Effects of Locally Delivered Morin Hydrate on Iodoacetate-induced Temporomandibular Joint Osteoarthritis in Rats

Authors

DOI:

https://doi.org/10.14295/bds.2020.v23i4.1904

Abstract

Objectives: morin hydrate has been reported to possess many beneficial pharmacological potentialities including antioxidant and anti-osteoarthritic effects. The antiosteoarthritic properties of locally administrated morin have not been investigated. The objective of this study is to evaluate the locally delivered morin on the temporomandibular joint osteoarthritis in rat.  Materials and methods: thirty young adult female Sprague Dawley rats were randomly arranged into three groups; control, osteoarthritis and osteoarthritis with morin. Both the iodoacetate for osteoarthritis induction and morin hydrate therapy were delivered unilaterally via intra-articular route. Results: morin reduced osteoarthritis manifestations with prominent thickening of both condylar fibrous layer and articular disc accompanied with discal cells hypertrophy that ultimately acquired chondrocytes features. The condylar cartilage matrix showed enhancement of extracellular matrix production with morin administration. Discussion: the present study has elucidated antiosteoarthritic effect of intraarticular injection of morin hydrate. Although morin has managed to prevent the propagation and advancing some of the recorded osteoarthritic manifestations; however, it showed some failure in managing others. The administration of morin hydrate modulated the structure of the joint rather than restore it back to its typical configuration. Conclusion: the morin hydrate administration to osteoarthritic animals showed relieve in some of osteoarthritic features and modulated the structure of some joint components to compensate the unhandled manifestations.

KEYWORDS

Iodoacetate; Morin; Osteoarthritis; OARSI Score;  Temporomandibular joint.

References

Liu F, Steinkeler A. Epidemiology, diagnosis, and treatment of temporomandibular disorders. Dent Clin North Am. 2013 Jul;57(3):465–79. doi:10.1016/j.cden.2013.04.006

Boyan BD, Tosi LL, Coutts RD, Enoka RM, Hart DA, Nicolella DP, et al. Addressing the gaps: sex differences in osteoarthritis of the knee. Biol Sex Differ. 2013 Feb 4;4(1):4. doi: 10.1186/2042-6410-4-4

Tanaka E, Detamore MS, Mercuri LG. Degenerative disorders of the temporomandibular joint: etiology, diagnosis, and treatment. J Dent Res. 2008;87(4):296–307. doi:10.1177/154405910808700406

Matsumoto R, Ioi H, Goto TK, Hara A, Nakata S, Nakasima A, et al. Relationship between the unilateral TMJ osteoarthritis/osteoarthrosis, mandibular asymmetry and the EMG activity of the masticatory muscles: a retrospective study. J Oral Rehabil. 2010; 37(2):85–92. doi:10.1111/j.1365-2842.2009.02026.x

Krisjane Z, Urtane I, Krumina G, Neimane L, Ragovska I. The prevalence of TMJ osteoarthritis in asymptomatic patients with dentofacial deformities: a cone-beam CT study. Int J Oral Maxillofac Surg. 2012;41(6):690–5. doi: 10.1016/j.ijom.2012.03.006

Wang XD, Zhang JN, Gan YH, Zhou YH. Current understanding of pathogenesis and treatment of TMJ osteoarthritis. J Dent Res. 2015;94(5):666-73. doi:10.1177/0022034515574770

Kuyinu EL, Narayanan G, Nair LS, Laurencin CT. Animal models of osteoarthritis: classification, update, and measurement of outcomes. J Orthop Surg Res. 2016; 11:19. doi: 10.1186/s13018-016-0346-5

Miyamoto S, Nakamura J, Ohtori S, Orita S, Omae T, Nakajima T, et al. Intra-articular injection of mono-iodoacetate induces osteoarthritis of the hip in rats. BMC Musculoskelet Disord. 2016 Mar; 18;17:132. doi: 10.1186/s12891-016-0985-z

Pitcher T, Sousa-Valente J, Malcangio M. The Monoiodoacetate Model of Osteoarthritis Pain in the Mouse. J Vis Exp. 2016 May;(111):53746. doi:10.3791/53746

Guingamp C, Gegout-Pottie P, Philippe L, Terlain B, Netter P, Gillet P. Mono-iodoacetate-induced experimental osteoarthritis: a dose-response study of loss of mobility, morphology, and biochemistry. Arthritis Rheum. 1997;40(9):1670–9. doi:10.1002/art.1780400917

