Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice
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 UNESP |
Texto Completo: | http://dx.doi.org/10.1007/s10266-023-00800-5 http://hdl.handle.net/11449/248520 |
Resumo: | Bone metabolism and repair are directly regulated by arachidonic acid metabolites. At present, we analyzed the dose–response effects of a selective cysteinyl leukotriene receptor type-1 antagonist during bone repair after tooth extraction and on non-injured skeleton. Sixty-three 129 Sv/Ev male mice composed the groups: C—Control (saline solution); MTK2—2 mg/Kg of Montelukast (MTK) and MTK4–4 mg/Kg of MTK, daily administered by mouth throughout all experimental periods set at 7, 14, and 21 days post-operative. Dental sockets were analyzed by computed microtomography (microCT), histopathology, and immunohistochemistry. Femurs, L5 vertebra and organs were also removed for observation. Blood was collected for plasma bone and liver markers. Histopathology and microCT analysis revealed early socket repair of MTK2 and MTK4 animals, with significant increased BV/TV at days 14 and 21 compared to C. Higher plasma calcium was detected at days 7 and 21 in MTK4 in comparison to C, while phosphate was significantly increased in MTK2 in the same periods in comparison to C and MTK4. No significant differences were found regarding plasma ALP and TRAP, neither for local TRAP and Runx2 immunolabeling at the healing sockets. Organs did not present histological abnormalities. Increased AST levels have been detected in distinct groups and periods. In general, femur phenotype was improved in MTK treated animals. Collectively, MTK promoted early bone formation after tooth extraction and increased bone quality of femurs and vertebra in a time-dose-dependent manner, and should be considered as an alternative therapy when improved post-extraction socket repair or skeleton preservation is required. |
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Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice5-LeukotrieneBone tissueCysteinyl leukotrienesDental socketMiceBone metabolism and repair are directly regulated by arachidonic acid metabolites. At present, we analyzed the dose–response effects of a selective cysteinyl leukotriene receptor type-1 antagonist during bone repair after tooth extraction and on non-injured skeleton. Sixty-three 129 Sv/Ev male mice composed the groups: C—Control (saline solution); MTK2—2 mg/Kg of Montelukast (MTK) and MTK4–4 mg/Kg of MTK, daily administered by mouth throughout all experimental periods set at 7, 14, and 21 days post-operative. Dental sockets were analyzed by computed microtomography (microCT), histopathology, and immunohistochemistry. Femurs, L5 vertebra and organs were also removed for observation. Blood was collected for plasma bone and liver markers. Histopathology and microCT analysis revealed early socket repair of MTK2 and MTK4 animals, with significant increased BV/TV at days 14 and 21 compared to C. Higher plasma calcium was detected at days 7 and 21 in MTK4 in comparison to C, while phosphate was significantly increased in MTK2 in the same periods in comparison to C and MTK4. No significant differences were found regarding plasma ALP and TRAP, neither for local TRAP and Runx2 immunolabeling at the healing sockets. Organs did not present histological abnormalities. Increased AST levels have been detected in distinct groups and periods. In general, femur phenotype was improved in MTK treated animals. Collectively, MTK promoted early bone formation after tooth extraction and increased bone quality of femurs and vertebra in a time-dose-dependent manner, and should be considered as an alternative therapy when improved post-extraction socket repair or skeleton preservation is required.Department of Oral Surgery and Dental Clinics Araçatuba School of Dentistry São Paulo State University—Unesp, Rua José Bonifácio 1192, São PauloDepartment of Basic Sciences Araçatuba School of Dentistry SãoPauloStateUniversity-Unesp, Rua José Bonifácio 1192, São PauloDepartment of DentistryEndodontics and Dental MaterialsSchool of Dentistry University of São Paulo Alameda Otávio Pinheiro Brisola, 9-20, São PauloSchool of Dentistry The University of Texas at Health Science Center at Houston (UTH), 1941 East RoadSchool of Podiatric Medicine The University of Texas at Rio Grande Valley (UTRGV), 2120 Treasure Hills Blvd. HarlingenDepartment of Oral Surgery and Dental Clinics Araçatuba School of Dentistry São Paulo State University—Unesp, Rua José Bonifácio 1192, São PauloDepartment of Basic Sciences Araçatuba School of Dentistry SãoPauloStateUniversity-Unesp, Rua José Bonifácio 1192, São PauloUniversidade Estadual Paulista (UNESP)Universidade de São Paulo (USP)The University of Texas at Health Science Center at Houston (UTH)The University of Texas at Rio Grande Valley (UTRGV)Ribeiro, Kim Henderson Carmo [UNESP]da Silva, Raquel Barroso Parra [UNESP]Roseno, Ana Carolyna Becher [UNESP]Barreto, Ana Julia Moreno [UNESP]Bacelar, Ana Carolina Zucon [UNESP]Ervolino, Edilson [UNESP]Duarte, Marco Antônio HúngaroFakhouri, Walid D.Chaves-Neto, Antonio Hernandes [UNESP]Biguetti, Cláudia CristinaMatsumoto, Mariza Akemi [UNESP]2023-07-29T13:46:16Z2023-07-29T13:46:16Z2023-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1007/s10266-023-00800-5Odontology.1618-12551618-1247http://hdl.handle.net/11449/24852010.1007/s10266-023-00800-52-s2.0-85150175626Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengOdontologyinfo:eu-repo/semantics/openAccess2024-09-19T14:03:04Zoai:repositorio.unesp.br:11449/248520Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-19T14:03:04Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
