Evidence map›Paper›PMID 37058498›Full record

ArticlePloS one2023

Probing microstructural changes in muscles of leptin-deficient zebrafish by non-invasive ex-vivo magnetic resonance microimaging.

Muhamed N Hashem Eeza, Rico Singer, Yi Ding, Junling He, Zain Zuberi, Hans J Baelde, Huub J M de Groot, Jörg Matysik, Herman P Spaink, A Alia

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. 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
0.5field-weighted citation impact, top 35% 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, 3 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

10 authors at 3 institutions in 2 countries.

Muhamed N Hashem EezaInstitute of Medical Physics and Biophysics, Leipzig University, Leipzig, Germany.ORCID 0000-0001-5246-5588
Rico SingerLeiden Institute of Chemistry, Leiden University, Leiden, The Netherlands.
Yi DingInstitute of Biology (IBL), Leiden University, Leiden, The Netherlands.
Junling HeInstitute of Biology (IBL), Leiden University, Leiden, The Netherlands.
Zain ZuberiLeiden Institute of Chemistry, Leiden University, Leiden, The Netherlands.
Hans J BaeldeDepartment of Pathology, Leiden University Medical Center, Leiden, The Netherlands.
Huub J M de GrootLeiden Institute of Chemistry, Leiden University, Leiden, The Netherlands.
Jörg MatysikInstitut für Analytische Chemie, Leipzig University, Leipzig, Germany.
Herman P SpainkInstitute of Biology (IBL), Leiden University, Leiden, The Netherlands.
A AliaInstitute of Medical Physics and Biophysics, Leipzig University, Leipzig, Germany.ORCID 0000-0002-4900-9749
Leiden University · NLLeipzig University · DELeiden University Medical Center · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leptin is a hormone that plays a key role in controlling food intake and energy homeostasis. Skeletal muscle is an important target for leptin and recent studies have shown that leptin deficiency may lead to muscular atrophy. However, leptin deficiency-induced structural changes in muscles are poorly understood. The zebrafish has emerged as an excellent model organism for studies of vertebrate diseases and hormone response mechanisms. In this study, we explored ex-vivo magnetic resonance microimaging (μMRI) methods to non-invasively assess muscle wasting in leptin-deficient (lepb-/-) zebrafish model. The fat mapping performed by using chemical shift selective imaging shows significant fat infiltration in muscles of lepb-/- zebrafish compared to control zebrafish. T2 relaxation measurements show considerably longer T2 values in the muscle of lepb-/- zebrafish. Multiexponential T2 analysis detected a significantly higher value and magnitude of long T2 component in the muscles of lepb-/- as compared to control zebrafish. For further zooming into the microstructural changes, we applied diffusion-weighted MRI. The results show a significant decrease in the apparent diffusion coefficient indicating increased constraints of molecular movements within the muscle regions of lepb-/- zebrafish. The use of the phasor transformation for the separation of diffusion-weighted decay signals showed a bi-component diffusion system which allows us to estimate each fraction on a voxel-wise basis. A substantial difference was found between the ratio of two components in lepb-/- and control zebrafish muscles, indicating alterations in diffusion behavior associated with the tissue microstructural changes in muscles of lepb-/- zebrafish as compared to control zebrafish. Taken together, our results demonstrate that the muscles of lepb-/- zebrafish undergo significant fat infiltration and microstructural changes leading to muscle wasting. This study also demonstrates that μMRI provides excellent means to non-invasively study the microstructural changes in the muscles of the zebrafish model.

Indexed as

LeptinZebrafishAnimalsDiffusion Magnetic Resonance ImagingMagnetic Resonance ImagingMagnetic Resonance SpectroscopyMuscle, SkeletalMuscular AtrophyLeptin

Identifiers

PMID37058498
PMCPMC10104282
OpenAlexW4365478932

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.