Allopurinol preconditioning attenuates renal ischemia/reperfusion injury by inhibiting HMGB1 expression in a rat model

Acta Cir Bras. 2016 Mar;31(3):176-82. doi: 10.1590/S0102-865020160030000005.

Abstract

Purpose: To investigate the potential effects of pretreatment with allopurinol on renal ischemia/reperfusion injury (IRI) in a rat model.

Methods: Twenty four rats were subjected to right kidney uninephrectomy were randomly distributed into the following three groups (n=8): Group A (sham-operated group); Group B (ischemic group) with 30 min of renal ischemia after surgery; and Group C (allopurinol + ischemia group) pretreated with allopurinol at 50 mg/kg for 14 days. At 72 h after renal reperfusion, the kidney was harvested to assess inflammation and apoptosis.

Results: Pretreatment with allopurinol significantly improved renal functional and histological grade scores following I/R injury (p<0.05). Compared with Group B, the expression levels of caspase-3 and Bax were markedly reduced in Group C, meanwhile, whereas expression of bcl-2 was clearly increased (p<0.05). A newly described marker of inflammation, High Mobility Group Box 1(HMGB1), showed reduced expression in Group C (p<0.05).

Conclusion: Pretreatment with allopurinol had a protective effect on kidney ischemia/reperfusion injury, which might be related to the inhibition of HMGB1 expression.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allopurinol / pharmacology*
  • Animals
  • Apoptosis / drug effects
  • Blood Urea Nitrogen
  • Disease Models, Animal
  • HMGB1 Protein / drug effects*
  • HMGB1 Protein / metabolism
  • Inflammation / metabolism
  • Ischemic Preconditioning / methods*
  • Kidney / blood supply*
  • Kidney / pathology
  • Male
  • Peroxidase / metabolism
  • Protective Agents / pharmacology*
  • Random Allocation
  • Rats, Sprague-Dawley
  • Reperfusion Injury / metabolism
  • Reperfusion Injury / prevention & control*
  • Superoxide Dismutase / drug effects

Substances

  • HMGB1 Protein
  • Protective Agents
  • Allopurinol
  • Peroxidase
  • Superoxide Dismutase