Guzman RE, Evans MG, Bove S, Morenko B, Kilgore K. Mono-iodoacetate-induced histologic changes in subchondral bone and articular cartilage of rat femorotibial joints: an animal model of osteoarthritis. Toxicol Pathol. 2003;31(6):619–24. doi:10.1080/01926230390241800

Gutiérrez RM, Mitchell S, Solis RV. Psidium guajava: a review of its traditional uses, phytochemistry and pharmacology. J Ethnopharmacol. 2008;117(1):1–27. doi:10.1016/j.jep.2008.01.025

Yue M, Zeng N, Xia Y, Wei Z, Dai Y. Morin exerts anti-arthritic effects by attenuating synovial angiogenesis via activation of peroxisome proliferator activated receptor-γ. Mol Nutr Food Res. 2018;62(21):e1800202. doi:10.1002/mnfr.201800202

Chen WP, Hu PF, Bao JP, Wu LD. Morin exerts anti-osteoarthritic properties: an in vitro and in vivo study. Exp Biol Med. 2012; 237: 380–6. doi: 10.1258/ebm.2011.011271

Pufe T, Harde V, Petersen W, Goldring MB, Tillmann B, Mentlein R. Vascular endothelial growth factor (VEGF) induces matrix metalloproteinase expression in immortalized chondrocytes. J Pathol. 2004;202(3):367-74. doi:10.1002/path.1527

Pritzker KPH, Gay S, Jimenez SA, Ostergaard K, Pelletier JP, Revell PA, et al. Osteoarthritis cartilage histopathology: grading and staging. Osteoarthritis Cartilage. 2006;14(1):13-29. doi:10.1016/j.joca.2005.07.014

Wang XD, Kou XX, He DQ, Zeng MM, Meng Z, Bi RY, et al. Progression of cartilage degradation, bone resorption and pain in rat temporomandibular joint osteoarthritis induced by injection of iodoacetate. PLoS One. 2012; 7(9):e45036. doi: 10.1371/journal.pone.0045036

Zeng N, Tong B, Zhang X, Dou Y, Wu X, Xia Y, et al. Antiarthritis Effect of Morin is Associated with Inhibition of Synovial Angiogensis. Drug Dev Res. 2015 ; 76(8):463-73. doi: 10.1002/ddr.21282

Walter JB, Hamilton MC, Israel MS. Principles of pathology for dental students. 3rd ed. Edinburgh: Churchill Livingstone; 1990. p. 464-5

Wang XD, Kou XX, Meng Z, Bi RY, Liu Y, Zhang JN, et al. Estrogen aggravates iodoacetate-induced temporomandibular joint osteoarthritis. J Dent Res. 2013 Oct;92(10):918-24. doi: 10.1177/0022034513501323

Heijink A, Gomoll AH, Madry H, Drobnič M, Filardo G, Espregueira-Mendes J, et al. Biomechanical considerations in the pathogenesis of osteoarthritis of the knee. Knee Surg Sports Traumatol Arthrosc. 2012 Mar;20(3):423–35. doi:10.1007/s00167-011-1818-0

Janusz MJ, Hookfin EB, Heitmeyer SA, Woessner JF, Freemont AJ, Hoyland JA, et al. Moderation of iodoacetate-induced experimental osteoarthritis in rats by matrix metalloproteinase inhibitors. Osteoarthritis Cartilage. 2001 Nov; 9(8): 751–60. doi:10.1053/joca.2001.0472

Dong Y, Wu G, Zhu T, Chen H, Zhu Y, Zhu G, et al. VEGF promotes cartilage angiogenesis by phospho-ERK1/2 activation of Dll4 signaling in temporomandibular joint osteoarthritis caused by chronic sleep disturbance in Wistar rats. Oncotarget. 2017 Mar; 8 (11):17849-61. doi: 10.18632/oncotarget.14874

Caselli A, Cirri P, Santi A, Paoli P. Morin: a promising natural drug. Curr Med Chem; 2016 Jan; 23(8):774-91. doi: 10.2174/0929867323666160106150821

Downloads

Published

2020-09-30

Issue

Section

Clinical or Laboratorial Research Manuscript