Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii

Detalhes bibliográficos
Ano de defesa: 2009
Autor(a) principal: Sylvio, Mirian de lattes
Orientador(a): Castro, Ana Maria de lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Goiás
Programa de Pós-Graduação: Programa de Pós-graduação em Medicina Tropical e Saúde Pública (IPTSP)
Departamento: Instituto de Patologia Tropical e Saúde Pública - IPTSP (RG)
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: http://repositorio.bc.ufg.br/tede/handle/tede/3567
Resumo: Infection with Toxoplasma gondii occurs throughout the globe, with a prevalence of up to 90% in the population. The physiological changes caused by this parasite are well studied in immunocompromised individuals and in cases of congenital transmission. In immunocompetent individuals the infection is usually asymptomatic and little explored by researchers. Experimental studies follow the pattern of human studies, and there fow mention about the biochemical changes (liver and kidney metabolisms) in the host infected by T. gondii. This study aimed the quantification of hepatic and kidney alterations caused by acute infections by T. gondii (non cystogenic strain – RH) and by chronic infections (cystogenic strain – ME-49). The control group was formed by mice without infection, only submitted to saline stress. Several enzymes were measured in serum and peritoneal exudate of mice infected and control such as: aspartate aminotransferase (AST), alanine aminotransferase (ALT), glutamyltransferase (GGT), alkaline phosphatase (ALP), urea, creatinine and lactate dehydrogenase, using an automated methodology. AST and ALT presented a significative difference in the serum of mice infected with RH strain when compared to controls indicating a destruction of liver cells. The peritoneal exudates did not present significative changes in relation to controls nor did the urea and creatinine levels. The séric lactate dehydrogenase showed gradual changes in all days of the infection in mice peritoneal exudates as early as this change was evident only in the fifth day of infection. All samples of the group infected with ME-49 strain showed changes in serum and peritoneal exudate during all days of analysis. Only ALT peritoneal exudates showed no change during all days of analysis. An increase in urea at all doses was observed, however, creatinine showed a change only within 120 days of infection. The LDH was altered in the serum in all days of analysis. In conclusion, the T. gondii infection may cause hepatic and kidney injuries either when caused by non-cystogenic as by cystogenic strains of the parasite.
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spelling Castro, Ana Maria dehttp://lattes.cnpq.br/9232309971000621Bezerra, José Clecildo Barreto BezerraVinaud, Marina Clarehttp://lattes.cnpq.br/1213426393403645Sylvio, Mirian de2014-11-07T11:29:38Z2009-12-15SYLVIO, Mirian de. Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii. 2009. 73 f. Dissertação (Mestrado em Medicina Tropical e Saúde Pública) - Universidade Federal de Goiás, Goiânia, 2009.http://repositorio.bc.ufg.br/tede/handle/tede/3567Infection with Toxoplasma gondii occurs throughout the globe, with a prevalence of up to 90% in the population. The physiological changes caused by this parasite are well studied in immunocompromised individuals and in cases of congenital transmission. In immunocompetent individuals the infection is usually asymptomatic and little explored by researchers. Experimental studies follow the pattern of human studies, and there fow mention about the biochemical changes (liver and kidney metabolisms) in the host infected by T. gondii. This study aimed the quantification of hepatic and kidney alterations caused by acute infections by T. gondii (non cystogenic strain – RH) and by chronic infections (cystogenic strain – ME-49). The control group was formed by mice without infection, only submitted to saline stress. Several enzymes were measured in serum and peritoneal exudate of mice infected and control such as: aspartate aminotransferase (AST), alanine aminotransferase (ALT), glutamyltransferase (GGT), alkaline phosphatase (ALP), urea, creatinine and lactate dehydrogenase, using an automated methodology. AST and ALT presented a significative difference in the serum of mice infected with RH strain when compared to controls indicating a destruction of liver cells. The peritoneal exudates did not present significative changes in relation to controls nor did the urea and creatinine levels. The séric lactate dehydrogenase showed gradual changes in all days of the infection in mice peritoneal exudates as early as this change was evident only in the fifth day of infection. All samples of the group infected with ME-49 strain showed changes in serum and peritoneal exudate during all days of analysis. Only ALT peritoneal exudates showed no change during all days of analysis. An increase in urea at all doses was observed, however, creatinine showed a change only within 120 days of infection. The LDH was altered in the serum in all days of analysis. In