Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis

Bibliographic Details
Main Author: Tavares, B. S. [UNESP]
Publication Date: 2021
Other Authors: Tsosura, T. V.S. [UNESP], Mattera, M. S.L.C. [UNESP], Santelli, J. O. [UNESP], Belardi, B. E. [UNESP], Chiba, F. Y. [UNESP], Cintra, L. T.A. [UNESP], Silva, C. C. [UNESP], Matsushita, D. H. [UNESP]
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1111/iej.13474
http://hdl.handle.net/11449/205770
Summary: Aim: To verify the effects of melatonin supplementation on insulin sensitivity, plasma concentrations of inflammatory cytokines, insulin signalling and inflammatory pathways in the soleus (SM) and extensor digitorum longus (EDL) muscles of rats with apical periodontitis (AP). Methodology: Seventy-two Wistar rats were distributed into 4 groups: (a) control (C), (b) control supplemented with melatonin (M), (c) AP (AP), and (d) AP supplemented with melatonin (AP + M). AP was induced by pulp exposure of the maxillary and mandibular right first and second molars to the oral environment. After AP induction, oral supplementation with 5 mg kg−1 melatonin (diluted in drinking water) for 60 days was initiated. At the end of the treatment, the following were analysed: (1) plasma concentrations of insulin and inflammatory cytokines (TNF-α, IL-6, IL-1β and IL-10) using ELISA kits; (2) glycaemia using enzymatic assay; (3) insulin resistance using homoeostasis model assessment of insulin resistance (HOMA-IR) index; and (4) phosphorylation status of pp185 tyrosine, Akt serine, IKKα/β, and JNK in SM and EDL using Western blot. Analysis of variance of two or three factors was performed, followed by the Bonferroni test. P values < 0.05 were considered statistically significant. Results: AP promoted insulin resistance, significantly increased (P < 0.05) plasma concentrations of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β), significantly decreased (P < 0.05) the concentration of anti-inflammatory cytokine IL-10, impaired insulin signalling in SM, and increased IKKα/β phosphorylation status in SM and EDL. Melatonin supplementation in rats with AP improved insulin sensitivity, significantly decreased (P < 0.05) TNF-α and IL-1β, significantly increased (P < 0.05) IL-10 plasma concentrations, and changed the insulin signalling in soleus muscle and IKKα/β phosphorylation status in SM and EDL muscles. Conclusions: Melatonin is a potent adjuvant treatment for improving apical periodontitis-associated changes in insulin sensitivity, insulin signalling and inflammatory pathways. In addition, the negative impact of AP on general health was also demonstrated.
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spelling Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitisapical periodontitisinflammationinsulin resistancemelatoninAim: To verify the effects of melatonin supplementation on insulin sensitivity, plasma concentrations of inflammatory cytokines, insulin signalling and inflammatory pathways in the soleus (SM) and extensor digitorum longus (EDL) muscles of rats with apical periodontitis (AP). Methodology: Seventy-two Wistar rats were distributed into 4 groups: (a) control (C), (b) control supplemented with melatonin (M), (c) AP (AP), and (d) AP supplemented with melatonin (AP + M). AP was induced by pulp exposure of the maxillary and mandibular right first and second molars to the oral environment. After AP induction, oral supplementation with 5 mg kg−1 melatonin (diluted in drinking water) for 60 days was initiated. At the end of the treatment, the following were analysed: (1) plasma concentrations of insulin and inflammatory cytokines (TNF-α, IL-6, IL-1β and IL-10) using ELISA kits; (2) glycaemia using enzymatic assay; (3) insulin resistance using homoeostasis model assessment of insulin resistance (HOMA-IR) index; and (4) phosphorylation status of pp185 tyrosine, Akt serine, IKKα/β, and JNK in SM and EDL using Western blot. Analysis of variance of two or three factors was performed, followed by the Bonferroni test. P values < 0.05 were considered statistically significant. Results: AP promoted insulin resistance, significantly increased (P < 0.05) plasma concentrations of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β), significantly decreased (P < 0.05) the concentration of anti-inflammatory cytokine IL-10, impaired insulin signalling in SM, and increased IKKα/β phosphorylation status in SM and EDL. Melatonin supplementation in rats with AP improved insulin sensitivity, significantly decreased (P < 0.05) TNF-α and IL-1β, significantly increased (P < 0.05) IL-10 plasma concentrations, and changed the insulin signalling in soleus muscle and IKKα/β phosphorylation status in SM and EDL muscles. Conclusions: Melatonin is a potent adjuvant treatment for improving apical periodontitis-associated changes in insulin sensitivity, insulin signalling and inflammatory pathways. In addition, the negative impact of AP on general health was also demonstrated.