Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats

Detalhes bibliográficos
Autor(a) principal: Pereira, Renato Felipe [UNESP]
Data de Publicação: 2017
Outros Autores: Cintra, Luciano Tavares Angelo [UNESP], Tessarin, Gestter Willian Lattari [UNESP], Chiba, Fernando Yamamoto [UNESP], de Lima Coutinho Mattera, Maria Sara [UNESP], Scaramele, Natalia Francisco [UNESP], Tsosura, Thais Verônica Saori [UNESP], Ervolino, Edilson [UNESP], de Oliveira, Sandra Helena Penha [UNESP], Sumida, Doris Hissako [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.joen.2017.01.030
http://hdl.handle.net/11449/178800
Resumo: Introduction Our previous studies have shown that periapical lesions (PLs) in rats cause systemic disorders such as increased tumor necrosis factor-α plasma levels, insulin resistance, and impairment in insulin signal transduction in muscle tissue. However, the mechanisms involved in these alterations are not fully understood. Under chronic inflammatory conditions such as obesity, it has been shown that the skeletal muscle is affected by inflammation, and the number of resident macrophages that are associated with impairments of insulin action and sensitivity is increased. This study aimed to investigate the presence of macrophages, activation of inflammatory pathways in muscle tissue, glycemia, and insulinemia of rats with PLs. Methods Sixty Wistar rats were distributed into a control group; a group with 1 PL (1PL), which was induced in the right maxillary first molar; and a group with 4 PLs (4PL), which were induced in the right upper and lower first and second molars. We quantified macrophage content by immunohistochemistry for the F4/80 protein. We evaluated Jun N-terminal kinase and IKKα/β phosphorylation status in the muscle tissue by Western blotting. Serum levels of lipopolysaccharide (LPS) and HSP70 and plasma levels of glucose and insulin were assessed by using commercial kits. Results The 1PL and 4PL groups showed increase in macrophage content, IKKα/β, and Jun N-terminal kinase phosphorylation status, serum LPS and HSP70 levels, and insulin resistance and no changes in glycemia and insulinemia compared with the control group. There was no difference in these parameters between the 1PL and 4PL groups. Conclusions PLs promoted an increase in macrophage infiltration, activation of inflammatory pathways in muscle tissue, and serum concentrations of HSP70 and LPS in rats. The present study improves the knowledge on the impact of oral inflammations on the development of systemic alteration, which can induce insulin resistance.
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spelling Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of RatsInflammationinsulin resistanceperiapical lesionsystemic disordersIntroduction Our previous studies have shown that periapical lesions (PLs) in rats cause systemic disorders such as increased tumor necrosis factor-α plasma levels, insulin resistance, and impairment in insulin signal transduction in muscle tissue. However, the mechanisms involved in these alterations are not fully understood. Under chronic inflammatory conditions such as obesity, it has been shown that the skeletal muscle is affected by inflammation, and the number of resident macrophages that are associated with impairments of insulin action and sensitivity is increased. This study aimed to investigate the presence of macrophages, activation of inflammatory pathways in muscle tissue, glycemia, and insulinemia of rats with PLs. Methods Sixty Wistar rats were distributed into a control group; a group with 1 PL (1PL), which was induced in the right maxillary first molar; and a group with 4 PLs (4PL), which were induced in the right upper and lower first and second molars. We quantified macrophage content by immunohistochemistry for the F4/80 protein. We evaluated Jun N-terminal kinase and IKKα/β phosphorylation status in the muscle tissue by Western blotting. Serum levels of lipopolysaccharide (LPS) and HSP70 and plasma levels of glucose and insulin were assessed by using commercial kits. Results The 1PL and 4PL groups showed increase in macrophage content, IKKα/β, and Jun N-terminal kinase phosphorylation status, serum LPS and HSP70 levels, and insulin resistance and no changes in glycemia and insulinemia compared with the control group. There was no difference in these parameters between the 1PL and 4PL groups. Conclusions PLs promoted an increase in macrophage infiltration, activation of inflammatory pathways in muscle tissue, and serum concentrations of HSP70 and LPS in rats. The present study improves the knowledge on the impact of oral inflammations on the development of systemic alteration, which can induce insulin resistance.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Programa de Pós-Graduação Multicêntrico em Ciências Fisiológicas-SBFis Department of Basic Sciences São Paulo State University (Unesp) School of DentistryDepartment of Restorative Dentistry São Paulo State University (Unesp) School of DentistryDepartment of Child and Social Dentistry São Paulo State University (Unesp) School of DentistryDepartment of Basic Sciences São Paulo State University (Unesp) School of DentistrySão Paulo State University (Unesp) Institute of BiosciencesPrograma de Pós-Graduação Multicêntrico em Ciências Fisiológicas-SBFis Department of Basic Sciences São Paulo State University (Unesp) School of DentistryDepartment of Restorative Dentistry São Paulo State University (Unesp) School of DentistryDepartment of Child and Social Dentistry São Paulo State University (Unesp) School of DentistryDepartment of Basic Sciences São Paulo State University (Unesp) School of DentistrySão Paulo State University (Unesp) Institute of BiosciencesFAPESP: 2014/17619-6Universidade Estadual Paulista (Unesp)Pereira, Renato