Evidence map›Paper›PMID 27648918›Full record

ArticleTranslational psychiatry2016

Antidepressive and BDNF effects of enriched environment treatment across ages in mice lacking BDNF expression through promoter IV.

S Jha, B E Dong, Y Xue, D F Delotterie, M G Vail, K Sakata

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 35 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

S JhaDepartment of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
B E DongDepartment of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
Y XueDepartment of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
D F DelotterieDepartment of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
M G VailDepartment of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
K SakataDepartment of Pharmacology, University of Tennessee Health Science Center, Memphis, TN, USA.
University of Tennessee Health Science Center · US

Funding

Neural Mechanisms of Inflexible Learning Caused by BDNF DeficiencyR21MH105567 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SAKATA, KAZUKO · 2014 to 2015
$375k
Antidepressive Effects and Gene Mechanisms of Early-life Enriched EnvironmentR03MH102445 · NIMH · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SAKATA, KAZUKO · 2014 to 2015
$148k
NIMH NIH HHS R03 MH102445NIMH NIH HHS R21 MH105567
6 · The paper itself

Abstract

Reduced promoter IV-driven expression of brain-derived neurotrophic factor (BDNF) is implicated in stress and major depression. We previously reported that defective promoter IV (KIV) caused depression-like behavior in young adult mice, which was reversed more effectively by enriched environment treatment (EET) than antidepressants. The effects of promoter IV-BDNF deficiency and EET over the life stages remain unknown. Since early-life development (ED) involves dynamic epigenetic processes, we hypothesized that EET during ED would provide maximum antidepressive effects that would persist later in life due to enhanced, long-lasting BDNF induction. We tested this hypothesis by determining EET effects across three life stages: ED (0-2 months), young adult (2-4 months), and old adult (12-14 months). KIV mice at all life stages showed depression-like behavior in the open-field and tail-suspension tests compared with wild-type mice. Two months of EET reduced depression-like behavior in ED and young adult, but not old adult mice, with the largest effect in ED KIV mice. This effect lasted for 1 month after discontinuance of EET only in ED mice. BDNF protein induction by EET in the hippocampus and frontal cortex was also the largest in ED mice and persisted only in the hippocampus of ED KIV mice after discontinuance of EET. No gender-specific effects were observed. The results suggest that defective promoter IV causes depression-like behavior, regardless of age and gender, and that EET during ED is particularly beneficial to individuals with promoter IV-BDNF deficiency, while additional treatment may be needed for older adults.

Indexed as

Behavior, AnimalSocial EnvironmentAnimalsBrain-Derived Neurotrophic FactorDepressionFemaleFrontal LobeGene Knock-In TechniquesHippocampusMaleMicePromoter Regions, GeneticBrain-Derived Neurotrophic Factor

Identifiers

PMID27648918
PMCPMC5048201
OpenAlexW2521848146

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.