Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys

Detalhes bibliográficos
Ano de defesa: 2014
Autor(a) principal: Dias, Cínthia Nóbrega de Sousa lattes
Orientador(a): Mascarenhas, Sandra Rodrigues lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal da Paraí­ba
Programa de Pós-Graduação: Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos
Departamento: Farmacologia
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufpb.br/jspui/handle/tede/6821
Resumo: Leishmaniasis is a complex of inserted parasitic diseases in the group of neglected tropical diseases. The drugs used primarily in the treatment of leishmaniasis are pentavalent antimonials and amphotericin B. However, these drugs are associated with serious side effects. Therefore, it is necessary to search for new antileishmanial drugs. In this context natural products are a source of new active molecules. This study, it was investigated the antileishmanial activity of the ethanol extract of Phyllanthus acuminatus and Justicidin B, lignan obtained from this plant and the ethanol extract, the dichloromethane phase and Hyptenolide obtained from Hyptis macrostachys in vitro experimental models. All samples assessed showed antileishmanial activity, initially demonstrated by inhibition of growth of L. amazonensis promastigotes in logarithmic growth phase. The concentration that inhibits 50% of growth (IC50) for the tested substances was 35.58 μg /mL for the ethanolic extract of P. acuminatus, 12.51 μg/mL for Justicidin B; 280.69 μg/mL for the ethanol extract of H. macrostachys, 55.3 μg/mL for dichloromethane phase of H. macrostachys and 22.67 μg/mL for Hyptenolide. These samples were also evaluated for cytotoxicity in murine peritoneal macrophages of swiss mice, which resulted in the measurement of the cytotoxic concentration for 50% macrophages (CC50), which were 39.62 μg/mL for the ethanolic extract of P. acuminatus, 58.56 μg/ml for Justicidin B; 121,36 μg/mL for the ethanol extract of H. macrostachys, 40.45 μg/mL for dichloromethane phase of H. macrostachys and 61.78 μg/ml for Hyptenolide. These data resulted in IC50 and CC50 resulted in a selectivity index of 1.11 for the ethanol extract of P. acuminatus; 4.68 for Justicidin B; 0.43 for the ethanol extract of H. macrostachys; 0.73 to dichloromethane phase of H. macrostachys and 2.72 to Hyptenolide. Given these results, we selected the lignan Justicidina B for further study of antileishmanial activity against L. amazonensis. In the evaluation of the DNA fragmentation pattern of L. amazonensis promastigotes, it was observed in higher concentration evaluated of Justicidin B (4x IC50) induction of DNA fragmentation similar to that observed in the positive control H2O2 (4mM). In infection model macrophage with L. amazonensis and treated with lignan Justicidin B showed reduction in both the percentage of infected macrophages as the number of amastigotes per infected macrophage, resulting in a reduction in the rate of infection compared to control, resulting decrease in the effective concentration for 50% of infection (EC50) of 9.14 and 3.58 for 24 hours and 72 hours after treatment. This result was correlated with an immunomodulatory activity of this lignan, associated with decreased levels of interleukin (IL) -10, and increased levels of nitric oxide (NO). It can be concluded that the lignan Justicidin B has significant activity antipromastigote and antiamastigote and presents immunomodulatory properties in models of infection in vitro.
