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.

Highlights

  • The vitamin A, through its main metabolite retinoic acid (RA), plays a key role in brain development by regulating neuronal differentiation, neurite outgrowth and the anteroposterior axis of the neural tube [1,2,3]

  • We demonstrate for the first time that 4 months of nutritional vitamin A supplementation started at midlife improve the spatial memory and the level of differentiation of newborn neurons in aged Wistar rats

  • Our results suggest that hippocampal cellular retinoic acidbinding proteins (CRABPs)-I expression which controls the intracellular availability of RA, may be an important regulator of neuronal differentiation processes in the aged hippocampus

Read more

Summary

Introduction

The vitamin A, through its main metabolite retinoic acid (RA), plays a key role in brain development by regulating neuronal differentiation, neurite outgrowth and the anteroposterior axis of the neural tube [1,2,3]. New neurons can be generated and survive in the adult dentate gyrus (cell proliferation, survival mechanisms and subsequent differentiation processes) but the neurogenenic rate declines precipitously from middle-age [16,17,18,19,20] These newly born neurons have been shown to be preferentially recruited into circuits supporting various types of learning and memory [21,22,23,24,25,26], providing evidence for a critical role of adult neurogenesis in hippocampus-dependent memory including spatial memory in the Morris Water Maze [27,28,29,30]. It has been reported that decreased neurogenesis correlates with aging-associated impairments in learning and memory [31,32] but some controversial studies have shown that poorer performance was associated to a better neuronal differentiation and survival [33,34]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call