Evidence map›Paper›PMID 26894468›Full record

ReviewCurrent opinion in pharmacology2016

Mitochondrial redox status as a target for cardiovascular disease.

James W Walters, Deborah Amos, Kristeena Ray, Nalini Santanam

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.7field-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

23 citing papers in PubMed, 50 citations in OpenAlex.

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  7. Pyk2/MCU Pathway as a New Target for Reversing Atherosclerosis.Frontiers in cell and developmental biology · 2021
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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

4 authors at 2 institutions in 1 country.

James W WaltersSchool of Arts & Sciences, Bluefield State College, Basic Science Building B213, 219 Rock Street, Bluefield, WV 24701, USA.
Deborah AmosDepartment of Pharmacology, Physiology & Toxicology, Joan C Edwards School of Medicine, Marshall University, One John Marshall Dr, Huntington, WV 25755, USA.
Kristeena RayDepartment of Pharmacology, Physiology & Toxicology, Joan C Edwards School of Medicine, Marshall University, One John Marshall Dr, Huntington, WV 25755, USA.
Nalini SantanamDepartment of Pharmacology, Physiology & Toxicology, Joan C Edwards School of Medicine, Marshall University, One John Marshall Dr, Huntington, WV 25755, USA. Electronic address: santanam@marshall.edu.
Marshall University · USBluefield State College · US

Funding

WV INBRE: The Inhibitor of Growth Family Member 4 (ING4) inhibits L-Type Amino Acid Transporter 1 (LAT1) expression to suppress Breast CancerP20GM103434 · NIGMS · MARSHALL UNIVERSITY · PI GARY O RANKIN · 2012 to 2026
$61.1M
WVU &MU NEW FACULTY GRANTSP20RR016477 · NCRR · MARSHALL UNIVERSITY · PI RANKIN, GARY O · 2001 to 2011
$35.5M
ADAR2 and Adipose Dysfunction in AgingR15AG051062 · NIA · MARSHALL UNIVERSITY · PI SANTANAM, NALINI · 2015 to 2015
$357k
NCRR NIH HHS P20 RR016477NIA NIH HHS 1R15AG051062-01NIA NIH HHS R15 AG051062NIGMS NIH HHS P20 GM103434NIGMS NIH HHS P20GM103434
6 · The paper itself

Abstract

Mitochondria are major players in cellular energetics, oxidative stress and programmed cell death. Mitochondrial dynamics regulate and integrate these functions. Mitochondrial dysfunction is involved in cardiac hypertrophy, hypertension and myocardial ischemia/reperfusion injury. Reactive oxygen species generation is modulated by the fusion-fission pathway as well as key proteins such as sirtuins that act as metabolic sensors of cellular energetics. Mitochondrial redox status has thus become a good target for therapy against cardiovascular diseases. Recently, there is an influx of studies garnered towards assessing the beneficial effects of mitochondrial targeted antioxidants, drugs modulating the fusion-fission proteins, sirtuins, and other mitochondrial processes as potential cardio-protecting agents.

Indexed as

AnimalsAntioxidantsCardiotonic AgentsCardiovascular DiseasesHumansMitochondriaOxidation-ReductionOxidative StressReactive Oxygen SpeciesAntioxidantsCardiotonic AgentsReactive Oxygen Species

Identifiers

PMID26894468
PMCPMC4808324
OpenAlexW2281269668

What OpenQuestion holds

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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.