Dexmedetomidine attenuates remote lung injury induced by renal ischemia-reperfusion in mice

Acta Anaesthesiol Scand. 2011 Nov;55(10):1272-8. doi: 10.1111/j.1399-6576.2011.02526.x. Epub 2011 Sep 26.

Abstract

Background: Renal ischemia-reperfusion (I/R) may cause acute lung injury (ALI). The mortality of combined acute kidney injury and ALI is extremely high. Dexmedetomidine, an α(2) adrenergic agonist, exerts potent anti-inflammatory and organoprotective effects in addition to its sedative and analgesic properties. We sought to elucidate whether dexmedetomidine can attenuate lung injury following renal I/R in a murine model of renal I/R.

Methods: Adult C57BL/6J male mice were randomized to five groups: sham-operated control (Sham); renal I/R (I/R); intraperitoneal injection of dexmedetomidine 25 μg/kg before ischemia (pre-dex) and after perfusion (post-dex); combination of α(2) adrenergic antagonist atipamezole 250 μg/kg prior to dexmedetomidine pre-treatment (atip-dex). Kidney I/R was induced by bilateral renal pedicle clamping for 45 min and followed by 6 h reperfusion. The pulmonary tissues were harvested for histopathological evaluation, wet/dry ratio measurement, biochemical analysis of myeloperoxidase (MPO), Polymerase chain reaction (PCR) determination of Inter-cellular adhesion molecule (ICAM-1) and Tumor necrosis factor - alpha (TNF-α) mRNA.

Results: Renal IR induced significant pulmonary injuries, increased wet/dry ratio together with the enhanced of MPO activities and increased ICAM-1 and TNF-α mRNA level. Both pre- and post-treatment with dexmedetomidine markedly reduced lung edema and inflammatory response and lowered MPO activity and ICAM-1 and TNF-α mRNA expression. The protective effects of dexmedetomidine in the lung were partially reversed by atipamezole, but there were no effect on ICAM-1 and TNF-α mRNA expression level.

Conclusions: Dexmedetomidine is capable of attenuating remote lung injury induced by renal IR via both α(2) adrenoceptors dependent and independent mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Agonists / therapeutic use*
  • Adrenergic alpha-Antagonists / pharmacology
  • Animals
  • Depression, Chemical
  • Dexmedetomidine / antagonists & inhibitors
  • Dexmedetomidine / therapeutic use*
  • Imidazoles / pharmacology
  • Immunohistochemistry
  • Intercellular Adhesion Molecule-1 / metabolism
  • Kidney Diseases / complications*
  • Lung Injury / drug therapy*
  • Lung Injury / etiology*
  • Lung Injury / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Organ Size / physiology
  • Paraffin Embedding
  • Peroxidase / antagonists & inhibitors
  • Peroxidase / metabolism
  • Real-Time Polymerase Chain Reaction
  • Reperfusion Injury / complications*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Adrenergic alpha-Agonists
  • Adrenergic alpha-Antagonists
  • Imidazoles
  • Tumor Necrosis Factor-alpha
  • atipamezole
  • Intercellular Adhesion Molecule-1
  • Dexmedetomidine
  • Peroxidase