Influence of late-life exposure to environmental enrichment or exercise on hippocampal function and CA1 senescent physiology

Neurobiol Aging. 2012 Apr;33(4):828.e1-17. doi: 10.1016/j.neurobiolaging.2011.06.023. Epub 2011 Aug 4.

Abstract

Aged (20-22 months) male Fischer 344 rats were randomly assigned to sedentary (A-SED), environmentally-enriched (A-ENR), or exercise (A-EX) conditions. After 10-12 weeks of differential experience, the 3 groups of aged rats and young sedentary controls were tested for physical and cognitive function. Spatial discrimination learning and memory consolidation, tested on the water maze, were enhanced in environmentally-enriched compared with sedentary. A-EX exhibited improved and impaired performance on the cue and spatial task, respectively. Impaired spatial learning in A-EX was likely due to a bias in response selection associated with exercise training, as object recognition memory improved for A-EX rats. An examination of senescent hippocampal physiology revealed that enrichment and exercise reversed age-related changes in long-term depression (LTD) and long-term potentiation (LTP). Rats in the enrichment group exhibited an increase in cell excitability compared with the other 2 groups of aged animals. The results indicate that differential experience biased the selection of a spatial or a response strategy and factors common across the 2 conditions, such as increased hippocampal activity associated with locomotion, contribute to reversal of senescent synaptic plasticity.

Publication types

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

MeSH terms

  • Age Factors
  • Aging / physiology*
  • Aldehydes / metabolism
  • Analysis of Variance
  • Animals
  • Biophysics
  • Brain-Derived Neurotrophic Factor / metabolism
  • CA1 Region, Hippocampal / physiology*
  • Cues
  • Discrimination, Psychological
  • Electric Stimulation
  • Environment*
  • Gene Expression Regulation / physiology
  • Glutathione Peroxidase / metabolism
  • Glutathione Peroxidase GPX1
  • In Vitro Techniques
  • Long-Term Potentiation / physiology
  • Long-Term Synaptic Depression / physiology
  • Male
  • Malondialdehyde / metabolism
  • Maze Learning
  • Memory / physiology
  • Muscle Strength
  • Patch-Clamp Techniques
  • Physical Conditioning, Animal*
  • Psychomotor Performance
  • Rats
  • Rats, Inbred F344
  • Statistics, Nonparametric
  • Superoxide Dismutase / metabolism
  • Superoxide Dismutase-1

Substances

  • Aldehydes
  • Brain-Derived Neurotrophic Factor
  • Malondialdehyde
  • Glutathione Peroxidase
  • Sod1 protein, rat
  • Superoxide Dismutase
  • Superoxide Dismutase-1
  • 4-hydroxy-2-nonenal
  • Glutathione Peroxidase GPX1
  • Gpx1 protein, rat