Evidence map›Paper›PMID 32407240›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2020

A time course for markers of protein synthesis and degradation with hindlimb unloading and the accompanying anabolic resistance to refeeding.

Paul A Roberson, Kevin L Shimkus, Jaclyn E Welles, Dandan Xu, Abigale L Whitsell, Eric M Kimball, Leonard S Jefferson, Scot R Kimball

Open access · greenAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Optimization of a pericyte therapy to improve muscle recovery after limb immobilization.Journal of applied physiology (Bethesda, Md. : 1985) · 2022
    Article
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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

8 authors at 1 institution in 1 country.

Paul A RobersonPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.ORCID 0000-0001-7696-7398
Kevin L ShimkusPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.
Jaclyn E WellesPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.
Dandan XuPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.
Abigale L WhitsellPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.
Eric M KimballPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.
Leonard S JeffersonPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.
Scot R KimballPennsylvania State University, Department of Cellular and Molecular Physiology, College of Medicine, Hershey, Pennsylvania.ORCID 0000-0002-2149-7189
Pennsylvania State University · US

Funding

REGULATION OF SKELETAL MUSCLE METABOLISMR01DK015658 · NIDDK · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI KIMBALL, SCOT R · 1986 to 2021
$7.4M
NIDDK NIH HHS R01 DK015658
6 · The paper itself

Abstract

Skeletal muscle atrophy is associated with disease, aging, and disuse. Hindlimb unloading (HU) in animals provides an experimental model to study muscle atrophy. A comprehensive time course for how HU affects biomarkers of protein synthesis and degradation acutely and chronically and the associated resistance to an anabolic stimulus following disuse remain undocumented. Sixteen-week-old C57BL/6 mice underwent 0, 1, 12, 24, 72, 168, or 336 h of HU. Following 336 h of HU, mice were reloaded for 1, 24, or 72 h. Another group of mice underwent 120 h of HU, were fasted or refed, and were then compared with similar condition control animals (CTL). Protein content and phosphorylation of biomarkers of protein synthesis, degradation, and autophagy were assessed in the soleus muscle. Gastrocnemius, soleus, and plantaris muscles atrophied within 120 h of HU. Protein synthesis trended toward decrease following 24 h of HU. p70S6K phosphorylation and protein synthesis increased with reloading. Following HU, changes in MAFbx and DEPTOR expression and DEPTOR phosphorylation were consistent with development of a catabolic state. DEPTOR expression recovered following reloading. Animals that underwent 120 h of HU exhibited attenuation of refeeding-induced p70S6K phosphorylation compared with CTL counterparts. Following 120 h of HU, protein synthesis, eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1) phosphorylation, and DEPTOR, MAFbx, and Sestrin1 expression indicated a catabolic state. Following 120 h of HU, autophagy markers, including p62 expression, REDD1 expression, LC3 ratio, and Unc-51-like autophagy-activating kinase 1 (ULK1) phosphorylation, indicated impaired autophagy. HU promotes a deleterious balance between protein synthesis and degradation. The time course herein provides scientists information about when the associated biomarkers become affected.

Indexed as

Hindlimb SuspensionMuscular AtrophyAnimalsBiomarkersHindlimbMiceMice, Inbred C57BLMuscle, SkeletalProtein BiosynthesisBiomarkersanabolic resistancedisuse atrophyhindlimb suspensionhindlimb unloadingskeletal muscle

Identifiers

PMID32407240
PMCPMC7469230
OpenAlexW3024603808

What Socratic holds

Textmetadata
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 Socratic graph.