Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar

Detalhes bibliográficos
Autor(a) principal: Vieira, Bárbara Martins
Data de Publicação: 2014
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UFG
Texto Completo: http://repositorio.bc.ufg.br/tede/handle/tede/4309
Resumo: The carbon tetrachloride (CCl4) is recognized as a classic hepatotoxin, being considered the best method to induce liver injury, commonly used as a model to test the hepatoprotective effect of drugs and natural substances and for investigation of hepatotoxicity, cytotoxicity and oxidative stress, in both in vivo and in vitro studies. This study aimed to standardize the lowest dose of CCl4 to cause acute liver injury by oxidative stress in Wistar rats. The in vivo experiment was carried out with 12 male Wistar rats (180-240g),which were maintained for 16 days under controlled environment and supplied with water and Purina® rodent ad libitum. The animals were separated into four groups: CG - control group; G0,5 - dose of 0.5 ml / kg body weight (bw); G0,75 - dose of 0.75 ml / kg bw and G1 - dose of 1 ml / kg bw. CCl4 was administered by intraperitoneal injection twice a week. 24h after the last CCl4 administration, all animals were anesthetized (xylazine: ketamine - 1: 1 v / v) for performing cardiac puncture, euthanasia and dissection of the liver for removal and analysis. Results obtained were subjected to normality test, and followed by the analysis of variance (ANOVA) and comparison of means (Tukey at 5% probability - post-hoc). It was observed that the mean weights of rats treated with CCl4 were higher than that of to the GC and the liver protein content (in g / 100 g) was lower in the treated groups, with no statistical difference between the test groups. Histopathological analysis showed changes in the structure, increased numbers of macrophages with intracellular lipid accumulation and increased cellular infiltration in groups treated with CCl4. By quantifying the enzymes alanine aminotransferase (ALT), aspartate and alanine aminotransferase (AST), it was found that the CCl4-treated groups showed significantly higher levels than CG, being higher in G1 compared to the other groups tested. All tested concentrations of CCl4 induced liver injury in vivo, in different degrees, and the concentration of 0.5 mL / kg bw, administered twice weekly, was the lowest dose tested that could cause changes in all the parameters evaluated. Therefore, this is the ideal dose for induction of acute liver injury, aiming to test the modulatory role of dietary and nutritional factors.
id UFG-2_acc891921928f3c8cceed3483be847f6
oai_identifier_str oai:repositorio.bc.ufg.br:tede/4309
network_acronym_str UFG-2
network_name_str Repositório Institucional da UFG
repository_id_str
spelling Naves, Maria Margareth Veloso http://lattes.cnpq.br/6563181057140270Cominetti, CristianeHorst, Maria AderuzaNaves, Maria Margareth VelosoCeles, Mara Rúbia Nuneshttp://lattes.cnpq.br/9945884989330825Vieira, Bárbara Martins2015-03-20T14:04:37Z2014-08-22VIEIRA, B. M. Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar. 2014. 53 f. Dissertação ( Mestrado em Nutrição e Saúde) - Universidade Federal de Goiás, Goiânia, 2014.http://repositorio.bc.ufg.br/tede/handle/tede/4309ark:/38995/0013000001srqThe carbon tetrachloride (CCl4) is recognized as a classic hepatotoxin, being considered the best method to induce liver injury, commonly used as a model to test the hepatoprotective effect of drugs and natural substances and for investigation of hepatotoxicity, cytotoxicity and oxidative stress, in both in vivo and in vitro studies. This study aimed to standardize the lowest dose of CCl4 to cause acute liver injury by oxidative stress in Wistar rats. The in vivo experiment was carried out with 12 male Wistar rats (180-240g),which were maintained for 16 days under controlled environment and supplied with water and