CC BY 4.0 · Eur J Dent 2024; 18(03): 841-851
DOI: 10.1055/s-0043-1776118
Original Article

Hyperbaric Oxygen Therapy to Minimize Orthodontic Relapse in Rabbits

1   Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
2   Department of Research and Development, Indonesian Naval Dental Institute R.E. Martadinata, Jakarta, Indonesia
,
Ani Melani Maskoen
3   Department of Oral Biology, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
,
Endah Mardiati
4   Department of Orthodontics, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
,
Ganesha Wandawa
2   Department of Research and Development, Indonesian Naval Dental Institute R.E. Martadinata, Jakarta, Indonesia
,
Amaliya Amaliya
5   Departement of Periodontology, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
6   Center Study for Military Dentistry, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
,
Ida Bagus Narmada
7   Department of Orthodontics, Faculty of Dentistry, Universitas Airlangga, Surabaya, Indonesia
,
Nina Djustiana
8   Department of Dental Material, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
,
Ida Ayu Evangelina
4   Department of Orthodontics, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
,
Rasmi Rikmasari
9   Department of Prosthodontics, Faculty of Dentistry, Universitas Padjadjaran, Bandung, Indonesia
,
Mas Rizky Anggun
10   Department of Biomedical Sciences, Faculty of Medicine, Universitas Padjadjaran, Bandung, Indonesia
› Author Affiliations

Abstract

Objectives The purpose of the present study was to discover how hyperbaric oxygen therapy (HBOT) could reduce orthodontic relapse by altering the expressions of hypoxia-inducible factor (HIF)-1 messenger ribonucleic acid (mRNA), type I collagen (Col I), and matrix metalloproteinase-1 (MMP-1) in the gingival supracrestal fibers in rabbits.

Materials and Methods This study involved 44 male rabbits (Oryctolagus cuniculus) randomly divided into the normal group (K0), the orthodontic group without HBOT (K1), and the orthodontic group with HBOT (K2). Following orthodontic separation of the two upper central incisors, a retention phase and relapse assessment were performed. The HBOT was performed for a period of 2, 4, 6, 8, and 10 days after retention. HIF-1α transcription was assessed employing real-time polymerase chain reaction, whereas Col I and MMP-1 proteins were examined using immunohistochemistry. The orthodontic relapse was measured clinically using a digital caliper.

Statistical Analysis We used the one-way analysis of variance followed by Tukey's post hoc for multiple comparisons to measure differences between pairs of means; a p-value of 0.05 was considered statistically significant.

Results HBOT significantly increased the HIF-1α mRNA expression (p = 0.0140), increased Col I (p = 0.0043) and MMP-1 (p = 0.0068) on the tensioned and pressured side of the gingival supracrestal fibers, respectively, and clinically decreased the relapse (p = 3.75 × 10−40).

Conclusion HBOT minimizes orthodontic relapse by influencing HIF-1α expression, collagen synthesis (Col I), and degradation (MMP-1). This result suggests that HBOT has the potential to be used as an adjunctive method in the orthodontic retention phase.



Publication History

Article published online:
10 January 2024

© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

Thieme Medical and Scientific Publishers Pvt. Ltd.
A-12, 2nd Floor, Sector 2, Noida-201301 UP, India

