Periapical Lesions Increase Macrophage Infiltration and Inflammatory Signaling in Muscle Tissue of Rats
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , |
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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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/openAccess2024-09-19T18:31:24Zoai:repositorio.unesp.br:11449/178800Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T18:31:24Repositório 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 |
repositoriounesp@unesp.br |
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1813546409978232832 |