Purina® rodent ad libitum. The animals were separated into four groups: CG - control group; G0,5 - dose of 0.5 ml / kg body weight (bw); G0,75 - dose of 0.75 ml / kg bw and G1 - dose of 1 ml / kg bw. CCl4 was administered by intraperitoneal injection twice a week. 24h after the last CCl4 administration, all animals were anesthetized (xylazine: ketamine - 1: 1 v / v) for performing cardiac puncture, euthanasia and dissection of the liver for removal and analysis. Results obtained were subjected to normality test, and followed by the analysis of variance (ANOVA) and comparison of means (Tukey at 5% probability - post-hoc). It was observed that the mean weights of rats treated with CCl4 were higher than that of to the GC and the liver protein content (in g / 100 g) was lower in the treated groups, with no statistical difference between the test groups. Histopathological analysis showed changes in the structure, increased numbers of macrophages with intracellular lipid accumulation and increased cellular infiltration in groups treated with CCl4. By quantifying the enzymes alanine aminotransferase (ALT), aspartate and alanine aminotransferase (AST), it was found that the CCl4-treated groups showed significantly higher levels than CG, being higher in G1 compared to the other groups tested. All tested concentrations of CCl4 induced liver injury in vivo, in different degrees, and the concentration of 0.5 mL / kg bw, administered twice weekly, was the lowest dose tested that could cause changes in all the parameters evaluated. Therefore, this is the ideal dose for induction of acute liver injury, aiming to test the modulatory role of dietary and nutritional factors.O Tetracloreto de Carbono (CCl4) é reconhecido como hepatotoxina clássica, sendo considerada a melhor substância para induzir lesão hepática, comumente utilizado como modelo para testar o efeito hepatoprotetor de drogas e substâncias naturais e para investigação de hepatotoxicidade, citotoxicidade e estresse oxidativo, tanto para estudos in vivo quanto in vitro. O presente estudo visou padronizar a menor dose de CCl4 capaz de provocar lesão hepática aguda por estresse oxidativo em ratos Wistar. O experimento in vivo foi realizado com 12 ratos Wistar adultos, machos, mantidos em condições de ambiente controladas e fornecimento de água e ração distribuídos ad libitum. O ensaio teve duração de 16 dias. Os animais foram separados em quatro grupos, sendo: GC – grupo controle; G0,5 – dose de 0,5 mL/kg de peso corporal (pc); G0,75 – dose de 0,75 mL/kg de pc e G1 – dose de 1 mL/kg de pc. O CCI4 foi administrado via injeção intraperitoneal, duas vezes por semana. Após 24h da última administração de CCI4, todos os animais foram anestesiados para realização de punção cardíaca, eutanásia e dissecação para retirada do fígado e análises. Os resultados obtidos foram submetidos ao teste de normalidade e, posteriormente, à análise de variância e comparação de médias. Observou-se que o peso do fígado dos ratos tratados com CCl4 foi maior em todos os grupos tratados em comparação ao GC e o teor protéico do fígado (em g/100g) foi menor nos grupos tratados, sem diferença estatística entre os grupos teste. As análises histopatológicas mostraram alteração na estrutura do tecido hepático, aumento do número de macrófagos com acúmulo intracelular de lipídeos e aumento do infiltrado celular nos grupos tratados com CCl4. Por meio da quantificação das enzimas alanina aminotransferase (ALT) e alanina aspartato aminotransferase (AST), verificou-se que os grupos tratados com CCl4 apresentaram concentrações significativamente mais elevadas em relação ao GC, sendo maiores no G1 em comparação aos demais grupos testados. Todas as concentrações de CCl4 testadas induziram lesão hepática, em diferentes graus, sendo a concentração de 0,5 mL/kg de pc, administrada duas vezes por semana, a menor dose testada que conseguiu provocar alterações