Evidence map›Paper›PMID 32492508›Full record

ArticleNeuroImage2020

Visualization of live, mammalian neurons during Kainate-infusion using magnetic resonance microscopy.

Jeremy J Flint, Kannan Menon, Brian Hansen, John Forder, Stephen J Blackband

Abstract 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 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Guideline
  2. Enhanced spatial resolution in magnetic resonance imaging by dynamic nuclear polarization at 5 K.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  3. 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.

Jeremy J FlintDepartment of Neuroscience, University of Florida, Gainesville, FL, USA; McKnight Brain Institute, University of Florida, Gainesville, FL, USA. Electronic address: jflint@mbi.ufl.edu.
Kannan MenonDepartment of Biomedical Engineering, University of Florida, Gainesville, FL, USA; McKnight Brain Institute, University of Florida, Gainesville, FL, USA.
Brian HansenCenter of Functionally Integrative Neuroscience, Aarhus University, Denmark.
John ForderDepartment of Biomedical Engineering, University of Florida, Gainesville, FL, USA; Department of Radiology, University of Florida, Gainesville, FL, USA; McKnight Brain Institute, University of Florida, Gainesville, FL, USA; National High Magnetic Field Laboratory, Tallahassee, FL, USA.
Stephen J BlackbandDepartment of Neuroscience, University of Florida, Gainesville, FL, USA; McKnight Brain Institute, University of Florida, Gainesville, FL, USA; Center for Structural Biology, University of Florida, Gainesville, FL, USA; National High Magnetic Field Laboratory, Tallahassee, FL, USA.

Funding

Diffusion functional imaging (DfMRI) of evoked neuronal activation at the cellular levelR21NS094061 · NINDS · UNIVERSITY OF FLORIDA · PI FLINT, JEREMY JOSEPH · 2016 to 2017
$413k
NINDS NIH HHS R21 NS094061
6 · The paper itself

Abstract

Since its first description and development in the late 20th century, diffusion magnetic resonance imaging (dMRI) has proven useful in describing the microstructural details of biological tissues. Signal generated from the protons of water molecules undergoing Brownian motion produces contrast based on the varied diffusivity of tissue types. Images employing diffusion contrast were first used to describe the diffusion characteristics of tissues, later used to describe the fiber orientations of white matter through tractography, and most recently proposed as a functional contrast method capable of delineating neuronal firing in the active brain. Thanks to the molecular origins of its signal source, diffusion contrast is inherently useful at describing features of the microenvironment; however, limitations in achievable resolution in magnetic resonance imaging (MRI) scans precluded direct visualization of tissue microstructure for decades following MRI's inception as an imaging modality. Even after advancements in MRI hardware had permitted the visualization of mammalian cells, these specialized systems could only accommodate fixed specimens that prohibited the observation and characterization of physiological processes. The goal of the current study was to visualize cellular structure and investigate the subcellular origins of the functional diffusion contrast mechanism (DfMRI) in living, mammalian tissue explants. Using a combination of ultra-high field spectrometers, micro radio frequency (RF) coils, and an MRI-compatible superfusion device, we are able to report the first live, mammalian cells-α-motor neurons-visualized with magnetic resonance microscopy (MRM). We are also able to report changes in the apparent diffusion of the stratum oriens within the hippocampus-a layer comprised primarily of pyramidal cell axons and basal dendrites-and the spinal cord's ventral horn following exposure to kainate.

Indexed as

AnimalsHippocampusImage Processing, Computer-AssistedKainic AcidMagnetic Resonance ImagingMicroscopyNeuronsRatsRats, Sprague-DawleySpinal CordKainic AcidAcute sliceDiffusion kurtosisHippocampusKainateMagnetic resonance microscopyα-motor

Identifiers

PMID32492508
PMCPMC7510773

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.