NFkB and MMP-13 expression in condylar cartilage of temporomandibular joint with occlusal disharmony in vivo
Downloads
Background: Temporomandibular disorder (TMD) is a collection of symptoms that causes pain and disturbs a person's life quality. One of the trigger factors is mechanical overloading. Mechanical overloading in occlusal disharmony conditions will lead to an inflammatory reaction in the temporomandibular joint (TMJ). This condition will induce nuclear factor Kappa Beta(NFkB) activation to transcribe proinflammatory cytokines and matrix metalloproteinase-13 (MMP13) and will also degrade condylar cartilage as a major factor in strengthening the TMJ. Purpose:The aim of this study was to analyze the expression of NFkB and MMP13 in the condylar cartilage of TMJ with occlusal disharmony. Methods: This research was an experimental study with post-test-only control group design. Twenty Rats (Rattus norvegicus) were divided into four groups: One control group without any intervention and three experimental groups. Occlusal-reducing intervention was due on the right molar ofthe experimental groups, which were divided into the 7th, 14th, and 21st days. Immunohistochemical staining was performed to determine the expression of NFkB and MMP13 in the condylar cartilage. The data were analyzed by using the Welch test and independent t-test.Results: There were significant differences in NFkB and MMP13 expression between the control and experimentexperimentalgroups (p<0.05). NFkB expression increased on the 7th, 14th, and 21st days of observation. The MMP13 expression showed a significant difference between the control and experimental groups (p<0.05).Conclusion:Occlusal disharmony increases NFkB and MMP13 expression and could affect TMJ integrity and induce TMD. These findings are important for describing the mechanism of TMJ damage and developing potential alternative therapies to prevent further TMD.
Downloads
Ogura N, Kondoh T. Molecular aspects in inflammatory events of temporomandibular joint: Microarray-based identification of mediators. Jpn Dent Sci Rev. 2015; 51(1): 10–24. doi: https://doi.org/10.1016/j.jdsr.2014.09.001
Chairunnisa R, Fadilla SD. Effectiveness of telemedicine approach as a treatment to reduce severity of temporomandibular disorders. Dent J. 2022; 55(4): 204–8. doi: https://doi.org/10.20473/j.djmkg.v55.i4.p204-208
Marpaung C, van Selms MKA, Lobbezoo F. Prevalence and risk indicators of pain"related temporomandibular disorders among Indonesian children and adolescents. Community Dent Oral Epidemiol. 2018; 46(4): 400–6. doi: https://doi.org/10.1111/cdoe.12382
Bugaighis I, Elgehani R, Orafi M, Elatrash A. The prevalence of temporomandibular disorders among a group of libyan dental students. Libyan Int Med Univ J. 2017; 2(1): 64–73. doi: https://doi.org/10.21502/limuj.009.02.2017
Dibello V, Panza F, Mori G, Ballini A, Di Cosola M, Lozupone M, Dibello A, Santarcangelo F, Vertucci V, Dioguardi M, Cantore S. Temporomandibular disorders as a risk factor for suicidal behavior: A systematic review. J Pers Med. 2022; 12(11): 1782. doi: https://doi.org/10.3390/jpm12111782
DzingutÄ— A, PileiÄikienÄ— G, BaltruÅ¡aitytÄ— A, Skirbutis G. Evaluation of the relationship between the occlusion parameters and symptoms of the temporomandibular joint disorder. Acta medica Litu. 2017; 24(3): 167–75. doi: https://doi.org/10.6001/actamedica.v24i3.3551
Al-Ani Z. Occlusion and temporomandibular disorders: A long-standing controversy in dentistry. Prim Dent J. 2020; 9(1): 43–8. doi: https://doi.org/10.1177/2050168420911029
