Evidence map›Paper›PMID 21235349›Full record

ReviewAntioxidants & redox signaling2011

Playing with cardiac "redox switches": the "HNO way" to modulate cardiac function.

Carlo G Tocchetti, Brian A Stanley, Christopher I Murray, Vidhya Sivakumaran, Sonia Donzelli, Daniele Mancardi, Pasquale Pagliaro, Wei Dong Gao, Jennifer van Eyk, David A Kass and 2 more

Open access · greenAbstract readReview
In one paragraph

Review in Antioxidants & redox signaling, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

49 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Proteomics of the heart.Physiological reviews · 2024
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Cardiovascular diagnosis and therapy · 2020
    Article
  12. Review
  13. Article
  14. Treatments targeting inotropy.European heart journal · 2019
    Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Review
  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

12 authors at 4 institutions in 3 countries.

Carlo G TocchettiDivision of Cardiology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA.
Brian A Stanley
Christopher I Murray
Vidhya Sivakumaran
Sonia Donzelli
Daniele Mancardi
Pasquale Pagliaro
Wei Dong Gao
Jennifer van Eyk
David A Kass
David A Wink
Nazareno Paolocci
Johns Hopkins University · USUniversity of Turin · ITNational Cancer Institute · USUniversität Hamburg · DE

Funding

Pathobiology of Cardiac Dyssynchrony &ResynchronizationP01HL077180 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KASS, DAVID ALAN · 2004 to 2014
$22.8M
STRUCTURE OF MITOCHONDRIAL K+ CHANNELSP01HL081427 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI VAN EYK, JENNIFER E · 2005 to 2009
$11.2M
Properties of redox modified NSAIDs in cancer prevention and treatmentZIABC010899 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WINK, DAVID · 2009 to 2025
$6.7M
CHemical Biology of Nitroxyl (HNO)ZIABC011190 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI WINK, DAVID · 2009 to 2025
$2.9M
Mechanisms Underlying Mitrochondrial Dysfunction in the Diabetic HeartR01HL091923 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI AKAR, FADI GABRIEL, AON, MIGUEL ANTONIO · 2009 to 2012
$1.9M
Nitroxyl cardiac effects are mediated by cAMP/PKA signalR01HL075265 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI PAOLOCCI, NAZARENO · 2005 to 2008
$1.5M
NHLBI NIH HHS HL075265NHLBI NIH HHS HL-077180NHLBI NIH HHS HL091923NHLBI NIH HHS P01-HL077180NHLBI NIH HHS P01-HL081427
6 · The paper itself

Abstract

The nitric oxide (NO(•)) sibling, nitroxyl or nitrosyl hydride (HNO), is emerging as a molecule whose pharmacological properties include providing functional support to failing hearts. HNO also preconditions myocardial tissue, protecting it against ischemia-reperfusion injury while exerting vascular antiproliferative actions. In this review, HNO's peculiar cardiovascular assets are discussed in light of its unique chemistry that distinguish HNO from NO(•) as well as from reactive oxygen and nitrogen species such as the hydroxyl radical and peroxynitrite. Included here is a discussion of the possible routes of HNO formation in the myocardium and its chemical targets in the heart. HNO has been shown to have positive inotropic/lusitropic effects under normal and congestive heart failure conditions in animal models. The mechanistic intricacies of the beneficial cardiac effects of HNO are examined in cellular models. In contrast to β-receptor/cyclic adenosine monophosphate/protein kinase A-dependent enhancers of myocardial performance, HNO uses its "thiophylic" nature as a vehicle to interact with redox switches such as cysteines, which are located in key components of the cardiac electromechanical machinery ruling myocardial function. Here, we will briefly review new features of HNO's cardiovascular effects that when combined with its positive inotropic/lusitropic action may render HNO donors an attractive addition to the current therapeutic armamentarium for treating patients with acutely decompensated congestive heart failure.

Indexed as

AnimalsHumansModels, BiologicalMyocardiumNitric Oxide SynthaseNitrogen OxidesOxidation-ReductionReactive Oxygen SpeciesReperfusion InjurySulfhydryl CompoundsNitric Oxide SynthaseNitrogen OxidesnitroxylReactive Oxygen SpeciesSulfhydryl Compounds

Identifiers

PMID21235349
PMCPMC3066693
OpenAlexW2064363834

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.