Evidence map›Paper›PMID 23792087›Full record

ReviewPharmacology & therapeutics2013

Multiplicity of effectors of the cardioprotective agent, diazoxide.

William A Coetzee

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Article
  6. Do KFrontiers in immunology · 2024
    Review
  7. KArhiv za farmaciju · 2024
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Mitochondrial connexin43 and mitochondrial KPflugers Archiv : European journal of physiology · 2023
    Article
  13. Article
  14. CL-705G: a novel chemical Kir6.2-specific KFrontiers in pharmacology · 2023
    Article
  15. Review
  16. Review
  17. Article
  18. iScience · 2022
    Article
  19. Editorial: Hypoxia in cardiovascular disease.Frontiers in cardiovascular medicine · 2022
    Article
  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

1 author at 1 institution in 1 country.

William A CoetzeeDepartment of Pediatrics, NYU School of Medicine, New York, NY 10016, United States; Department of Physiology & Neuroscience, NYU School of Medicine, New York, NY 10016, United States; Department of Biochemistry and Molecular Pharmacology, NYU School of Medicine, New York, NY 10016, United States. Electronic address: william.coetzee@nyu.edu.
New York University · US

Funding

Potassium Channels as Macromolecular ComplexesR01HL085820 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COETZEE, WILLIAM A, NEUBERT, THOMAS A · 2008 to 2013
$3.2M
KATP Channel Trafficking and CardioprotectionR01HL126905 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COETZEE, WILLIAM A · 2015 to 2018
$2.7M
Conditional knockout mice lacking K(ATP) channel subunitsR21HL093563 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI COETZEE, WILLIAM A · 2009 to 2010
$465k
NHLBI NIH HHS HL093563NHLBI NIH HHS R01 HL085820NHLBI NIH HHS R01 HL126905NHLBI NIH HHS R21 HL093563
6 · The paper itself

Abstract

Diazoxide has been identified over the past 50years to have a number of physiological effects, including lowering the blood pressure and rectifying hypoglycemia. Today it is used clinically to treat these conditions. More recently, another important mode of action emerged: diazoxide has powerful protective properties against cardiac ischemia. The heart has intrinsic protective mechanisms against ischemia injury; one of which is ischemic preconditioning. Diazoxide mimics ischemic preconditioning. The purpose of this treatise is to review the literature in an attempt to identify the many effectors of diazoxide and discuss how they may contribute to diazoxide's cardioprotective properties. Particular emphasis is placed on the concentration ranges in which diazoxide affects its different targets and how this compares with the concentrations commonly used to study cardioprotection. It is concluded that diazoxide may have several potential effectors that may potentially contribute to cardioprotection, including KATP channels in the pancreas, smooth muscle, endothelium, neurons and the mitochondrial inner membrane. Diazoxide may also affect other ion channels and ATPases and may directly regulate mitochondrial energetics. It is possible that the success of diazoxide lies in this promiscuity and that the compound acts to rebalance multiple physiological processes during cardiac ischemia.

Indexed as

AnimalsCardiotonic AgentsDiazoxideHumansInsulin-Secreting CellsKATP ChannelsMitochondriaMyocardial IschemiaMyocytes, Smooth MuscleSarcolemmaCardiotonic AgentsDiazoxideKATP Channels2,4-dinitrophenol5HD5-hydroxydecanoateATP-sensitive K(+) channelCardioprotectionDiazoxideDNPIPCI/R injuryIschemiaischemia/reperfusion injuryischemic preconditioningIschemic preconditioningK(ATP) channelK(ATP) channelsMitochondriamitochondrial membrane potentialreactive oxygen speciesROSSDHsuccinate dehydrogenaseΔΨm

Identifiers

PMID23792087
PMCPMC3795896
OpenAlexW2041149609

What OpenQuestion holds

Textmetadata
LicenceTDM
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.