Cordray FE. The telationship between ccclusion and TMD. Open J Stomatol. 2017; 07(01): 35–80. doi: https://doi.org/10.4236/ojst.2017.71003
Ekuni D, Yoneda T, Endo Y, Kasuyama K, Irie K, Mizutani S, Azuma T, Tomofuji T, Morita M. Occlusal disharmony accelerates the initiation of atherosclerosis in apoE knockout rats. Lipids Health Dis. 2014; 13(1): 144. doi: https://doi.org/10.1186/1476-511X-13-144
Kartha S, Zhou T, Granquist EJ, Winkelstein BA. Development of a rat model of mechanically induced tunable pain and associated temporomandibular joint responses. J Oral Maxillofac Surg. 2016; 74(1): 54.e1-54.e10. doi: https://doi.org/10.1016/j.joms.2015.09.005
Lin X, Xie J, Sun S, Ren X, Kong J, Ji P. Toll-like receptor 4 (TLR4) stimulates synovial injury of temporomandibular joint in rats through the activation of p38 mitogen-activated protein kinase (MAPK) signaling pathway. Med Sci Monit. 2018; 24: 4405–12. doi: https://doi.org/10.12659/MSM.908526
Watanabe S, Ogura N, Akutsu M, Kawashima M, Hattori T, Yano T, Ito K, Kondoh T. Interleukin-1β and tumor necrosis Factor-α synergistically induce expression of colony stimulating factors in synovial fibroblasts from the human temporomandibular joint. Int J Oral-Medical Sci. 2017; 15(3–4): 74–84. doi: https://doi.org/10.5466/ijoms.15.74
Chen Y-J, Chan D-C, Chiang C-K, Wang C-C, Yang T-H, Lan K-C, Chao S-C, Tsai K-S, Yang R-S, Liu S-H. Advanced glycation end-products induced VEGF production and inflammatory responses in human synoviocytes via RAGE-NF-κB pathway activation. J Orthop Res. 2016; 34(5): 791–800. doi: https://doi.org/10.1002/jor.23083
Perotto JH, Camejo F de A, Doetzer AD, Almeida LE, Azevedo M, Olandoski M, Noronha L, Trevilatto PC. Expression of MMP-13 in human temporomandibular joint disc derangement and osteoarthritis. Cranio®. 2018; 36(3): 161–6. doi: https://doi.org/10.1080/08869634.2017.1315511
Ogston SA, Lemeshow S, Hosmer DW, Klar J, Lwanga SK. Adequacy of sample size in health studies. Biometrics. 1991; 47(1): 347. doi: https://doi.org/10.2307/2532527
Long H-Q, Tian P-F, Guan Y-X, Liu L-X, Wu X-P, Li B. Expression of Ihh signaling pathway in condylar cartilage after bite-raising in adult rats. J Mol Histol. 2019; 50(5): 459–70. doi: https://doi.org/10.1007/s10735-019-09840-0
Xu L, Sun C, Zhang S, Xu X, Zhai L, Wang Y, Wang S, Liu Z, Cheng H, Xiao M, Tao R, Zhang D. Sam68 promotes NF-κB activation and apoptosis signaling in articular chondrocytes during osteoarthritis. Inflamm Res. 2015; 64(11): 895–902. doi: https://doi.org/10.1007/s00011-015-0872-3
Barnabei L, Laplantine E, Mbongo W, Rieux-Laucat F, Weil R. NF-κB: At the borders of autoimmunity and inflammation. Front Immunol. 2021; 12: 1–27. doi: https://doi.org/10.3389/fimmu.2021.716469
Hutami IR, Tanaka E, Izawa T. Crosstalk between Fas and S1P1 signaling via NF-kB in osteoclasts controls bone destruction in the TMJ due to rheumatoid arthritis. Jpn Dent Sci Rev. 2019; 55(1): 12–9. doi: https://doi.org/10.1016/j.jdsr.2018.09.004
Yuan J, Ding W, Wu N, Jiang S, Li W. Protective effect of genistein on condylar cartilage through downregulating NF- κ B expression in experimentally created osteoarthritis rats. Biomed Res Int. 2019; 2019: 1–6. doi: https://doi.org/10.1155/2019/2629791
Pribadi N, Rahmawati R, Rukmo M, Tandadjaja AK, Kurniawan HJ, Hadi RP. The expression of nuclear factor of activated T cell c1 and receptor activator of nuclear factor kappa β induced by Enterococcus faecalis in osteoclastogenesis (laboratory experiment on Wistar rats). Dent J. 2019; 52(4): 172–6. doi: https://doi.org/10.20473/j.djmkg.v52.i4.p172-176
