N-methyl-N-nitrosourea toxicology: data from a rat model
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2021 |
| Outros Autores: | , , , , |
| 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. |
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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 |
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2021-01-01T00:00:00Z 2022-01-31T16:18:47Z 2022-01-31 |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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http://hdl.handle.net/10174/31028 http://hdl.handle.net/10174/31028 |
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http://hdl.handle.net/10174/31028 |
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eng |
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eng |
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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 |
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openAccess |
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III Jornadas Ibéricas de Toxicologia |
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III Jornadas Ibéricas de Toxicologia |
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