conclusion, the T. gondii infection may cause hepatic and kidney injuries either when caused by non-cystogenic as by cystogenic strains of the parasite.A infecção pelo Toxoplasma gondii ocorre em todo o mundo, com prevalência de até 90% na população conforme seus hábitos culturais e condições socioeconômicas. As alterações fisiopatológicas provocadas por este parasito são muito estudadas nos indivíduos imunocomprometidos, nos casos de transmissão congênita, e nos indivíduos imunocompetentes a infecção é, geralmente, assintomática e pouco explorada pelos pesquisadores. Experimentalmente, os estudos seguem o padrão dos estudos humanos, e há pouca referência sobre as alterações bioquímicas (hepáticas e renais) no hospedeiro infectado pelo T. gondii. Este trabalho objetivou avaliar as alterações hepáticas e renais causadas por esse parasito em camundongos na fase aguda, usando a cepa não cistogênica (RH), e na fase crônica, com a cepa cistogênica (ME-49), tendo como controles camundongos sem infecção, somente submetidos ao estresse de inoculação com salina. Foram dosadas no soro e no exsudato peritoneal dos camundongos infectados e controles os níveis das enzimas Aspartato aminotransferase (AST), Alanina aminotransferase (ALT), Gamaglutamiltransferase (GGT), Fosfatase alcalina (FAL), desidrogenase lática (DHL) e dos seguintes compostos: uréia e creatinina, por metodologia automatizada. As enzimas AST e ALT apresentaram diferença significativa no soro de camundongos infectados com cepa RH, demonstraram alterações em relação aos controles indicando uma destruição das células hepáticas. No exsudato peritoneal não foram demonstradas alterações em relação aos controles. A uréia e creatinina dosadas não demonstraram alteração significativa. A enzima lactato desidrogenase sérica apresentou alterações gradativas em todos os dias de infecção do camundongo no soro, já no exsudato peritoneal essa alteração foi evidenciada somente no quinto dia da infecção, mostrando que com o aumento de parasitos e a destruição celular causada por esse, essa enzima presente em várias células é responsável por demonstrar aumentos consideráveis. Todas as amostras de soro analisadas do grupo infectado com a cepa ME-49 demonstraram alterações durante todo período de acompanhamento. Enquanto que no exsudato peritoneal não mostrou nenhuma alteração durante todo período analisado. Houve aumento crescente na uréia em todos os dias de analises, porém, a creatinina não apresentou nenhuma alteração. A LDH mostrou-se alterada no soro em todos os dias de analisado. Conclui-se que a infecção pelo T. gondii pode provocar alterações hepáticas e renais ao longo do curso de infecção, tanto em infecções com cepa cistogênica quanto com cepa não cistogênica.application/pdfhttp://repositorio.bc.ufg.br/tede/retrieve/11957/Disserta%c3%a7%c3%a3o%20-%20Mirian%20de%20Sylvio%20-%202009.pdf.jpgporUniversidade Federal de GoiásPrograma de Pós-graduação em Medicina Tropical e Saúde Pública (IPTSP)UFGBrasilInstituto de Patologia Tropical e Saúde Pública - IPTSP (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessAspartato aminotransferasesAlanina aminotransferasesGamaglutamiltransferaseFosfatase alcalinaLactato desidrogenaseGama - GTUréiaCreatininaToxoplasma gondiiAspartate aminotransferaseAlanine aminotransferaseGlutamyltransferaseAlkaline phosphataseLactate dehydrogenaseGamma - GTUreaCreatinineToxoplasma gondiiCLINICA MEDICA::DOENCAS INFECCIOSAS E PARASITARIASAnálises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondiiinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis8197219506590464977600600600-77690114445645562881767748423488408711reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGLICENSElicense.txtlicense.txttext/plain; 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dc.title.por.fl_str_mv Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
title Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
spellingShingle Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
Sylvio, Mirian de
Aspartato aminotransferases
Alanina aminotransferases
Gamaglutamiltransferase
Fosfatase alcalina
Lactato desidrogenase
Gama - GT
Uréia
Creatinina
Toxoplasma gondii
Aspartate aminotransferase
Alanine aminotransferase
Glutamyltransferase
Alkaline phosphatase
Lactate dehydrogenase
Gamma - GT
Urea
Creatinine
Toxoplasma gondii
CLINICA MEDICA::DOENCAS INFECCIOSAS E PARASITARIAS
title_short Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
title_full Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
title_fullStr Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
title_full_unstemmed Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
title_sort Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii
author Sylvio, Mirian de
author_facet Sylvio, Mirian de
author_role author
dc.contributor.advisor1.fl_str_mv Castro, Ana Maria de
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/9232309971000621
dc.contributor.advisor-co1.fl_str_mv Bezerra, José Clecildo Barreto Bezerra
dc.contributor.advisor-co2.fl_str_mv Vinaud, Marina Clare
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/1213426393403645
