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Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption

OBJECTIVES: Dipeptidyl peptidase-4 (DPP-4) inhibitors are used as a treatment for type 2 diabetes mellitus and have also recently been applied to enhance bone quality and density, and increase the expression of bone markers. This study aimed to investigate the effect of a DPP-4 inhibitor on orthodon...

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Autores principales: Qi, Jiawei, Kitaura, Hideki, Shen, Wei-Ren, Ogawa, Saika, Ohori, Fumitoshi, Noguchi, Takahiro, Marahleh, Aseel, Nara, Yasuhiko, Adya, Pramusita, Mizoguchi, Itaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453249/
https://www.ncbi.nlm.nih.gov/pubmed/32923485
http://dx.doi.org/10.1155/2020/7189084
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author Qi, Jiawei
Kitaura, Hideki
Shen, Wei-Ren
Ogawa, Saika
Ohori, Fumitoshi
Noguchi, Takahiro
Marahleh, Aseel
Nara, Yasuhiko
Adya, Pramusita
Mizoguchi, Itaru
author_facet Qi, Jiawei
Kitaura, Hideki
Shen, Wei-Ren
Ogawa, Saika
Ohori, Fumitoshi
Noguchi, Takahiro
Marahleh, Aseel
Nara, Yasuhiko
Adya, Pramusita
Mizoguchi, Itaru
author_sort Qi, Jiawei
collection PubMed
description OBJECTIVES: Dipeptidyl peptidase-4 (DPP-4) inhibitors are used as a treatment for type 2 diabetes mellitus and have also recently been applied to enhance bone quality and density, and increase the expression of bone markers. This study aimed to investigate the effect of a DPP-4 inhibitor on orthodontic tooth movement (OTM) and related root resorption in a mouse model. MATERIALS AND METHODS: Mice were randomly divided into three groups: those undergoing OTM with the addition of a DPP-4 inhibitor (30 μg), those undergoing OTM and receiving phosphate-buffered saline (PBS), and those without force loading (control group). OTM was achieved by means of a nickel–titanium closed coil spring that moved the first molar in a mesial direction for 12 days. The distance of OTM was measured using silicone impression. Maxillae were removed for histological analysis or real-time PCR analysis. RESULTS: The distance of OTM and the number of osteoclasts were significantly decreased after administration of the DPP-4 inhibitor, which also significantly suppressed the number of odontoclasts and root resorption after OTM. Furthermore, the mRNA expression of tumour necrosis factor-α (TNF-α) and the receptor activator of nuclear factor kappa-B ligand (RANKL) were decreased in DPP-4 inhibitor-treated mice compared with those receiving PBS and control animals. CONCLUSION: The DPP-4 inhibitor inhibited tooth movement and associated root resorption by blocking the formation of osteoclasts and odontoclasts, respectively. It also appeared to inhibit osteoclastogenesis and odontoclastogenesis by suppressing the expression of TNF-α and/or RANKL.
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spelling pubmed-74532492020-09-11 Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption Qi, Jiawei Kitaura, Hideki Shen, Wei-Ren Ogawa, Saika Ohori, Fumitoshi Noguchi, Takahiro Marahleh, Aseel Nara, Yasuhiko Adya, Pramusita Mizoguchi, Itaru Biomed Res Int Research Article OBJECTIVES: Dipeptidyl peptidase-4 (DPP-4) inhibitors are used as a treatment for type 2 diabetes mellitus and have also recently been applied to enhance bone quality and density, and increase the expression of bone markers. This study aimed to investigate the effect of a DPP-4 inhibitor on orthodontic tooth movement (OTM) and related root resorption in a mouse model. MATERIALS AND METHODS: Mice were randomly divided into three groups: those undergoing OTM with the addition of a DPP-4 inhibitor (30 μg), those undergoing OTM and receiving phosphate-buffered saline (PBS), and those without force loading (control group). OTM was achieved by means of a nickel–titanium closed coil spring that moved the first molar in a mesial direction for 12 days. The distance of OTM was measured using silicone impression. Maxillae were removed for histological analysis or real-time PCR analysis. RESULTS: The distance of OTM and the number of osteoclasts were significantly decreased after administration of the DPP-4 inhibitor, which also significantly suppressed the number of odontoclasts and root resorption after OTM. Furthermore, the mRNA expression of tumour necrosis factor-α (TNF-α) and the receptor activator of nuclear factor kappa-B ligand (RANKL) were decreased in DPP-4 inhibitor-treated mice compared with those receiving PBS and control animals. CONCLUSION: The DPP-4 inhibitor inhibited tooth movement and associated root resorption by blocking the formation of osteoclasts and odontoclasts, respectively. It also appeared to inhibit osteoclastogenesis and odontoclastogenesis by suppressing the expression of TNF-α and/or RANKL. Hindawi 2020-08-18 /pmc/articles/PMC7453249/ /pubmed/32923485 http://dx.doi.org/10.1155/2020/7189084 Text en Copyright © 2020 Jiawei Qi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Qi, Jiawei
Kitaura, Hideki
Shen, Wei-Ren
Ogawa, Saika
Ohori, Fumitoshi
Noguchi, Takahiro
Marahleh, Aseel
Nara, Yasuhiko
Adya, Pramusita
Mizoguchi, Itaru
Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption
title Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption
title_full Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption
title_fullStr Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption
title_full_unstemmed Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption
title_short Effect of a DPP-4 Inhibitor on Orthodontic Tooth Movement and Associated Root Resorption
title_sort effect of a dpp-4 inhibitor on orthodontic tooth movement and associated root resorption
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453249/
https://www.ncbi.nlm.nih.gov/pubmed/32923485
http://dx.doi.org/10.1155/2020/7189084
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