N-methyl-N-nitrosourea toxicology: data from a rat model

Detalhes bibliográficos
Autor(a) principal: Vala, Helena
Data de Publicação: 2021
Outros Autores: Vasconcelos-Nóbrega, Carmen, Gama, Adelina, Ferreira, Rita, Oliveira, Paula Alexandra, Faustino-Rocha, Ana Isabel
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: http://hdl.handle.net/10174/31028
Resumo: Introduction: N-methyl-N-nitrosourea (MNU) is the oldest member of the nitroso-compounds that can alkylate DNA. MNU induces tumor development in several organs, depending on the animals’ specie and strain, dose, route, and age at administration. Aims: This study aimed to address the toxicological effects of MNU administration in female rats. Methods: Twelve Sprague-Dawley female rats were divided into two experimental groups: MNU (n=10) and control (n=2). At seven weeks of age, animals from group MNU received an intraperitoneal administration of the carcinogen MNU, at a dose of 50 mg/Kg. Animals from group control received an administration of vehicle (saline solution 0.9%). Animals were humanely sacrificed 18 weeks after MNU or vehicle administration by intraperitoneal injection of xylazine and ketamine, followed by exsanguination by cardiac puncture. A complete necropsy was performed. Heart, lungs, liver, spleen, kidneys, adrenal glands, clitoral glands, and lymph nodes were removed and immersed in buffered formalin for histopathological analysis. Results: Animals from group MNU developed a total of 21 mammary tumors., The organs of animals from group MNU presented a higher number of lesions with higher grade, when compared with the organs of animals from group control. Hyalinization, coagulative myocytolysis, congestion hemorrhage and hyperemia were observed in the heart. Lungs exhibited interstitial inflammation, arteriolosclerosis, arteriosclerosis, congestion, and hyperemia. Interstitial inflammation, congestion and cholestasis were observed in the liver. The spleen presented interstitial inflammation, congestion, hemosiderosis and hyperemia. Congestion, hyperemia, blebbing, hydropic degenerescence, hyaline casts and cystic dilations were found in the kidneys. Adrenal glands presented hyperplasia, congestion, and hydropic degeneration; while clitoral glands presented interstitial fibrosis, ductal dilation, interstitial inflammation, and hyperemia. Infiltrate and congestion were observed in the lymph nodes. Conclusions: The higher number and higher grade of the lesions in group MNU were due to the carcinogenic action of the chemical agent MNU.
id RCAP_6529ead850d8cd7e33db87eeb6e89101
oai_identifier_str oai:dspace.uevora.pt:10174/31028
network_acronym_str RCAP
network_name_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository_id_str https://opendoar.ac.uk/repository/7160
spelling N-methyl-N-nitrosourea toxicology: data from a rat modelIntroduction: N-methyl-N-nitrosourea (MNU) is the oldest member of the nitroso-compounds that can alkylate DNA. MNU induces tumor development in several organs, depending on the animals’ specie and strain, dose, route, and age at administration. Aims: This study aimed to address the toxicological effects of MNU administration in female rats. Methods: Twelve Sprague-Dawley female rats were divided into two experimental groups: MNU (n=10) and control (n=2). At seven weeks of age, animals from group MNU received an intraperitoneal administration of the carcinogen MNU, at a dose of 50 mg/Kg. Animals from group control received an administration of vehicle (saline solution 0.9%). Animals were humanely sacrificed 18 weeks after MNU or vehicle administration by intraperitoneal injection of xylazine and ketamine, followed by exsanguination by cardiac puncture. A complete necropsy was performed. Heart, lungs, liver, spleen, kidneys, adrenal glands, clitoral glands, and lymph nodes were removed and immersed in buffered formalin for histopathological analysis. Results: Animals from group MNU developed a total of 21 mammary tumors., The organs of animals from group MNU presented a higher number of lesions with higher grade, when compared with the organs of animals from group control. Hyalinization, coagulative myocytolysis, congestion hemorrhage and hyperemia were observed in the heart. Lungs exhibited interstitial inflammation, arteriolosclerosis, arteriosclerosis, congestion, and hyperemia. Interstitial inflammation, congestion and cholestasis were observed in the liver. The spleen presented interstitial inflammation, congestion, hemosiderosis and hyperemia. Congestion, hyperemia, blebbing, hydropic degenerescence, hyaline casts and cystic dilations were found in the kidneys. Adrenal glands presented hyperplasia, congestion, and hydropic degeneration; while clitoral glands presented interstitial fibrosis, ductal dilation, interstitial inflammation, and hyperemia. Infiltrate and congestion were observed in the lymph nodes. Conclusions: