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Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats

Studies have revealed that severe apical root resorption during tooth movement is caused by the noninfective inflammatory reaction of apical root tissues. We hypothesized that loxoprofen can suppress apical root resorption during tooth movement. Cyclic tensile force (CTF) of 10 kPa was applied to th...

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Autores principales: Yamamoto, Taeko, Kaku, Masato, Sumi, Hiromi, Yashima, Yuka, Izumino, Jin, Tanimoto, Kotaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919005/
https://www.ncbi.nlm.nih.gov/pubmed/29694352
http://dx.doi.org/10.1371/journal.pone.0194453
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author Yamamoto, Taeko
Kaku, Masato
Sumi, Hiromi
Yashima, Yuka
Izumino, Jin
Tanimoto, Kotaro
author_facet Yamamoto, Taeko
Kaku, Masato
Sumi, Hiromi
Yashima, Yuka
Izumino, Jin
Tanimoto, Kotaro
author_sort Yamamoto, Taeko
collection PubMed
description Studies have revealed that severe apical root resorption during tooth movement is caused by the noninfective inflammatory reaction of apical root tissues. We hypothesized that loxoprofen can suppress apical root resorption during tooth movement. Cyclic tensile force (CTF) of 10 kPa was applied to the human pulp cells for 48 hours by the Flexcell Strain Unit. Loxoprofen (10 and 100 μM) was added to the culture cells, and expression of cyclooxygenase (COX)-1, COX-2, interleukin (IL)-1β, receptor activator of nuclear factor kappa-B ligand (RANKL), tumor necrosis factor (TNF)-α, and macrophage colony-stimulating factor (M-CSF) were examined. To determine the effects of loxoprofen sodium on apical root reabsorption during tooth movement, the upper first molars of 7-week-old rats were subjected to mesial movement by 10g force for 30 days with or without the oral administration of loxoprofen. Gene expression and protein concentration of COX-1, COX-2, IL-1β, TNF-α, RANKL and M-CSF were significantly higher in the CTF group than in the control group. However, these levels were decreased by loxoprofen administration. After orthodontic tooth movement, the expression of IL-1β, TNF-α, RANKL and M-CSF decreased in the loxoprofen group than in the control group by immunohistochemical staining. In comparison to control group, less number of odontoclasts and a decrease in the amount of apical root resorption was observed in the loxoprofen group. Many osteoclasts became visible on the pressure side of the alveolar bone in the both groups, and the amount of tooth movement did not show a significant difference. These findings demonstrate that severe apical root resorption may be suppressed by loxoprofen administration, without a disturbance of tooth movement.
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spelling pubmed-59190052018-05-05 Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats Yamamoto, Taeko Kaku, Masato Sumi, Hiromi Yashima, Yuka Izumino, Jin Tanimoto, Kotaro PLoS One Research Article Studies have revealed that severe apical root resorption during tooth movement is caused by the noninfective inflammatory reaction of apical root tissues. We hypothesized that loxoprofen can suppress apical root resorption during tooth movement. Cyclic tensile force (CTF) of 10 kPa was applied to the human pulp cells for 48 hours by the Flexcell Strain Unit. Loxoprofen (10 and 100 μM) was added to the culture cells, and expression of cyclooxygenase (COX)-1, COX-2, interleukin (IL)-1β, receptor activator of nuclear factor kappa-B ligand (RANKL), tumor necrosis factor (TNF)-α, and macrophage colony-stimulating factor (M-CSF) were examined. To determine the effects of loxoprofen sodium on apical root reabsorption during tooth movement, the upper first molars of 7-week-old rats were subjected to mesial movement by 10g force for 30 days with or without the oral administration of loxoprofen. Gene expression and protein concentration of COX-1, COX-2, IL-1β, TNF-α, RANKL and M-CSF were significantly higher in the CTF group than in the control group. However, these levels were decreased by loxoprofen administration. After orthodontic tooth movement, the expression of IL-1β, TNF-α, RANKL and M-CSF decreased in the loxoprofen group than in the control group by immunohistochemical staining. In comparison to control group, less number of odontoclasts and a decrease in the amount of apical root resorption was observed in the loxoprofen group. Many osteoclasts became visible on the pressure side of the alveolar bone in the both groups, and the amount of tooth movement did not show a significant difference. These findings demonstrate that severe apical root resorption may be suppressed by loxoprofen administration, without a disturbance of tooth movement. Public Library of Science 2018-04-25 /pmc/articles/PMC5919005/ /pubmed/29694352 http://dx.doi.org/10.1371/journal.pone.0194453 Text en © 2018 Yamamoto et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Yamamoto, Taeko
Kaku, Masato
Sumi, Hiromi
Yashima, Yuka
Izumino, Jin
Tanimoto, Kotaro
Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
title Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
title_full Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
title_fullStr Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
title_full_unstemmed Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
title_short Effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
title_sort effects of loxoprofen on the apical root resorption during orthodontic tooth movement in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5919005/
https://www.ncbi.nlm.nih.gov/pubmed/29694352
http://dx.doi.org/10.1371/journal.pone.0194453
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