Evidence map›Paper›PMID 26136648›Full record

ArticleFrontiers in neuroscience2015

Gene expression patterns and environmental enrichment-induced effects in the hippocampi of mice suggest importance of Lsamp in plasticity.

Indrek Heinla, Este Leidmaa, Karina Kongi, Airi Pennert, Jürgen Innos, Kaarel Nurk, Triin Tekko, Katyayani Singh, Taavi Vanaveski, Riin Reimets and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  9. Exercising New Neurons to Vanquish Alzheimer Disease.Brain plasticity (Amsterdam, Netherlands) · 2018
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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

16 authors at 2 institutions in 2 countries.

Indrek HeinlaDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Este LeidmaaDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia ; Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry Munich, Germany.
Karina KongiDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Airi PennertDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Jürgen InnosDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Kaarel NurkDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Triin TekkoDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Katyayani SinghDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Taavi VanaveskiDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Riin ReimetsDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Merle MandelDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Aavo LangDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Kersti LilleväliDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Allen KaasikDepartment of Pharmacology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Eero VasarDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
Mari-Anne PhilipsDepartment of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu Tartu, Estonia.
University of Tartu · EEMax Planck Institute of Psychiatry · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Limbic system associated membrane protein (Lsamp) gene is involved in behavioral adaptation in social and anxiogenic environments and has been associated with a broad spectrum of psychiatric diseases. Here we studied the activity of alternative promoters of Lsamp gene in mice in three rearing conditions (standard housing, environmental enrichment and social isolation) and in two different genetic backgrounds (129S6/SvEv and C57BL/6). Isolation had no effect on the expression levels of Lsamp. Environmental enrichment elevated the expression levels of Lsamp 1b transcript specifically in the hippocampus in B6 mice, and the same tendency existed across both mouse lines and both transcripts. Furthermore, we showed that the density of cells exhibiting 1b promoter activity is remarkably higher in the subgranular zone of the dentate gyrus in the hippocampal formation which is a specific area of enrichment-induced neurogenesis in adult rodents. On the contrary to 1b, 1a promoter is selectively active in the pyramidal and granule cell layers. We provide evidence that Lsamp modulates enrichment-induced activation of Bdnf as the enrichment-induced elevation of Bdnf in the hippocampus is significantly diminished in Lsamp-deficient mice; furthermore, a significant correlation was found between the expression levels of Lsamp and Bdnf transcripts in the hippocampus and frontal cortex. Significant strain differences in Lsamp expression were detected in the hippocampus, frontal cortex and thalamus that could be related to the different behavioral phenotype of B6 and 129Sv mice. Our data provides further evidence that LSAMP is implicated in the hippocampal connectivity and plasticity thereby modulating adaptability in changing environments.

Indexed as

129SvB6BdnfenrichmenthippocampusisolationLsampmice

Identifiers

PMID26136648
PMCPMC4470440
OpenAlexW1553908542

What OpenQuestion holds

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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.