em todos os parâmentos avaliados. Portanto, esta é a dose mais indicada para indução de lesão hepática aguda, objetivando testar o papel modulador de fatores alimentares e nutricionais.Submitted by Cássia Santos (cassia.bcufg@gmail.com) on 2015-03-17T11:16:45Z No. of bitstreams: 2 Dissertação - Barbara Martins Vieira - 2014.pdf: 1451459 bytes, checksum: 595a3718c8c4e83f9334cf6513f85119 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2015-03-20T14:04:37Z (GMT) No. of bitstreams: 2 Dissertação - Barbara Martins Vieira - 2014.pdf: 1451459 bytes, checksum: 595a3718c8c4e83f9334cf6513f85119 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)Made available in DSpace on 2015-03-20T14:04:37Z (GMT). No. of bitstreams: 2 Dissertação - Barbara Martins Vieira - 2014.pdf: 1451459 bytes, checksum: 595a3718c8c4e83f9334cf6513f85119 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) Previous issue date: 2014-08-22Conselho Nacional de Pesquisa e Desenvolvimento Científico e Tecnológico - CNPqapplication/pdfhttp://repositorio.bc.ufg.br/tede/retrieve/17991/Disserta%c3%a7%c3%a3o%20-%20Barbara%20Martins%20Vieira%20-%202014.pdf.jpgporUniversidade Federal de GoiásPrograma de Pós-graduação em Nutrição e Saúde (FANUT)UFGBrasilFaculdade de Nutrição - FANUT (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessFígadoModeloCCl4RatosHepatotoxicidadeHepatotoxicityLiverModelRatsCIENCIAS DA SAUDE::NUTRICAOPadronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos WistarCarbon tetrachloride dose standardization of liver injury model acute oxidative stress in ratsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis-30109707181642501066006006006009028001981735587154-1073001350029933100-2555911436985713659reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGLICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://repositorio.bc.ufg.br/tede/bitstreams/3e61bdc7-d288-475e-80ab-69885be0b0cf/downloadbd3efa91386c1718a7f26a329fdcb468MD51CC-LICENSElicense_urllicense_urltext/plain; charset=utf-849http://repositorio.bc.ufg.br/tede/bitstreams/18f3df51-0084-4eeb-897d-0efb1f2f9fa7/download4afdbb8c545fd630ea7db775da747b2fMD52license_textlicense_texttext/html; charset=utf-822376http://repositorio.bc.ufg.br/tede/bitstreams/0cbd0825-cc81-4c95-9baf-4b8c35e8271a/downloadb292a83e42bd8ad62533bba1395b83ffMD53license_rdflicense_rdfapplication/rdf+xml; charset=utf-823148http://repositorio.bc.ufg.br/tede/bitstreams/be7ba135-6a50-4c4a-98c7-5ce55a2e6e3a/download9da0b6dfac957114c6a7714714b86306MD54ORIGINALDissertação - Barbara Martins Vieira - 2014.pdfDissertação - Barbara Martins Vieira - 2014.pdfapplication/pdf1451459http://repositorio.bc.ufg.br/tede/bitstreams/958c3cd8-9f2d-48f3-8437-f95aa492bebb/download595a3718c8c4e83f9334cf6513f85119MD55TEXTDissertação - Barbara Martins Vieira - 2014.pdf.txtDissertação - Barbara Martins Vieira - 2014.pdf.txtExtracted Texttext/plain100127http://repositorio.bc.ufg.br/tede/bitstreams/624c4775-98fe-4879-9b45-24cf90023233/downloada4e57b39365f05f6bd5e93a63eea258dMD56THUMBNAILDissertação - Barbara Martins Vieira - 2014.pdf.jpgDissertação - Barbara Martins Vieira - 2014.pdf.jpgGenerated Thumbnailimage/jpeg1943http://repositorio.bc.ufg.br/tede/bitstreams/7838fd91-ad94-4b02-af22-2c0125513a6a/downloadcc73c4c239a4c332d642ba1e7c7a9fb2MD57tede/43092015-03-21 03:00:54.863http://creativecommons.org/licenses/by-nc-nd/4.0/Acesso Abertoopen.accessoai:repositorio.bc.ufg.br:tede/4309http://repositorio.bc.ufg.br/tedeRepositório InstitucionalPUBhttp://repositorio.bc.ufg.br/oai/requesttasesdissertacoes.bc@ufg.bropendoar:2015-03-21T06:00:54Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)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
dc.title.por.fl_str_mv Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
dc.title.alternative.eng.fl_str_mv Carbon tetrachloride dose standardization of liver injury model acute oxidative stress in rats
title Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
spellingShingle Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
Vieira, Bárbara Martins
Fígado
Modelo
CCl4
Ratos
Hepatotoxicidade
Hepatotoxicity
Liver
Model
Rats
CIENCIAS DA SAUDE::NUTRICAO
title_short Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
title_full Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
title_fullStr Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
title_full_unstemmed Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
title_sort Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar
author Vieira, Bárbara Martins
author_facet Vieira, Bárbara Martins
author_role author
dc.contributor.advisor1.fl_str_mv Naves, Maria Margareth Veloso
dc.contributor.advisor1Lattes.fl_str_mv  http://lattes.cnpq.br/6563181057140270
dc.contributor.referee1.fl_str_mv Cominetti, Cristiane
dc.contributor.referee2.fl_str_mv Horst, Maria Aderuza
dc.contributor.referee3.fl_str_mv Naves, Maria Margareth Veloso
dc.contributor.advisor2.fl_str_mv Celes, Mara Rúbia Nunes
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/9945884989330825
dc.contributor.author.fl_str_mv Vieira, Bárbara Martins
contributor_str_mv Naves, Maria Margareth Veloso
Cominetti, Cristiane
Horst, Maria Aderuza
Naves, Maria Margareth Veloso
Celes, Mara Rúbia Nunes
dc.subject.por.fl_str_mv Fígado
Modelo
CCl4
Ratos
Hepatotoxicidade
Hepatotoxicity
topic Fígado
Modelo
CCl4
Ratos
Hepatotoxicidade
Hepatotoxicity
Liver
Model
Rats
CIENCIAS DA SAUDE::NUTRICAO
dc.subject.eng.fl_str_mv Liver
Model
Rats
dc.subject.cnpq.fl_str_mv CIENCIAS DA SAUDE::NUTRICAO
description The carbon tetrachloride (CCl4) is recognized as a classic hepatotoxin, being considered the best method to induce liver injury, commonly used as a model to test the hepatoprotective effect of drugs and natural substances and for investigation of hepatotoxicity, cytotoxicity and oxidative stress, in both in vivo and in vitro studies. This study aimed to standardize the lowest dose of CCl4 to cause acute liver injury by oxidative stress in Wistar rats. The in vivo experiment was carried out with 12 male Wistar rats (180-240g),which were maintained for 16 days under controlled environment and supplied with water and Purina® rodent ad libitum. The animals were separated into four groups: CG - control group; G0,5 - dose of 0.5 ml / kg body weight (bw); G0,75 - dose of 0.75 ml / kg bw and G1 - dose of 1 ml / kg bw. CCl4 was administered by intraperitoneal injection twice a week. 24h after the last CCl4 administration, all animals were anesthetized (xylazine: ketamine - 1: 1 v / v) for performing cardiac puncture, euthanasia and dissection of the liver for removal and analysis. Results obtained were subjected to normality test, and followed by the analysis of variance (ANOVA) and comparison of means (Tukey at 5% probability - post-hoc). It was observed that the mean weights of rats treated with CCl4 were higher than that of to the GC and the liver protein content (in g / 100 g) was lower in the treated groups, with no statistical difference between the test groups. Histopathological analysis showed changes in the structure, increased numbers of macrophages with intracellular lipid accumulation and increased cellular infiltration in groups treated with CCl4. By quantifying the enzymes alanine aminotransferase (ALT), aspartate and alanine aminotransferase (AST), it was found that the CCl4-treated groups showed significantly higher levels than CG, being higher in G1 compared to the other groups tested. All tested concentrations of CCl4 induced liver injury in vivo, in different degrees, and the concentration of 0.5 mL / kg bw, administered twice weekly, was the lowest dose tested that could cause changes in all the parameters evaluated. Therefore, this is the ideal dose for induction of acute liver injury, aiming to test the modulatory role of dietary and nutritional factors.
