Evidence map›Paper›PMID 25753480›Full record

ArticleScientific reports2015

Visualization of synaptic domains in the Drosophila brain by magnetic resonance microscopy at 10 micron isotropic resolution.

Choong H Lee, Stephen J Blackband, Pedro Fernandez-Funez

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

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

  1. Guideline
  2. Article
  3. Article
  4. Experimental demonstration of diffusion limitations on resolution and SNR in MR microscopy.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Probing the brain with molecular fMRI.Current opinion in neurobiology · 2018
    Review
  9. Low-temperature magnetic resonance imaging with 2.8 μm isotropic resolution.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Micron-scale magnetic resonance imaging of both liquids and solids.Journal of magnetic resonance (San Diego, Calif. : 1997) · 2015
    Article
  14. Journal of orthopaedic translation · 2015
    Article
  15. 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

3 authors.

Choong H LeeDepartment of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL. 32611, USA.
Stephen J Blackband1] Department of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL. 32611, USA [2] National High Magnetic Field Laboratory, University of Florida, Gainesville, FL. 32611, USA.
Pedro Fernandez-Funez1] Department of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, FL. 32611, USA [2] Department of Neurology, Genetics Institute, and Center for Translational Research on Neurodegenerative Diseases, University of Florida, Gainesville, FL 32611, USA.

Funding

Development of MR Microscopy at the Cellular LevelR01EB012874 · NIBIB · UNIVERSITY OF FLORIDA · PI BLACKBAND, STEPHEN J. · 2010 to 2013
$2.1M
NIBIB NIH HHS 1R01EB012874-01NIBIB NIH HHS R01 EB012874
6 · The paper itself

Abstract

Understanding the complex architecture, connectivity, and pathology of the human brain is a major application of magnetic resonance imaging (MRI). However, the cellular basis of MR signal is still poorly understood. The advent of MR microscopy (MRM) enables imaging biological samples at cellular resolution, helping to interpret the nature of MR signal at the cellular level. In this regard, the small Drosophila brain can reveal key aspects of MR signal through the visualization of complex, intact neuronal structures in their native spatial arrangement. Applying state-of-the-art MR technology, we imaged fixed Drosophila heads at 10 μm isotropic resolution by two endogenously contrasted MRM sequences. The improved MRM sensitivity described here delivered the highest 3D resolution of an intact animal head reported so far. 3D fast low angle shot (FLASH) revealed strong signal in most internal tissues, particularly in the brain cortex, which contains the cell bodies of neurons and glia. Remarkably, 3D diffusion weighted imaging (DWI) delivered unprecedented contrast within the modular brain neuropil, revealing hyperintense signal in synapse-rich microdomains. Thus, the complex Drosophila brain revealed unknown features of FLASH and DWI with potential applications in characterizing the structure and pathology of the mammalian brain.

Indexed as

AnimalsBrainBrain MappingDrosophilaHumansImage Interpretation, Computer-AssistedMagnetic Resonance ImagingMicroscopyNeurons

Identifiers

PMID25753480
PMCPMC4649768

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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.