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Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count

Curcuma longa (turmeric) rhizomes contains curcumin, an active compound which possesses anti-inflammatory effects. Collagen-induced arthritis (CIA) is an accepted experimental animal model of rheumatoid arthritis. The present study aimed to observe the histological changes in the joints of experimen...

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Autores principales: Kamarudin, Taty Anna, Othman, Faizah, Mohd Ramli, Elvy Suhana, Md Isa, Nurismah, Das, Srijit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928023/
https://www.ncbi.nlm.nih.gov/pubmed/27366139
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author Kamarudin, Taty Anna
Othman, Faizah
Mohd Ramli, Elvy Suhana
Md Isa, Nurismah
Das, Srijit
author_facet Kamarudin, Taty Anna
Othman, Faizah
Mohd Ramli, Elvy Suhana
Md Isa, Nurismah
Das, Srijit
author_sort Kamarudin, Taty Anna
collection PubMed
description Curcuma longa (turmeric) rhizomes contains curcumin, an active compound which possesses anti-inflammatory effects. Collagen-induced arthritis (CIA) is an accepted experimental animal model of rheumatoid arthritis. The present study aimed to observe the histological changes in the joints of experimental arthritic rats treated with curcumin. Twenty four male Sprague-Dawley (approximately 7 weeks-old) rats were randomly divided into four groups. Three groups were immunized with 150 µg collagen. All rats with established CIA, with arthritis scores exceeding 1, were orally treated with betamethasone (0.5 mg/ml/kg body weight), curcumin (110 mg/ml/kg body weight) or olive oil (1.0 ml/kg body weight) daily, for two weeks. One remaining group was kept as normal control. Treatment with 110 mg/ml/kg curcumin showed significant mean differences in the average white blood cell (WBC) count (p<0.05), cell infiltration, bone and cartilage erosion scores (p<0.05) compared to the olive oil treated group. Pannus formation scores showed that curcumin supplementation successfully suppressed the pannus formation process that occurred in the articular cartilage of the CIA joints. The mean difference for histological scores for the curcumin group was insignificant compared to the betamethasone treated group. It is concluded that supplementation of curcumin has protective effect on the histopathological and degenerative changes in the joints of CIA rats which was at par with betamethasone.
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spelling pubmed-49280232016-06-30 Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count Kamarudin, Taty Anna Othman, Faizah Mohd Ramli, Elvy Suhana Md Isa, Nurismah Das, Srijit EXCLI J Original Article Curcuma longa (turmeric) rhizomes contains curcumin, an active compound which possesses anti-inflammatory effects. Collagen-induced arthritis (CIA) is an accepted experimental animal model of rheumatoid arthritis. The present study aimed to observe the histological changes in the joints of experimental arthritic rats treated with curcumin. Twenty four male Sprague-Dawley (approximately 7 weeks-old) rats were randomly divided into four groups. Three groups were immunized with 150 µg collagen. All rats with established CIA, with arthritis scores exceeding 1, were orally treated with betamethasone (0.5 mg/ml/kg body weight), curcumin (110 mg/ml/kg body weight) or olive oil (1.0 ml/kg body weight) daily, for two weeks. One remaining group was kept as normal control. Treatment with 110 mg/ml/kg curcumin showed significant mean differences in the average white blood cell (WBC) count (p<0.05), cell infiltration, bone and cartilage erosion scores (p<0.05) compared to the olive oil treated group. Pannus formation scores showed that curcumin supplementation successfully suppressed the pannus formation process that occurred in the articular cartilage of the CIA joints. The mean difference for histological scores for the curcumin group was insignificant compared to the betamethasone treated group. It is concluded that supplementation of curcumin has protective effect on the histopathological and degenerative changes in the joints of CIA rats which was at par with betamethasone. Leibniz Research Centre for Working Environment and Human Factors 2012-05-15 /pmc/articles/PMC4928023/ /pubmed/27366139 Text en Copyright © 2012 Kamarudin et al. http://www.excli.de/documents/assignment_of_rights.pdf This is an Open Access article distributed under the following Assignment of Rights http://www.excli.de/documents/assignment_of_rights.pdf. You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Kamarudin, Taty Anna
Othman, Faizah
Mohd Ramli, Elvy Suhana
Md Isa, Nurismah
Das, Srijit
Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
title Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
title_full Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
title_fullStr Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
title_full_unstemmed Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
title_short Protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
title_sort protective effect of curcumin on experimentally induced arthritic rats: detailed histopathological study of the joints and white blood cell count
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928023/
https://www.ncbi.nlm.nih.gov/pubmed/27366139
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