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, Cármen, Gama, Adelina, Ferreira, Rita, Oliveira, Paula Alexandra, Faustino-Rocha, Ana Isabel
Tipo de documento: Artigo de conferência
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10174/32769
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_43c612bc137155b03948e9a6b2f2612c
oai_identifier_str oai:dspace.uevora.pt:10174/32769
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str
spelling N-methyl-N-nitrosourea toxicology: data from a rat modelMNUIntroduction: 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.2022-11-17T17:01:16Z2022-11-172021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjecthttp://hdl.handle.net/10174/32769http://hdl.handle.net/10174/32769engVala 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, 4 a 5 de junho.naonaosimndndndndndanafaustino@uevora.pt206Vala, HelenaVasconcelos-Nóbrega, CármenGama, AdelinaFerreira, RitaOliveira, Paula AlexandraFaustino-Rocha, Ana Isabelinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-08-08T04:42:51ZPortal AgregadorONG
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
MNU
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, Cármen
Gama, Adelina
Ferreira, Rita
Oliveira, Paula Alexandra
Faustino-Rocha, Ana Isabel
author_role author
author2 Vasconcelos-Nóbrega, Cármen
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, Cármen
Gama, Adelina
Ferreira, Rita
Oliveira, Paula Alexandra
Faustino-Rocha, Ana Isabel
dc.subject.por.fl_str_mv MNU
topic MNU
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
2022-11-17T17:01:16Z
2022-11-17
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/conferenceObject
format conferenceObject
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/32769
http://hdl.handle.net/10174/32769
url http://hdl.handle.net/10174/32769
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, 4 a 5 de junho.
nao
nao
sim
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.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1777304655957590016