The higher number and higher grade of the lesions in group MNU were due to the carcinogenic action of the chemical agent MNU.III Jornadas Ibéricas de Toxicologia2022-01-31T16:18:47Z2022-01-312021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10174/31028http://hdl.handle.net/10174/31028engVala H, Vasconcelos-Nóbrega C, Gama A, Ferreira R, Oliveira PA, Faustino-Rocha AI. 2021. N-methyl-N-nitrosourea toxicology: data from a rat model. III Jornadas Ibéricas de Toxicologia, p. 240, 4 a 5 de junho.240-241ndndndndndanafaustino@uevora.pt206Vala, HelenaVasconcelos-Nóbrega, CarmenGama, AdelinaFerreira, RitaOliveira, Paula AlexandraFaustino-Rocha, Ana Isabelinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-01-03T19:27:40Zoai:dspace.uevora.pt:10174/31028Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T12:24:44.975038Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv N-methyl-N-nitrosourea toxicology: data from a rat model
title N-methyl-N-nitrosourea toxicology: data from a rat model
spellingShingle N-methyl-N-nitrosourea toxicology: data from a rat model
Vala, Helena
title_short N-methyl-N-nitrosourea toxicology: data from a rat model
title_full N-methyl-N-nitrosourea toxicology: data from a rat model
title_fullStr N-methyl-N-nitrosourea toxicology: data from a rat model
title_full_unstemmed N-methyl-N-nitrosourea toxicology: data from a rat model
title_sort N-methyl-N-nitrosourea toxicology: data from a rat model
author Vala, Helena
author_facet Vala, Helena
Vasconcelos-Nóbrega, Carmen
Gama, Adelina
Ferreira, Rita
Oliveira, Paula Alexandra
Faustino-Rocha, Ana Isabel
author_role author
author2 Vasconcelos-Nóbrega, Carmen
Gama, Adelina
Ferreira, Rita
Oliveira, Paula Alexandra
Faustino-Rocha, Ana Isabel
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Vala, Helena
Vasconcelos-Nóbrega, Carmen
Gama, Adelina
Ferreira, Rita
Oliveira, Paula Alexandra
Faustino-Rocha, Ana Isabel
description Introduction: N-methyl-N-nitrosourea (MNU) is the oldest member of the nitroso-compounds that can alkylate DNA. MNU induces tumor development in several organs, depending on the animals’ specie and strain, dose, route, and age at administration. Aims: This study aimed to address the toxicological effects of MNU administration in female rats. Methods: Twelve Sprague-Dawley female rats were divided into two experimental groups: MNU (n=10) and control (n=2). At seven weeks of age, animals from group MNU received an intraperitoneal administration of the carcinogen MNU, at a dose of 50 mg/Kg. Animals from group control received an administration of vehicle (saline solution 0.9%). Animals were humanely sacrificed 18 weeks after MNU or vehicle administration by intraperitoneal injection of xylazine and ketamine, followed by exsanguination by cardiac puncture. A complete necropsy was performed. Heart, lungs, liver, spleen, kidneys, adrenal glands, clitoral glands, and lymph nodes were removed and immersed in buffered formalin for histopathological analysis. Results: Animals from group MNU developed a total of 21 mammary tumors., The organs of animals from group MNU presented a higher number of lesions with higher grade, when compared with the organs of animals from group control. Hyalinization, coagulative myocytolysis, congestion hemorrhage and hyperemia were observed in the heart. Lungs exhibited interstitial inflammation, arteriolosclerosis, arteriosclerosis, congestion, and hyperemia. Interstitial inflammation, congestion and cholestasis were observed in the liver. The spleen presented interstitial inflammation, congestion, hemosiderosis and hyperemia. Congestion, hyperemia, blebbing, hydropic degenerescence, hyaline casts and cystic dilations were found in the kidneys. Adrenal glands presented hyperplasia, congestion, and hydropic degeneration; while clitoral glands presented interstitial fibrosis, ductal dilation, interstitial inflammation, and hyperemia. Infiltrate and congestion were observed in the lymph nodes. Conclusions: The higher number and higher grade of the lesions in group MNU were due to the carcinogenic action of the chemical agent MNU.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-01T00:00:00Z
2022-01-31T16:18:47Z
2022-01-31
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://hdl.handle.net/10174/31028
http://hdl.handle.net/10174/31028
url http://hdl.handle.net/10174/31028
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Vala H, Vasconcelos-Nóbrega C, Gama A, Ferreira R, Oliveira PA, Faustino-Rocha AI. 2021. N-methyl-N-nitrosourea toxicology: data from a rat model. III Jornadas Ibéricas de Toxicologia, p. 240, 4 a 5 de junho.
240-241
nd
nd
nd
nd
nd
anafaustino@uevora.pt
206
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv III Jornadas Ibéricas de Toxicologia
publisher.none.fl_str_mv III Jornadas Ibéricas de Toxicologia
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
_version_ 1833592796685008896