id UFPB-2_91d85555fbf3e7b5c4420c4807b3bb7b
oai_identifier_str oai:repositorio.ufpb.br:tede/6821
network_acronym_str UFPB-2
network_name_str Repositório Institucional da UFPB
repository_id_str
spelling 2015-05-14T13:00:03Z2018-07-21T00:25:21Z2014-10-222018-07-21T00:25:21Z2014-06-27DIAS, Cínthia Nóbrega de Sousa. Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys. 2014. 114 f. Dissertação (Mestrado em Produtos Naturais e Sintéticos Bioativos) - Universidade Federal da Paraí­ba, João Pessoa, 2014.https://repositorio.ufpb.br/jspui/handle/tede/6821Leishmaniasis is a complex of inserted parasitic diseases in the group of neglected tropical diseases. The drugs used primarily in the treatment of leishmaniasis are pentavalent antimonials and amphotericin B. However, these drugs are associated with serious side effects. Therefore, it is necessary to search for new antileishmanial drugs. In this context natural products are a source of new active molecules. This study, it was investigated the antileishmanial activity of the ethanol extract of Phyllanthus acuminatus and Justicidin B, lignan obtained from this plant and the ethanol extract, the dichloromethane phase and Hyptenolide obtained from Hyptis macrostachys in vitro experimental models. All samples assessed showed antileishmanial activity, initially demonstrated by inhibition of growth of L. amazonensis promastigotes in logarithmic growth phase. The concentration that inhibits 50% of growth (IC50) for the tested substances was 35.58 μg /mL for the ethanolic extract of P. acuminatus, 12.51 μg/mL for Justicidin B; 280.69 μg/mL for the ethanol extract of H. macrostachys, 55.3 μg/mL for dichloromethane phase of H. macrostachys and 22.67 μg/mL for Hyptenolide. These samples were also evaluated for cytotoxicity in murine peritoneal macrophages of swiss mice, which resulted in the measurement of the cytotoxic concentration for 50% macrophages (CC50), which were 39.62 μg/mL for the ethanolic extract of P. acuminatus, 58.56 μg/ml for Justicidin B; 121,36 μg/mL for the ethanol extract of H. macrostachys, 40.45 μg/mL for dichloromethane phase of H. macrostachys and 61.78 μg/ml for Hyptenolide. These data resulted in IC50 and CC50 resulted in a selectivity index of 1.11 for the ethanol extract of P. acuminatus; 4.68 for Justicidin B; 0.43 for the ethanol extract of H. macrostachys; 0.73 to dichloromethane phase of H. macrostachys and 2.72 to Hyptenolide. Given these results, we selected the lignan Justicidina B for further study of antileishmanial activity against L. amazonensis. In the evaluation of the DNA fragmentation pattern of L. amazonensis promastigotes, it was observed in higher concentration evaluated of Justicidin B (4x IC50) induction of DNA fragmentation similar to that observed in the positive control H2O2 (4mM). In infection model macrophage with L. amazonensis and treated with lignan Justicidin B showed reduction in both the percentage of infected macrophages as the number of amastigotes per infected macrophage, resulting in a reduction in the rate of infection compared to control, resulting decrease in the effective concentration for 50% of infection (EC50) of 9.14 and 3.58 for 24 hours and 72 hours after treatment. This result was correlated with an immunomodulatory activity of this lignan, associated with decreased levels of interleukin (IL) -10, and increased levels of nitric oxide (NO). It can be concluded that the lignan Justicidin B has significant activity antipromastigote and antiamastigote and presents immunomodulatory properties in models of infection in vitro.As leishmanioses são um complexo de doenças parasitárias inseridas no grupo de doenças tropicais negligenciadas. Os principais medicamentos utilizados na