Evidence map›Paper›PMID 38103626›Full record

ArticlePhysiology & behavior2024

Cognitive trajectories in longitudinally trained 3xTg-AD mice.

Michael R Duggan, Zoe Steinberg, Tara Peterson, Tara-Jade Francois, Vinay Parikh

Open access · greenAbstract read
In one paragraph

Article in Physiology & behavior, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Experimental laboratory models as tools for understanding modifiable dementia risk.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Review
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

5 authors at 1 institution in 1 country.

Michael R DugganDepartment of Psychology and Neuroscience Program, Temple University, Philadelphia, PA 19122, United States.
Zoe SteinbergDepartment of Psychology and Neuroscience Program, Temple University, Philadelphia, PA 19122, United States.
Tara PetersonDepartment of Psychology and Neuroscience Program, Temple University, Philadelphia, PA 19122, United States.
Tara-Jade FrancoisDepartment of Psychology and Neuroscience Program, Temple University, Philadelphia, PA 19122, United States.
Vinay ParikhDepartment of Psychology and Neuroscience Program, Temple University, Philadelphia, PA 19122, United States. Electronic address: vinay.parikh@temple.edu.
Temple University · US

Funding

Cholinergic overload and resilience to attentional capacities in agingR21AG046580 · NIA · TEMPLE UNIV OF THE COMMONWEALTH · PI PARIKH, VINAY · 2015 to 2016
$421k
NIA NIH HHS R21 AG046580
6 · The paper itself

Abstract

Preclinical studies in Alzheimer's disease (AD) often rely on cognitively naïve animal models in cross-sectional designs that can fail to reflect the cognitive exposures across the lifespan and heterogeneous neurobehavioral features observed in humans. To determine whether longitudinal cognitive training may affect cognitive capacities in a well-characterized AD mouse model, 3xTg and wild-type mice (n = 20) were exposed daily to a training variant of the Go-No-Go (GNG) operant task from 3 to 9 months old. At 3, 6, and 9 months, performance on a testing variant of the GNG task and anxiety-like behaviors were measured, while long-term recognition memory was also assessed at 9 months. In general, GNG training improved performance with increasing age across genotypes. At 3 months old, 3xTg mice showed slight deficits in inhibitory control that were accompanied by minor improvements in signal detection and decreased anxiety-like behavior, but these differences did not persist at 6 and 9 months old. At 9 months old, 3xTg mice displayed minor deficits in signal detection, and long-term recognition memory capacity was comparable with wild-type subjects. Our findings indicate that longitudinal cognitive training can render 3xTg mice with cognitive capacities that are on par with their wild-type counterparts, potentially reflecting functional compensation in subjects harboring AD genetic mutations.

Indexed as

Alzheimer DiseaseAnimalsCognitionCross-Sectional StudiesDisease Models, AnimalHumansInfantMiceMice, Inbred C57BLMice, TransgenicRecognition, Psychologytau Proteinstau Proteins3xTgAlzheimer's diseaseCognitive trainingGo-No-GoResilience

Identifiers

PMID38103626
PMCPMC10872326
OpenAlexW4389720793

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.