Evidence map›Paper›PMID 27293517›Full record

ArticleOxidative medicine and cellular longevity2016

Efficacy of Mitochondrial Antioxidant Plastoquinonyl-decyl-triphenylphosphonium Bromide (SkQ1) in the Rat Model of Autoimmune Arthritis.

Alexander A Andreev-Andrievskiy, Nataliya G Kolosova, Natalia A Stefanova, Maxim V Lovat, Maxim V Egorov, Vasily N Manskikh, Roman A Zinovkin, Ivan I Galkin, Anastasia S Prikhodko, Maxim V Skulachev and 1 more

Abstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

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  11. Mitochondria and sensory processing in inflammatory and neuropathic pain.Frontiers in pain research (Lausanne, Switzerland) · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Serum bilirubin and the risk of rheumatoid arthritis.Journal of clinical laboratory analysis · 2017
    Article
  17. 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

11 authors.

Alexander A Andreev-AndrievskiyInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia; Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia.
Nataliya G KolosovaInstitute of Cytology and Genetics, Novosibirsk, Russia.
Natalia A StefanovaInstitute of Cytology and Genetics, Novosibirsk, Russia.
Maxim V LovatInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia.
Maxim V EgorovInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia.
Vasily N ManskikhInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia.
Roman A ZinovkinInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia; Faculty of Biology, Lomonosov Moscow State University, Moscow, Russia; Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia.
Ivan I GalkinBelozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia.
Anastasia S PrikhodkoInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia.
Maxim V SkulachevInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia.
Alexander N LukashevInstitute of Mitoengineering, Lomonosov Moscow State University, Moscow, Russia; Martsinovsky Institute of Medical Parasitology and Tropical Medicine, Sechenov First Moscow State Medical University, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis is one of the most common autoimmune diseases. Many antioxidants have been tested in arthritis, but their efficacy was, at best, marginal. In this study, a novel mitochondria-targeted antioxidant, plastoquinonyl-decyl-triphenylphosphonium bromide (SkQ1), was tested in vivo to prevent and cure experimental autoimmune arthritis. In conventional Wistar rats, SkQ1 completely prevented the development of clinical signs of arthritis if administered with food before induction. Further, SkQ1 significantly reduced the fraction of animals that developed clinical signs of arthritis and severity of pathological lesions if administration began immediately after induction of arthritis or at the onset of first symptoms (day 14 after induction). In specific pathogen-free Wistar rats, SkQ1 administered via gavage after induction of arthritis did not reduce the fraction of animals with arthritis but decreased the severity of lesions upon pathology examination in a dose-dependent manner. Efficacious doses of SkQ1 were in the range of 0.25-1.25 nmol/kg/day (0.13-0.7 μg/kg/day), which is much lower than doses commonly used for conventional antioxidants. SkQ1 promoted apoptosis of neutrophils in vitro, which may be one of the mechanisms underlying its pharmacological activity. Considering its low toxicity and the wide therapeutic window, SkQ1 may be a valuable additional therapy for rheumatoid arthritis.

Indexed as

AnimalsAntioxidantsAntirheumatic AgentsApoptosisArthritis, ExperimentalCell LineCollagen Type IIDose-Response Relationship, DrugHumansJointsMitochondriaNeutrophilsOxidative StressPlastoquinoneRats, WistarTime Factors10-(6'-plastoquinonyl)decyltriphenylphosphoniumAntioxidantsAntirheumatic AgentsCollagen Type IIPlastoquinone

Identifiers

PMID27293517
PMCPMC4887630

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Registered trials

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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.