Izawa T, Mori H, Shinohara T, Mino-Oka A, Hutami IR, Iwasa A, Tanaka E. Rebamipide attenuates mandibular condylar degeneration in a murine model of TMJ-OA by mediating a chondroprotective effect and by downregulating RANKL-mediated osteoclastogenesis. Tang C-H, editor. PLoS One. 2016; 11(4): e0154107. doi: https://doi.org/10.1371/journal.pone.0154107
Almeida LE, Hresko K, Sorenson A, Butcher S, Tayebi L, Leonardi R, Loreto C, Bosio J, Camejo F, Doetzer A. Immunohistochemical expression of TLR-4 in temporomandibular joint dysfunction. Cranio®. 2019; 37(5): 323–8. doi: https://doi.org/10.1080/08869634.2018.1446770
Liu W, Sun Y, He Y, Zhang H, Zheng Y, Yao Y, Zhang Z. IL-1β impedes the chondrogenic differentiation of synovial fluid mesenchymal stem cells in the human temporomandibular joint. Int J Mol Med. 2017; 39(2): 317–26. doi: https://doi.org/10.3892/ijmm.2016.2832
Izach AI, Christnawati C, Susantyo D. The effects of unilateral posterior crossbite toward the superficial masseter and anterior temporalis on muscle activity during mastication: A surface electromyographic study. Dent J. 2022; 55(1): 38–43. doi: https://doi.org/10.20473/j.djmkg.v55.i1.p38-43
Momcheva I, Kazmin I, Hristova S, Madgova V. The role of inflammation in the pathogenesis of osteoarthritis. Rheumatol. 2021; 29(2): 56–60. web: https://www.rheumatologybg.org/journal/index.php?journal=revmatologiia&page=article&op=view&path%5B%5D=97
Li H, Wang D, Yuan Y, Min J. New insights on the MMP-13 regulatory network in the pathogenesis of early osteoarthritis. Arthritis Res Ther. 2017; 19(1): 248. doi: https://doi.org/10.1186/s13075-017-1454-2
Asakawa-Tanne Y, Su S, Kunimatsu R, Hirose N, Mitsuyoshi T, Okamoto Y, Tanaka E, Tanne K, Tanimoto K. Effects of enzymatic degradation after loading in temporomandibular joint. J Dent Res. 2015; 94(2): 337–43. doi: https://doi.org/10.1177/0022034514560588
Shrivastava M, Battaglino R, Ye L. A comprehensive review on biomarkers associated with painful temporomandibular disorders. Int J Oral Sci. 2021; 13(1): 23. doi: https://doi.org/10.1038/s41368-021-00129-1
Ishizuka Y, Shibukawa Y, Nagayama M, Decker R, Kinumatsu T, Saito A, Pacifici M, Koyama E. TMJ degeneration in SAMP8 mice is accompanied by deranged Ihh signaling. J Dent Res. 2014; 93(3): 281–7. doi: https://doi.org/10.1177/0022034513519649
Hartono CK, Hendrijantini N, Soekobagiono. Bilateral mandibular posterior edentulous rehabilitation for unstable occlusion patient with bilateral attachment retained mandibular removable partial denture. Acta Med Philipp. 2019; 53(6): 547–57. doi: https://doi.org/10.47895/amp.v53i6.709
Herm L, Haxhia A, de Alcantara Camejo F, Tayebi L, Almeida LE. Matrix metalloproteinases and temporomandibular joint disorder: A review of the literature. Appl Sci. 2019; 9(21): 4508. doi: https://doi.org/10.3390/app9214508
Copyright (c) 2024 Dental Journal
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.
- Every manuscript submitted to must observe the policy and terms set by the Dental Journal (Majalah Kedokteran Gigi).
- Publication rights to manuscript content published by the Dental Journal (Majalah Kedokteran Gigi) is owned by the journal with the consent and approval of the author(s) concerned.
- Full texts of electronically published manuscripts can be accessed free of charge and used according to the license shown below.
- The Dental Journal (Majalah Kedokteran Gigi) is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License