Evidence map›Paper›PMID 32464290›Full record

ArticleNeuroImage2020

A longitudinal, multi-parametric functional MRI study to determine age-related changes in the rodent brain.

Andrew Crofts, Melissa Trotman-Lucas, Justyna Janus, Michael Kelly, Claire L Gibson

Open access · goldAbstract read
In one paragraph

Article in NeuroImage, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 1 country.

Andrew CroftsDepartment of Neuroscience, Psychology & Behaviour, University of Leicester, Leicester, UK; Preclinical Imaging Facility, Core Biotechnology Services, University of Leicester, Leicester, UK.
Melissa Trotman-LucasDepartment of Neuroscience, Psychology & Behaviour, University of Leicester, Leicester, UK; School of Psychology, University of Nottingham, Nottingham, UK.
Justyna JanusPreclinical Imaging Facility, Core Biotechnology Services, University of Leicester, Leicester, UK.
Michael KellyPreclinical Imaging Facility, Core Biotechnology Services, University of Leicester, Leicester, UK.
Claire L GibsonDepartment of Neuroscience, Psychology & Behaviour, University of Leicester, Leicester, UK; School of Psychology, University of Nottingham, Nottingham, UK. Electronic address: claire.gibson@nottingham.ac.uk.
University of Leicester · GBUniversity of Nottingham · GB

Funding

Medical Research Council MR/N013913/1
6 · The paper itself

Abstract

As the population ages, the incidence of age-related neurological diseases and cognitive decline increases. To further understand disease-related changes in brain function it is advantageous to examine brain activity changes in healthy aging rodent models to permit mechanistic investigation. Here, we examine the suitability, in rodents, of using a novel, minimally invasive anaesthesia protocol in combination with a functional MRI protocol to assess alterations in neuronal activity due to physiological aging. 11 Wistar Han female rats were studied at 7, 9, 12, 15 and 18 months of age. Under an intravenous infusion of propofol, animals underwent functional magnetic resonance imaging (fMRI) and functional magnetic resonance spectroscopy (fMRS) with forepaw stimulation to quantify neurotransmitter activity, and resting cerebral blood flow (CBF) quantification using arterial spin labelling (ASL) to study changes in neurovascular coupling over time. Animals showed a significant decrease in size of the active region with age (P ​< ​0.05). fMRS results showed a significant decrease in glutamate change with stimulation (ΔGlu) with age (P ​< ​0.05), and ΔGlu became negative from 12 months onwards. Global CBF remained constant for the duration of the study. This study shows age related changes in the blood oxygen level dependent (BOLD) response in rodents that correlate with those seen in humans. The results also suggest that a reduction in synaptic glutamate turnover with age may underlie the reduction in the BOLD response, while CBF is preserved.

Indexed as

Models, AnimalAgingAnesthetics, IntravenousAnimalsBrainFemaleLongitudinal StudiesMagnetic Resonance ImagingMagnetic Resonance SpectroscopyNeuroimagingPropofolRatsRats, WistarAnesthetics, IntravenousPropofolAgingfMRIfMRSImagingPreclinical models

Identifiers

PMID32464290
PMCPMC7422839
OpenAlexW3026969124

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.