Evidence map›Paper›PMID 16707719›Full record

ArticleJournal of neurophysiology2006

Restoration of long-term potentiation in middle-aged hippocampus after induction of brain-derived neurotrophic factor.

Christopher S Rex, Julie C Lauterborn, Ching-Yi Lin, Eniko A Kramár, Gary A Rogers, Christine M Gall, Gary Lynch

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 158 citations in OpenAlex.

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18 more citing papers are in PubMed but not listed here.

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

7 authors at 1 institution in 1 country.

Christopher S RexDepartment of Neurobiology and Behavior, University of California at Irvine, 92697-4292, USA.
Julie C Lauterborn
Ching-Yi Lin
Eniko A Kramár
Gary A Rogers
Christine M Gall
Gary Lynch
University of California, Irvine · US

Funding

TISSUE REPOSITORY COREP01AG000538 · NIA · UNIVERSITY OF CALIFORNIA-IRVINE · PI COTMAN, CARL WAYNE · 1985 to 2018
$24.8M
The Spine Cytoskeleton and Memory DisordersP01NS045260 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GALL, CHRISTINE M · 2003 to 2015
$14.4M
Integrins and LTP consolidationR01NS051823 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI LYNCH, GARY S · 2005 to 2008
$1.0M
Training Program in Neural PlasticityT32MH014599 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI CAREW, THOMAS J · 1985 to 2007
$600k
INFLUENCE OF AGE AND RACE ON BONE HEALTHK08AG000358 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF CUNY · PI MEIER, DIANE E · 1987 to 1991
–
NIA NIH HHS AG-00358NIA NIH HHS P01 AG000538NIMH NIH HHS 5-T32-MH-14599-27NIMH NIH HHS T32 MH014599NINDS NIH HHS NS-051823NINDS NIH HHS NS-45260NINDS NIH HHS P01 NS045260NINDS NIH HHS R01 NS051823
6 · The paper itself

Abstract

Restoration of neuronal viability and synaptic plasticity through increased trophic support is widely regarded as a potential therapy for the cognitive declines that characterize aging. Previous studies have shown that in the hippocampal CA1 basal dendritic field deficits in the stabilization of long-term potentiation (LTP) are evident by middle age. The present study tested whether increasing endogenous brain-derived neurotrophic factor (BDNF) could reverse this age-related change. We report here that in middle-aged (8- to 10-mo-old) rats, in vivo treatments with a positive AMPA-type glutamate receptor modulator both increase BDNF protein levels in the cortical telencephalon and restore stabilization of basal dendritic LTP as assessed in acute hippocampal slices 18 h after the last drug treatment. These effects were not attributed to enhanced synaptic transmission or to facilitation of burst responses used to induce LTP. Increasing extracellular levels of BDNF by exogenous application to slices of middle-aged rats was also sufficient to rescue the stabilization of basal dendritic LTP. Finally, otherwise stable LTP in ampakine-treated middle-aged rats can be eliminated by infusion of the extracellular BDNF scavenger TrkB-Fc. Together these results indicate that increases in endogenous BDNF signaling can offset deficits in the postinduction processes that stabilize LTP.

Indexed as

AgingAnimalsBlotting, WesternBrain-Derived Neurotrophic FactorElectroencephalographyElectrophysiologyEnzyme-Linked Immunosorbent AssayExcitatory Postsynaptic PotentialsHippocampusIn Vitro TechniquesLong-Term PotentiationMaleProsencephalonRatsRats, Sprague-DawleyReceptors, AMPABrain-Derived Neurotrophic FactorReceptors, AMPA

Identifiers

PMID16707719
PMCPMC1554892
OpenAlexW2066250553

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.