Evidence map›Paper›PMID 30604029›Full record

ArticleMetabolic brain disease2019

Enriched environment modulates behavior, myelination and augments molecules governing the plasticity in the forebrain region of rats exposed to chronic immobilization stress.

Gangadharan Thamizhoviya, Arambakkam Janardhanam Vanisree

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Article in Metabolic brain disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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10citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Gangadharan ThamizhoviyaDepartment of Biochemistry, University of Madras, Guindy Campus, Chennai, 600025, India.
Arambakkam Janardhanam VanisreeDepartment of Biochemistry, University of Madras, Guindy Campus, Chennai, 600025, India. journalsvuom@gmail.com.ORCID 0000-0001-8909-6552

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, several reports on chronic stress have shown that prolonged exposure to stress contributes to psychological and neurological complications. However, the impact of stress-induced alterations in myelination remains to be unexplored. Therefore, in the current study, the rats were subjected to immobilization stress (IS) followed by enriched environment (EE) and the behavioral, neurochemical changes pertaining to neuronal survival pathway, in addition, to the ultrastructural changes in myelin in forebrain (FB) region of rats were analyzed. Immobilization stress-exposed rats (4 h/day IS, for 28 days) exhibited increased anhedonia, anxiety, immobility, and reduced social interaction, which could be reflected in increased levels of corticosterone. In contrast, exposure to EE (4 h IS+2 h EE/day, for 28 days) was found to minimize anhedonic state, supress the depressive-like features, enhance social interaction and also reduce the levels of corticosterone. The ultrastructural changes in the FB region of the brain revealed that IS group showed enhanced g-ratio indicating decreased myelin thickness, while EE group exhibited reduced g-ratio manifesting increased myelination. Further, the study revealed that IS exposed group showed decreased levels of NGF, TrkA, PI3K, AKT, ERK, CREB, and MBP in FB regions whereas EE group could preserve normal protein and mRNA levels of these neuronal survival molecules. The results from this study suggest that EE exerts a positive impact by improving myelination in rats exposed to chronic immobilization stress.

Indexed as

EnvironmentStress, PsychologicalAnimalsAnxietyBehavior, AnimalCorticosteroneHippocampusMaleMyelin SheathNeuronal PlasticityRats, WistarCorticosteroneBehavioral plasticityCorticosteroneEnriched environmentImmobilization stressMyelinationMyelin basic proteinNeurotrophic growth factor

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.