Vitamin A deficiency impairs contextual fear memory in rats: Abnormalities in the glucocorticoid pathway

J Neuroendocrinol. 2019 Nov;31(11):e12802. doi: 10.1111/jne.12802. Epub 2019 Nov 13.

Abstract

Vitamin A and its active metabolite, retinoic acid (RA), play a key role in the maintenance of cognitive functions in the adult brain. Depletion of RA using the vitamin A deficiency (VAD) model in Wistar rats leads to spatial memory deficits in relation to elevated intrahippocampal basal corticosterone (CORT) levels and increased hippocampal 11β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) activity. All of these effects are normalised by vitamin A supplementation. However, it is unknown whether vitamin A status also modulates contextual fear conditioning (CFC) in a glucocorticoid-associated fear memory task dependent on the functional integrity of the hippocampus. In the present study, we investigated the impact of VAD and vitamin A supplementation in adult male rats on fear memory processing, plasma CORT levels, hippocampal retinoid receptors and 11β-HSD1 expression following a novelty-induced stress. We also examined whether vitamin A supplementation or a single injection of UE2316, a selective 11β-HSD1 inhibitor, known to modulate local glucocorticoid levels, had any beneficial effects on contextual fear memory and biochemical parameters in VAD rats. We provide evidence that VAD rats exhibit a decreased fear conditioning response during training with a poor contextual fear memory 24 hours later. These VAD-induced cognitive impairments are associated with elevated plasma CORT levels under basal conditions, as well as following a stressful event, with saturated CORT release, altered hippocampal retinoid receptors and 11β-HSD1 expression. Vitamin A supplementation normalises VAD-induced fear conditioning training deficits and all biochemical effects, although it cannot prevent fear memory deficits. Moreover, a single injection of UE2316 not only impairs contextual fear memory, but also reduces plasma CORT levels, regardless of the vitamin A status and decreases slightly hippocampal 11β-HSD1 activity in VAD rats following stress. The present study highlights the importance of vitamin A status with respect to modulating fear memory conditioning in relation to plasma CORT levels and hippocampal 11β-HSD1.

Keywords: 11β-hydroxysteroid dehydrogenase type 1; contextual fear memory; glucocorticoid; hippocampus; retinoic acid receptor; vitamin A.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cognition / drug effects
  • Cognition / physiology
  • Conditioning, Psychological / drug effects
  • Corticosterone / blood
  • Dietary Supplements
  • Fear* / drug effects
  • Fear* / psychology
  • Glucocorticoids / metabolism*
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Male
  • Memory Disorders / blood
  • Memory Disorders / etiology*
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Spatial Memory / drug effects
  • Spatial Memory / physiology
  • Stress, Psychological
  • Vitamin A / pharmacology
  • Vitamin A / therapeutic use
  • Vitamin A Deficiency / complications*
  • Vitamin A Deficiency / diet therapy
  • Vitamin A Deficiency / pathology
  • Vitamin A Deficiency / psychology*

Substances

  • Glucocorticoids
  • Vitamin A
  • Corticosterone