A mid-life vitamin A supplementation prevents age-related spatial memory deficits and hippocampal neurogenesis alterations through CRABP-I

PLoS One. 2013 Aug 19;8(8):e72101. doi: 10.1371/journal.pone.0072101. eCollection 2013.

Abstract

Age-related memory decline including spatial reference memory is considered to begin at middle-age and coincides with reduced adult hippocampal neurogenesis. Moreover, a dysfunction of vitamin A hippocampal signalling pathway has been involved in the appearance of age-related memory deficits but also in adult hippocampal neurogenesis alterations. The present study aims at testing the hypothesis that a mid-life vitamin A supplementation would be a successful strategy to prevent age-related memory deficits. Thus, middle-aged Wistar rats were submitted to a vitamin A enriched diet and were tested 4 months later in a spatial memory task. In order to better understand the potential mechanisms mediating the effects of vitamin A supplementation on hippocampal functions, we studied different aspects of hippocampal adult neurogenesis and evaluated hippocampal CRABP-I expression, known to modulate differentiation processes. Here, we show that vitamin A supplementation from middle-age enhances spatial memory and improves the dendritic arborisation of newborn immature neurons probably resulting in a better survival and neuronal differentiation in aged rats. Moreover, our results suggest that hippocampal CRABP-I expression which controls the intracellular availability of retinoic acid (RA), may be an important regulator of neuronal differentiation processes in the aged hippocampus. Thus, vitamin A supplementation from middle-age could be a good strategy to maintain hippocampal plasticity and functions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / drug effects
  • Animals
  • Cell Proliferation
  • Cell Survival
  • Dietary Supplements
  • Hippocampus / drug effects*
  • Hippocampus / metabolism
  • Hippocampus / physiopathology
  • Male
  • Maze Learning / drug effects
  • Memory
  • Memory Disorders / prevention & control*
  • Neurogenesis / drug effects*
  • Neurons / drug effects
  • Neurons / physiology
  • Rats
  • Rats, Wistar
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / metabolism*
  • Vitamin A / administration & dosage*
  • Vitamin A / pharmacokinetics

Substances

  • Receptors, Retinoic Acid
  • retinoic acid binding protein I, cellular
  • Vitamin A

Grants and funding

This work was supported by University of Bordeaux 1 and Bordeaux 2, the Conseil Regional d’Aquitaine and the French National Institute Of Food Processing (INRA). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.