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Programa de Pós-graduação Multicêntrico em Ciências Fisiológicas PPGMCF SBFis Department of Basic Sciences School of Dentistry São Paulo State University (UNESP)Department of Preventive and Restorative Dentistry School of Dentistry São Paulo State University (UNESP)Programa de Pós-graduação Multicêntrico em Ciências Fisiológicas PPGMCF SBFis Department of Basic Sciences School of Dentistry São Paulo State University (UNESP)Department of Preventive and Restorative Dentistry School of Dentistry São Paulo State University (UNESP)FAPESP: #2018/23346-3FAPESP: #2019/12995-3FAPESP: #2019/18589-7Universidade Estadual Paulista (Unesp)Tavares, B. S. [UNESP]Tsosura, T. V.S. [UNESP]Mattera, M. S.L.C. [UNESP]Santelli, J. O. [UNESP]Belardi, B. E. [UNESP]Chiba, F. Y. [UNESP]Cintra, L. T.A. [UNESP]Silva, C. C. [UNESP]Matsushita, D. H. [UNESP]2021-06-25T10:20:58Z2021-06-25T10:20:58Z2021-06-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article926-940http://dx.doi.org/10.1111/iej.13474International Endodontic Journal, v. 54, n. 6, p. 926-940, 2021.1365-25910143-2885http://hdl.handle.net/11449/20577010.1111/iej.134742-s2.0-85099762414Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengInternational Endodontic Journalinfo:eu-repo/semantics/openAccess2021-10-22T17:11:50Zoai:repositorio.unesp.br:11449/205770Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-22T17:11:50Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
title Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
spellingShingle Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
Tavares, B. S. [UNESP]
apical periodontitis
inflammation
insulin resistance
melatonin
title_short Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
title_full Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
title_fullStr Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
title_full_unstemmed Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
title_sort Effects of melatonin on insulin signaling and inflammatory pathways of rats with apical periodontitis
author Tavares, B. S. [UNESP]
author_facet Tavares, B. S. [UNESP]
Tsosura, T. V.S. [UNESP]
Mattera, M. S.L.C. [UNESP]
Santelli, J. O. [UNESP]
Belardi, B. E. [UNESP]
Chiba, F. Y. [UNESP]
Cintra, L. T.A. [UNESP]
Silva, C. C. [UNESP]
Matsushita, D. H. [UNESP]
author_role author
author2 Tsosura, T. V.S. [UNESP]
Mattera, M. S.L.C. [UNESP]
Santelli, J. O. [UNESP]
Belardi, B. E. [UNESP]
Chiba, F. Y. [UNESP]
Cintra, L. T.A. [UNESP]
Silva, C. C. [UNESP]
Matsushita, D. H. [UNESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Tavares, B. S. [UNESP]
Tsosura, T. V.S. [UNESP]
Mattera, M. S.L.C. [UNESP]
Santelli, J. O. [UNESP]
Belardi, B. E. [UNESP]
Chiba, F. Y. [UNESP]
Cintra, L. T.A. [UNESP]
Silva, C. C. [UNESP]
Matsushita, D. H. [UNESP]
dc.subject.por.fl_str_mv apical periodontitis
inflammation
insulin resistance
melatonin
topic apical periodontitis
inflammation
insulin resistance
melatonin
description Aim: To verify the effects of melatonin supplementation on insulin sensitivity, plasma concentrations of inflammatory cytokines, insulin signalling and inflammatory pathways in the soleus (SM) and extensor digitorum longus (EDL) muscles of rats with apical periodontitis (AP). Methodology: Seventy-two Wistar rats were distributed into 4 groups: (a) control (C), (b) control supplemented with melatonin (M), (c) AP (AP), and (d) AP supplemented with melatonin (AP + M). AP was induced by pulp exposure of the maxillary and mandibular right first and second molars to the oral environment. After AP induction, oral supplementation with 5 mg kg−1 melatonin (diluted in drinking water) for 60 days was initiated. At the end of the treatment, the following were analysed: (1) plasma concentrations of insulin and inflammatory cytokines (TNF-α, IL-6, IL-1β and IL-10) using ELISA kits; (2) glycaemia using enzymatic assay; (3) insulin resistance using homoeostasis model assessment of insulin resistance (HOMA-IR) index; and (4) phosphorylation status of pp185 tyrosine, Akt serine, IKKα/β, and JNK in SM and EDL using Western blot. Analysis of variance of two or three factors was performed, followed by the Bonferroni test. P values < 0.05 were considered statistically significant. Results: AP promoted insulin resistance, significantly increased (P < 0.05) plasma concentrations of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β), significantly decreased (P < 0.05) the concentration of anti-inflammatory cytokine IL-10, impaired insulin signalling in SM, and increased IKKα/β phosphorylation status in SM and EDL. Melatonin supplementation in rats with AP improved insulin sensitivity, significantly decreased (P < 0.05) TNF-α and IL-1β, significantly increased (P < 0.05) IL-10 plasma concentrations, and changed the insulin signalling in soleus muscle and IKKα/β phosphorylation status in SM and EDL muscles. Conclusions: Melatonin is a potent adjuvant treatment for improving apical periodontitis-associated changes in insulin sensitivity, insulin signalling and inflammatory pathways. In addition, the negative impact of AP on general health was also demonstrated.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T10:20:58Z
2021-06-25T10:20:58Z
2021-06-01
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/10.1111/iej.13474
International Endodontic Journal, v. 54, n. 6, p. 926-940, 2021.
1365-2591
0143-2885
http://hdl.handle.net/11449/205770
10.1111/iej.13474
2-s2.0-85099762414
url http://dx.doi.org/10.1111/iej.13474
http://hdl.handle.net/11449/205770
identifier_str_mv International Endodontic Journal, v. 54, n. 6, p. 926-940, 2021.
1365-2591
0143-2885
10.1111/iej.13474
2-s2.0-85099762414
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv International Endodontic Journal
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 926-940
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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