Quercetin improves hypoxia-ischemia induced cognitive deficits via promoting remyelination in neonatal rat

Brain Res. 2014 Mar 17:1553:31-40. doi: 10.1016/j.brainres.2014.01.035. Epub 2014 Jan 28.

Abstract

Myelination failure is associated with perinatal cerebral hypoxia-ischemia (PHI) induced brain injury in premature infants. How to efficiently promote remyelination is crucial for improving cognitive deficits caused by brain injury. Here, we demonstrated that quercetin (Que), a kind of flavonoids, significantly improved cognitive deficits and the behavior of PHI-rat in Morris water maze and open field tasks. After administration of Que to PHI-rat, the number of neogenetic Olig2⁺ oligodendrocyte progenitor cells (OPCs) was evidently increased in the subventricular zone. Additionally, in corpus callosum (CC), the expression of MBP (myelin basic protein) was increased, and the myelin sheaths reached normal level at 30 days with more compact while less damaged myelin sheaths and more mature oligodendrocytes (OLs) repopulating the CC compared with PHI groups. In a word, our findings indicated that Que could remarkably improve both cognition performance and myelination in the context of PHI-induced brain injury by promoting the proliferation of OPCs and strengthening survival of OLs in vivo.

Keywords: Cognitive deficit; Oligodendrocyte; Oligodendrocyte progenitor cell; Perinatal cerebral hypoxia-ischemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Proliferation / drug effects
  • Cognition Disorders / drug therapy
  • Cognition Disorders / etiology
  • Cognition Disorders / pathology
  • Cognition Disorders / physiopathology
  • Corpus Callosum / drug effects
  • Corpus Callosum / pathology
  • Corpus Callosum / physiopathology
  • Exploratory Behavior / drug effects
  • Exploratory Behavior / physiology
  • Gene Expression / drug effects
  • Hippocampus / drug effects
  • Hippocampus / pathology
  • Hippocampus / physiopathology
  • Hypoxia-Ischemia, Brain / complications
  • Hypoxia-Ischemia, Brain / drug therapy*
  • Hypoxia-Ischemia, Brain / pathology
  • Hypoxia-Ischemia, Brain / physiopathology*
  • Locomotion / drug effects
  • Locomotion / physiology
  • Maze Learning / drug effects
  • Myelin Basic Protein / metabolism
  • Myelin Sheath / drug effects*
  • Myelin Sheath / pathology
  • Myelin Sheath / physiology*
  • Nerve Tissue Proteins / metabolism
  • Neural Stem Cells / drug effects
  • Neural Stem Cells / pathology
  • Neural Stem Cells / physiology
  • Neuroprotective Agents / pharmacology*
  • Oligodendrocyte Transcription Factor 2
  • Oligodendroglia / drug effects
  • Oligodendroglia / pathology
  • Oligodendroglia / physiology
  • Quercetin / pharmacology*
  • Rats

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Mbp protein, rat
  • Myelin Basic Protein
  • Nerve Tissue Proteins
  • Neuroprotective Agents
  • Olig2 protein, rat
  • Oligodendrocyte Transcription Factor 2
  • Quercetin