Evidence map›Paper›PMID 35817772›Full record

ArticleNPJ microgravity2022

Mitigating sarcoplasmic reticulum stress limits disuse-induced muscle loss in hindlimb unloaded mice.

Amir Ali Khan, Muhammad Tehsil Gul, Asima Karim, Anu Ranade, Muhammad Azeem, Zeinab Ibrahim, Gopika Ramachandran, Vidhya A Nair, Firdos Ahmad, Adel Elmoselhi and 1 more

Open access · goldAbstract read
In one paragraph

Article in NPJ microgravity, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  6. The emerging roles of necroptosis in skeletal muscle health and disease.Pflugers Archiv : European journal of physiology · 2024
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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

11 authors at 1 institution in 1 country.

Amir Ali KhanDepartment of Applied Biology, College of Sciences, University of Sharjah, Sharjah, 27272, UAE.
Muhammad Tehsil GulDepartment of Applied Biology, College of Sciences, University of Sharjah, Sharjah, 27272, UAE.ORCID http://orcid.org/0000-0002-5318-008X
Asima KarimDepartment of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, 27272, UAE.ORCID http://orcid.org/0000-0002-6288-0686
Anu RanadeDepartment of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, 27272, UAE.
Muhammad AzeemDepartment of Applied Physics and Astronomy, College of Sciences, University of Sharjah, Sharjah, 27272, UAE.
Zeinab IbrahimCardiovascular research group, Sharjah Institute for Medical Research, University of Sharjah, Sharjah, 27272, UAE.ORCID http://orcid.org/0000-0002-0320-4127
Gopika RamachandranCardiovascular research group, Sharjah Institute for Medical Research, University of Sharjah, Sharjah, 27272, UAE.
Vidhya A NairCardiovascular research group, Sharjah Institute for Medical Research, University of Sharjah, Sharjah, 27272, UAE.
Firdos AhmadDepartment of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, 27272, UAE.ORCID http://orcid.org/0000-0001-6530-6068
Adel ElmoselhiDepartment of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, 27272, UAE.
Rizwan QaisarDepartment of Basic Medical Sciences, College of Medicine, University of Sharjah, Sharjah, 27272, UAE. rqaisar@sharjah.ac.ae.
University of Sharjah · AE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Muscle disuse in the hindlimb unloaded (HU) mice causes significant atrophy and weakness. However, the cellular and molecular mechanisms driving disuse-muscle atrophy remain elusive. We investigated the potential contribution of proteins dysregulation by sarcoplasmic reticulum (SR), a condition called SR stress, to muscle loss during HU. Male, c57BL/6j mice were assigned to ground-based controls or HU groups treated with vehicle or 4-phenylbutyrate (4-PBA), a potent inhibitor of SR stress, once a day for three weeks. We report that the 4-PBA reduced the SR stress and partly reversed the muscle atrophy and weakness in the HU mice. Transcriptome analysis revealed that several genes were switched on (n = 3688) or differentially expressed (n = 1184) due to HU. GO, and KEGG term analysis revealed alterations in pathways associated with the assembly of cilia and microtubules, extracellular matrix proteins regulation, calcium homeostasis, and immune modulation during HU. The muscle restoration with 4-PBA partly reversed these changes along with differential and unique expression of several genes. The analysis of genes among the two comparisons (HU-v vs. control and HU-t vs. HU-v.) shows 841 genes were overlapped between the two comparisons and they may be regulated by 4-PBA. Altogether, our findings suggest that the pharmacological suppression of SR stress may be an effective strategy to prevent disuse-induced muscle weakness and atrophy.

Identifiers

PMID35817772
PMCPMC9273600
OpenAlexW4285010523

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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.