publishDate 2014
dc.date.issued.fl_str_mv 2014-08-22
dc.date.accessioned.fl_str_mv 2015-03-20T14:04:37Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv VIEIRA, B. M. Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar. 2014. 53 f. Dissertação ( Mestrado em Nutrição e Saúde) - Universidade Federal de Goiás, Goiânia, 2014.
dc.identifier.uri.fl_str_mv http://repositorio.bc.ufg.br/tede/handle/tede/4309
dc.identifier.dark.fl_str_mv ark:/38995/0013000001srq
identifier_str_mv VIEIRA, B. M. Padronização de dose de tetracloreto de carbono em modelo de lesão hepática aguda por estresse oxidativo em ratos Wistar. 2014. 53 f. Dissertação ( Mestrado em Nutrição e Saúde) - Universidade Federal de Goiás, Goiânia, 2014.
ark:/38995/0013000001srq
url http://repositorio.bc.ufg.br/tede/handle/tede/4309
dc.language.iso.fl_str_mv por
language por
dc.relation.program.fl_str_mv -3010970718164250106
dc.relation.confidence.fl_str_mv 600
600
600
600
dc.relation.department.fl_str_mv 9028001981735587154
dc.relation.cnpq.fl_str_mv -1073001350029933100
dc.relation.sponsorship.fl_str_mv -2555911436985713659
dc.rights.driver.fl_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Goiás
dc.publisher.program.fl_str_mv Programa de Pós-graduação em Nutrição e Saúde (FANUT)
dc.publisher.initials.fl_str_mv UFG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Faculdade de Nutrição - FANUT (RG)
publisher.none.fl_str_mv Universidade Federal de Goiás
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFG
instname:Universidade Federal de Goiás (UFG)
instacron:UFG
instname_str Universidade Federal de Goiás (UFG)
instacron_str UFG
institution UFG
reponame_str Repositório Institucional da UFG
collection Repositório Institucional da UFG
bitstream.url.fl_str_mv http://repositorio.bc.ufg.br/tede/bitstreams/3e61bdc7-d288-475e-80ab-69885be0b0cf/download
http://repositorio.bc.ufg.br/tede/bitstreams/18f3df51-0084-4eeb-897d-0efb1f2f9fa7/download
http://repositorio.bc.ufg.br/tede/bitstreams/0cbd0825-cc81-4c95-9baf-4b8c35e8271a/download
http://repositorio.bc.ufg.br/tede/bitstreams/be7ba135-6a50-4c4a-98c7-5ce55a2e6e3a/download
http://repositorio.bc.ufg.br/tede/bitstreams/958c3cd8-9f2d-48f3-8437-f95aa492bebb/download
http://repositorio.bc.ufg.br/tede/bitstreams/624c4775-98fe-4879-9b45-24cf90023233/download
http://repositorio.bc.ufg.br/tede/bitstreams/7838fd91-ad94-4b02-af22-2c0125513a6a/download
bitstream.checksum.fl_str_mv bd3efa91386c1718a7f26a329fdcb468
4afdbb8c545fd630ea7db775da747b2f
b292a83e42bd8ad62533bba1395b83ff
9da0b6dfac957114c6a7714714b86306
595a3718c8c4e83f9334cf6513f85119
a4e57b39365f05f6bd5e93a63eea258d
cc73c4c239a4c332d642ba1e7c7a9fb2
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)
repository.mail.fl_str_mv tasesdissertacoes.bc@ufg.br
_version_ 1811721341359882240