Evidence map›Paper›PMID 38605461›Full record

ArticleThe Journal of comparative neurology2024

Cerebellum Purkinje cell vulnerability in aged rats with memory impairment.

C'iana P Cooper, Liam H Cheng, Jafar A Bhatti, Edward L Rivera, Derek Huell, Cristina Banuelos, Evelyn J Perez, Jeffrey M Long, Peter R Rapp

Open access · hybridAbstract read
In one paragraph

Article in The Journal of comparative neurology, 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
2.4field-weighted citation impact, top 12% 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, 9 citations in OpenAlex.

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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

9 authors at 1 institution in 1 country.

C'iana P CooperNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.ORCID 0000-0002-3384-706X
Liam H ChengNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.
Jafar A BhattiNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.ORCID 0000-0002-9645-2356
Edward L RiveraNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.
Derek HuellNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.ORCID 0000-0002-9658-8800
Cristina BanuelosNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.
Evelyn J PerezNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.
Jeffrey M LongNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.
Peter R RappNeurocognitive Aging Section, Laboratory of Behavioral Neuroscience, National Institute on Aging, Baltimore, Maryland, USA.ORCID 0000-0002-0983-3944
Institute on Aging · US

Funding

Neurocognitive Aging: Experience-Dependent Dynamics, Plasticity and Network ContributionsZIAAG000350 · NIA · NATIONAL INSTITUTE ON AGING · PI RAPP, PETER R · 2009 to 2025
$30.9M
Intramural NIH HHS ZIA AG000350
6 · The paper itself

Abstract

The cerebellum is involved in higher order cognitive function and is susceptible to age-related atrophy. However, limited evidence has directly examined the cerebellum's role in cognitive aging. To interrogate potential substrates of the relationship between cerebellar structure and memory in aging, here we target the Purkinje cells (PCs). The sole output neurons of the cerebellum, PC loss and/or degeneration underlie a variety of behavioral abnormalities. Using a rat model of normal cognitive aging, we immunostained sections through the cerebellum for the PC-specific protein, calbindin-D28k. Although morphometric quantification revealed no significant difference in total PC number as a function of age or cognitive status, regional cell number was a more robust correlate of memory performance in the young cerebellum than in aged animals. Parallel biochemical analysis of PC-specific protein levels in whole cerebellum additionally revealed that calbindin-D28k and Purkinje cell protein-2 (pcp-2) levels were lower selectively in aged rats with spatial memory impairment compared to both young animals and aged rats with intact memory. These results suggest that cognitive aging is associated with cerebellum vulnerability, potentially reflecting disruption of the cerebellum-medial temporal lobe network.

Indexed as

Purkinje CellsS100 Calcium Binding Protein GAnimalsCalbindin 1CerebellumNeuronsRatsCalbindin 1S100 Calcium Binding Protein GagingcalbindincerebellumneurocognitivePurkinje cellratspatial memory

Identifiers

PMID38605461
PMCPMC11027960
OpenAlexW4394757838

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.