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Differential Recovery Patterns of the Maxilla and Mandible After Eliminating Nasal Obstruction in Growing Rats

Overview
Journal J Clin Med
Specialty General Medicine
Date 2022 Dec 23
PMID 36555975
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Abstract

Although nasal obstruction (NO) during growth causes maxillofacial growth suppression, it remains unclear whether eliminating the NO affects maxillary and mandibular growth differentially. We aimed to clarify whether eliminating NO can help regain normal maxillofacial growth and to determine the optimal intervention timing. Forty-two 4-week-old male Wistar rats were randomly divided into six groups. Their left nostril was sutured to simulate NO over different durations in the experimental groups; the sutures were later removed to resume nasal breathing. Maxillofacial morphology was assessed using microcomputed tomography. Immunohistochemical changes in hypoxia-inducible factor (HIF)-1α, osteoprotegerin (OPG), and receptor activator of nuclear factor kappa-B ligand (RANKL) of the condylar cartilage were evaluated to reveal the underlying mechanisms of these changes. Maxillary length was significantly lower in rats with NO for ≥5 weeks. In groups with NO for ≥7 weeks, the posterior mandibular length, ramus height, thickness of the hypertrophic cell layer in the condylar cartilage, HIF-1α levels, and RANKL levels were significantly lower and OPG levels and RANKL/OPG were significantly higher than those in the control group. Our findings suggest that eliminating NO is effective in regaining maxillofacial growth. Moreover, the optimal timing of intervention differed between the maxilla and mandible.

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References
1.
Knowles H . Hypoxic regulation of osteoclast differentiation and bone resorption activity. Hypoxia (Auckl). 2016; 3:73-82. PMC: 5045091. DOI: 10.2147/HP.S95960. View

2.
Grimaud E, Soubigou L, Couillaud S, Coipeau P, Moreau A, Passuti N . Receptor activator of nuclear factor kappaB ligand (RANKL)/osteoprotegerin (OPG) ratio is increased in severe osteolysis. Am J Pathol. 2003; 163(5):2021-31. PMC: 1892410. DOI: 10.1016/s0002-9440(10)63560-2. View

3.
Shirakura M, Tanimoto K, Eguchi H, Miyauchi M, Nakamura H, Hiyama K . Activation of the hypoxia-inducible factor-1 in overloaded temporomandibular joint, and induction of osteoclastogenesis. Biochem Biophys Res Commun. 2010; 393(4):800-5. DOI: 10.1016/j.bbrc.2010.02.086. View

4.
Zettergren-Wijk L, Forsberg C, Linder-Aronson S . Changes in dentofacial morphology after adeno-/tonsillectomy in young children with obstructive sleep apnoea--a 5-year follow-up study. Eur J Orthod. 2006; 28(4):319-26. DOI: 10.1093/ejo/cji119. View

5.
Kilic N, Oktay H . Effects of rapid maxillary expansion on nasal breathing and some naso-respiratory and breathing problems in growing children: a literature review. Int J Pediatr Otorhinolaryngol. 2008; 72(11):1595-601. DOI: 10.1016/j.ijporl.2008.07.014. View