dc.contributor.author.fl_str_mv Sylvio, Mirian de
contributor_str_mv Castro, Ana Maria de
Bezerra, José Clecildo Barreto Bezerra
Vinaud, Marina Clare
dc.subject.por.fl_str_mv Aspartato aminotransferases
Alanina aminotransferases
Gamaglutamiltransferase
Fosfatase alcalina
Lactato desidrogenase
Gama - GT
Uréia
Creatinina
Toxoplasma gondii
topic Aspartato aminotransferases
Alanina aminotransferases
Gamaglutamiltransferase
Fosfatase alcalina
Lactato desidrogenase
Gama - GT
Uréia
Creatinina
Toxoplasma gondii
Aspartate aminotransferase
Alanine aminotransferase
Glutamyltransferase
Alkaline phosphatase
Lactate dehydrogenase
Gamma - GT
Urea
Creatinine
Toxoplasma gondii
CLINICA MEDICA::DOENCAS INFECCIOSAS E PARASITARIAS
dc.subject.eng.fl_str_mv Aspartate aminotransferase
Alanine aminotransferase
Glutamyltransferase
Alkaline phosphatase
Lactate dehydrogenase
Gamma - GT
Urea
Creatinine
Toxoplasma gondii
dc.subject.cnpq.fl_str_mv CLINICA MEDICA::DOENCAS INFECCIOSAS E PARASITARIAS
description Infection with Toxoplasma gondii occurs throughout the globe, with a prevalence of up to 90% in the population. The physiological changes caused by this parasite are well studied in immunocompromised individuals and in cases of congenital transmission. In immunocompetent individuals the infection is usually asymptomatic and little explored by researchers. Experimental studies follow the pattern of human studies, and there fow mention about the biochemical changes (liver and kidney metabolisms) in the host infected by T. gondii. This study aimed the quantification of hepatic and kidney alterations caused by acute infections by T. gondii (non cystogenic strain – RH) and by chronic infections (cystogenic strain – ME-49). The control group was formed by mice without infection, only submitted to saline stress. Several enzymes were measured in serum and peritoneal exudate of mice infected and control such as: aspartate aminotransferase (AST), alanine aminotransferase (ALT), glutamyltransferase (GGT), alkaline phosphatase (ALP), urea, creatinine and lactate dehydrogenase, using an automated methodology. AST and ALT presented a significative difference in the serum of mice infected with RH strain when compared to controls indicating a destruction of liver cells. The peritoneal exudates did not present significative changes in relation to controls nor did the urea and creatinine levels. The séric lactate dehydrogenase showed gradual changes in all days of the infection in mice peritoneal exudates as early as this change was evident only in the fifth day of infection. All samples of the group infected with ME-49 strain showed changes in serum and peritoneal exudate during all days of analysis. Only ALT peritoneal exudates showed no change during all days of analysis. An increase in urea at all doses was observed, however, creatinine showed a change only within 120 days of infection. The LDH was altered in the serum in all days of analysis. In conclusion, the T. gondii infection may cause hepatic and kidney injuries either when caused by non-cystogenic as by cystogenic strains of the parasite.
publishDate 2009
dc.date.issued.fl_str_mv 2009-12-15
dc.date.accessioned.fl_str_mv 2014-11-07T11:29:38Z
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dc.identifier.citation.fl_str_mv SYLVIO, Mirian de. Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii. 2009. 73 f. Dissertação (Mestrado em Medicina Tropical e Saúde Pública) - Universidade Federal de Goiás, Goiânia, 2009.
dc.identifier.uri.fl_str_mv http://repositorio.bc.ufg.br/tede/handle/tede/3567
identifier_str_mv SYLVIO, Mirian de. Análises das comparações bioquímicas no soro e exsudato peritoneal de camundongos BALB/c inoculados com cepa cistogênica e não cistogênica de Toxoplasma gondii. 2009. 73 f. Dissertação (Mestrado em Medicina Tropical e Saúde Pública) - Universidade Federal de Goiás, Goiânia, 2009.
url http://repositorio.bc.ufg.br/tede/handle/tede/3567
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language por
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600
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dc.publisher.none.fl_str_mv Universidade Federal de Goiás
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dc.publisher.initials.fl_str_mv UFG
dc.publisher.country.fl_str_mv Brasil
dc.publisher.department.fl_str_mv Instituto de Patologia Tropical e Saúde Pública - IPTSP (RG)
publisher.none.fl_str_mv Universidade Federal de Goiás
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http://repositorio.bc.ufg.br/tede/bitstreams/316471d3-6e69-44c9-91a2-c4ccd2205a6e/download
http://repositorio.bc.ufg.br/tede/bitstreams/bf15c78d-a459-4f23-8642-2ab846bd2f69/download
http://repositorio.bc.ufg.br/tede/bitstreams/d595c31d-c669-4a8b-807f-8e1a8300f20f/download
http://repositorio.bc.ufg.br/tede/bitstreams/8b6dfee6-b1fb-4151-bee5-ca758f1173cd/download
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repository.name.fl_str_mv Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)
repository.mail.fl_str_mv grt.bc@ufg.br
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