terapêutica das leishmanioses são antimoniais pentavalentes e anfotericina B. Contudo, esses medicamentos estão associados a sérios efeitos colaterais. Portanto, é necessária a busca de novas drogas leishmanicidas. Nesse contexto, os produtos naturais são uma fonte de novas moléculas ativas. Neste trabalho, investigou-se a atividade antileishmania do extrato etanólico de Phyllanthus acuminatus e Justicidina B, lignana obtida dessa planta, bem como o extrato etanólico, a fase diclorometano e o Hiptenolideo, obtidos de Hyptis macrostachys em modelos experimentais in vitro. Todas as amostras avaliadas apresentaram atividade antileishmania, demonstrada inicialmente pela inibição de crescimento de formas promastigotas de L. amazonensis em fase logarítmica de crescimento. A concentração que inibe 50% do crescimento (CI50) para as substâncias avaliadas foi de 35,58μg/mL para o extrato etanólico de P. acuminatus, 12,51μg/mL para Justicidina B; 280,69μg/mL para o extrato etanólico de H. macrostachys, 55,3μg/mL para fase diclorometano de H. macrostachys e 22,67μg/mL para o Hiptenolideo. Essas amostras também foram avaliadas quanto à citotoxicidade em macrófagos peritoneais murinos de camundongos suíços, o que resultou na medida da concentração citotóxica para 50% dos macrófagos (CC50), que foram de 39,62μg/mL para o extrato etanólico de P. acuminatus, 58,56μg/mL para Justicidina B; 121,36μg/mL para o extrato etanólico de H. macrostachys, 40,45μg/mL para fase diclorometano de H. macrostachys e 61,78μg/mL para o Hiptenolideo. Esses dados de CI50 e CC50 resultaram no Índice de Seletividade que foram de 1,11 para o extrato etanólico de P. acuminatus; 4,68 para Justicidina B; 0,43 para o extrato etanólico de H. macrostachys; 0,73 para fase diclorometano de H. macrostachys e 2,72 para o Hiptenolideo. Diante desses resultados, foi selecionada a lignana Justicidina B para aprofundar os estudos de atividade antileishmania sobre L. amazonensis. Na avaliação do padrão de fragmentação do DNA de formas promastigotas de L. amazonensis observou-se que a Justicidina B na maior concentração avaliada (4x IC50) foi capaz de induzir a fragmentação do DNA semelhante ao observado no controle positivo H2O2 (4mM). Em modelo de infecção de macrófagos com L. amazonensis e tratados com a lignana Justicidina B observou-se redução tanto da porcentagem de macrófagos infectados quanto do número de amastigotas por macrófago infectado, resultando em uma redução no índice de infecção quando comparados ao controle, resultando em concentração efetiva para diminuir 50% da infecção (EC50) de 9,14 e 3,58 para 24 horas e 72 horas de tratamento. Esse resultado foi correlacionado com uma atividade imunomoduladora dessa lignana, associada à diminuição nos níveis de interleucina (IL)-10, e a um aumento nos níveis de óxido nítrico (NO). Pode-se concluir que a lignana Justicidina B possui significativa atividade antipromastigota e antiamastigota e apresenta propriedades imunomodulatórias em modelos de infecção in vitroMade available in DSpace on 2015-05-14T13:00:03Z (GMT). No. of bitstreams: 1 arquivototal.pdf: 2069742 bytes, checksum: 30969d68a1c51eddd37190cde04e71ac (MD5) Previous issue date: 2014-06-27Made available in DSpace on 2018-07-21T00:25:21Z (GMT). No. of bitstreams: 2 arquivototal.pdf: 2069742 bytes, checksum: 30969d68a1c51eddd37190cde04e71ac (MD5) arquivototal.pdf.jpg: 1958 bytes, checksum: 6b0e6c395f859c99d75a8548d6d79ba6 (MD5) Previous issue date: 2014-06-27Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal da Paraí­baPrograma de Pós-Graduação em Produtos Naturais e Sintéticos BioativosUFPBBRFarmacologiaLeishmania amazonensisLignanaJusticidina BAntileishmaniaImunomodulaçãoLeishmania amazonensisLignan, Justicidin