Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/5684 |
Resumo: | Miltefosine (MT) is a alkylphospholipid originally developed for treatment of breast cancer and other solid tumors. It is currently used in the treatment of leishmaniasis, an infectious parasitic disease caused by protozoa of the genus Leishmania, being the first oral drug adopted for this purpose. However, its mechanism of action remains unclear. Electron paramagnetic resonance (EPR) spectroscopy of a spin-labeled lipid (5-DOXIL stearate) and a thiol-specific spin label (4-maleimido-TEMPO) in the membrane of axenic amastigotes of L.(Leishmania) amazonensis and peritoneal macrophages from Balb/c mice showed that MT causes significant increase in membrane dynamics at similar concentrations that inhibit parasite growth or are cytotoxic to macrophage. Although these alterations can be detected using a spin-labeled lipid, our experimental results indicated that MT interacts predominantly with the protein component of the membrane. Using a method for the rapid incorporation of MT into the membrane, these effects were measured immediately after treatment. Cytotoxicity, estimated via microscopic counting of living and dead cells, indicated ~80% parasites and macrophages death at the concentration of MT at which EPR spectroscopy detected a significant change in membrane dynamics. Cell viability, analyzed using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide tetrazolium) reduction assay, showed that 50% inhibitory concentration (IC50) of MT depends on the cell concentration used in the assay. This dependence was analyzed using a theoretical equation involving biophysical parameters such as the partition coefficient of watermembrane and MT concentrations on the membrane and in the aqueous medium. The data showed that cells more sensitive to MT are respectively: erythrocytes, Leishmania promastigotes and Leishmania amastigotes and macrophage. The IC50 value of MT for 4 x 107 parasites/mL was 24,35 M. For the same cell concentration, a significant alteration was detected in the membrane lipid fluidity of parasites to 15 M of MT. The EPR spectra of spinlabeled membrane-bound proteins were consistent with more expanded and solvent exposed protein conformations, suggesting a detergent-like action, with a possible formation of micelle-like structures around polypeptide chains. |
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Alonso, Antoniohttp://lattes.cnpq.br/5013069863616789Dorta, Miriam Cristina Leandrottp://lattes.cnpq.br/3933395097851681Alonso, AntonioDorta, Miriam Cristina LeandroIzumi, ErikaSouza, Paulo Eduardo Narcizo deOliveira, Valéria dehttp://lattes.cnpq.br/5214388420773954Fernandes, Kelly de Souza2016-06-10T13:24:18Z2016-02-15FERNANDES, K. S. Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais. 2016. 146 f. Tese (Doutorado em Física) - Universidade Federal de Goiás, Goiânia, 2016.http://repositorio.bc.ufg.br/tede/handle/tede/5684Miltefosine (MT) is a alkylphospholipid originally developed for treatment of breast cancer and other solid tumors. It is currently used in the treatment of leishmaniasis, an infectious parasitic disease caused by protozoa of the genus Leishmania, being the first oral drug adopted for this purpose. However, its mechanism of action remains unclear. Electron paramagnetic resonance (EPR) spectroscopy of a spin-labeled lipid (5-DOXIL stearate) and a thiol-specific spin label (4-maleimido-TEMPO) in the membrane of axenic amastigotes of L.(Leishmania) amazonensis and peritoneal macrophages from Balb/c mice showed that MT causes significant increase in membrane dynamics at similar concentrations that inhibit parasite growth or are cytotoxic to macrophage. Although these alterations can be detected using a spin-labeled lipid, our experimental results indicated that MT interacts predominantly with the protein component of the membrane. Using a method for the rapid incorporation of MT into the membrane, these effects were measured immediately after treatment. Cytotoxicity, estimated via microscopic counting of living and dead cells, indicated ~80% parasites and macrophages death at the concentration of MT at which EPR spectroscopy detected a significant change in membrane dynamics. Cell viability, analyzed using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide tetrazolium) reduction assay, showed that 50% inhibitory concentration (IC50) of MT depends on the cell concentration used in the assay. This dependence was analyzed using a theoretical equation involving biophysical parameters such as the partition coefficient of watermembrane and MT concentrations on the membrane and in the aqueous medium. The data showed that cells more sensitive to MT are respectively: erythrocytes, Leishmania promastigotes and Leishmania amastigotes and macrophage. The IC50 value of MT for 4 x 107 parasites/mL was 24,35 M. For the same cell concentration, a significant alteration was detected in the membrane lipid fluidity of parasites to 15 M of MT. The EPR spectra of spinlabeled membrane-bound proteins were consistent with more expanded and solvent exposed protein conformations, suggesting a detergent-like action, with a possible formation of micelle-like structures around polypeptide chains.A Miltefosina (MT) é um alquilfosfolipídio originalmente desenvolvido para o tratamento de câncer de mama