Literature DB >> 12096231

Selective COX-2 inhibition prevents proinflammatory cytokine-induced cartilage damage.

S C Mastbergen1, F P J G Lafeber, J W J Bijlsma.   

Abstract

OBJECTIVES: This study evaluated the in vitro effect of the selective cyclooxygenase-2 (COX) inhibitor celecoxib on cartilage matrix turnover under normal and inflammatory conditions.
METHODS: Healthy human articular cartilage tissue alone, in co-culture with peripheral blood mononuclear cells (PBMC) or in the presence of interleukin 1 (IL-1beta) plus tumour necrosis factor alpha (TNF-alpha) was cultured for 7 days in the presence of celecoxib. Changes in cartilage matrix turnover were measured.
RESULTS: No direct effects of celecoxib on healthy normal cartilage were found. Both PBMC and IL-1beta plus TNF-alpha induced strong inhibition of cartilage proteoglycan synthesis and significant enhancement of the release of proteoglycans, diminishing proteoglycan content. Celecoxib was able to reverse these adverse effects up to complete normalization.
CONCLUSIONS: The results suggest that, under the influence of inflammation, COX-2 is up-regulated, which results in disturbance of cartilage matrix turnover. Celecoxib, by diminishing COX-2 activity, prevents these adverse effects without having a direct effect on healthy cartilage.

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Year:  2002        PMID: 12096231     DOI: 10.1093/rheumatology/41.7.801

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  20 in total

1.  Biomechanical signals suppress proinflammatory responses in cartilage: early events in experimental antigen-induced arthritis.

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Journal:  Rheumatol Int       Date:  2006-01-26       Impact factor: 2.631

Review 3.  COX-2 inhibitors as adjunctive therapy in schizophrenia: rationale for use and evidence to date.

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Journal:  CNS Drugs       Date:  2005       Impact factor: 5.749

4.  Radiation synovectomy with yttrium-90 for persisting arthritis has direct harmful effects on human cartilage that cannot be prevented by co-administration of glucocorticoids: an in vitro study.

Authors:  Z N Jahangier; K M G Jacobs; J W J Bijlsma; F P J G Lafeber
Journal:  Ann Rheum Dis       Date:  2006-04-27       Impact factor: 19.103

5.  The effects of NSAIDs on types I, II, and III collagen metabolism in a rat osteoarthritis model.

Authors:  Yun-Sheng Ou; Chao Tan; Hong An; Dian-Ming Jiang; Zheng-Xue Quan; Ke Tang; Xiao-Ji Luo
Journal:  Rheumatol Int       Date:  2011-06-17       Impact factor: 2.631

6.  The influence of scaffold material on chondrocytes under inflammatory conditions.

Authors:  Heenam Kwon; Lin Sun; Dana M Cairns; Roshni S Rainbow; Rucsanda C Preda; David L Kaplan; Li Zeng
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7.  Endoplasmic reticulum stress induces the expression of COX-2 through activation of eIF2α, p38-MAPK and NF-κB in advanced glycation end products stimulated human chondrocytes.

Authors:  Zafar Rasheed; Tariq M Haqqi
Journal:  Biochim Biophys Acta       Date:  2012-09-06

8.  Selective COX-2 inhibitor ameliorates osteoarthritis by repressing apoptosis of chondrocyte.

Authors:  Yunsheng Ou; Chao Tan; Hong An; Dianming Jiang; Zhengxue Quan; Ke Tang; Xiaoji Luo
Journal:  Med Sci Monit       Date:  2012-06

9.  Antirheumatic drug response signatures in human chondrocytes: potential molecular targets to stimulate cartilage regeneration.

Authors:  Kristin Andreas; Thomas Häupl; Carsten Lübke; Jochen Ringe; Lars Morawietz; Anja Wachtel; Michael Sittinger; Christian Kaps
Journal:  Arthritis Res Ther       Date:  2009-02-03       Impact factor: 5.156

10.  Meta-analysis Comparing Celecoxib with Diclofenac Sodium in Patients with Knee Osteoarthritis.

Authors:  Hetao Huang; Minghui Luo; Haodong Liang; Jianke Pan; Weiyi Yang; Lingfeng Zeng; Guihong Liang; Senrong Hou; Jinlong Zhao; Jun Liu
Journal:  Pain Med       Date:  2021-02-23       Impact factor: 3.750

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