BAntileishmaniaImmunomodulationCIENCIAS BIOLOGICAS::FARMACOLOGIAAvaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachysEvaluation of the antileishmanial activity of natural products isolated from phyllanthus acuminatus and hyptis macrostachysinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisMascarenhas, Sandra RodriguesCPF:05334211799http://lattes.cnpq.br/4300081489772959CPF:09434718484http://lattes.cnpq.br/1124643706763396Dias, Cínthia Nóbrega de Sousahttp://tede.biblioteca.ufpb.br:8080/retrieve/16545/arquivototal.pdf.jpginfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFPBinstname:Universidade Federal da Paraíba (UFPB)instacron:UFPBTEXTarquivototal.pdf.txtarquivototal.pdf.txtExtracted texttext/plain197226https://repositorio.ufpb.br/jspui/bitstream/tede/6821/4/arquivototal.pdf.txt0d148959850cc6b5f8a3dfd5a038240dMD54LICENSElicense.txtlicense.txttext/plain; charset=utf-81867https://repositorio.ufpb.br/jspui/bitstream/tede/6821/3/license.txt07956d2f9f6879bad6c75289be248398MD53THUMBNAILarquivototal.pdf.jpgarquivototal.pdf.jpgIM Thumbnailimage/jpeg3270https://repositorio.ufpb.br/jspui/bitstream/tede/6821/5/arquivototal.pdf.jpg5380b37266de8d368add5a7492556ba0MD55ORIGINALarquivototal.pdfapplication/pdf2069742https://repositorio.ufpb.br/jspui/bitstream/tede/6821/1/arquivototal.pdf30969d68a1c51eddd37190cde04e71acMD51tede/68212018-09-05 23:04:50.7oai:repositorio.ufpb.br:tede/6821TElDRU7Dh0EgREUgRElTVFJJQlVJw4fDg08gTsODTy1FWENMVVNJVkEKCkNvbSBhIGFwcmVzZW50YcOnw6NvIGRlc3RhIGxpY2Vuw6dhLCB2b2PDqiAobyBhdXRvciAoZXMpIG91IG8gdGl0dWxhciBkb3MgZGlyZWl0b3MgZGUgYXV0b3IpIGNvbmNlZGUgw6AgVW5pdmVyc2lkYWRlIApGZWRlcmFsIGRhIFBhcmHDrWJhIChVRlBCKSBvIGRpcmVpdG8gbsOjby1leGNsdXNpdm8gZGUgcmVwcm9kdXppciwgIHRyYWR1emlyIChjb25mb3JtZSBkZWZpbmlkbyBhYmFpeG8pLCBlL291IGRpc3RyaWJ1aXIgYSAKc3VhIHB1YmxpY2HDp8OjbyAoaW5jbHVpbmRvIG8gcmVzdW1vKSBwb3IgdG9kbyBvIG11bmRvIG5vIGZvcm1hdG8gaW1wcmVzc28gZSBlbGV0csO0bmljbyBlIGVtIHF1YWxxdWVyIG1laW8sIGluY2x1aW5kbyBvcyAKZm9ybWF0b3Mgw6F1ZGlvIG91IHbDrWRlby4KClZvY8OqIGNvbmNvcmRhIHF1ZSBhIFVGUEIgcG9kZSwgc2VtIGFsdGVyYXIgbyBjb250ZcO6ZG8sIHRyYW5zcG9yIGEgc3VhIHB1YmxpY2HDp8OjbyBwYXJhIHF1YWxxdWVyIG1laW8gb3UgZm9ybWF0byAKcGFyYSBmaW5zIGRlIHByZXNlcnZhw6fDo28uCgpWb2PDqiB0YW1iw6ltIGNvbmNvcmRhIHF1ZSBhIFVGUEIgcG9kZSBtYW50ZXIgbWFpcyBkZSB1bWEgY8OzcGlhIGRlIHN1YSBwdWJsaWNhw6fDo28gcGFyYSBmaW5zIGRlIHNlZ3VyYW7Dp2EsIGJhY2stdXAgCmUgcHJlc2VydmHDp8Ojby4KClZvY8OqIGRlY2xhcmEgcXVlIGEgc3VhIHB1YmxpY2HDp8OjbyDDqSBvcmlnaW5hbCBlIHF1ZSB2b2PDqiB0ZW0gbyBwb2RlciBkZSBjb25jZWRlciBvcyBkaXJlaXRvcyBjb250aWRvcyBuZXN0YSBsaWNlbsOnYS4gClZvY8OqIHRhbWLDqW0gZGVjbGFyYSBxdWUgbyBkZXDDs3NpdG8gZGEgc3VhIHB1YmxpY2HDp8OjbyBuw6NvLCBxdWUgc2VqYSBkZSBzZXUgY29uaGVjaW1lbnRvLCBpbmZyaW5nZSBkaXJlaXRvcyBhdXRvcmFpcyAKZGUgbmluZ3XDqW0uCgpDYXNvIGEgc3VhIHB1YmxpY2HDp8OjbyBjb250ZW5oYSBtYXRlcmlhbCBxdWUgdm9jw6ogbsOjbyBwb3NzdWkgYSB0aXR1bGFyaWRhZGUgZG9zIGRpcmVpdG9zIGF1dG9yYWlzLCB2b2PDqiBkZWNsYXJhIHF1ZSAKb2J0ZXZlIGEgcGVybWlzc8OjbyBpcnJlc3RyaXRhIGRvIGRldGVudG9yIGRvcyBkaXJlaXRvcyBhdXRvcmFpcyBwYXJhIGNvbmNlZGVyIGFvIERlcG9zaXRhIG9zIGRpcmVpdG9zIGFwcmVzZW50YWRvcyAKbmVzdGEgbGljZW7Dp2EsIGUgcXVlIGVzc2UgbWF0ZXJpYWwgZGUgcHJvcHJpZWRhZGUgZGUgdGVyY2Vpcm9zIGVzdMOhIGNsYXJhbWVudGUgaWRlbnRpZmljYWRvIGUgcmVjb25oZWNpZG8gbm8gdGV4dG8gCm91IG5vIGNvbnRlw7pkbyBkYSBwdWJsaWNhw6fDo28gb3JhIGRlcG9zaXRhZGEuCgpDQVNPIEEgUFVCTElDQcOHw4NPIE9SQSBERVBPU0lUQURBIFRFTkhBIFNJRE8gUkVTVUxUQURPIERFIFVNIFBBVFJPQ8ONTklPIE9VIEFQT0lPIERFIFVNQSBBR8OKTkNJQSBERSBGT01FTlRPIE9VIE9VVFJPIApPUkdBTklTTU8sIFZPQ8OKIERFQ0xBUkEgUVVFIFJFU1BFSVRPVSBUT0RPUyBFIFFVQUlTUVVFUiBESVJFSVRPUyBERSBSRVZJU8ODTyBDT01PIFRBTULDiU0gQVMgREVNQUlTIE9CUklHQcOHw5VFUyAKRVhJR0lEQVMgUE9SIENPTlRSQVRPIE9VIEFDT1JETy4KCkEgVUZQQiBzZSBjb21wcm9tZXRlIGEgaWRlbnRpZmljYXIgY2xhcmFtZW50ZSBvIHNldSBub21lIChzKSBvdSBvKHMpIG5vbWUocykgZG8ocykgZGV0ZW50b3IoZXMpIGRvcyBkaXJlaXRvcyAKYXV0b3JhaXMgZGEgcHVibGljYcOnw6NvLCBlIG7Do28gZmFyw6EgcXVhbHF1ZXIgYWx0ZXJhw6fDo28sIGFsw6ltIGRhcXVlbGFzIGNvbmNlZGlkYXMgcG9yIGVzdGEgbGljZW7Dp2EuCg==Repositório InstitucionalPUBhttps://repositorio.ufpb.br/oai/requestdiretoria@ufpb.br||bdtd@biblioteca.ufpb.bropendoar:25462018-09-06T02:04:50Repositório Institucional da UFPB - Universidade Federal da Paraíba (UFPB)false
