Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations
Autor(a) principal: | |
---|---|
Data de Publicação: | 2005 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1128/AAC.49.4.1521-1528.2005 http://repositorio.unifesp.br/handle/11600/28205 |
Resumo: | Chagas' disease, caused by Trypanosoma cruzi infection, is one of the main causes of death due to heart failure in Latin American countries. Benznidazole, the chemotherapeutic agent most often used for the treatment of chagasic patients, is highly toxic and has limited efficacy, especially in the chronic phase of the disease. in the present study we used a mouse model of chronic Chagas' disease to investigate the effects of benznidazole treatment during the chronic phase on disease progression. the hearts of benznidazole-treated mice had decreased parasitism and myocarditis compared to the hearts of untreated chagasic mice. Both groups of Trypanosoma cruzi-infected mice had significant alterations in their electrocardiograms compared to those of the healthy mice. However, untreated mice had significantly higher cardiac conduction disturbances than benznidazole-treated mice, including intraventricular conduction disturbances, atrioventricular blocks, and extrasystoles. the levels of antibodies against T. cruzi antigens (epimastigote extract, P-2 beta, and trans-sialidase) as well as antibodies against peptides of the second extracellular loops beta(1)-adrenergic and M-2-muscarinic cardiac receptors were also lower in the sera from benznidazole-treated mice than in the sera from untreated mice. These results demonstrate that treatment with benznidazole in the chronic phase of infection prevents the development of severe chronic cardiomyopathy, despite the lack of complete parasite eradication. in addition, our data highlight the role of parasite persistence in the development of chronic Chagas' disease and reinforce the importance of T. cruzi elimination in order to decrease or prevent the development of severe chagasic cardiomyopathy. |
id |
UFSP_19fe869f26ae869b77a3b768fa0f0648 |
---|---|
oai_identifier_str |
oai:repositorio.unifesp.br/:11600/28205 |
network_acronym_str |
UFSP |
network_name_str |
Repositório Institucional da UNIFESP |
repository_id_str |
3465 |
spelling |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterationsChagas' disease, caused by Trypanosoma cruzi infection, is one of the main causes of death due to heart failure in Latin American countries. Benznidazole, the chemotherapeutic agent most often used for the treatment of chagasic patients, is highly toxic and has limited efficacy, especially in the chronic phase of the disease. in the present study we used a mouse model of chronic Chagas' disease to investigate the effects of benznidazole treatment during the chronic phase on disease progression. the hearts of benznidazole-treated mice had decreased parasitism and myocarditis compared to the hearts of untreated chagasic mice. Both groups of Trypanosoma cruzi-infected mice had significant alterations in their electrocardiograms compared to those of the healthy mice. However, untreated mice had significantly higher cardiac conduction disturbances than benznidazole-treated mice, including intraventricular conduction disturbances, atrioventricular blocks, and extrasystoles. the levels of antibodies against T. cruzi antigens (epimastigote extract, P-2 beta, and trans-sialidase) as well as antibodies against peptides of the second extracellular loops beta(1)-adrenergic and M-2-muscarinic cardiac receptors were also lower in the sera from benznidazole-treated mice than in the sera from untreated mice. These results demonstrate that treatment with benznidazole in the chronic phase of infection prevents the development of severe chronic cardiomyopathy, despite the lack of complete parasite eradication. in addition, our data highlight the role of parasite persistence in the development of chronic Chagas' disease and reinforce the importance of T. cruzi elimination in order to decrease or prevent the development of severe chagasic cardiomyopathy.Fundacao Oswaldo Cruz, Ctr Pesquisas Goncalo Moniz, BR-40295001 Salvador, BA, BrazilUniv Fed Rio de Janeiro, Inst Biofis Carlos Chagas Filho, BR-21941 Rio de Janeiro, BrazilHosp Santa Izabel, Salvador, BA, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, São Paulo, BrazilUniversidade Federal de São Paulo, Escola Paulista Med, São Paulo, BrazilWeb of ScienceAmer Soc MicrobiologyFundacao Oswaldo CruzUniversidade Federal do Rio de Janeiro (UFRJ)Hosp Santa IzabelUniversidade Federal de São Paulo (UNIFESP)Garcia, SimoneRamos, Carolina O.Senra, Juliana FVVilas-Boas, FabioRodrigues, Maurício M. [UNIFESP]Campos-De-Carvalho, Antonio C.Ribeiro-Dos-Santos, RicardoSoares, Milena BP2016-01-24T12:37:44Z2016-01-24T12:37:44Z2005-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1521-1528application/pdfhttp://dx.doi.org/10.1128/AAC.49.4.1521-1528.2005Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 49, n. 4, p. 1521-1528, 2005.10.1128/AAC.49.4.1521-1528.2005WOS000228082500038.pdf0066-4804http://repositorio.unifesp.br/handle/11600/28205WOS:000228082500038engAntimicrobial Agents and Chemotherapyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-07T01:13:28Zoai:repositorio.unifesp.br/:11600/28205Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-07T01:13:28Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
