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Probiotics ameliorate alveolar bone loss by regulating gut microbiota
OBJECTIVES: Oestrogen deficiency is an aetiological factor of postmenopausal osteoporosis (PMO), which not only decreases bone density in vertebrae and long bone but also aggravates inflammatory alveolar bone loss. Recent evidence has suggested the critical role of gut microbiota in osteoimmunology...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249787/ https://www.ncbi.nlm.nih.gov/pubmed/34101283 http://dx.doi.org/10.1111/cpr.13075 |
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author | Jia, Leming Tu, Ye Jia, Xiaoyue Du, Qian Zheng, Xin Yuan, Quan Zheng, Liwei Zhou, Xuedong Xu, Xin |
author_facet | Jia, Leming Tu, Ye Jia, Xiaoyue Du, Qian Zheng, Xin Yuan, Quan Zheng, Liwei Zhou, Xuedong Xu, Xin |
author_sort | Jia, Leming |
collection | PubMed |
description | OBJECTIVES: Oestrogen deficiency is an aetiological factor of postmenopausal osteoporosis (PMO), which not only decreases bone density in vertebrae and long bone but also aggravates inflammatory alveolar bone loss. Recent evidence has suggested the critical role of gut microbiota in osteoimmunology and its influence on bone metabolisms. The present study aimed to evaluate the therapeutic effects of probiotics on alveolar bone loss under oestrogen‐deficient condition. MATERIALS AND METHODS: Inflammatory alveolar bone loss was established in ovariectomized (OVX) rats, and rats were daily intragastrically administered with probiotics until sacrifice. Gut microbiota composition, intestinal permeability, systemic immune status and alveolar bone loss were assessed to reveal the underlying correlation between gut microbiota and bone metabolisms. RESULTS: We found administration of probiotics significantly prevented inflammatory alveolar bone resorption in OVX rats. By enriching butyrate‐producing genera and enhancing gut butyrate production, probiotics improved intestinal barrier and decreased gut permeability in the OVX rats. Furthermore, the oestrogen deprivation‐induced inflammatory responses were suppressed in probiotics‐treated OVX rats, as reflected by reduced serum levels of inflammatory cytokines and a balanced distribution of CD4(+)IL‐17A(+) Th17 cells and CD4(+)CD25(+)Foxp3(+) Treg cells in the bone marrow. CONCLUSIONS: This study demonstrated that probiotics can effectively attenuate alveolar bone loss by modulating gut microbiota and further regulating osteoimmune response and thus represent a promising adjuvant in the treatment of alveolar bone loss under oestrogen deficiency. |
format | Online Article Text |
id | pubmed-8249787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82497872021-07-09 Probiotics ameliorate alveolar bone loss by regulating gut microbiota Jia, Leming Tu, Ye Jia, Xiaoyue Du, Qian Zheng, Xin Yuan, Quan Zheng, Liwei Zhou, Xuedong Xu, Xin Cell Prolif Original Articles OBJECTIVES: Oestrogen deficiency is an aetiological factor of postmenopausal osteoporosis (PMO), which not only decreases bone density in vertebrae and long bone but also aggravates inflammatory alveolar bone loss. Recent evidence has suggested the critical role of gut microbiota in osteoimmunology and its influence on bone metabolisms. The present study aimed to evaluate the therapeutic effects of probiotics on alveolar bone loss under oestrogen‐deficient condition. MATERIALS AND METHODS: Inflammatory alveolar bone loss was established in ovariectomized (OVX) rats, and rats were daily intragastrically administered with probiotics until sacrifice. Gut microbiota composition, intestinal permeability, systemic immune status and alveolar bone loss were assessed to reveal the underlying correlation between gut microbiota and bone metabolisms. RESULTS: We found administration of probiotics significantly prevented inflammatory alveolar bone resorption in OVX rats. By enriching butyrate‐producing genera and enhancing gut butyrate production, probiotics improved intestinal barrier and decreased gut permeability in the OVX rats. Furthermore, the oestrogen deprivation‐induced inflammatory responses were suppressed in probiotics‐treated OVX rats, as reflected by reduced serum levels of inflammatory cytokines and a balanced distribution of CD4(+)IL‐17A(+) Th17 cells and CD4(+)CD25(+)Foxp3(+) Treg cells in the bone marrow. CONCLUSIONS: This study demonstrated that probiotics can effectively attenuate alveolar bone loss by modulating gut microbiota and further regulating osteoimmune response and thus represent a promising adjuvant in the treatment of alveolar bone loss under oestrogen deficiency. John Wiley and Sons Inc. 2021-06-07 /pmc/articles/PMC8249787/ /pubmed/34101283 http://dx.doi.org/10.1111/cpr.13075 Text en © 2021 The Authors. Cell Proliferation published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Jia, Leming Tu, Ye Jia, Xiaoyue Du, Qian Zheng, Xin Yuan, Quan Zheng, Liwei Zhou, Xuedong Xu, Xin Probiotics ameliorate alveolar bone loss by regulating gut microbiota |
title | Probiotics ameliorate alveolar bone loss by regulating gut microbiota |
title_full | Probiotics ameliorate alveolar bone loss by regulating gut microbiota |
title_fullStr | Probiotics ameliorate alveolar bone loss by regulating gut microbiota |
title_full_unstemmed | Probiotics ameliorate alveolar bone loss by regulating gut microbiota |
title_short | Probiotics ameliorate alveolar bone loss by regulating gut microbiota |
title_sort | probiotics ameliorate alveolar bone loss by regulating gut microbiota |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8249787/ https://www.ncbi.nlm.nih.gov/pubmed/34101283 http://dx.doi.org/10.1111/cpr.13075 |
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