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Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes

OBJECTIVES: To observe the elongation of the axial tooth movement in the unopposed rodent molar model with type 1 diabetes mellitus and explore the pathological changes of periodontal ligament and alveolar bone, and their correlation with tooth axial movement. METHODS: The 80 C57BL/6J mice were rand...

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Autores principales: Li, Wenjin, Zheng, Jing, Xu, Yao, Niu, Weiran, Guo, Dong, Cui, Jianing, Bian, Wenjin, Wang, Xiaohui, Niu, Jinliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900130/
https://www.ncbi.nlm.nih.gov/pubmed/36755916
http://dx.doi.org/10.3389/fendo.2023.1098702
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author Li, Wenjin
Zheng, Jing
Xu, Yao
Niu, Weiran
Guo, Dong
Cui, Jianing
Bian, Wenjin
Wang, Xiaohui
Niu, Jinliang
author_facet Li, Wenjin
Zheng, Jing
Xu, Yao
Niu, Weiran
Guo, Dong
Cui, Jianing
Bian, Wenjin
Wang, Xiaohui
Niu, Jinliang
author_sort Li, Wenjin
collection PubMed
description OBJECTIVES: To observe the elongation of the axial tooth movement in the unopposed rodent molar model with type 1 diabetes mellitus and explore the pathological changes of periodontal ligament and alveolar bone, and their correlation with tooth axial movement. METHODS: The 80 C57BL/6J mice were randomly divided into the streptozotocin(STZ)-injected group (n = 50) and the control group (n = 30). Mice in the streptozotocin(STZ)-injected group were injected intraperitoneal with streptozotocin (STZ), and mice in the control group were given intraperitoneal injection of equal doses of sodium citrate buffer. Thirty mice were randomly selected from the successful models as the T1DM group. The right maxillary molar teeth of mice were extracted under anesthesia, and allowed mandibular molars to super-erupt. Mice were sacrificed at 0, 3, 6,9, and 12 days. Tooth elongation and bone mineral density (BMD) were evaluated by micro-CT analysis(0,and 12 days mice). Conventional HE staining, Masson staining and TRAP staining were used to observe the changes in periodontal tissue(0, 3, 6, 9, and 12 days mice). The expression differences of SPARC, FGF9, BMP4, NOGGIN, and type I collagen were analyzed by RT-qPCR. RESULTS: After 12 days of tooth extraction, our data showed significant super-eruption of mandibular mouse molars of the two groups. The amount of molar super-eruption in the T1DM group was 0.055mm( ± 0.014mm), and in the control group was 0.157( ± 0.017mm). The elongation of the T1DM mice was less than that of the control mice(P<0.001). It was observed that the osteoclasts and BMD increased gradually in both groups over time. Compared with the control group, the collagen arrangement was more disordered, the number of osteoclasts was higher (P<0.05), and the increase of bone mineral density was lower(2.180 ± 0.007g/cm(3) vs. 2.204 ± 0.006g/cm(3), P<0.001) in the T1DM group. The relative expression of SPARC, FGF9, BMP4, and type I collagen in the two groups increased with the extension of tooth extraction time while NOGGIN decreased. The relative expression of all of SPARC, FGF9, BMP4, and type I collagen in the T1DM group were significantly lower, and the expression of NOGGIN was higher than that in the control group (P<0.05). CONCLUSION: The axial tooth movement was inhibited in type 1 diabetic mice. The result may be associated with the changes of periodontal ligament osteoclastogenic effects and alveolar bone remodeling regulated by the extracellular matrix and osteogenesis-related factors.
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spelling pubmed-99001302023-02-07 Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes Li, Wenjin Zheng, Jing Xu, Yao Niu, Weiran Guo, Dong Cui, Jianing Bian, Wenjin Wang, Xiaohui Niu, Jinliang Front Endocrinol (Lausanne) Endocrinology OBJECTIVES: To observe the elongation of the axial tooth movement in the unopposed rodent molar model with type 1 diabetes mellitus and explore the pathological changes of periodontal ligament and alveolar bone, and their correlation with tooth axial movement. METHODS: The 80 C57BL/6J mice were randomly divided into the streptozotocin(STZ)-injected group (n = 50) and the control group (n = 30). Mice in the streptozotocin(STZ)-injected group were injected intraperitoneal with streptozotocin (STZ), and mice in the control group were given intraperitoneal injection of equal doses of sodium citrate buffer. Thirty mice were randomly selected from the successful models as the T1DM group. The right maxillary molar teeth of mice were extracted under anesthesia, and allowed mandibular molars to super-erupt. Mice were sacrificed at 0, 3, 6,9, and 12 days. Tooth elongation and bone mineral density (BMD) were evaluated by micro-CT analysis(0,and 12 days mice). Conventional HE staining, Masson staining and TRAP staining were used to observe the changes in periodontal tissue(0, 3, 6, 9, and 12 days mice). The expression differences of SPARC, FGF9, BMP4, NOGGIN, and type I collagen were analyzed by RT-qPCR. RESULTS: After 12 days of tooth extraction, our data showed significant super-eruption of mandibular mouse molars of the two groups. The amount of molar super-eruption in the T1DM group was 0.055mm( ± 0.014mm), and in the control group was 0.157( ± 0.017mm). The elongation of the T1DM mice was less than that of the control mice(P<0.001). It was observed that the osteoclasts and BMD increased gradually in both groups over time. Compared with the control group, the collagen arrangement was more disordered, the number of osteoclasts was higher (P<0.05), and the increase of bone mineral density was lower(2.180 ± 0.007g/cm(3) vs. 2.204 ± 0.006g/cm(3), P<0.001) in the T1DM group. The relative expression of SPARC, FGF9, BMP4, and type I collagen in the two groups increased with the extension of tooth extraction time while NOGGIN decreased. The relative expression of all of SPARC, FGF9, BMP4, and type I collagen in the T1DM group were significantly lower, and the expression of NOGGIN was higher than that in the control group (P<0.05). CONCLUSION: The axial tooth movement was inhibited in type 1 diabetic mice. The result may be associated with the changes of periodontal ligament osteoclastogenic effects and alveolar bone remodeling regulated by the extracellular matrix and osteogenesis-related factors. Frontiers Media S.A. 2023-01-23 /pmc/articles/PMC9900130/ /pubmed/36755916 http://dx.doi.org/10.3389/fendo.2023.1098702 Text en Copyright © 2023 Li, Zheng, Xu, Niu, Guo, Cui, Bian, Wang and Niu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Li, Wenjin
Zheng, Jing
Xu, Yao
Niu, Weiran
Guo, Dong
Cui, Jianing
Bian, Wenjin
Wang, Xiaohui
Niu, Jinliang
Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
title Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
title_full Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
title_fullStr Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
title_full_unstemmed Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
title_short Remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
title_sort remodeling of the periodontal ligament and alveolar bone during axial tooth movement in mice with type 1 diabetes
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900130/
https://www.ncbi.nlm.nih.gov/pubmed/36755916
http://dx.doi.org/10.3389/fendo.2023.1098702
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