Effect of N-Feruloylserotonin and Methotrexate on Severity of Experimental Arthritis and on Messenger RNA Expression of Key Proinflammatory Markers in Liver
Language English Country Egypt Media print-electronic
Document type Journal Article
PubMed
27556049
PubMed Central
PMC4983360
DOI
10.1155/2016/7509653
Knihovny.cz E-resources
- MeSH
- Arachidonate Lipoxygenases genetics metabolism MeSH
- Arthritis, Experimental drug therapy genetics pathology MeSH
- Biomarkers MeSH
- C-Reactive Protein MeSH
- Time Factors MeSH
- Cytokines blood genetics metabolism MeSH
- Liver drug effects metabolism MeSH
- Rats MeSH
- Inflammation Mediators * MeSH
- Methotrexate pharmacology MeSH
- Disease Models, Animal MeSH
- Organ Specificity MeSH
- Gene Expression Regulation drug effects MeSH
- Serotonin analogs & derivatives pharmacology MeSH
- Severity of Illness Index MeSH
- Transcriptome * MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Arachidonate Lipoxygenases MeSH
- Biomarkers MeSH
- C-Reactive Protein MeSH
- Cytokines MeSH
- Inflammation Mediators * MeSH
- Methotrexate MeSH
- N-feruloylserotonin MeSH Browser
- Serotonin MeSH
Rheumatoid arthritis (RA) is a chronic inflammatory disease, leading to progressive destruction of joints and extra-articular tissues, including organs such as liver and spleen. The purpose of this study was to compare the effects of a potential immunomodulator, natural polyphenol N-feruloylserotonin (N-f-5HT), with methotrexate (MTX), the standard in RA therapy, in the chronic phase of adjuvant-induced arthritis (AA) in male Lewis rats. The experiment included healthy controls (CO), arthritic animals (AA), AA given N-f-5HT (AA-N-f-5HT), and AA given MTX (AA-MTX). N-f-5HT did not affect the body weight change and clinical parameters until the 14th experimental day. Its positive effect was rising during the 28-day experiment, indicating a delayed onset of N-f-5HT action. Administration of either N-f-5HT or MTX caused reduction of inflammation measured as the level of CRP in plasma and the activity of LOX in the liver. mRNA transcription of TNF-α and iNOS in the liver was significantly attenuated in both MTX and N-f-5HT treated groups of arthritic rats. Interestingly, in contrast to MTX, N-f-5HT significantly lowered the level of IL-1β in plasma and IL-1β mRNA expression in the liver and spleen of arthritic rats. This speaks for future investigations of N-f-5HT as an agent in the treatment of RA in combination therapy with MTX.
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