 
  • References

  • 1 Littlewood SJ, Kandasamy S, Huang G. Retention and relapse in clinical practice. Aust Dent J 2017; 62 (Suppl. 01) 51-57
  • 2 Kaan M, Madléna M. Retention and relapse. Review of the literature [in Hungarian]. Fogorv Sz 2011; 104 (04) 139-146
  • 3 Proffit W. Contemporary orthodontics. 5th ed. Published by Oxford University Press on behalf of the European Orthodontic Society. St. Louis, MO: Elsevier Inc.; 2012: 213-214
  • 4 Vaida L, Todor BI, Lile IE, Mut A, Mihaiu A, Todor L. Contention following the orthodontic treatment and prevalence of relapse. Hum Vet Med Int J Bioflux Soc 2019; 11: 37-42
  • 5 Redlich M, Reichenberg E, Harari D, Zaks B, Shoshan S, Palmon A. The effect of mechanical force on mRNA levels of collagenase, collagen type I, and tissue inhibitors of metalloproteinases in gingivae of dogs. J Dent Res 2001; 80 (12) 2080-2084
  • 6 Redlich M, Rahamim E, Gaft A, Shoshan S. The response of supraalveolar gingival collagen to orthodontic rotation movement in dogs. Am J Orthod Dentofacial Orthop 1996; 110 (03) 247-255
  • 7 Redlich M, Palmon A, Zaks B, Geremi E, Rayzman S, Shoshan S. The effect of centrifugal force on the transcription levels of collagen type I and collagenase in cultured canine gingival fibroblasts. Arch Oral Biol 1998; 43 (04) 313-316
  • 8 Redlich M, Shoshan S, Palmon A. Gingival response to orthodontic force. Am J Orthod Dentofacial Orthop 1999; 116 (02) 152-158
  • 9 Zinad K, Schols AMWJ, Schols JGJH. Another way of looking at treatment stability. Angle Orthod 2016; 86 (05) 721-726
  • 10 Al Yami EA, Kuijpers-Jagtman AM, van 't Hof MA. Stability of orthodontic treatment outcome: follow-up until 10 years postretention. Am J Orthod Dentofacial Orthop 1999; 115 (03) 300-304
  • 11 Kaan M, Madléna M. Retention and relapse. Review of the literature. Fogorv Sz 2011; 104 (04) 139-146
  • 12 de Bernabé PG, Montiel-Company JM, Paredes-Gallardo V, Gandía-Franco JL, Bellot-Arcís C. Orthodontic treatment stability predictors: a retrospective longitudinal study. Angle Orthod 2017; 87 (02) 223-229
  • 13 Stewart DR, Sherick P, Kramer S, Breining P. Use of relaxin in orthodontics. Ann N Y Acad Sci 2005; 1041: 379-387
  • 14 Salehi P, Heidari S, Tanideh N, Torkan S. Effect of low-level laser irradiation on the rate and short-term stability of rotational tooth movement in dogs. Am J Orthod Dentofacial Orthop 2015; 147 (05) 578-586
  • 15 Jahanbin A, Ramazanzadeh B, Ahrari F, Forouzanfar A, Beidokhti M. Effectiveness of Er:YAG laser-aided fiberotomy and low-level laser therapy in alleviating relapse of rotated incisors. Am J Orthod Dentofacial Orthop 2014; 146 (05) 565-572
  • 16 Edwards JG. A long-term prospective evaluation of the circumferential supracrestal fiberotomy in alleviating orthodontic relapse. Am J Orthod Dentofacial Orthop 1988; 93 (05) 380-387
  • 17 Meng M, Lv C, Yang Q. et al. Expression of proteins of elastic fibers and collagen type I in orthodontically rotated teeth in rats. Am J Orthod Dentofacial Orthop 2018; 154 (02) 249-259
  • 18 Weed T, Bill T, Gampper TJ. Hyperbaric oxygen therapy. In: Biomedical Technology and Devices Handbook. 2nd ed. London, UK: CRC Press; 2003
  • 19 Sen CK. Wound healing essentials: let there be oxygen. Wound Repair Regen 2009; 17 (01) 1-18
  • 20 Neuman TS, Thom SR. Physiology and Medicine of Hyperbaric Oxygen Therapy. In: Meloni D. ed. 1st ed. Philadelphia: Saunders/Elsevier; 2008: 606
  • 21 Fosen KM, Thom SR. Hyperbaric oxygen, vasculogenic stem cells, and wound healing. Antioxid Redox Signal 2014; 21 (11) 1634-1647
  • 22 Thom SR. Hyperbaric oxygen: its mechanisms and efficacy. Plast Reconstr Surg 2011; 127 (Suppl 1, Suppl 1): 131S-141S
  • 23 Gokce S, Bengi AO, Akin E. et al. Effects of hyperbaric oxygen during experimental tooth movement. Angle Orthod 2008; 78 (02) 304-308
  • 24 Salah H, Eid E-D. Effect of hyperbaric oxygen on mobility of orthodontically treated teeth. Egypt Orthod J 2010; 38: 107-124
