Literature DB >> 25503611

Effects of enzymatic degradation after loading in temporomandibular joint.

Y Asakawa-Tanne1, S Su1, R Kunimatsu1, N Hirose1, T Mitsuyoshi1, Y Okamoto1, E Tanaka2, K Tanne1, K Tanimoto3.   

Abstract

Synovial fluid of the joint decreases friction between the cartilage surfaces and reduces cartilage wear during articulation. Characteristic changes of synovial fluid have been shown in patients with osteoarthritis (OA) in the temporomandibular joint (TMJ). OA is generally considered to be induced by excessive mechanical stress. However, whether the changes in synovial fluid precede the mechanical overloading or vice versa remains unclear. In the present study, our purpose was to examine if the breakdown of joint lubrication affects the frictional properties of mandibular condylar cartilage and leads to subsequent degenerative changes in TMJ. We measured the frictional coefficient in porcine TMJ by a pendulum device after digestion with hyaluronidase (HAase) or trypsin. Gene expressions of interleukin-1β (IL-1β), cyclooxygenase-2 (COX-2), matrix metalloproteinases (MMPs), type II collagen, and histology were examined after prolonged cyclic loading by an active pendulum system. The results showed that the frictional coefficient increased significantly after HAase (35%) or trypsin (74%) treatment. Gene expression of IL-1β, COX-2, and MMPs-1, -3, and -9 increased significantly in enzyme-treated TMJs after cyclic loading. The increase in the trypsin-treated group was greater than that in the HAase-treated group. Type II collagen expression was reduced in both enzyme-treated groups. Histology revealed surface fibrillation and increased MMP-1 in the trypsin-treated group, as well as increased IL-1β in both enzyme-treated groups after cyclic loading. The findings demonstrated that the compromised lubrication in TMJ is associated with altered frictional properties and surface wear of condylar cartilage, accompanied by release of pro-inflammatory and matrix degradation mediators under mechanical loading. © International & American Associations for Dental Research 2014.

Entities:  

Keywords:  cyclic loading; hyaluronan; lubrication; matrix metalloproteases; osteoarthritis; superficial zone protein

Mesh:

Substances:

Year:  2014        PMID: 25503611      PMCID: PMC4438732          DOI: 10.1177/0022034514560588

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  32 in total

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Journal:  Arthritis Rheum       Date:  2012-02
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3.  Expressing human SHOX in Shox2SHOX KI/KI mice leads to congenital osteoarthritis‑like disease of the temporomandibular joint in postnatal mice.

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4.  Is quality of life affected by temporomandibular disorders?

Authors:  Débora de Melo Trize; Marcela Pagani Calabria; Solange de Oliveira Braga Franzolin; Carolina Ortigosa Cunha; Sara Nader Marta
Journal:  Einstein (Sao Paulo)       Date:  2018-11-29

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6.  The Antioxidant Resveratrol Protects against Chondrocyte Apoptosis by Regulating the COX-2/NF-κB Pathway in Created Temporomandibular Osteoarthritis.

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7.  ANGPTL2 Promotes Inflammation via Integrin α5β1 in Chondrocytes.

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8.  Gene Mutations Associated with Temporomandibular Joint Disorders: A Systematic Review.

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Journal:  OAlib       Date:  2015-06-03

9.  Lubricin in synovial fluid of mild and severe temporomandibular joint internal derangements.

Authors:  R Leonardi; R-E Perrotta; L-E Almeida; C Loreto; G Musumeci
Journal:  Med Oral Patol Oral Cir Bucal       Date:  2016-11-01

10.  TLR4 contributes to the damage of cartilage and subchondral bone in discectomy-induced TMJOA mice.

Authors:  Xin Liu; Heng-Xing Cai; Pin-Yin Cao; Yaping Feng; Heng-Hua Jiang; Li Liu; Jin Ke; Xing Long
Journal:  J Cell Mol Med       Date:  2020-09-11       Impact factor: 5.310

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