Evidence map›Paper›PMID 37878529›Full record

ArticleThe Journal of physiology2023

Modulation of sarcopenia phenotypes by glutathione peroxidase 4 overexpression in mice.

Hongyang Xu, Agnieszka Czyżowska, Holly Van Remmen, Jacob L Brown

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. iPLAScience advances · 2026
    Article
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  4. Review
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  10. Reactive oxygen species in the pathogenesis of sarcopenia.Free radical biology & medicine · 2025
    Review
  11. Review
  12. Article
  13. 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

4 authors at 1 institution in 1 country.

Hongyang XuAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.ORCID 0000-0001-8878-0600
Agnieszka CzyżowskaAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.ORCID 0000-0003-3398-4475
Holly Van RemmenAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Jacob L BrownAging and Metabolism Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.ORCID 0000-0003-0912-7924
Oklahoma Medical Research Foundation · US

Funding

PROJECT 3: Neuromuscular redox homeostasis in mice lacking SOD1 and aging wild type mice subcontract at University of LiverpoolP01AG051442 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JACKSON, MALCOLM JOSEPH · 2016 to 2020
$8.9M
GEROSCIENCE TRAINING PROGRAM IN OKLAHOMAT32AG052363 · NIA · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI Benjamin Francis Miller, William Edmund Sonntag · 2017 to 2026
$3.6M
Defining the relative roles of pre- and post-synaptic events in the initiation and progression of sarcopeniaR01AG050676 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BROOKS, SUSAN V, VAN REMMEN, HOLLY · 2016 to 2020
$3.3M
A novel role for oxidized lipid mediators as effectors of muscle atrophy and weakness in agingR01AG077812 · NIA · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI Kenneth M Humphries · 2022 to 2026
$2.8M
Lipid hydroperoxides in sarcopenia and muscle wasting: mechanisms and interventionIK2BX005620 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI BROWN, JACOB LEVI · 2022 to 2025
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BLR&D Research Career Scientist Award ApplicationIK6BX005234 · VA · OKLAHOMA CITY VA MEDICAL CENTER · PI VAN REMMEN, HOLLY · 2020 to 2024
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BLRD VA I01 BX002595BLRD VA I01 BX004453BLRD VA IK2 BX005620BLRD VA IK6 BX005234NIA NIH HHS P01 AG051442NIA NIH HHS R01 AG050676NIA NIH HHS R01 AG077812NIA NIH HHS R01AG077812NIA NIH HHS T32 AG052363
6 · The paper itself

Abstract

Our laboratory previously showed lipid hydroperoxides and oxylipin levels are elevated in response to loss of skeletal muscle innervation and are associated with muscle pathologies. To elucidate the pathological impact of lipid hydroperoxides, we overexpressed glutathione peroxidase 4 (GPx4), an enzyme that targets reduction of lipid hydroperoxides in membranes, in adult CuZn superoxide dismutase knockout (Sod1KO) mice that show accelerated muscle atrophy associated with loss of innervation. The gastrocnemius muscle from Sod1KO mice shows reduced mitochondrial respiration and elevated oxidative stress (F

Indexed as

SarcopeniaAdenosine TriphosphatasesAnimalsCalciumGlutathioneGlutathione PeroxidaseHydrogen PeroxideLipidsMiceMice, KnockoutMuscle, SkeletalPhenotypePhospholipid Hydroperoxide Glutathione PeroxidaseSuperoxide DismutaseSuperoxide Dismutase-1Adenosine TriphosphatasesCalciumGlutathioneGlutathione Peroxidaseglutathione peroxidase 4, mouseHydrogen PeroxideLipidsPhospholipid Hydroperoxide Glutathione PeroxidaseSuperoxide DismutaseSuperoxide Dismutase-1Ca2+ sensitivityE-C couplinglipid peroxidationmitochondriamuscle functionoxidative stressSERCA activity

Identifiers

PMID37878529
PMCPMC10871152
OpenAlexW4387949846

What OpenQuestion holds

Textmetadata
LicenceTDM
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.