Evidence map›Paper›PMID 30946636›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2019

Angiotensin II suppresses autophagy and disrupts ultrastructural morphology and function of mitochondria in mouse skeletal muscle.

Kleiton Augusto Santos Silva, Thaysa Ghiarone, Kathy Schreiber, DeAna Grant, Tommi White, Madlyn I Frisard, Sergiy Sukhanov, Bysani Chandrasekar, Patrice Delafontaine, Tadashi Yoshida

Open access · bronzeAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2019. 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
2.6field-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

16 citing papers in PubMed, 30 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Kleiton Augusto Santos SilvaDepartment of Medicine, University of Missouri School of Medicine, Columbia, Missouri.ORCID 0000-0001-8230-0012
Thaysa GhiaroneDalton Cardiovascular Research Center, University of Missouri , Columbia, Missouri.
Kathy SchreiberCell and Immunobiology Core, University of Missouri , Columbia, Missouri.
DeAna GrantElectron Microcopy Core Facility, University of Missouri , Columbia, Missouri.
Tommi WhiteElectron Microcopy Core Facility, University of Missouri , Columbia, Missouri.
Madlyn I FrisardDepartment of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia.
Sergiy SukhanovDepartment of Medicine, University of Missouri School of Medicine, Columbia, Missouri.
Bysani ChandrasekarDepartment of Medicine, University of Missouri School of Medicine, Columbia, Missouri.
Patrice DelafontaineDepartment of Medicine, University of Missouri School of Medicine, Columbia, Missouri.
Tadashi YoshidaDepartment of Medicine, University of Missouri School of Medicine, Columbia, Missouri.
University of Missouri · USHarry S. Truman Memorial Veterans' Hospital · USVirginia Tech · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI JUDD E SHELLITO · 2012 to 2026
$69.1M
The role of the CMV-associated reactive oxygen species in age-relatedP20GM103629 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI SAMMARCO, MIMI C · 2012 to 2021
$22.4M
Insulin-Like Growth Factor-1and AtherosclerosisR01HL070241 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI PATRICE DELAFONTAINE · 2003 to 2026
$10.1M
Translational Research in Hypertension and Renal BiologyP30GM103337 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI NAVAR, LUIS GABRIEL · 2012 to 2016
$5.8M
ANGIOTENSIN II, IGF-1 AND SKELETAL MUSCLE ATROPHYR01HL080682 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI DELAFONTAINE, PATRICE · 2007 to 2015
$3.3M
TRAF3IP2 in Adverse Cardiac Remodeling and Heart FailureI01BX004220 · VA · HARRY S. TRUMAN MEMORIAL VA HOSPITAL · PI BYSANI, CHANDRASEKAR · 2018 to 2021
–
BLRD Research Career Scientist Award ApplicationIK6BX004016 · VA · HARRY S. TRUMAN MEMORIAL VA HOSPITAL · PI Chandrasekar Bysani · 2018 to 2026
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BLRD VA I01 BX004220BLRD VA IK6 BX004016NHLBI NIH HHS R01 HL070241NHLBI NIH HHS R01 HL080682NIGMS NIH HHS P20 GM103629NIGMS NIH HHS P30 GM103337NIGMS NIH HHS U54 GM104940
6 · The paper itself

Abstract

Angiotensin II (ANG II)-induced skeletal muscle wasting is characterized by activation of the ubiquitin-proteasome system. However, the potential involvement of proteolytic system macroautophagy/autophagy in this wasting process remains elusive. Autophagy is precisely regulated to maintain cell survival and homeostasis; thus its dysregulation (i.e., overactivation or persistent suppression) could lead to detrimental outcomes in skeletal muscle. Here we show that infusion of ANG II for 7 days in male FVB mice suppressed autophagy in skeletal muscle. ANG II blunted microtubule-associated protein 1 light chain 3B (LC3B)-I-to-LC3B-II conversion (an autophagosome marker), increased p62/SQSTM1 (an autophagy cargo receptor) protein expression, and decreased the number of autophagic vacuoles. ANG II inhibited UNC-51-like kinase 1 via inhibition of 5'-AMP-activated kinase and activation of mechanistic target of rapamycin complex 1, leading to reduced phosphorylation of beclin-1

Indexed as

Angiotensin IIAnimalsAutophagosomesAutophagyBeclin-1MaleMiceMitochondriaMuscle, SkeletalMuscular AtrophyPhosphorylationProtein Serine-Threonine KinasesSignal TransductionAngiotensin IIBeclin-1Protein Serine-Threonine Kinasesautophagosomebeclin-1LC3Bmitochondrial respirationproteolysis

Identifiers

PMID30946636
PMCPMC6620657
OpenAlexW2933251640

What OpenQuestion 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 OpenQuestion graph.