Global brain atrophy after unilateral parietal lesion and its prevention by erythropoietin

Brain. 2006 Feb;129(Pt 2):480-9. doi: 10.1093/brain/awh703. Epub 2005 Dec 9.

Abstract

In humans, neurotrauma is suspected to cause brain atrophy and accelerate slowly progressive neurodegenerative disorders, such as Alzheimer's disease or schizophrenia. However, a direct link between brain injury and subsequent delayed global neurodegeneration has remained elusive. Here we show that juvenile (4-week-old) mice that are given a discrete unilateral lesion of the parietal cortex, develop to adulthood without obvious clinical symptoms. However, when monitored 3 and 9 months after lesioning, using high-resolution three-dimensional MRI and behavioural testing, the same mice display global neurodegenerative changes. Surprisingly, erythropoietin, a haematopoietic growth factor with potent neuroprotective activity, prevents behavioural abnormalities, cognitive dysfunction and brain atrophy when given for 2 weeks after acute brain injury. This demonstrates that a localized brain lesion is a primary cause of delayed global neurodegeneration that can be efficiently counteracted by neuroprotection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Atrophy
  • Brain / pathology*
  • Brain Injuries / complications
  • Brain Injuries / drug therapy*
  • Brain Injuries / pathology*
  • Erythropoietin / therapeutic use*
  • Magnetic Resonance Imaging
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Models, Animal
  • Neurodegenerative Diseases / diagnosis
  • Neurodegenerative Diseases / etiology
  • Neurodegenerative Diseases / prevention & control*
  • Neuropsychological Tests
  • Time Factors

Substances

  • Erythropoietin