TY - JOUR
T1 - Hyperbaric Oxygen Therapy to Minimize Orthodontic Relapse in Rabbits
AU - Akbar, Yun Mukmin
AU - Maskoen, Ani Melani
AU - Mardiati, Endah
AU - Wandawa, Ganesha
AU - Amaliya, Amaliya
AU - Narmada, Ida Bagus
AU - Djustiana, Nina
AU - Evangelina, Ida Ayu
AU - Rikmasari, Rasmi
AU - Anggun, Mas Rizky
N1 - Publisher Copyright:
© 2024 Georg Thieme Verlag. All rights reserved.
PY - 2024
Y1 - 2024
N2 - 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.
AB - 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.
KW - animal model
KW - collagen synthesis and degradation
KW - hyperbaric oxygen therapy
KW - orthodontic relapse
KW - supracrestal gingival fibers
UR - http://www.scopus.com/inward/record.url?scp=85182718725&partnerID=8YFLogxK
U2 - 10.1055/s-0043-1776118
DO - 10.1055/s-0043-1776118
M3 - Article
AN - SCOPUS:85182718725
SN - 1305-7456
JO - European Journal of Dentistry
JF - European Journal of Dentistry
ER -