Meclizine Preconditioning Protects the Kidney Against Ischemia-Reperfusion Injury

EBioMedicine. 2015 Jul 29;2(9):1090-101. doi: 10.1016/j.ebiom.2015.07.035. eCollection 2015 Sep.

Abstract

Global or local ischemia contributes to the pathogenesis of acute kidney injury (AKI). Currently there are no specific therapies to prevent AKI. Potentiation of glycolytic metabolism and attenuation of mitochondrial respiration may decrease cell injury and reduce reactive oxygen species generation from the mitochondria. Meclizine, an over-the-counter anti-nausea and -dizziness drug, was identified in a 'nutrient-sensitized' chemical screen. Pretreatment with 100 mg/kg of meclizine, 17 h prior to ischemia protected mice from IRI. Serum creatinine levels at 24 h after IRI were 0.13 ± 0.06 mg/dl (sham, n = 3), 1.59 ± 0.10 mg/dl (vehicle, n = 8) and 0.89 ± 0.11 mg/dl (meclizine, n = 8). Kidney injury was significantly decreased in meclizine treated mice compared with vehicle group (p < 0.001). Protection was also seen when meclizine was administered 24 h prior to ischemia. Meclizine reduced inflammation, mitochondrial oxygen consumption, oxidative stress, mitochondrial fragmentation, and tubular injury. Meclizine preconditioned kidney tubular epithelial cells, exposed to blockade of glycolytic and oxidative metabolism with 2-deoxyglucose and NaCN, had reduced LDH and cytochrome c release. Meclizine upregulated glycolysis in glucose-containing media and reduced cellular ATP levels in galactose-containing media. Meclizine inhibited the Kennedy pathway and caused rapid accumulation of phosphoethanolamine. Phosphoethanolamine recapitulated meclizine-induced protection both in vitro and in vivo.

Keywords: Acute kidney injury; Glycolysis; Kennedy pathway; Mitochondria; Oxidative phosphorylation; Phosphoethanolamine.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Kidney Injury / complications
  • Acute Kidney Injury / drug therapy
  • Acute Kidney Injury / pathology
  • Adenosine Triphosphate / metabolism
  • Animals
  • Cell Respiration / drug effects
  • Cytochromes c / metabolism
  • Deoxyglucose / pharmacology
  • Disease Models, Animal
  • Epithelial Cells / drug effects
  • Epithelial Cells / pathology
  • Ethanolamines / metabolism
  • Galactose / pharmacology
  • Glycolysis / drug effects
  • Humans
  • Inflammation / complications
  • Inflammation / pathology
  • Ischemic Preconditioning*
  • Kidney / blood supply*
  • Kidney / drug effects
  • Kidney / pathology*
  • Kidney Tubules / drug effects
  • Kidney Tubules / metabolism
  • Kidney Tubules / pathology
  • L-Lactate Dehydrogenase / metabolism
  • LLC-PK1 Cells
  • Male
  • Meclizine / pharmacology
  • Meclizine / therapeutic use*
  • Meclizine / toxicity
  • Mice, Inbred C57BL
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / ultrastructure
  • Protective Agents / pharmacology
  • Protective Agents / therapeutic use*
  • Reperfusion Injury / complications
  • Reperfusion Injury / drug therapy*
  • Reperfusion Injury / pathology
  • Sodium Cyanide / pharmacology
  • Swine
  • Up-Regulation / drug effects

Substances

  • Ethanolamines
  • Protective Agents
  • Meclizine
  • phosphorylethanolamine
  • Adenosine Triphosphate
  • Cytochromes c
  • Deoxyglucose
  • L-Lactate Dehydrogenase
  • Sodium Cyanide
  • Galactose