Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis

Detalhes bibliográficos
Autor(a) principal: Cargnin, Simone Tasca
Data de Publicação: 2019
Outros Autores: Staudt, Andressa Finkler, Menezes, Camila Braz, Santos, Ana Paula de Azevedo dos, Fialho, Saara Neri, Tasca, Tiana, Teles, Carolina Bioni Garcia, Gnoatto, Simone Cristina Baggio
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/212581
Resumo: Trichomonas vaginalis and Leishmania spp. are protozoal species responsible for millions of cases of parasitic diseases worldwide. Considering the potential of natural products and the need for more effective and less toxic alternatives to treat trichomoniasis and leishmaniasis, this study aimed to evaluate the effect of two series of triterpenes derivatives with different modifications at C-3 and C-28 positions of the ursolic acid (UA) and betulinic acid (BA) against trophozoites of Trichomonas vaginalis and promastigotes forms of Leishmania (L.) amazonensis. The compounds modified just at C-3 were the most active. The 3β-acetyl betulinic acid (1b) reduced the trophozoites viability of T. vaginalis at 74%, followed by the 3-oxo ursolic acid and 3-oxo betulinic acid (3a and 3b) compounds (55% of reduction). The compound 3β-isobutyl ursolic acid (7a) inhibited the viability of L. amazonensis promastigotes by 55%. Therefore, analyzing the structure-activity relationship and the data of literature, it is possible to suppose that the inclusion of polar groups in the skeletons could improve the antiprotozoal activity. Overall, further studies are necessary to develop triterpenic derivatives with more powerful trichomonicidal and leishmanicidal properties.
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spelling Cargnin, Simone TascaStaudt, Andressa FinklerMenezes, Camila BrazSantos, Ana Paula de Azevedo dosFialho, Saara NeriTasca, TianaTeles, Carolina Bioni GarciaGnoatto, Simone Cristina Baggio2020-08-04T03:38:40Z20191984-8250http://hdl.handle.net/10183/212581001116212Trichomonas vaginalis and Leishmania spp. are protozoal species responsible for millions of cases of parasitic diseases worldwide. Considering the potential of natural products and the need for more effective and less toxic alternatives to treat trichomoniasis and leishmaniasis, this study aimed to evaluate the effect of two series of triterpenes derivatives with different modifications at C-3 and C-28 positions of the ursolic acid (UA) and betulinic acid (BA) against trophozoites of Trichomonas vaginalis and promastigotes forms of Leishmania (L.) amazonensis. The compounds modified just at C-3 were the most active. The 3β-acetyl betulinic acid (1b) reduced the trophozoites viability of T. vaginalis at 74%, followed by the 3-oxo ursolic acid and 3-oxo betulinic acid (3a and 3b) compounds (55% of reduction). The compound 3β-isobutyl ursolic acid (7a) inhibited the viability of L. amazonensis promastigotes by 55%. Therefore, analyzing the structure-activity relationship and the data of literature, it is possible to suppose that the inclusion of polar groups in the skeletons could improve the antiprotozoal activity. Overall, further studies are necessary to develop triterpenic derivatives with more powerful trichomonicidal and leishmanicidal properties.application/pdfengBrazilian journal of pharmaceutical sciences. Vol. 55 (2019), e17481, [7 p.]FarmáciaTrichomonas vaginalisBetulinic acideLeishmania amazonensisSemisynthesisUrsolic acidEvaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalisinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001116212.pdf.txt001116212.pdf.txtExtracted Texttext/plain25492http://www.lume.ufrgs.br/bitstream/10183/212581/2/001116212.pdf.txt5adf1d533adce628fbeea45c45d6e880MD52ORIGINAL001116212.pdfTexto completo (inglês)application/pdf834447http://www.lume.ufrgs.br/bitstream/10183/212581/1/001116212.pdf05743e4aeb18ac142ec3944de392a4acMD5110183/2125812020-08-05 03:39:06.937316oai:www.lume.ufrgs.br:10183/212581Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2020-08-05T06:39:06Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
title Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
spellingShingle Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
Cargnin, Simone Tasca
Farmácia
Trichomonas vaginalis
Betulinic acide
Leishmania amazonensis
Semisynthesis
Ursolic acid
title_short Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
title_full Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
title_fullStr Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
title_full_unstemmed Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
title_sort Evaluation of triterpenes derivatives in the viability of Leishmania amazonensis and Trichomonas vaginalis
author Cargnin, Simone Tasca
author_facet Cargnin, Simone Tasca
Staudt, Andressa Finkler
Menezes, Camila Braz
Santos, Ana Paula de Azevedo dos
Fialho, Saara Neri
Tasca, Tiana
Teles, Carolina Bioni Garcia
Gnoatto, Simone Cristina Baggio
author_role author
author2 Staudt, Andressa Finkler
Menezes, Camila Braz
Santos, Ana Paula de Azevedo dos
Fialho, Saara Neri
Tasca, Tiana
Teles, Carolina Bioni Garcia
Gnoatto, Simone Cristina Baggio
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Cargnin, Simone Tasca
Staudt, Andressa Finkler
Menezes, Camila Braz
Santos, Ana Paula de Azevedo dos
Fialho, Saara Neri
Tasca, Tiana
Teles, Carolina Bioni Garcia
Gnoatto, Simone Cristina Baggio
dc.subject.por.fl_str_mv Farmácia
Trichomonas vaginalis
topic Farmácia
Trichomonas vaginalis
Betulinic acide
Leishmania amazonensis
Semisynthesis
Ursolic acid
dc.subject.eng.fl_str_mv Betulinic acide
Leishmania amazonensis
Semisynthesis
Ursolic acid
description Trichomonas vaginalis and Leishmania spp. are protozoal species responsible for millions of cases of parasitic diseases worldwide. Considering the potential of natural products and the need for more effective and less toxic alternatives to treat trichomoniasis and leishmaniasis, this study aimed to evaluate the effect of two series of triterpenes derivatives with different modifications at C-3 and C-28 positions of the ursolic acid (UA) and betulinic acid (BA) against trophozoites of Trichomonas vaginalis and promastigotes forms of Leishmania (L.) amazonensis. The compounds modified just at C-3 were the most active. The 3β-acetyl betulinic acid (1b) reduced the trophozoites viability of T. vaginalis at 74%, followed by the 3-oxo ursolic acid and 3-oxo betulinic acid (3a and 3b) compounds (55% of reduction). The compound 3β-isobutyl ursolic acid (7a) inhibited the viability of L. amazonensis promastigotes by 55%. Therefore, analyzing the structure-activity relationship and the data of literature, it is possible to suppose that the inclusion of polar groups in the skeletons could improve the antiprotozoal activity. Overall, further studies are necessary to develop triterpenic derivatives with more powerful trichomonicidal and leishmanicidal properties.
publishDate 2019
dc.date.issued.fl_str_mv 2019
dc.date.accessioned.fl_str_mv 2020-08-04T03:38:40Z
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10183/212581
dc.identifier.issn.pt_BR.fl_str_mv 1984-8250
dc.identifier.nrb.pt_BR.fl_str_mv 001116212
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dc.relation.ispartof.pt_BR.fl_str_mv Brazilian journal of pharmaceutical sciences. Vol. 55 (2019), e17481, [7 p.]
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dc.source.none.fl_str_mv reponame:Repositório Institucional da UFRGS
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