Modulation of blood redox status by the progression of induced apical periodontitis in rats

Detalhes bibliográficos
Autor(a) principal: Frazão, Deborah Ribeiro
Data de Publicação: 2023
Outros Autores: Mendes, Paulo Fernando Santos, Silva, Daiane Claydes Baia da, Moura, João Daniel Mendonça de, Santos, Vinicius Ruan Neves, Sousa, José Mário Matos, Balbinot, Gabriela de Souza, Guimarães, Douglas M., Collares, Fabrício Mezzomo, Lima, Rafael Rodrigues
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/271816
Resumo: This study aimed to investigate if apical periodontitis in different periods changes systemic levels of the antioxidant and pro-oxidant parameters in Wistar rats. Twenty-four rats were randomly allocated into healthy animals, apical periodontitis at 14 days (AP14) and apical periodontitis at 28 days (AP28). The first mandibular molars were accessed in the AP groups, and the pulp chamber was exposed to the oral environment, inducing the apical lesion. After 14 and 28 days, the animals were anesthetized, euthanized, and hemimandibles were collected for micro-computed tomography (micro-CT) analysis to measure lesion volume, bone volume (BV), percent of bone to total tissue volume (BV/TV), trabecular thickness (Tb.Th), trabecular number (Tb.N), and trabecular space (Tb.Sp). A histological examination of the remaining bone was also performed. Finally, blood samples were collected for oxidative biochemistry analysis, investigating glutathione (GSH), Trolox equivalent antioxidant capacity (TEAC), and lipid peroxidation (TBARS). The lesion volume was greater at 28 than at 14 days, as shown by micro-CT. AP14 and AP28 had decreased BV and Tb.Th, but only AP28 showed a reduction in BV/TV. Tb.N and Tb. Sp were increased in apical periodontitis at 28 days. In the histopathological analysis, AP14 had focal regions of moderate mononuclear inflammatory infiltrate, and AP28 had an intense inflammatory infiltrate with bacterial colonies. In the biochemical evaluation, GSH, TEAC, and TBARS were increased after 14 days. However, GSH returned to control levels, TEAC was similar to AP14, and TBARS increased significantly after 28 days. Therefore, the oxidative biochemistry response was modulated according to the progression of periapical damage. After 14 days, the organism could still react to the injury. However, at 28 days, the antioxidant response decreased, associated with an increase in TBARS
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spelling Frazão, Deborah RibeiroMendes, Paulo Fernando SantosSilva, Daiane Claydes Baia daMoura, João Daniel Mendonça deSantos, Vinicius Ruan NevesSousa, José Mário MatosBalbinot, Gabriela de SouzaGuimarães, Douglas M.Collares, Fabrício MezzomoLima, Rafael Rodrigues2024-02-09T05:08:25Z20231664-042Xhttp://hdl.handle.net/10183/271816001194679This study aimed to investigate if apical periodontitis in different periods changes systemic levels of the antioxidant and pro-oxidant parameters in Wistar rats. Twenty-four rats were randomly allocated into healthy animals, apical periodontitis at 14 days (AP14) and apical periodontitis at 28 days (AP28). The first mandibular molars were accessed in the AP groups, and the pulp chamber was exposed to the oral environment, inducing the apical lesion. After 14 and 28 days, the animals were anesthetized, euthanized, and hemimandibles were collected for micro-computed tomography (micro-CT) analysis to measure lesion volume, bone volume (BV), percent of bone to total tissue volume (BV/TV), trabecular thickness (Tb.Th), trabecular number (Tb.N), and trabecular space (Tb.Sp). A histological examination of the remaining bone was also performed. Finally, blood samples were collected for oxidative biochemistry analysis, investigating glutathione (GSH), Trolox equivalent antioxidant capacity (TEAC), and lipid peroxidation (TBARS). The lesion volume was greater at 28 than at 14 days, as shown by micro-CT. AP14 and AP28 had decreased BV and Tb.Th, but only AP28 showed a reduction in BV/TV. Tb.N and Tb. Sp were increased in apical periodontitis at 28 days. In the histopathological analysis, AP14 had focal regions of moderate mononuclear inflammatory infiltrate, and AP28 had an intense inflammatory infiltrate with bacterial colonies. In the biochemical evaluation, GSH, TEAC, and TBARS were increased after 14 days. However, GSH returned to control levels, TEAC was similar to AP14, and TBARS increased significantly after 28 days. Therefore, the oxidative biochemistry response was modulated according to the progression of periapical damage. After 14 days, the organism could still react to the injury. However, at 28 days, the antioxidant response decreased, associated with an increase in TBARSapplication/pdfengFrontiers in Physiology. Lausanne. Vol. 14, (2023), p. 1 - 12Periodontite periapicalEstresse oxidativoRatos WistarMicrotomografia por raio-xPeriapical periodontitisOxidative stressWistar ratsMicroCTInflammationModulation of blood redox status by the progression of induced apical periodontitis in ratsEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001194679.pdf.txt001194679.pdf.txtExtracted Texttext/plain59875http://www.lume.ufrgs.br/bitstream/10183/271816/2/001194679.pdf.txtb038cec694925f80a181b5c088073c8cMD52ORIGINAL001194679.pdfTexto completo (inglês)application/pdf3006797http://www.lume.ufrgs.br/bitstream/10183/271816/1/001194679.pdfdc0b750c2acaac7ebabf00b507deb484MD5110183/2718162024-02-10 06:09:34.28353oai:www.lume.ufrgs.br:10183/271816Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-02-10T08:09:34Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Modulation of blood redox status by the progression of induced apical periodontitis in rats
title Modulation of blood redox status by the progression of induced apical periodontitis in rats
spellingShingle Modulation of blood redox status by the progression of induced apical periodontitis in rats
Frazão, Deborah Ribeiro
Periodontite periapical
Estresse oxidativo
Ratos Wistar
Microtomografia por raio-x
Periapical periodontitis
Oxidative stress
Wistar rats
MicroCT
Inflammation
title_short Modulation of blood redox status by the progression of induced apical periodontitis in rats
title_full Modulation of blood redox status by the progression of induced apical periodontitis in rats
title_fullStr Modulation of blood redox status by the progression of induced apical periodontitis in rats
title_full_unstemmed Modulation of blood redox status by the progression of induced apical periodontitis in rats
title_sort Modulation of blood redox status by the progression of induced apical periodontitis in rats
author Frazão, Deborah Ribeiro
author_facet Frazão, Deborah Ribeiro
Mendes, Paulo Fernando Santos
Silva, Daiane Claydes Baia da
Moura, João Daniel Mendonça de
Santos, Vinicius Ruan Neves
Sousa, José Mário Matos
Balbinot, Gabriela de Souza
Guimarães, Douglas M.
