Effect of enriched environment and predictable chronic stress on spatial memory in adolescent rats: Predominant expression of BDNF, nNOS, and interestingly malondialdehyde in the right hippocampus.
Age Factors
Animals
Brain
/ metabolism
Brain-Derived Neurotrophic Factor
/ metabolism
Corticosterone
/ metabolism
Environment
Hippocampus
/ metabolism
Male
Malondialdehyde
/ metabolism
Maze Learning
Neuronal Plasticity
/ physiology
Nitric Oxide Synthase Type I
/ metabolism
Rats
Rats, Sprague-Dawley
Spatial Memory
/ physiology
Stress, Psychological
/ metabolism
Temporal Lobe
/ metabolism
Adolescence
Enriched environment
Hippocampal asymmetry
Predictable chronic stress
Spatial memory
Journal
Brain research
ISSN: 1872-6240
Titre abrégé: Brain Res
Pays: Netherlands
ID NLM: 0045503
Informations de publication
Date de publication:
15 10 2019
15 10 2019
Historique:
received:
26
02
2019
revised:
27
05
2019
accepted:
07
07
2019
pubmed:
13
7
2019
medline:
2
10
2020
entrez:
13
7
2019
Statut:
ppublish
Résumé
Little is known about the mechanisms that promote divergence of function between left and right in the hippocampus, which is most affected by external factors and critical for spatial memory. We investigated the levels of memory-related mediators in the left and right hippocampus and spatial memory in rats exposed to predictable chronic stress (PCS) and an enriched environment (EE) during adolescence. Twenty-eight-day-old Sprague-Dawley rats were divided into control (standard cages), PCS (15 min/day immobilization stress for four weeks), and EE (one hour/day environmentally enriched cages for four weeks) groups. After the applications, spatial memory was tested with the Morris water maze, and the serum levels of corticosterone were evaluated. The levels of brain-derived neurotrophic factor (BDNF) and neuronal nitric oxide synthase (nNOS), which are critical for synaptic plasticity; malondialdehyde (MDA; lipid-peroxidation indicator); protein carbonyl (protein-oxidation indicator); and superoxide dismutase (antioxidant enzyme) were evaluated in the left and right hippocampus. Corticosterone levels in both the PCS and EE groups did not change compared with control. In both the PCS and EE groups, spatial memory improved and BDNF was increased in both halves of the hippocampus, still there was an asymmetry. nNOS levels were increased in the dentate gyrus and CA1 regions of the right hippocampus in both PCS and EE groups. MDA levels were increased but PCO levels were decreased in the right hippocampus in both the PCS and EE groups, but SOD did not change in either half of the hippocampus. Our results suggest that both PCS and EE improved spatial memory by increasing BDNF and nNOS in the right hippocampus and that, interestingly; MDA could be the physiological signal molecule in the right hippocampus for spatial memory process.
Identifiants
pubmed: 31299186
pii: S0006-8993(19)30372-5
doi: 10.1016/j.brainres.2019.146326
pii:
doi:
Substances chimiques
Brain-Derived Neurotrophic Factor
0
Malondialdehyde
4Y8F71G49Q
Nitric Oxide Synthase Type I
EC 1.14.13.39
Nos1 protein, mouse
EC 1.14.13.39
Corticosterone
W980KJ009P
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
146326Informations de copyright
Published by Elsevier B.V.