Establishing a new alveolar cleft model in rats to investigate the influence of jaw reconstructions on orthodontic tooth movement.


Journal

Annals of anatomy = Anatomischer Anzeiger : official organ of the Anatomische Gesellschaft
ISSN: 1618-0402
Titre abrégé: Ann Anat
Pays: Germany
ID NLM: 100963897

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 28 09 2020
revised: 03 02 2021
accepted: 11 02 2021
pubmed: 7 3 2021
medline: 3 11 2021
entrez: 6 3 2021
Statut: ppublish

Résumé

The aim of the present investigation was to develop a new cleft model in rats that allows alveolar cleft repair and subsequent tooth movement. A complete continuity-interrupting alveolar cleft was performed on the left-side maxillae of 33 rats through ultrasonic surgery. The clefts were filled with bone wax, and microCT scans were done to analyze the cleft size. After four weeks, the cleft repair was completed using autologous, xenogeneic (human), or synthetic bone substitute. After an additional four weeks, the orthodontic tooth movement was initiated. Fourteen rats died during the research, and the study design was constantly adapted accordingly. The main reasons for death included breathing problems during or immediately after the experimental activities (eight animals), followed by two deaths due to circulatory failures. In the remaining 19 animals, the average cleft size was about 2.70 ± 0.46 × 2.01 ± 0.25 × 1.18 ± 0.20 mm, and the mean velocity of orthodontic tooth movement after seven days was between 0.21 ± 0.08 mm in the autologous group and 0.50 ± 0.54 mm in the xenogeneic group. After 56 days, the mean values ranged between 0.67 ± 0.27 mm in the autologous group and 0.82 ± 0.72 mm in the synthetic group. Surgical interventions in the oral cavity of rats requires a stronger anesthesia and lead to increased risk of coolant and coagulated blood aspiration. The new alveolar cleft model in rats allows for subsequent orthodontic tooth movement after cleft repair, but only in the mesial root of the first molar.

Sections du résumé

BACKGROUND BACKGROUND
The aim of the present investigation was to develop a new cleft model in rats that allows alveolar cleft repair and subsequent tooth movement.
METHODS METHODS
A complete continuity-interrupting alveolar cleft was performed on the left-side maxillae of 33 rats through ultrasonic surgery. The clefts were filled with bone wax, and microCT scans were done to analyze the cleft size. After four weeks, the cleft repair was completed using autologous, xenogeneic (human), or synthetic bone substitute. After an additional four weeks, the orthodontic tooth movement was initiated.
RESULTS RESULTS
Fourteen rats died during the research, and the study design was constantly adapted accordingly. The main reasons for death included breathing problems during or immediately after the experimental activities (eight animals), followed by two deaths due to circulatory failures. In the remaining 19 animals, the average cleft size was about 2.70 ± 0.46 × 2.01 ± 0.25 × 1.18 ± 0.20 mm, and the mean velocity of orthodontic tooth movement after seven days was between 0.21 ± 0.08 mm in the autologous group and 0.50 ± 0.54 mm in the xenogeneic group. After 56 days, the mean values ranged between 0.67 ± 0.27 mm in the autologous group and 0.82 ± 0.72 mm in the synthetic group.
CONCLUSIONS CONCLUSIONS
Surgical interventions in the oral cavity of rats requires a stronger anesthesia and lead to increased risk of coolant and coagulated blood aspiration. The new alveolar cleft model in rats allows for subsequent orthodontic tooth movement after cleft repair, but only in the mesial root of the first molar.

Identifiants

pubmed: 33675947
pii: S0940-9602(21)00039-X
doi: 10.1016/j.aanat.2021.151713
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

151713

Informations de copyright

Copyright © 2021 Elsevier GmbH. All rights reserved.

Auteurs

Stephan Christian Möhlhenrich (SC)

Department of Orthodontics, University of Witten/Herdecke, Alfred-Herrhausen Str. 45, 58455 Witten, Germany; Department of Oral and Maxillofacial Surgery, University Hospital of Aachen, Pauwelsstraße 30, 52074 Aachen, Germany. Electronic address: stephan.moehlhenrich@uni-wh.de.

Marius Heitzer (M)

Department of Oral and Maxillofacial Surgery, University Hospital of Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.

Zuzanna Magnuska (Z)

Institute for Experimental Molecular Imaging, Department of Nanomedicine and Theragnostic RWTH Aachen University, Forckenbeckstrasse 55, 52074 Aachen, Germany.

Felix Gremse (F)

Institute for Experimental Molecular Imaging, Department of Nanomedicine and Theragnostic RWTH Aachen University, Forckenbeckstrasse 55, 52074 Aachen, Germany.

Sachin Chhatwani (S)

Department of Orthodontics, University of Witten/Herdecke, Alfred-Herrhausen Str. 45, 58455 Witten, Germany.

Gholamreza Danesh (G)

Department of Orthodontics, University of Witten/Herdecke, Alfred-Herrhausen Str. 45, 58455 Witten, Germany.

Frank Hölzle (F)

Department of Oral and Maxillofacial Surgery, University Hospital of Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.

Ali Modabber (A)

Department of Oral and Maxillofacial Surgery, University Hospital of Aachen, Pauwelsstraße 30, 52074 Aachen, Germany.

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