during ischemia and the first 30 min of reperfusion. During the same period, glycerol was also higher in the IRI group than in the nitrite group (464 ± 38 μmol/L vs 367 ± 31 μmol/L, P = 0.049). With respect to histology, there were more signs of tissue damage in the I/R group than in the nitrite group, and 29% of the animals in the I/R group exhibited necrosis compared with none in the nitrite group. Inducible nitric oxide synthase transcription increased between early ischemia (t = 15) and the end of reperfusion in both groups.

Conclusion: Nitrite administered before liver ischemia in the rat liver reduces anaerobic metabolism and cell necrosis, which could be important in the clinical setting.

Keywords: Inducible nitric oxide synthase; Ischemia-reperfusion injury; Liver ischemia; Liver surgery; Microdialysis; Nitric oxide; Nitrite.

MeSH terms

  • Animals
  • Biomarkers / blood
  • Cytoprotection
  • Disease Models, Animal
  • Energy Metabolism / drug effects
  • Injections, Intravenous
  • Liver / blood supply*
  • Liver / drug effects*
  • Liver / metabolism
  • Liver / pathology
  • Liver / surgery
  • Male
  • Necrosis
  • Rats, Sprague-Dawley
  • Reperfusion Injury / blood
  • Reperfusion Injury / pathology
  • Reperfusion Injury / prevention & control*
  • Sodium Nitrite / administration & dosage*
  • Time Factors

Substances

  • Biomarkers
  • Sodium Nitrite