dc.title.por.fl_str_mv Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
dc.title.alternative.eng.fl_str_mv Evaluation of the antileishmanial activity of natural products isolated from phyllanthus acuminatus and hyptis macrostachys
title Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
spellingShingle Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
Dias, Cínthia Nóbrega de Sousa
Leishmania amazonensis
Lignana
Justicidina B
Antileishmania
Imunomodulação
Leishmania amazonensis
Lignan, Justicidin B
Antileishmania
Immunomodulation
CIENCIAS BIOLOGICAS::FARMACOLOGIA
title_short Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
title_full Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
title_fullStr Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
title_full_unstemmed Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
title_sort Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys
author Dias, Cínthia Nóbrega de Sousa
author_facet Dias, Cínthia Nóbrega de Sousa
author_role author
dc.contributor.advisor1.fl_str_mv Mascarenhas, Sandra Rodrigues
dc.contributor.advisor1ID.fl_str_mv CPF:05334211799
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/4300081489772959
dc.contributor.authorID.fl_str_mv CPF:09434718484
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/1124643706763396
dc.contributor.author.fl_str_mv Dias, Cínthia Nóbrega de Sousa
contributor_str_mv Mascarenhas, Sandra Rodrigues
dc.subject.por.fl_str_mv Leishmania amazonensis
Lignana
Justicidina B
Antileishmania
Imunomodulação
topic Leishmania amazonensis
Lignana
Justicidina B
Antileishmania
Imunomodulação
Leishmania amazonensis
Lignan, Justicidin B
Antileishmania
Immunomodulation
CIENCIAS BIOLOGICAS::FARMACOLOGIA
dc.subject.eng.fl_str_mv Leishmania amazonensis
Lignan, Justicidin B
Antileishmania
Immunomodulation
dc.subject.cnpq.fl_str_mv CIENCIAS BIOLOGICAS::FARMACOLOGIA
description Leishmaniasis is a complex of inserted parasitic diseases in the group of neglected tropical diseases. The drugs used primarily in the treatment of leishmaniasis are pentavalent antimonials and amphotericin B. However, these drugs are associated with serious side effects. Therefore, it is necessary to search for new antileishmanial drugs. In this context natural products are a source of new active molecules. This study, it was investigated the antileishmanial activity of the ethanol extract of Phyllanthus acuminatus and Justicidin B, lignan obtained from this plant and the ethanol extract, the dichloromethane phase and Hyptenolide obtained from Hyptis macrostachys in vitro experimental models. All samples assessed showed antileishmanial activity, initially demonstrated by inhibition of growth of L. amazonensis promastigotes in logarithmic growth phase. The concentration that inhibits 50% of growth (IC50) for the tested substances was 35.58 μg /mL for the ethanolic extract of P. acuminatus, 12.51 μg/mL for Justicidin B; 280.69 μg/mL for the ethanol extract of H. macrostachys, 55.3 μg/mL for dichloromethane phase of H. macrostachys and 22.67 μg/mL for Hyptenolide. These samples were also evaluated for cytotoxicity in murine peritoneal macrophages of swiss mice, which resulted in the measurement of the cytotoxic concentration for 50% macrophages (CC50), which were 39.62 μg/mL for the ethanolic extract of P. acuminatus, 58.56 μg/ml for Justicidin B; 