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Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats

In the present study, we evaluated the effects of individual administration of methionine or glucosamine (GlcN) and compared with the combined administration of methionine and GlcN on the adjuvant arthritis model of rheumatoid arthritis in rats. Adjuvant arthritis was induced in female Lewis rats by...

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Autores principales: YAMAGISHI, YOSHIE, IGARASHI, MAMORU, SUZUKI, ATSUKO, SUGURO, SHIORI, HIRANO, SHIN-ICHI, NAGAOKA, ISAO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501438/
https://www.ncbi.nlm.nih.gov/pubmed/23170118
http://dx.doi.org/10.3892/etm.2012.668
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author YAMAGISHI, YOSHIE
IGARASHI, MAMORU
SUZUKI, ATSUKO
SUGURO, SHIORI
HIRANO, SHIN-ICHI
NAGAOKA, ISAO
author_facet YAMAGISHI, YOSHIE
IGARASHI, MAMORU
SUZUKI, ATSUKO
SUGURO, SHIORI
HIRANO, SHIN-ICHI
NAGAOKA, ISAO
author_sort YAMAGISHI, YOSHIE
collection PubMed
description In the present study, we evaluated the effects of individual administration of methionine or glucosamine (GlcN) and compared with the combined administration of methionine and GlcN on the adjuvant arthritis model of rheumatoid arthritis in rats. Adjuvant arthritis was induced in female Lewis rats by injecting Freund’s complete adjuvant (FCA) into the right hind paws, and methionine (200 mg/kg body weight/day) and/or GlcN (400 mg/kg/day) were orally administered for 21 days. The progression of the adjuvant arthritis was clinically evaluated for characteristic signs and symptoms by employing an arthritis score. The administration of methionine combined with GlcN suppressed the swelling of FCA-uninjected left hind paws and the arthritis score. Additionally, histopathological examination revealed that the combined administration of methionine and GlcN markedly suppressed synovial hyperplasia and the destruction of the cartilage surface and articular meniscus of the knee joints of FCA-injected right hind paws. Furthermore, combined methionine and GlcN administration suppressed the increase in the levels of nitric oxide, prostaglandin E(2) and hyaluronic acid in the plasma of rats with adjuvant arthritis. By contrast, individual administration of methionine or GlcN suppressed arthritis only slightly. These observations suggest that the combined administration of methionine and GlcN is more effective compared with individual administrations of methionine or GlcN in suppressing the progression of adjuvant arthritis (identified as swelling of joints and arthritis score), possibly by synergistically inhibiting synovial inflammation (identified as synovial hyperplasia and the destruction of the cartilage surface and articular meniscus) and the production of inflammatory mediators.
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spelling pubmed-35014382013-10-01 Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats YAMAGISHI, YOSHIE IGARASHI, MAMORU SUZUKI, ATSUKO SUGURO, SHIORI HIRANO, SHIN-ICHI NAGAOKA, ISAO Exp Ther Med Articles In the present study, we evaluated the effects of individual administration of methionine or glucosamine (GlcN) and compared with the combined administration of methionine and GlcN on the adjuvant arthritis model of rheumatoid arthritis in rats. Adjuvant arthritis was induced in female Lewis rats by injecting Freund’s complete adjuvant (FCA) into the right hind paws, and methionine (200 mg/kg body weight/day) and/or GlcN (400 mg/kg/day) were orally administered for 21 days. The progression of the adjuvant arthritis was clinically evaluated for characteristic signs and symptoms by employing an arthritis score. The administration of methionine combined with GlcN suppressed the swelling of FCA-uninjected left hind paws and the arthritis score. Additionally, histopathological examination revealed that the combined administration of methionine and GlcN markedly suppressed synovial hyperplasia and the destruction of the cartilage surface and articular meniscus of the knee joints of FCA-injected right hind paws. Furthermore, combined methionine and GlcN administration suppressed the increase in the levels of nitric oxide, prostaglandin E(2) and hyaluronic acid in the plasma of rats with adjuvant arthritis. By contrast, individual administration of methionine or GlcN suppressed arthritis only slightly. These observations suggest that the combined administration of methionine and GlcN is more effective compared with individual administrations of methionine or GlcN in suppressing the progression of adjuvant arthritis (identified as swelling of joints and arthritis score), possibly by synergistically inhibiting synovial inflammation (identified as synovial hyperplasia and the destruction of the cartilage surface and articular meniscus) and the production of inflammatory mediators. D.A. Spandidos 2012-10 2012-08-16 /pmc/articles/PMC3501438/ /pubmed/23170118 http://dx.doi.org/10.3892/etm.2012.668 Text en Copyright © 2012, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
YAMAGISHI, YOSHIE
IGARASHI, MAMORU
SUZUKI, ATSUKO
SUGURO, SHIORI
HIRANO, SHIN-ICHI
NAGAOKA, ISAO
Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
title Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
title_full Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
title_fullStr Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
title_full_unstemmed Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
title_short Evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
title_sort evaluation of the effect of methionine and glucosamine on adjuvant arthritis in rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501438/
https://www.ncbi.nlm.nih.gov/pubmed/23170118
http://dx.doi.org/10.3892/etm.2012.668
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