title |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
spellingShingle |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice Ribeiro, Kim Henderson Carmo [UNESP] 5-Leukotriene Bone tissue Cysteinyl leukotrienes Dental socket Mice |
title_short |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
title_full |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
title_fullStr |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
title_full_unstemmed |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
title_sort |
Dose–response effect of Montelukast on post-extraction dental socket repair and skeletal phenotype of mice |
author |
Ribeiro, Kim Henderson Carmo [UNESP] |
author_facet |
Ribeiro, Kim Henderson Carmo [UNESP] da Silva, Raquel Barroso Parra [UNESP] Roseno, Ana Carolyna Becher [UNESP] Barreto, Ana Julia Moreno [UNESP] Bacelar, Ana Carolina Zucon [UNESP] Ervolino, Edilson [UNESP] Duarte, Marco Antônio Húngaro Fakhouri, Walid D. Chaves-Neto, Antonio Hernandes [UNESP] Biguetti, Cláudia Cristina Matsumoto, Mariza Akemi [UNESP] |
author_role |
author |
author2 |
da Silva, Raquel Barroso Parra [UNESP] Roseno, Ana Carolyna Becher [UNESP] Barreto, Ana Julia Moreno [UNESP] Bacelar, Ana Carolina Zucon [UNESP] Ervolino, Edilson [UNESP] Duarte, Marco Antônio Húngaro Fakhouri, Walid D. Chaves-Neto, Antonio Hernandes [UNESP] Biguetti, Cláudia Cristina Matsumoto, Mariza Akemi [UNESP] |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (UNESP) Universidade de São Paulo (USP) The University of Texas at Health Science Center at Houston (UTH) The University of Texas at Rio Grande Valley (UTRGV) |
dc.contributor.author.fl_str_mv |
Ribeiro, Kim Henderson Carmo [UNESP] da Silva, Raquel Barroso Parra [UNESP] Roseno, Ana Carolyna Becher [UNESP] Barreto, Ana Julia Moreno [UNESP] Bacelar, Ana Carolina Zucon [UNESP] Ervolino, Edilson [UNESP] Duarte, Marco Antônio Húngaro Fakhouri, Walid D. Chaves-Neto, Antonio Hernandes [UNESP] Biguetti, Cláudia Cristina Matsumoto, Mariza Akemi [UNESP] |
dc.subject.por.fl_str_mv |
5-Leukotriene Bone tissue Cysteinyl leukotrienes Dental socket Mice |
topic |
5-Leukotriene Bone tissue Cysteinyl leukotrienes Dental socket Mice |
description |
Bone metabolism and repair are directly regulated by arachidonic acid metabolites. At present, we analyzed the dose–response effects of a selective cysteinyl leukotriene receptor type-1 antagonist during bone repair after tooth extraction and on non-injured skeleton. Sixty-three 129 Sv/Ev male mice composed the groups: C—Control (saline solution); MTK2—2 mg/Kg of Montelukast (MTK) and MTK4–4 mg/Kg of MTK, daily administered by mouth throughout all experimental periods set at 7, 14, and 21 days post-operative. Dental sockets were analyzed by computed microtomography (microCT), histopathology, and immunohistochemistry. Femurs, L5 vertebra and organs were also removed for observation. Blood was collected for plasma bone and liver markers. Histopathology and microCT analysis revealed early socket repair of MTK2 and MTK4 animals, with significant increased BV/TV at days 14 and 21 compared to C. Higher plasma calcium was detected at days 7 and 21 in MTK4 in comparison to C, while phosphate was significantly increased in MTK2 in the same periods in comparison to C and MTK4. No significant differences were found regarding plasma ALP and TRAP, neither for local TRAP and Runx2 immunolabeling at the healing sockets. Organs did not present histological abnormalities. Increased AST levels have been detected in distinct groups and periods. In general, femur phenotype was improved in MTK treated animals. Collectively, MTK promoted early bone formation after tooth extraction and increased bone quality of femurs and vertebra in a time-dose-dependent manner, and should be considered as an alternative therapy when improved post-extraction socket repair or skeleton preservation is required. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023-07-29T13:46:16Z 2023-07-29T13:46:16Z 2023-01-01 |
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/10.1007/s10266-023-00800-5 Odontology. 1618-1255 1618-1247 http://hdl.handle.net/11449/248520 10.1007/s10266-023-00800-5 2-s2.0-85150175626 |
url |
http://dx.doi.org/10.1007/s10266-023-00800-5 http://hdl.handle.net/11449/248520 |
identifier_str_mv |
Odontology. 1618-1255 1618-1247 10.1007/s10266-023-00800-5 2-s2.0-85150175626 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Odontology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
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 |
_version_ |
1813546482083561472 |