Evidence map›Paper›PMID 23831688›Full record

ArticleThe Journal of biological chemistry2013

Angiotensin II inhibits satellite cell proliferation and prevents skeletal muscle regeneration.

Tadashi Yoshida, Sarah Galvez, Sumit Tiwari, Bashir M Rezk, Laura Semprun-Prieto, Yusuke Higashi, Sergiy Sukhanov, Zipora Yablonka-Reuveni, Patrice Delafontaine

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

53 citing papers in PubMed, 82 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Chronic hypoxia impairs skeletal muscle repair via HIF-2α stabilization.Journal of cachexia, sarcopenia and muscle · 2024
    Article
  5. Angiotensin-(1-7) improves skeletal muscle regeneration.European journal of translational myology · 2023
    Article
  6. Review
  7. Review
  8. Review
  9. Skeletal Muscle Regeneration in Cardiotoxin-Induced Muscle Injury Models.International journal of molecular sciences · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Current Thoughts of Notch's Role in Myoblast Regulation and Muscle-Associated Disease.International journal of environmental research and public health · 2021
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
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

9 authors at 2 institutions in 1 country.

Tadashi YoshidaHeart and Vascular Institute, Tulane University School of Medicine, New Orleans, Louisiana 70112, USA.
Sarah Galvez
Sumit Tiwari
Bashir M Rezk
Laura Semprun-Prieto
Yusuke Higashi
Sergiy Sukhanov
Zipora Yablonka-Reuveni
Patrice Delafontaine
Tulane University · USUniversity of Washington · US

Funding

Tracking & Evaluation CoreU54GM104940 · NIGMS · LSU PENNINGTON BIOMEDICAL RESEARCH CTR · PI Peter Todd Katzmarzyk · 2012 to 2026
$69.1M
VASCULAR SMOOTH MUSCLE PLASTICITY IN NITRIC OXIDEP20RR018766 · NCRR · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2003 to 2011
$18.5M
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
Myogenic Stem Cell Function in Aging Skeletal MuscleR01AG021566 · NIA · UNIVERSITY OF WASHINGTON · PI YABLONKA-REUVENI, ZIPORA · 2002 to 2012
$3.6M
ANGIOTENSIN II, IGF-1 AND SKELETAL MUSCLE ATROPHYR01HL080682 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI DELAFONTAINE, PATRICE · 2007 to 2015
$3.3M
MENTORING IN CARDIOVASCULAR BIOLOGYP20GM103514 · NIGMS · LSU HEALTH SCIENCES CENTER · PI KAPUSTA, DANIEL R · 2012 to 2012
$2.0M
Myogenic stem cells in extraocular musclesR01AG035377 · NIA · UNIVERSITY OF WASHINGTON · PI YABLONKA-REUVENI, ZIPORA · 2009 to 2014
$1.6M
12/15-LIPOXYGENASE, INSULIN-LIKE GROWTH FACTOR-1 AND ATHEROSCLEROSISR21HL113705 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI SUKHANOV, SERGIY · 2013 to 2014
$399k
Intra-arterial delivery of skeletal muscle stem cellsR21AR057794 · NIAMS · UNIVERSITY OF WASHINGTON · PI YABLONKA-REUVENI, ZIPORA · 2010 to 2011
$395k
NCRR NIH HHS P20 RR018766NCRR NIH HHS P20-RR018766NHLBI NIH HHS R01 HL070241NHLBI NIH HHS R01-HL070241NHLBI NIH HHS R01 HL080682NHLBI NIH HHS R01-HL080682NHLBI NIH HHS R21 HL113705NIAMS NIH HHS R21 AR057794NIAMS NIH HHS R21AR057794NIA NIH HHS R01 AG021566NIA NIH HHS R01AG021566NIA NIH HHS R01 AG035377NIA NIH HHS R01AG035377NIGMS NIH HHS P20 GM103514NIGMS NIH HHS P20-GM103514NIGMS NIH HHS P30 GM103337NIGMS NIH HHS P30-GM103337NIGMS NIH HHS U54 GM104940NIGMS NIH HHS U54-GM104940
6 · The paper itself

Abstract

Cachexia is a serious complication of many chronic diseases, such as congestive heart failure (CHF) and chronic kidney disease (CKD). Although patients with advanced CHF or CKD often have increased angiotensin II (Ang II) levels and cachexia and Ang II causes skeletal muscle wasting in rodents, the potential effects of Ang II on muscle regeneration are unknown. Muscle regeneration is highly dependent on the ability of a pool of muscle stem cells (satellite cells) to proliferate and to repair damaged myofibers or form new myofibers. Here we show that Ang II reduced skeletal muscle regeneration via inhibition of satellite cell (SC) proliferation. Ang II reduced the number of regenerating myofibers and decreased expression of SC proliferation/differentiation markers (MyoD, myogenin, and active-Notch) after cardiotoxin-induced muscle injury in vivo and in SCs cultured in vitro. Ang II depleted the basal pool of SCs, as detected in Myf5(nLacZ/+) mice and by FACS sorting, and this effect was inhibited by Ang II AT1 receptor (AT1R) blockade and in AT1aR-null mice. AT1R was highly expressed in SCs, and Notch activation abrogated the AT1R-mediated antiproliferative effect of Ang II in cultured SCs. In mice that developed CHF postmyocardial infarction, there was skeletal muscle wasting and reduced SC numbers that were inhibited by AT1R blockade. Ang II inhibition of skeletal muscle regeneration via AT1 receptor-dependent suppression of SC Notch and MyoD signaling and proliferation is likely to play an important role in mechanisms leading to cachexia in chronic disease states such as CHF and CKD.

Indexed as

Angiotensin IIAnimalsCell CountCell Cycle ProteinsCell ProliferationDisease Models, AnimalHeart FailureMiceMuscle, SkeletalReceptor, Angiotensin, Type 1Receptors, NotchRegenerationSatellite Cells, Skeletal MuscleSignal TransductionWasting SyndromeAngiotensin IICell Cycle ProteinsReceptor, Angiotensin, Type 1Receptors, NotchAngiotensin IICachexiaMyocardial InfarctionRegenerationSatellite CellsSkeletal MuscleStem Cells

Identifiers

PMID23831688
PMCPMC3745329
OpenAlexW1974909493

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.