Modulation of blood redox status by the progression of induced apical periodontitis in rats
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Outros Autores: | , , , , , , , , |
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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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 info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
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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1664-042X 001194679 |
url |
http://hdl.handle.net/10183/271816 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Frontiers in Physiology. Lausanne. Vol. 14, (2023), p. 1 - 12 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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