Evidence map›Paper›PMID 29289553›Full record

ArticleExperimental gerontology2018

Advanced aging causes diaphragm functional abnormalities, global proteome remodeling, and loss of mitochondrial cysteine redox flexibility in mice.

Rachel C Kelley, Brian McDonagh, Leonardo F Ferreira

Abstract read
In one paragraph

Article in Experimental gerontology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Effects of aging on diaphragm hyperemia and blood flow distribution in male and female Fischer 344 rats.American journal of physiology. Regulatory, integrative and comparative physiology · 2024
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  7. Satellite cell depletion does not affect diaphragm adaptations to hypoxia.Journal of applied physiology (Bethesda, Md. : 1985) · 2022
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  12. A chronic high-fat diet exacerbates contractile dysfunction with impaired intracellular CaJournal of applied physiology (Bethesda, Md. : 1985) · 2020
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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

3 authors at 2 institutions in 2 countries.

Rachel C KelleyDept. of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL, USA.
Brian McDonaghDept. of Physiology, School of Medicine, NUI, Galway, Ireland. Electronic address: brian.mcdonagh@nuigalway.ie.
Leonardo F FerreiraDept. of Applied Physiology and Kinesiology, University of Florida, Gainesville, FL, USA. Electronic address: ferreira@hhp.ufl.edu.
University of Florida · USOllscoil na Gaillimhe – University of Galway · IE

Funding

Breathing Research and Therapeutics (BREATHE)T32HL134621 · NHLBI · UNIVERSITY OF FLORIDA · PI Gordon S. Mitchell · 2017 to 2026
$3.4M
Mechanisms of Respiratory Muscle Dysfunction in Heart FailureR00HL098453 · NHLBI · UNIVERSITY OF FLORIDA · PI FERREIRA, LEONARDO · 2011 to 2013
$735k
Mechanisms of reduced regenerative potential in aging skeletal muscleR03AG040400 · NIA · UNIVERSITY OF FLORIDA · PI FERREIRA, LEONARDO · 2012 to 2013
$142k
NHLBI NIH HHS R00 HL098453NHLBI NIH HHS T32 HL134621NIA NIH HHS R03 AG040400
6 · The paper itself

Abstract

aimInspiratory muscle (diaphragm) function declines with age, contributing to exercise intolerance and impaired airway clearance. Studies of diaphragm dysfunction in rodents have focused on moderate aging (~24months); thus, the impact of advanced age on the diaphragm and potential mechanisms of dysfunction are less clear. Therefore, we aimed to define the effects of advanced age on the mechanics, morphology, and global and redox proteome of the diaphragm.

methodsWe studied diaphragm from young (6months) and very old male mice (30months). Diaphragm function was evaluated using isolated muscle bundles. Proteome analyses followed LC-MS/MS processing of diaphragm muscle.

resultsAdvanced aging decreased diaphragm peak power by ~35% and maximal isometric specific force by ~15%, and prolonged time to peak twitch tension by ~30% (P<0.05). These changes in contractile properties were accompanied, and might be caused by, decreases in abundance of calsequestrin, sarcoplasmic reticulum C

conclusionOur novel findings are that the most pronounced impact of advanced aging on the diaphragm is loss of peak power and disrupted cysteine redox homeostasis in metabolic enzymes and mitochondrial proteins.

Indexed as

AgingAnimalsCysteineDiaphragmMaleMiceMice, Inbred C57BLMitochondriaMitochondrial ProteinsOxidation-ReductionPhysical Conditioning, AnimalProteomeProteomicsCysteineMitochondrial ProteinsProteomeProtein oxidationProteomicsSkeletal muscleStiffnessWeakness

Identifiers

PMID29289553
PMCPMC6880408
OpenAlexW2777785648

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.