Evidence map›Paper›PMID 28067251›Full record

ArticleScientific reports2017

Analgesic and Anti-Inflammatory Effects of the Novel Semicarbazide-Sensitive Amine-Oxidase Inhibitor SzV-1287 in Chronic Arthritis Models of the Mouse.

Ádám Horváth, Awt Menghis, Bálint Botz, Éva Borbély, Ágnes Kemény, Valéria Tékus, Janka Zsófia Csepregi, Attila Mócsai, Tamás Juhász, Róza Zákány and 5 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

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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

15 authors at 5 institutions in 3 countries.

Ádám HorváthDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Awt MenghisInstitute of Pharmaceutical Science, King's College London, London, United Kingdom.
Bálint BotzDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Éva BorbélyDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Ágnes KeményDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Valéria TékusDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Janka Zsófia CsepregiDepartment of Physiology &MTA-SE 'Lendület' Inflammation Physiology Research Group of the Hungarian Academy of Sciences, Semmelweis University, Budapest, Hungary.
Attila MócsaiDepartment of Physiology &MTA-SE 'Lendület' Inflammation Physiology Research Group of the Hungarian Academy of Sciences, Semmelweis University, Budapest, Hungary.
Tamás JuhászDepartment of Anatomy, Histology and Embryology, Medical School, University of Debrecen, Debrecen, Hungary.
Róza ZákányDepartment of Anatomy, Histology and Embryology, Medical School, University of Debrecen, Debrecen, Hungary.
Dóra BogdánDepartment of Organic Chemistry, Faculty of Pharmacology, Semmelweis University, Budapest, Hungary.
Péter MátyusDepartment of Organic Chemistry, Faculty of Pharmacology, Semmelweis University, Budapest, Hungary.
Julie KeebleInstitute of Pharmaceutical Science, King's College London, London, United Kingdom.
Erika PintérDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Zsuzsanna HelyesDepartment of Pharmacology and Pharmacotherapy, Medical School; János Szentágothai Research Centre &Centre for Neuroscience, University of Pécs, Pécs, Hungary.
Pharmac · NZSemmelweis University · HUUniversity of Pecs · HUKing's College London · GBUniversity of Debrecen · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Semicarbazide-sensitive amine oxidase (SSAO) catalyses oxidative deamination of primary amines. Since there is no data about its function in pain and arthritis mechanisms, we investigated the effects of our novel SSAO inhibitor SzV-1287 in chronic mouse models of joint inflammation. Effects of SzV-1287 (20 mg/kg i.p./day) were investigated in the K/BxN serum-transfer and complete Freund's adjuvant (CFA)-evoked active immunization models compared to the reference SSAO inhibitor LJP-1207. Mechanonociception was assessed by aesthesiometry, oedema by plethysmometry, clinical severity by scoring, joint function by grid test, myeloperoxidase activity by luminescence, vascular leakage by fluorescence in vivo imaging, histopathological changes by semiquantitative evaluation, and cytokines by Luminex assay. SzV-1287 significantly inhibited hyperalgesia and oedema in both models. Plasma leakage and keratinocyte chemoattractant production in the tibiotarsal joint, but not myeloperoxidase activity was significantly reduced by SzV-1287 in K/BxN-arthritis. SzV-1287 did not influence vascular and cellular mechanisms in CFA-arthritis, but significantly decreased histopathological alterations. There was no difference in the anti-hyperalgesic and anti-inflammatory actions of SzV-1287 and LJP-1207, but only SzV-1287 decreased CFA-induced tissue damage. Unlike SzV-1287, LJP-1207 induced cartilage destruction, which was confirmed in vitro. SzV-1287 exerts potent analgesic and anti-inflammatory actions in chronic arthritis models of distinct mechanisms, without inducing cartilage damage.

Indexed as

Amine Oxidase (Copper-Containing)Analgesics, Non-NarcoticAnimalsAnti-Inflammatory AgentsArthritisCells, CulturedChronic DiseaseDisease Models, AnimalDisease ProgressionFreund's AdjuvantHumansHydrazinesJointsMiceMice, Inbred StrainsMice, Transgenic3-(4,5-diphenyl-1,3-oxazol-2-yl)propanal oximeAmine Oxidase (Copper-Containing)Analgesics, Non-NarcoticAnti-Inflammatory AgentsFreund's AdjuvantHydrazinesN'-(2-phenylallyl)hydrazineOxazolesOximes

Identifiers

PMID28067251
PMCPMC5220351
OpenAlexW2571440756

What OpenQuestion holds

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LicenceCC BY
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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.