Evidence map›Paper›PMID 25394677›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2015

Resveratrol prevents pathological but not physiological cardiac hypertrophy.

Vernon W Dolinsky, Carrie-Lynn M Soltys, Kyle J Rogan, Anita Y M Chan, Jeevan Nagendran, Shaohua Wang, Jason R B Dyck

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

22 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
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  7. Article
  8. Linderae radix ethanol extract attenuates alcoholic liver injury via attenuating inflammation and regulating gut microbiota in rats.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2019
    Article
  9. Article
  10. Article
  11. miR-133: A Suppressor of Cardiac Remodeling?Frontiers in pharmacology · 2018
    Review
  12. Sirtinol abrogates late phase of cardiac ischemia preconditioning in rats.The journal of physiological sciences : JPS · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. New Treatment Strategies for Alcohol-Induced Heart Damage.International journal of molecular sciences · 2016
    Review
  18. Biology of the cardiac myocyte in heart disease.Molecular biology of the cell · 2016
    Review
  19. Review
  20. 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

7 authors at 1 institution in 1 country.

Vernon W DolinskyCardiovascular Research Centre, Faculty of Medicine and Dentistry, Mazankowski Alberta Heart Institute, University of Alberta, Edmonton, AB, Canada.
Carrie-Lynn M Soltys
Kyle J Rogan
Anita Y M Chan
Jeevan Nagendran
Shaohua Wang
Jason R B Dyck
University of Alberta · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

unlabelledThe mechanisms responsible for how resveratrol inhibits pathological left ventricular hypertrophy (LVH) but not physiological LVH have not been elucidated. Herein, we show that in rat cardiomyocytes, lower concentrations of resveratrol (0.1 and 1 μM) are efficient at selectively inhibiting important regulators involved in pathological LVH (such as nuclear factor of activated T cells (NFAT)) while not affecting pathways involved in physiological LVH (Akt and p70S6 kinase (p70S6K)). These differential responses are also observed in both mouse and rat models of in vivo physiological and pathological LVH. Interestingly, in all of the experiments involving a low concentration of resveratrol (1 μM), the observed effects on Akt, p70S6K, and NFAT were independent from AMP-activated protein kinase (AMPK) activation while these effects at higher concentrations of resveratrol (50 μM) were potentiated by AMPK activation. In summary, we show that resveratrol can concentration/dose selectively inhibit various pro-hypertrophic signaling pathways and that resveratrol has differential effects on the modification of these signaling cascades in response to pathological stimuli versus physiological stimuli. This has important clinical implications as our findings support the concept that resveratrol may be useful in the selective treatment of pathological LVH. KEY MESSAGE: Resveratrol differentially regulates pathological and physiological cardiac hypertrophy. Resveratrol dose selectively inhibits pathological cardiac signaling pathways. Resveratrol inhibits NFAT-dependent transcription. At low concentrations, effects of resveratrol are AMPK-independent. Resveratrol may be used to selectively treat pathological cardiac hypertrophy.

Indexed as

AMP-Activated Protein KinasesAnimalsAntioxidantsCells, CulturedExerciseHeart VentriclesHumansHypertrophy, Left VentricularInsulin-Like Growth Factor IMice, Inbred C57BLMyocytes, CardiacNFATC Transcription FactorsRatsResveratrolRibosomal Protein S6 Kinases, 70-kDaSignal TransductionAMP-Activated Protein KinasesAntioxidantsInsulin-Like Growth Factor INFATC Transcription FactorsResveratrolRibosomal Protein S6 Kinases, 70-kDaStilbenes

Identifiers

PMID25394677
OpenAlexW1990101410

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.