  • 25 Prayogo RD, Sandy BN, Sujarwo H. et al. The changes of fibroblast and periodontal ligament characteristics in orthodontic tooth movement with adjuvant HBOT and propolis: a study in Guinea pigs. Padjadjaran J Dent. 2020; 32: 48
  • 26 Akbar YM, Maskoen AM, Mardiati E, Wandawa G, Setiawan AS. Potential use of hyperbaric oxygen therapy in orthodontic treatment: a systematic review of animal studies. Eur J Dent 2023; 17 (01) 16-23
  • 27 Inuzuka Y, Edo N, Araki Y. et al. Decompression illness treated with the Hart-Kindwall protocol in a monoplace chamber. Am J Case Rep 2022; 23: e935534
  • 28 The Norwegian National Reserach Ethics Committees. Ethical Guidelines for the Use of Animals in Research [Internet]. 2018: 12 Accessed September 24, 2023 at: www.etikkom.no
  • 29 Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Δ Δ C(T)) Method. Methods 2001; 25 (04) 402-408
  • 30 Zhang Q, Chang Q, Cox RA, Gong X, Gould LJ. Hyperbaric oxygen attenuates apoptosis and decreases inflammation in an ischemic wound model. J Invest Dermatol 2008; 128 (08) 2102-2112
  • 31 Sunkari VG, Lind F, Botusan IR. et al. Hyperbaric oxygen therapy activates hypoxia-inducible factor 1 (HIF-1), which contributes to improved wound healing in diabetic mice. Wound Repair Regen 2015; 23 (01) 98-103
  • 32 Růžička J, Dejmek J, Bolek L, Beneš J, Kuncová J. Hyperbaric oxygen influences chronic wound healing – a cellular level review. Physiol Res 2021; 70: 261-273
  • 33 Lindenmann J, Kamolz L, Graier W. Smolle J, Smolle-Juettner F-M. Hyperbaric oxygen therapy and tissue regeneration : a literature survey. Biomedicines 2022; 10 (12) 3145
  • 34 Sun L, Marti HH, Veltkamp R. Hyperbaric oxygen reduces tissue hypoxia and hypoxia-inducible factor-1 α expression in focal cerebral ischemia. Stroke 2008; 39 (03) 1000-1006
  • 35 Zhang L, Ke J, Min S. et al. Hyperbaric oxygen therapy represses the Warburg effect and epithelial – mesenchymal transition in hypoxic NSCLC cells via the HIF-1 a / PFKP axis. Front Oncol 2021; 11: 1-9
  • 36 Chen CA, Huang YC, Lo JJ, Wang SH, Huang SH, Wu SH. Hyperbaric oxygen therapy attenuates burn-induced denervated muscle atrophy. Int J Med Sci 2021; 18 (16) 3821-3830
  • 37 Sari DR, Meiliana ID, Sakti D, Kinasih S, Kurniasari H, Rejeki PS. Hyperbaric oxygen therapy as an adjuvant treatment in hydrochloric acid poisoning: a literature review. Biomorphology J. 2023; 33: 52-58
  • 38 Hadanny A, Efrati S. The hyperoxic-hypoxic paradox. Biomolecules 2020; 10 (06) 1-17
  • 39 Stegen S, Laperre K, Eelen G. et al. HIF-1α metabolically controls collagen synthesis and modification in chondrocytes. Nature 2019; 565 (7740): 511-515
  • 40 Guo F, Carter DE, Leask A. Mechanical tension increases CCN2 / CTGF expression and proliferation in gingival fibroblasts via a TGF b - dependent mechanism. PLoS One 2011; 6: 1-10
  • 41 Jeon Y-M, Kook S-H, Son Y-O. et al. Role of MAPK in mechanical force-induced up-regulation of type I collagen and osteopontin in human gingival fibroblasts. Mol Cell Biochem 2009; 320 (1-2): 45-52
  • 42 Kook SH, Son YO, Hwang JM. et al. Mechanical force inhibits osteoclastogenic potential of human periodontal ligament fibroblasts through OPG production and ERK-mediated signaling. J Cell Biochem 2009; 106 (06) 1010-1019
  • 43 Mallikarjunappa AS, George S, Aghanashini S, Bhat D, Mundinamane DB. Collagen—the skeleton of the periodontium: a review. J Sci Dent 2021; 11: 1-5
  • 44 Sandhu SV, Gupta S, Singla K. Collagen in health and disease. J Orofac Res. 2012; 2: 153-159
  • 45 Deshmukh SN, Dive AM, Moharil R, Munde P. Enigmatic insight into collagen. J Oral Maxillofac Pathol 2016; 20 (02) 276-283
  • 46 Nan LAN, Zheng YI, Liao NI, Li S, Wang YAO, Chen Z. Mechanical force promotes the proliferation and extracellular matrix synthesis of human gingival fibroblasts cultured on 3D PLGA scaffolds via TGF-β expression. Mol Med Rep 2019; 19 (01) 2107-2114