title |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
spellingShingle |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations Garcia, Simone |
title_short |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
title_full |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
title_fullStr |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
title_full_unstemmed |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
title_sort |
Treatment with benznidazole during the chronic phase of experimental Chagas' disease decreases cardiac alterations |
author |
Garcia, Simone |
author_facet |
Garcia, Simone Ramos, Carolina O. Senra, Juliana FV Vilas-Boas, Fabio Rodrigues, Maurício M. [UNIFESP] Campos-De-Carvalho, Antonio C. Ribeiro-Dos-Santos, Ricardo Soares, Milena BP |
author_role |
author |
author2 |
Ramos, Carolina O. Senra, Juliana FV Vilas-Boas, Fabio Rodrigues, Maurício M. [UNIFESP] Campos-De-Carvalho, Antonio C. Ribeiro-Dos-Santos, Ricardo Soares, Milena BP |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Fundacao Oswaldo Cruz Universidade Federal do Rio de Janeiro (UFRJ) Hosp Santa Izabel Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Garcia, Simone Ramos, Carolina O. Senra, Juliana FV Vilas-Boas, Fabio Rodrigues, Maurício M. [UNIFESP] Campos-De-Carvalho, Antonio C. Ribeiro-Dos-Santos, Ricardo Soares, Milena BP |
description |
Chagas' disease, caused by Trypanosoma cruzi infection, is one of the main causes of death due to heart failure in Latin American countries. Benznidazole, the chemotherapeutic agent most often used for the treatment of chagasic patients, is highly toxic and has limited efficacy, especially in the chronic phase of the disease. in the present study we used a mouse model of chronic Chagas' disease to investigate the effects of benznidazole treatment during the chronic phase on disease progression. the hearts of benznidazole-treated mice had decreased parasitism and myocarditis compared to the hearts of untreated chagasic mice. Both groups of Trypanosoma cruzi-infected mice had significant alterations in their electrocardiograms compared to those of the healthy mice. However, untreated mice had significantly higher cardiac conduction disturbances than benznidazole-treated mice, including intraventricular conduction disturbances, atrioventricular blocks, and extrasystoles. the levels of antibodies against T. cruzi antigens (epimastigote extract, P-2 beta, and trans-sialidase) as well as antibodies against peptides of the second extracellular loops beta(1)-adrenergic and M-2-muscarinic cardiac receptors were also lower in the sera from benznidazole-treated mice than in the sera from untreated mice. These results demonstrate that treatment with benznidazole in the chronic phase of infection prevents the development of severe chronic cardiomyopathy, despite the lack of complete parasite eradication. in addition, our data highlight the role of parasite persistence in the development of chronic Chagas' disease and reinforce the importance of T. cruzi elimination in order to decrease or prevent the development of severe chagasic cardiomyopathy. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-04-01 2016-01-24T12:37:44Z 2016-01-24T12:37:44Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1128/AAC.49.4.1521-1528.2005 Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 49, n. 4, p. 1521-1528, 2005. 10.1128/AAC.49.4.1521-1528.2005 WOS000228082500038.pdf 0066-4804 http://repositorio.unifesp.br/handle/11600/28205 WOS:000228082500038 |
url |
http://dx.doi.org/10.1128/AAC.49.4.1521-1528.2005 http://repositorio.unifesp.br/handle/11600/28205 |
identifier_str_mv |
Antimicrobial Agents and Chemotherapy. Washington: Amer Soc Microbiology, v. 49, n. 4, p. 1521-1528, 2005. 10.1128/AAC.49.4.1521-1528.2005 WOS000228082500038.pdf 0066-4804 WOS:000228082500038 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Antimicrobial Agents and Chemotherapy |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
1521-1528 application/pdf |
dc.publisher.none.fl_str_mv |
Amer Soc Microbiology |
publisher.none.fl_str_mv |
Amer Soc Microbiology |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268426656415744 |