Felipe [UNESP]Cintra, Luciano Tavares Angelo [UNESP]Tessarin, Gestter Willian Lattari [UNESP]Chiba, Fernando Yamamoto [UNESP]de Lima Coutinho Mattera, Maria Sara [UNESP]Scaramele, Natalia Francisco [UNESP]Tsosura, Thais Verônica Saori [UNESP]Ervolino, Edilson [UNESP]de Oliveira, Sandra Helena Penha [UNESP]Sumida, Doris Hissako [UNESP]2018-12-11T17:32:10Z2018-12-11T17:32:10Z2017-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article982-988application/pdfhttp://dx.doi.org/10.1016/j.joen.2017.01.030Journal of Endodontics, v. 43, n. 6, p. 982-988, 2017.0099-2399http://hdl.handle.net/11449/17880010.1016/j.joen.2017.01.0302-s2.0-850174505312-s2.0-85017450531.pdf440809551734684692357430816673620000-0003-4859-0583Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Endodontics1,585info:eu-repo/semantics/openAccess2023-10-24T06:06:35Zoai:repositorio.unesp.br:11449/178800Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T15:48:49.511904Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
title Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
spellingShingle Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
Pereira, Renato Felipe [UNESP]
Inflammation
insulin resistance
periapical lesion
systemic disorders
title_short Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
title_full Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
title_fullStr Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
title_full_unstemmed Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
title_sort Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
author Pereira, Renato Felipe [UNESP]
author_facet Pereira, Renato Felipe [UNESP]
Cintra, Luciano Tavares Angelo [UNESP]
Tessarin, Gestter Willian Lattari [UNESP]
Chiba, Fernando Yamamoto [UNESP]
de Lima Coutinho Mattera, Maria Sara [UNESP]
Scaramele, Natalia Francisco [UNESP]
Tsosura, Thais Verônica Saori [UNESP]
Ervolino, Edilson [UNESP]
de Oliveira, Sandra Helena Penha [UNESP]
Sumida, Doris Hissako [UNESP]
author_role author
author2 Cintra, Luciano Tavares Angelo [UNESP]
Tessarin, Gestter Willian Lattari [UNESP]
Chiba, Fernando Yamamoto [UNESP]
de Lima Coutinho Mattera, Maria Sara [UNESP]
Scaramele, Natalia Francisco [UNESP]
Tsosura, Thais Verônica Saori [UNESP]
Ervolino, Edilson [UNESP]
de Oliveira, Sandra Helena Penha [UNESP]
Sumida, Doris Hissako [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Pereira, Renato Felipe [UNESP]
Cintra, Luciano Tavares Angelo [UNESP]
Tessarin, Gestter Willian Lattari [UNESP]
Chiba, Fernando Yamamoto [UNESP]
de Lima Coutinho Mattera, Maria Sara [UNESP]
Scaramele, Natalia Francisco [UNESP]
Tsosura, Thais Verônica Saori [UNESP]
Ervolino, Edilson [UNESP]
de Oliveira, Sandra Helena Penha [UNESP]
Sumida, Doris Hissako [UNESP]
dc.subject.por.fl_str_mv Inflammation
insulin resistance
periapical lesion
systemic disorders
topic Inflammation
insulin resistance
periapical lesion
systemic disorders
description Introduction Our previous studies have shown that periapical lesions (PLs) in rats cause systemic disorders such as increased tumor necrosis factor-α plasma levels, insulin resistance, and impairment in insulin signal transduction in muscle tissue. However, the mechanisms involved in these alterations are not fully understood. Under chronic inflammatory conditions such as obesity, it has been shown that the skeletal muscle is affected by inflammation, and the number of resident macrophages that are associated with impairments of insulin action and sensitivity is increased. This study aimed to investigate the presence of macrophages, activation of inflammatory pathways in muscle tissue, glycemia, and insulinemia of rats with PLs. Methods Sixty Wistar rats were distributed into a control group; a group with 1 PL (1PL), which was induced in the right maxillary first molar; and a group with 4 PLs (4PL), which were induced in the right upper and lower first and second molars. We quantified macrophage content by immunohistochemistry for the F4/80 protein. We evaluated Jun N-terminal kinase and IKKα/β phosphorylation status in the muscle tissue by Western blotting. Serum levels of lipopolysaccharide (LPS) and HSP70 and plasma levels of glucose and insulin were assessed by using commercial kits. Results The 1PL and 4PL groups showed increase in macrophage content, IKKα/β, and Jun N-terminal kinase phosphorylation status, serum LPS and HSP70 levels, and insulin resistance and no changes in glycemia and insulinemia compared with the control group. There was no difference in these parameters between the 1PL and 4PL groups. Conclusions PLs promoted an increase in macrophage infiltration, activation of inflammatory pathways in muscle tissue, and serum concentrations of HSP70 and LPS in rats. The present study improves the knowledge on the impact of oral inflammations on the development of systemic alteration, which can induce insulin resistance.
publishDate 2017
dc.date.none.fl_str_mv 2017-06-01
2018-12-11T17:32:10Z
2018-12-11T17:32:10Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.joen.2017.01.030
Journal of Endodontics, v. 43, n. 6, p. 982-988, 2017.
0099-2399
http://hdl.handle.net/11449/178800
10.1016/j.joen.2017.01.030
2-s2.0-85017450531
2-s2.0-85017450531.pdf
4408095517346846
9235743081667362
0000-0003-4859-0583
url http://dx.doi.org/10.1016/j.joen.2017.01.030
http://hdl.handle.net/11449/178800
identifier_str_mv Journal of Endodontics, v. 43, n. 6, p. 982-988, 2017.
0099-2399
10.1016/j.joen.2017.01.030
2-s2.0-85017450531
2-s2.0-85017450531.pdf
4408095517346846
9235743081667362
0000-0003-4859-0583
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of Endodontics
1,585
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 982-988
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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