Collares, Fabrício Mezzomo
Lima, Rafael Rodrigues
author_role author
author2 Mendes, Paulo Fernando Santos
Silva, Daiane Claydes Baia da
Moura, João Daniel Mendonça de
Santos, Vinicius Ruan Neves
Sousa, José Mário Matos
Balbinot, Gabriela de Souza
Guimarães, Douglas M.
Collares, Fabrício Mezzomo
Lima, Rafael Rodrigues
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Frazão, Deborah Ribeiro
Mendes, Paulo Fernando Santos
Silva, Daiane Claydes Baia da
Moura, João Daniel Mendonça de
Santos, Vinicius Ruan Neves
Sousa, José Mário Matos
Balbinot, Gabriela de Souza
Guimarães, Douglas M.
Collares, Fabrício Mezzomo
Lima, Rafael Rodrigues
dc.subject.por.fl_str_mv Periodontite periapical
Estresse oxidativo
Ratos Wistar
Microtomografia por raio-x
topic Periodontite periapical
Estresse oxidativo
Ratos Wistar
Microtomografia por raio-x
Periapical periodontitis
Oxidative stress
Wistar rats
MicroCT
Inflammation
dc.subject.eng.fl_str_mv Periapical periodontitis
Oxidative stress
Wistar rats
MicroCT
Inflammation
description This study aimed to investigate if apical periodontitis in different periods changes systemic levels of the antioxidant and pro-oxidant parameters in Wistar rats. Twenty-four rats were randomly allocated into healthy animals, apical periodontitis at 14 days (AP14) and apical periodontitis at 28 days (AP28). The first mandibular molars were accessed in the AP groups, and the pulp chamber was exposed to the oral environment, inducing the apical lesion. After 14 and 28 days, the animals were anesthetized, euthanized, and hemimandibles were collected for micro-computed tomography (micro-CT) analysis to measure lesion volume, bone volume (BV), percent of bone to total tissue volume (BV/TV), trabecular thickness (Tb.Th), trabecular number (Tb.N), and trabecular space (Tb.Sp). A histological examination of the remaining bone was also performed. Finally, blood samples were collected for oxidative biochemistry analysis, investigating glutathione (GSH), Trolox equivalent antioxidant capacity (TEAC), and lipid peroxidation (TBARS). The lesion volume was greater at 28 than at 14 days, as shown by micro-CT. AP14 and AP28 had decreased BV and Tb.Th, but only AP28 showed a reduction in BV/TV. Tb.N and Tb. Sp were increased in apical periodontitis at 28 days. In the histopathological analysis, AP14 had focal regions of moderate mononuclear inflammatory infiltrate, and AP28 had an intense inflammatory infiltrate with bacterial colonies. In the biochemical evaluation, GSH, TEAC, and TBARS were increased after 14 days. However, GSH returned to control levels, TEAC was similar to AP14, and TBARS increased significantly after 28 days. Therefore, the oxidative biochemistry response was modulated according to the progression of periapical damage. After 14 days, the organism could still react to the injury. However, at 28 days, the antioxidant response decreased, associated with an increase in TBARS
publishDate 2023
dc.date.issued.fl_str_mv 2023
dc.date.accessioned.fl_str_mv 2024-02-09T05:08:25Z
dc.type.driver.fl_str_mv Estrangeiro
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/271816
dc.identifier.issn.pt_BR.fl_str_mv 1664-042X
dc.identifier.nrb.pt_BR.fl_str_mv 001194679
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dc.language.iso.fl_str_mv eng
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dc.relation.ispartof.pt_BR.fl_str_mv Frontiers in Physiology. Lausanne. Vol. 14, (2023), p. 1 - 12
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