121,36 μg/mL for the ethanol extract of H. macrostachys, 40.45 μg/mL for dichloromethane phase of H. macrostachys and 61.78 μg/ml for Hyptenolide. These data resulted in IC50 and CC50 resulted in a selectivity index of 1.11 for the ethanol extract of P. acuminatus; 4.68 for Justicidin B; 0.43 for the ethanol extract of H. macrostachys; 0.73 to dichloromethane phase of H. macrostachys and 2.72 to Hyptenolide. Given these results, we selected the lignan Justicidina B for further study of antileishmanial activity against L. amazonensis. In the evaluation of the DNA fragmentation pattern of L. amazonensis promastigotes, it was observed in higher concentration evaluated of Justicidin B (4x IC50) induction of DNA fragmentation similar to that observed in the positive control H2O2 (4mM). In infection model macrophage with L. amazonensis and treated with lignan Justicidin B showed reduction in both the percentage of infected macrophages as the number of amastigotes per infected macrophage, resulting in a reduction in the rate of infection compared to control, resulting decrease in the effective concentration for 50% of infection (EC50) of 9.14 and 3.58 for 24 hours and 72 hours after treatment. This result was correlated with an immunomodulatory activity of this lignan, associated with decreased levels of interleukin (IL) -10, and increased levels of nitric oxide (NO). It can be concluded that the lignan Justicidin B has significant activity antipromastigote and antiamastigote and presents immunomodulatory properties in models of infection in vitro.
publishDate 2014
dc.date.available.fl_str_mv 2014-10-22
2018-07-21T00:25:21Z
dc.date.issued.fl_str_mv 2014-06-27
dc.date.accessioned.fl_str_mv 2015-05-14T13:00:03Z
2018-07-21T00:25:21Z
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 DIAS, Cínthia Nóbrega de Sousa. Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys. 2014. 114 f. Dissertação (Mestrado em Produtos Naturais e Sintéticos Bioativos) - Universidade Federal da Paraí­ba, João Pessoa, 2014.
dc.identifier.uri.fl_str_mv https://repositorio.ufpb.br/jspui/handle/tede/6821
identifier_str_mv DIAS, Cínthia Nóbrega de Sousa. Avaliação da atividade antileishmania de produtos naturais isolados de phyllanthus acuminatus e de hyptis macrostachys. 2014. 114 f. Dissertação (Mestrado em Produtos Naturais e Sintéticos Bioativos) - Universidade Federal da Paraí­ba, João Pessoa, 2014.
url https://repositorio.ufpb.br/jspui/handle/tede/6821
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal da Paraí­ba
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos
dc.publisher.initials.fl_str_mv UFPB
dc.publisher.country.fl_str_mv BR
dc.publisher.department.fl_str_mv Farmacologia
publisher.none.fl_str_mv Universidade Federal da Paraí­ba
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFPB
instname:Universidade Federal da Paraíba (UFPB)
instacron:UFPB
instname_str Universidade Federal da Paraíba (UFPB)
instacron_str UFPB
institution UFPB
reponame_str Repositório Institucional da UFPB
collection Repositório Institucional da UFPB
bitstream.url.fl_str_mv https://repositorio.ufpb.br/jspui/bitstream/tede/6821/4/arquivototal.pdf.txt
https://repositorio.ufpb.br/jspui/bitstream/tede/6821/3/license.txt
https://repositorio.ufpb.br/jspui/bitstream/tede/6821/5/arquivototal.pdf.jpg
https://repositorio.ufpb.br/jspui/bitstream/tede/6821/1/arquivototal.pdf
bitstream.checksum.fl_str_mv 0d148959850cc6b5f8a3dfd5a038240d
07956d2f9f6879bad6c75289be248398
5380b37266de8d368add5a7492556ba0
30969d68a1c51eddd37190cde04e71ac
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFPB - Universidade Federal da Paraíba (UFPB)
repository.mail.fl_str_mv diretoria@ufpb.br||bdtd@biblioteca.ufpb.br
_version_ 1877597321880928256