Evidence map›Paper›PMID 25989111›Full record

ArticleThe European journal of neuroscience2015

Sex-dependent modulation of age-related cognitive decline by the L-type calcium channel gene Cacna1c (Cav 1.2).

Panos Zanos, Shambhu Bhat, Chantelle E Terrillion, Robert J Smith, Leonardo H Tonelli, Todd D Gould

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Neuronal deletion of CaScientific reports · 2022
    Article
  8. Review
  9. Aging, hormones and receptors.Physiological research · 2020
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Vitamin D, reactive oxygen species and calcium signalling in ageing and disease.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2016
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Panos ZanosDepartment of Psychiatry, University of Maryland School of Medicine, MSTF 936, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Shambhu BhatDepartment of Psychiatry, University of Maryland School of Medicine, MSTF 936, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Chantelle E TerrillionDepartment of Psychiatry, University of Maryland School of Medicine, MSTF 936, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Robert J SmithDepartment of Psychiatry, University of Maryland School of Medicine, MSTF 936, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Leonardo H TonelliDepartment of Psychiatry, University of Maryland School of Medicine, MSTF 936, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
Todd D GouldDepartment of Psychiatry, University of Maryland School of Medicine, MSTF 936, 685 W. Baltimore Street, Baltimore, MD 21201, USA.
University of Maryland, Baltimore · US

Funding

The Effects of Kynurenine Aminotransferase Inhibition in People with SchizophreniaP50MH103222 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI SCHWARCZ, ROBERT · 2014 to 2023
$25.2M
Regulatory Role of CACNA1C Intronic DNA Variation Relevant to Psychiatric DiseaseR21MH103847 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI CHANG, YEN PEI CHRISTY, GOULD, TODD D · 2014 to 2015
$422k
Gonadal Hormones and Depression:The Role of Mood Disorder Risk Gene CACNA1CR21MH093967 · NIMH · UNIVERSITY OF MARYLAND BALTIMORE · PI GOULD, TODD D · 2011 to 2012
$413k
NIMH NIH HHS L30 MH091729NIMH NIH HHS MH093967NIMH NIH HHS P50 MH103222NIMH NIH HHS R21 MH093967NIMH NIH HHS R21 MH103847
6 · The paper itself

Abstract

Increased calcium influx through L-type voltage-gated calcium channels has been implicated in the neuronal dysfunction underlying age-related memory declines. The present study aimed to test the specific role of Cacna1c (which encodes Cav 1.2) in modulating age-related memory dysfunction. Short-term, spatial and contextual/emotional memory was evaluated in young and aged, wild-type as well as mice with one functional copy of Cacna1c (haploinsufficient), using the novel object recognition, Y-maze and passive avoidance tasks, respectively. Hippocampal expression of Cacna1c mRNA was measured by quantitative polymerase chain reaction. Ageing was associated with object recognition and contextual/emotional memory deficits, and a significant increase in hippocampal Cacna1c mRNA expression. Cacna1c haploinsufficiency was associated with decreased Cacna1c mRNA expression in both young and old animals. However, haploinsufficient mice did not manifest an age-related increase in expression of this gene. Behaviourally, Cacna1c haploinsufficiency prevented object recognition deficits during ageing in both male and female mice. A significant correlation between higher Cacna1c levels and decreased object recognition performance was observed in both sexes. Also, a sex-dependent protective role of decreased Cacna1c levels in contextual/emotional memory loss has been observed, specifically in male mice. These data provide evidence for an association between increased hippocampal Cacna1c expression and age-related cognitive decline. Additionally, they indicate an interaction between the Cacna1c gene and sex in the modulation of age-related contextual memory declines.

Indexed as

Sex CharacteristicsAgingAnimalsAvoidance LearningCalcium Channels, L-TypeCognitionCognition DisordersEmotionsFemaleHaploinsufficiencyHippocampusMaleMaze LearningMemory DisordersMice, Inbred C57BLMice, TransgenicCACNA1C protein, mouseCalcium Channels, L-TypeRNA, Messengerageingcognitionhippocampusmemorymice

Identifiers

PMID25989111
PMCPMC4615431
OpenAlexW1555844632

What OpenQuestion holds

Textmetadata
LicenceTDM
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.