Acute hyperglycemia prevents dexmedetomidine-induced preconditioning against renal ischemia-reperfusion injury

Acta Cir Bras. 2014 Dec;29(12):812-8. doi: 10.1590/S0102-86502014001900008.

Abstract

Purpose: To investigate the effects of acute hyperglycemia on dexmedetomidine-induced preconditioning against renal ischemia-reperfusion injury.

Methods: Sprague-Dawley rats were randomly arranged to the normoglycemic (NG) or hyperglycemic group (HG), with each group further divided into sham (no I/R injury), I/R (ischemia-reperfusion) and dex (given by dexmedetomidine) groups. Acute hyperglycemia was induced by intraperitoneal injection (i.p.) of 25% glucose (3 g/kg) 45 min before ischemia. Dexmedetomidine (50 μg/kg, i.p.) was administrated 30 min before induction of ischemia. Renal function, histology, apoptosis, expression of Bax, Bcl-2 and phosphorylated AKT (p-AKT) were detected.

Results: I/R insult significantly increased the serum levels of blood urea nitrogen and creatinine, apoptotic tubular epithelial cells, expression of Bax and p-AKT, but decreased Bcl-2 expression. All these changes were further enhanced by hyperglycemia (p<0.05). In hyperglycemic condition, there was no statistically difference between the I/R group and Dex group in all the aforementioned detection indexes (p>0.05).

Conclusion: Acute hyperglycemia attenuates dexmedetomidine-induced preconditioning against renal ischemia-reperfusion injury in non-diabetic rats.

MeSH terms

  • Acute Disease
  • Animals
  • Apoptosis / drug effects
  • Blood Glucose
  • Creatinine / blood
  • Dexmedetomidine / pharmacology*
  • Hyperglycemia / chemically induced
  • Hyperglycemia / physiopathology*
  • Ischemia / chemically induced*
  • Ischemia / drug therapy
  • Ischemic Preconditioning*
  • Kidney / blood supply*
  • Kidney Tubules / drug effects
  • Kidney Tubules / pathology
  • Male
  • Models, Animal
  • Nephrectomy
  • Proto-Oncogene Proteins c-akt / metabolism
  • Random Allocation
  • Rats, Sprague-Dawley
  • Reperfusion Injury / prevention & control*
  • Urea / blood

Substances

  • Blood Glucose
  • Dexmedetomidine
  • Urea
  • Creatinine
  • Proto-Oncogene Proteins c-akt