Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Anais da Academia Brasileira de Ciências (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652012000300016 |
Resumo: | The effects of acute and chronic infection caused by Toxoplasma gondii on duodenal myenteric neurons were analyzed. Eighteen rats were assigned into four groups: Acute Control Group (ACG, n=4); Acute Experimental Group (AEG, n=4); Chronic Control Group (CCG, n=5); and Chronic Experimental Group (CEG, n=5). Rats from the AEG and CEG were inoculated orally with 105 genotype III (BTU-II strain) tachyzoites of T. gondii isolated from a dog with neurological signs. Acute groups were killed after 24 hours after the inoculation and the chronic groups after 30 days. Whole-mount from the duodenum were stained with Giemsa. The population density of myenteric neurons, as well the body cell, nuclear and cytoplasmic area were analyzed. Both acute and chronic toxoplasmic infection did not provoke neuronal loss. On the other hand, plastic alterations were observed: decreasing of the nuclear and cytoplasmic area during the acute phase and neuronal hypertrophy during the chronic phase. |
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Anais da Academia Brasileira de Ciências (Online) |
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Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of ratsenteric nervous systeminfectionparasitetoxoplasmosisThe effects of acute and chronic infection caused by Toxoplasma gondii on duodenal myenteric neurons were analyzed. Eighteen rats were assigned into four groups: Acute Control Group (ACG, n=4); Acute Experimental Group (AEG, n=4); Chronic Control Group (CCG, n=5); and Chronic Experimental Group (CEG, n=5). Rats from the AEG and CEG were inoculated orally with 105 genotype III (BTU-II strain) tachyzoites of T. gondii isolated from a dog with neurological signs. Acute groups were killed after 24 hours after the inoculation and the chronic groups after 30 days. Whole-mount from the duodenum were stained with Giemsa. The population density of myenteric neurons, as well the body cell, nuclear and cytoplasmic area were analyzed. Both acute and chronic toxoplasmic infection did not provoke neuronal loss. On the other hand, plastic alterations were observed: decreasing of the nuclear and cytoplasmic area during the acute phase and neuronal hypertrophy during the chronic phase.Academia Brasileira de Ciências2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652012000300016Anais da Academia Brasileira de Ciências v.84 n.3 2012reponame:Anais da Academia Brasileira de Ciências (Online)instname:Academia Brasileira de Ciências (ABC)instacron:ABC10.1590/S0001-37652012005000052info:eu-repo/semantics/openAccessPapazian-Cabanas,Rodrigo M.Araújo,Eduardo J.A.Silva,Aristeu V. daSant'Ana,Débora M.G.eng2012-08-06T00:00:00Zoai:scielo:S0001-37652012000300016Revistahttp://www.scielo.br/aabchttps://old.scielo.br/oai/scielo-oai.php||aabc@abc.org.br1678-26900001-3765opendoar:2012-08-06T00:00Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC)false |
dc.title.none.fl_str_mv |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
title |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
spellingShingle |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats Papazian-Cabanas,Rodrigo M. enteric nervous system infection parasite toxoplasmosis |
title_short |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
title_full |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
title_fullStr |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
title_full_unstemmed |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
title_sort |
Myenteric neuronal plasticity induced by Toxoplasma gondii (genotype III) on the duodenum of rats |
author |
Papazian-Cabanas,Rodrigo M. |
author_facet |
Papazian-Cabanas,Rodrigo M. Araújo,Eduardo J.A. Silva,Aristeu V. da Sant'Ana,Débora M.G. |
author_role |
author |
author2 |
Araújo,Eduardo J.A. Silva,Aristeu V. da Sant'Ana,Débora M.G. |
author2_role |
author author author |
dc.contributor.author.fl_str_mv |
Papazian-Cabanas,Rodrigo M. Araújo,Eduardo J.A. Silva,Aristeu V. da Sant'Ana,Débora M.G. |
dc.subject.por.fl_str_mv |
enteric nervous system infection parasite toxoplasmosis |
topic |
enteric nervous system infection parasite toxoplasmosis |
description |
The effects of acute and chronic infection caused by Toxoplasma gondii on duodenal myenteric neurons were analyzed. Eighteen rats were assigned into four groups: Acute Control Group (ACG, n=4); Acute Experimental Group (AEG, n=4); Chronic Control Group (CCG, n=5); and Chronic Experimental Group (CEG, n=5). Rats from the AEG and CEG were inoculated orally with 105 genotype III (BTU-II strain) tachyzoites of T. gondii isolated from a dog with neurological signs. Acute groups were killed after 24 hours after the inoculation and the chronic groups after 30 days. Whole-mount from the duodenum were stained with Giemsa. The population density of myenteric neurons, as well the body cell, nuclear and cytoplasmic area were analyzed. Both acute and chronic toxoplasmic infection did not provoke neuronal loss. On the other hand, plastic alterations were observed: decreasing of the nuclear and cytoplasmic area during the acute phase and neuronal hypertrophy during the chronic phase. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-09-01 |
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://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652012000300016 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652012000300016 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0001-37652012005000052 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Academia Brasileira de Ciências |
publisher.none.fl_str_mv |
Academia Brasileira de Ciências |
dc.source.none.fl_str_mv |
Anais da Academia Brasileira de Ciências v.84 n.3 2012 reponame:Anais da Academia Brasileira de Ciências (Online) instname:Academia Brasileira de Ciências (ABC) instacron:ABC |
instname_str |
Academia Brasileira de Ciências (ABC) |
instacron_str |
ABC |
institution |
ABC |
reponame_str |
Anais da Academia Brasileira de Ciências (Online) |
collection |
Anais da Academia Brasileira de Ciências (Online) |
repository.name.fl_str_mv |
Anais da Academia Brasileira de Ciências (Online) - Academia Brasileira de Ciências (ABC) |
repository.mail.fl_str_mv |
||aabc@abc.org.br |
_version_ |
1754302859102388224 |