Evidence map›Paper›PMID 18481283›Full record

ArticleHippocampus2008

Brief novelty exposure facilitates dentate gyrus LTP in aged rats.

Demetrio Sierra-Mercado, Dario Dieguez, Edwin J Barea-Rodriguez

Abstract read
In one paragraph

Article in Hippocampus, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
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  9. Article
  10. Article
  11. Review
  12. Article
  13. Dopamine modulates synaptic plasticity in dendrites of rat and human dentate granule cells.Proceedings of the National Academy of Sciences of the United States of America · 2010
    Article
  14. Article
  15. Review
  16. Article
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

3 authors.

Demetrio Sierra-MercadoNeurobiology of Aging Laboratory, Department of Biology, The University of Texas, San Antonio, Texas 78249-0662, USA.
Dario Dieguez
Edwin J Barea-Rodriguez

Funding

ZOLEDRONATE VS AREDIA IN MULTIPLE MYELOMA/BREAST CANCER W /BONE DISORDERSM01RR001346 · NCRR · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FERRER, ROBERT L · 1985 to 2008
$23.1M
UTSA Maximizing Access to Research Careers Research Training Program - Admin SupplementT34GM007717 · NIGMS · UNIVERSITY OF TEXAS SAN ANTONIO · PI BAREA-RODRIGUEZ, EDWIN J · 1985 to 2021
$9.5M
Texas Consortium Program in Behavioral NeuroscienceT32MH065728 · NIMH · UNIVERSITY OF TEXAS AUSTIN · PI GONZALEZ-LIMA, FRANCISCO · 2002 to 2009
$4.9M
NCRR NIH HHS G12RR1346-02-RCMINCRR NIH HHS M01 RR001346NIGMS NIH HHS GM07717NIGMS NIH HHS T34 GM007717NIMH NIH HHS T32 MH065728NIMH NIH HHS T32-MH65728
6 · The paper itself

Abstract

Aging is associated with a decreased capacity for dentate gyrus (DG) granule cell depolarization as well as reduced perforant path activation. Although it is well established that the maintenance of DG long-term potentiation (LTP) over days is impaired in aged, as compared to young animals, the threshold for inducing this LTP has never been investigated in aged, awake animals. In addition, although exposure to novelty prior to theta-burst stimulation (TBS) increases both the induction and longevity of DG LTP in adult rats, the effects of exposure to novelty on LTP in aged rats have never been investigated. Here, we report that although TBS delivered in the home cage induces robust and long-lasting DG LTP in young rats, TBS fails to induce DG LTP in aged rats. Interestingly, delivery of TBS to aged rats exploring novel environments induces robust and long-lasting LTP, with the induction, but not the longevity, of this LTP being similar in magnitude to that observed in young rats delivered TBS in the home cage. These results indicate that although TBS-induced DG LTP is impaired in aged, as compared to young rats, TBS during exploration of novel environments is sufficient to rescue age-related deficits in DG LTP. We discuss these observations in the context of previous findings suggesting that the facilitation of LTP by exposure to novel environments results as a consequence of reduced network inhibition in the DG and we suggest that, in spite of age-related changes in the DG, this capacity persists in aged rats and represents a nondietary and nonpharmacological way to facilitate DG LTP during aging.

Indexed as

AgingAnimalsDentate GyrusElectrophysiologyExcitatory Postsynaptic PotentialsExploratory BehaviorLong-Term PotentiationMaleRatsRats, Inbred F344Time Factors

Identifiers

PMID18481283
PMCPMC2910321

What OpenQuestion holds

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Read underepoch 390

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.