Evidence map›Paper›PMID 36296709›Full record

ArticleMolecules (Basel, Switzerland)2022

Combination Therapy of Carnosic Acid and Methotrexate Effectively Suppressed the Inflammatory Markers and Oxidative Stress in Experimental Arthritis.

Martin Chrastina, Silvester Poništ, Jaroslav Tóth, Szilvia Czigle, Ľudmila Pašková, Veronika Vyletelová, Karol Švík, Katarína Bauerová

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
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  9. Nutrients · 2023
    Article
  10. 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

8 authors at 2 institutions in 1 country.

Martin ChrastinaInstitute of Experimental Pharmacology and Toxicology, Centre of Experimental Medicine, Slovak Academy of Sciences, Dúbravská cesta 5826/9, SK-841 41 Bratislava, Slovakia.
Silvester PoništInstitute of Experimental Pharmacology and Toxicology, Centre of Experimental Medicine, Slovak Academy of Sciences, Dúbravská cesta 5826/9, SK-841 41 Bratislava, Slovakia.
Jaroslav TóthDepartment of Pharmacognosy and Botany, Faculty of Pharmacy, Comenius University Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.ORCID 0000-0002-6417-9586
Szilvia CzigleDepartment of Pharmacognosy and Botany, Faculty of Pharmacy, Comenius University Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.ORCID 0000-0002-4634-3311
Ľudmila PaškováDepartment of Cell and Molecular Biology of Drugs, Faculty of Pharmacy, Comenius University Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.ORCID 0000-0001-8732-7054
Veronika VyletelováDepartment of Cell and Molecular Biology of Drugs, Faculty of Pharmacy, Comenius University Bratislava, Odbojárov 10, SK-832 32 Bratislava, Slovakia.
Karol ŠvíkInstitute of Experimental Pharmacology and Toxicology, Centre of Experimental Medicine, Slovak Academy of Sciences, Dúbravská cesta 5826/9, SK-841 41 Bratislava, Slovakia.
Katarína BauerováInstitute of Experimental Pharmacology and Toxicology, Centre of Experimental Medicine, Slovak Academy of Sciences, Dúbravská cesta 5826/9, SK-841 41 Bratislava, Slovakia.
Comenius University Bratislava · SKSlovak Academy of Sciences · SK

Funding

Ministry of educatioon, science, research and sport of the Slovak Republic VEGA 1/0429/21Ministry of educatioon, science, research and sport of the Slovak Republic VEGA 2/0136*20Slovak Research and Development Agency 15-0308
6 · The paper itself

Abstract

backgroundCombination therapy with methotrexate (MTX) is the most common therapeutic strategy used for the treatment of patients with rheumatoid arthritis (RA). In this study, we combined the natural compound carnosic acid (CA) with MTX to reduce inflammation and oxidative stress in adjuvant arthritis (AA).

methodsAA was induced in 6-8 rats per group. MTX was administrated twice a week at a dose of 0.3 mg/kg b.w., while CA was administered daily at a dose of 100 mg/kg both in monotherapy and in combination with MTX. Plasma samples were collected on the 14th, 21st, and 28th day. Body weight and hind paw volume were measured once a week.

resultsWe found that, mainly, the CA + MTX combination significantly reduced the hind paw swelling, the levels of IL-17A, MMP-9, and MCP-1 in plasma, and GGT activity in joint homogenates. The mRNA expression of HO-1, catalase, and IL-1β in the liver were significantly improved by CA + MTX only. Our results indicate that adding CA to MTX treatment could be a good therapeutic option for patients suffering from RA.

conclusionsThe addition of CA to methotrexate treatment significantly improved its efficacy in decreasing the development of AA by inhibiting the markers of inflammation and oxidative stress.

Indexed as

Arthritis, ExperimentalArthritis, RheumatoidAbietanesAnimalsBiomarkersCatalaseDrug Therapy, CombinationInflammationInterleukin-17Matrix Metalloproteinase 9MethotrexateOxidative StressRatsRNA, MessengerAbietanesBiomarkersCatalaseInterleukin-17Matrix Metalloproteinase 9MethotrexateRNA, Messengersalvinadjuvant arthritisautoimmune diseasecarnosic acidcombination therapyinflammationmethotrexateoxidative stress

Identifiers

PMID36296709
PMCPMC9612293
OpenAlexW4307261872

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.