Literature DB >> 21681568

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

Yun-Sheng Ou1, Chao Tan, Hong An, Dian-Ming Jiang, Zheng-Xue Quan, Ke Tang, Xiao-Ji Luo.   

Abstract

The effects of long-term use of celecoxib, ibuprofen, and indomethacin on types I, II, and III collagen metabolism were evaluated in rat osteoarthritis (OA) model. One hundred and thirty wistar rats were randomly divided into 4 groups: the celecoxib group, the ibuprofen group, the indomethacin group, and the normal saline group. The osteoarthritis was induced by the excision of the left Achilles tendon. In the 3rd, 6th, and 9th month of treatment after surgically induced osteoarthritis, the articular cartilage was observed with microscope using HE staining. The expression of proteoglycans was semiquantified using toluidine blue staining. And, the expressions of types I, II, and III collagen in chondrocytes were examined using immunohistochemistry. The results suggested that celecoxib had no remarkable effects on the expression of types I, II, and III collagen. Ibuprofen upgraded the expression of types I, II, and III collagen and increased the synthesis of collagen. Indomethacin suppressed the expression of type II collagen and enhanced the expression of types I and III collagen. Therefore, during the long-term use of NSAIDs in osteoarthritis, celecoxib may have no remarkable influences on collagen metabolism of the articular cartilage and may be the ideal choice in the treatment of chronic destructive joint disease when anti-inflammatory drugs need to be used for a prolonged period. Ibuprofen may be unfavorable, and indomethacin may be harmful to collagen metabolism in OA treatment.

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Year:  2011        PMID: 21681568     DOI: 10.1007/s00296-011-1978-8

Source DB:  PubMed          Journal:  Rheumatol Int        ISSN: 0172-8172            Impact factor:   2.631


  19 in total

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  5 in total

Review 1.  Immune modulation to improve tissue engineering outcomes for cartilage repair in the osteoarthritic joint.

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Journal:  Tissue Eng Part B Rev       Date:  2014-08-04       Impact factor: 6.389

Review 2.  Molecular basis of intervertebral disc degeneration and herniations: what are the important translational questions?

Authors:  Tiffany Kadow; Gwendolyn Sowa; Nam Vo; James D Kang
Journal:  Clin Orthop Relat Res       Date:  2015-06       Impact factor: 4.176

3.  NSAID use in intervertebral disc degeneration: what are the effects on matrix homeostasis in vivo?

Authors:  Nicholas Vaudreuil; Tiffany Kadow; Takashi Yurube; Robert Hartman; Kevin Ngo; Qing Dong; Pedro Pohl; J Paulo Coelho; James Kang; Nam Vo; Gwendolyn Sowa
Journal:  Spine J       Date:  2017-04-14       Impact factor: 4.166

4.  Regulation of gene expression by MF63, a selective inhibitor of microsomal PGE synthase 1 (mPGES1) in human osteoarthritic chondrocytes.

Authors:  Lauri Tuure; Antti Pemmari; Mari Hämäläinen; Teemu Moilanen; Eeva Moilanen
Journal:  Br J Pharmacol       Date:  2020-08-10       Impact factor: 8.739

5.  Curcumin Inhibits Proliferation of Synovial Cells by Downregulating Expression of Matrix Metalloproteinase-3 in Osteoarthritis.

Authors:  Jian-Jun Zeng; Hai-Dong Wang; Zhong-Wei Shen; Xiao-Dong Yao; Cheng-Jun Wu; Tao Pan
Journal:  Orthop Surg       Date:  2018-12-17       Impact factor: 2.071

  5 in total

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