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Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection

This study aimed to explore periodontal and systemic immune response of overweight hosts to periodontitis. Forty C57 BL/6J male mice were divided into high (HF) or low fat (LF) diet groups and fed with the two diets, respectively, for 8 weeks. Each diet group was then divided into periodontitis (P)...

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Autores principales: Yu, Ting, Zhao, Li, Huang, Xin, Xie, Baoyi, Zhang, Jincai, Xuan, Dongying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335672/
https://www.ncbi.nlm.nih.gov/pubmed/30719451
http://dx.doi.org/10.1155/2019/9042542
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author Yu, Ting
Zhao, Li
Huang, Xin
Xie, Baoyi
Zhang, Jincai
Xuan, Dongying
author_facet Yu, Ting
Zhao, Li
Huang, Xin
Xie, Baoyi
Zhang, Jincai
Xuan, Dongying
author_sort Yu, Ting
collection PubMed
description This study aimed to explore periodontal and systemic immune response of overweight hosts to periodontitis. Forty C57 BL/6J male mice were divided into high (HF) or low fat (LF) diet groups and fed with the two diets, respectively, for 8 weeks. Each diet group was then divided into periodontitis (P) or control (C) groups (n = 10 per group) for 10-day ligation or sham-ligation. Overweight-related parameters including body weight were measured. Alveolar bone loss (ABL) was morphometrically analyzed and periodontal osteoclasts were stained. Periodontal immune response including leukocyte and macrophage number and inflammatory cytokines were analyzed by histology and quantitative PCR. Serum cytokine and lipid levels were quantified using electrochemiluminescence immunoassays, enzyme-linked immunosorbent assays, and biochemistry. It was found that HF group had 14.4% body weight gain compared with LF group (P < 0.01). ABL and periodontal osteoclast, leukocyte, and macrophage number were higher in P group than C group regardless of diet (P < 0.05). ABL and periodontal osteoclast number were not affected by diet regardless of ligation or sham-ligation. Leukocyte and macrophage number and protein level of tumor necrosis factor α (TNF-α) in periodontium and serum interleukin-6 level were downregulated by HF diet in periodontitis mice (P < 0.05). Periodontal protein level of TNF-α was highly correlated with serum interleukin-6 and low-density lipoprotein cholesterol levels (P < 0.01). These findings indicated that impaired immune response occurs both periodontally and systemically in preobesity overweight individuals. Given a well-reported exacerbating effect of obesity on periodontitis, overweight, if let uncontrolled, might place the individuals at potential risk for future periodontal tissue damage.
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spelling pubmed-63356722019-02-04 Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection Yu, Ting Zhao, Li Huang, Xin Xie, Baoyi Zhang, Jincai Xuan, Dongying Biomed Res Int Research Article This study aimed to explore periodontal and systemic immune response of overweight hosts to periodontitis. Forty C57 BL/6J male mice were divided into high (HF) or low fat (LF) diet groups and fed with the two diets, respectively, for 8 weeks. Each diet group was then divided into periodontitis (P) or control (C) groups (n = 10 per group) for 10-day ligation or sham-ligation. Overweight-related parameters including body weight were measured. Alveolar bone loss (ABL) was morphometrically analyzed and periodontal osteoclasts were stained. Periodontal immune response including leukocyte and macrophage number and inflammatory cytokines were analyzed by histology and quantitative PCR. Serum cytokine and lipid levels were quantified using electrochemiluminescence immunoassays, enzyme-linked immunosorbent assays, and biochemistry. It was found that HF group had 14.4% body weight gain compared with LF group (P < 0.01). ABL and periodontal osteoclast, leukocyte, and macrophage number were higher in P group than C group regardless of diet (P < 0.05). ABL and periodontal osteoclast number were not affected by diet regardless of ligation or sham-ligation. Leukocyte and macrophage number and protein level of tumor necrosis factor α (TNF-α) in periodontium and serum interleukin-6 level were downregulated by HF diet in periodontitis mice (P < 0.05). Periodontal protein level of TNF-α was highly correlated with serum interleukin-6 and low-density lipoprotein cholesterol levels (P < 0.01). These findings indicated that impaired immune response occurs both periodontally and systemically in preobesity overweight individuals. Given a well-reported exacerbating effect of obesity on periodontitis, overweight, if let uncontrolled, might place the individuals at potential risk for future periodontal tissue damage. Hindawi 2019-01-03 /pmc/articles/PMC6335672/ /pubmed/30719451 http://dx.doi.org/10.1155/2019/9042542 Text en Copyright © 2019 Ting Yu et al. https://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
Yu, Ting
Zhao, Li
Huang, Xin
Xie, Baoyi
Zhang, Jincai
Xuan, Dongying
Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection
title Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection
title_full Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection
title_fullStr Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection
title_full_unstemmed Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection
title_short Aberrant Periodontal and Systemic Immune Response of Overweight Rodents to Periodontal Infection
title_sort aberrant periodontal and systemic immune response of overweight rodents to periodontal infection
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335672/
https://www.ncbi.nlm.nih.gov/pubmed/30719451
http://dx.doi.org/10.1155/2019/9042542
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