e outros tumores sólidos. Atualmente é utilizada no tratamento da leishmaniose, uma doença infecto-parasitária causada pelo protozoário do gênero Leishmania, sendo o primeiro fármaco de uso oral aprovado para tal fim. No entanto, seu mecanismo de ação ainda é pouco conhecido. A espectroscopia de Ressonância Paramagnética Eletrônica (RPE) de um marcador de spin lipídico (5-DOXIL estearato) e outro específico de grupo tiol (4-maleimido-TEMPO) na membrana de amastigotas axênicas de L. (Leishmania) amazonensis e de macrófagos extraídos de peritônio de camundongos BALB/c, mostrou que a MT causa um aumento significativo na dinâmica destas membranas para concentrações similares àquelas que inibem o crescimento do parasito ou que são citotóxicas ao macrófago. Embora essas alterações possam ser detectadas usando um marcador de spin lipídico, nossos resultados experimentais indicaram que a MT interage predominantemente com a componente proteica da membrana. Utilizando um método para incorporação rápida da MT na membrana, esses efeitos foram medidos imediatamente após o tratamento. Ensaios de citotoxicidade, estimada via contagem microscópica de células vivas e mortas, indicaram que ~80% dos parasitos e dos macrófagos estão mortos na concentração de MT no qual a espectroscopia de RPE detectou uma mudança significativa na dinâmica da membrana. A viabilidade celular, quantificada pela redução do sal MTT ((3-4,5- Dimetiltiazol-2yl)-2,5 difenil brometo de tetrazolina), mostrou que a concentração de MT que inibe 50% da proliferação celular (IC50) depende da concentração celular usada no ensaio. Esta dependência foi analisada utilizando uma equação teórica envolvendo parâmetros biofísicos tais como o coeficiente de partição membrana-água e concentrações de MT na membrana e no meio aquoso. Os dados mostraram que as células mais sensíveis à MT são respectivamente: eritrócitos, formas promastigotas e amastigotas da Leishmania e macrófagos. O valor do IC50 da MT para 4 x 107 parasitos/mL foi de 24,35 M. Para esta mesma concentração de células, foi detectada uma alteração significativa na fluidez lipídica da membrana dos parasitos com 15 M de MT. Os espectros de RPE do marcador de spin ligados a proteínas da membrana foram consistentes com as conformações mais expandidas e dinâmicas das proteínas expostas no solvente, sugerindo uma ação semelhante à de detergente, com uma possível formação de estruturas tipo micelas em volta das cadeias polipeptídicas.Submitted by Cláudia Bueno (claudiamoura18@gmail.com) on 2016-06-09T21:26:35Z No. of bitstreams: 2 Dissertação - Kelly de Souza Fernandes - 2016: 2715711 bytes, checksum: a2c065301e1443bb424fa23c738e43d2 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2016-06-10T13:24:18Z (GMT) No. of bitstreams: 2 Dissertação - Kelly de Souza Fernandes - 2016: 2715711 bytes, checksum: a2c065301e1443bb424fa23c738e43d2 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5)Made available in DSpace on 2016-06-10T13:24:18Z (GMT). No. of bitstreams: 2 Dissertação - Kelly de Souza Fernandes - 2016: 2715711 bytes, checksum: a2c065301e1443bb424fa23c738e43d2 (MD5) license_rdf: 23148 bytes, checksum: 9da0b6dfac957114c6a7714714b86306 (MD5) Previous issue date: 2016-02-15Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Fisica (IF)UFGBrasilInstituto de Física - IF (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessMiltefosinaL. (L.) amazonensisMacrófagos peritoneaisRPEMarcador de spinMiltefosineL. (L.) amazonensisPeritoneal macrophagesEPRSpin labelFISICA::FISICA GERALEstudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneaisStudy of interactions of Miltefosine with membranes of L. (Leishmania) amazonensis and peritoneal macrophagesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesis3162138865744262028600600600600-402965885365204930646527873527626978302075167498588264571reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGCC-LICENSElicense_urllicense_urltext/plain; charset=utf-849http://repositorio.bc.ufg.br/tede/bitstreams/6114ca55-b51c-4bbd-b229-1bdb84ce499a/download4afdbb8c545fd630ea7db775da747b2fMD52license_textlicense_texttext/html; charset=utf-822064http://repositorio.bc.ufg.br/tede/bitstreams/97a7762f-a78b-4756-a34a-5a12914e92f1/downloadef48816a10f2d45f2e2fee2f478e2fafMD53license_rdflicense_rdfapplication/rdf+xml; charset=utf-823148http://repositorio.bc.ufg.br/tede/bitstreams/90747a89-3222-4ccb-b495-8c87cd05c3e4/download9da0b6dfac957114c6a7714714b86306MD54LICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://repositorio.bc.ufg.br/tede/bitstreams/8b8027fc-0f7c-4812-b2e7-58f8078230bc/downloadbd3efa91386c1718a7f26a329fdcb468MD51ORIGINALDissertação - Kelly de Souza Fernandes - 2016Dissertação - Kelly de Souza Fernandes - 2016application/pdf2715711http://repositorio.bc.ufg.br/tede/bitstreams/52febf49-108a-4083-aa52-3b20dbf2fc51/downloada2c065301e1443bb424fa23c738e43d2MD55tede/56842016-06-10 10:24:18.32http://creativecommons.org/licenses/by-nc-nd/4.0/Acesso Abertoopen.accessoai:repositorio.bc.ufg.br:tede/5684http://repositorio.bc.ufg.br/tedeRepositório InstitucionalPUBhttp://repositorio.bc.ufg.br/oai/requesttasesdissertacoes.bc@ufg.bropendoar:2016-06-10T13:24:18Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)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 |
dc.title.por.fl_str_mv |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
dc.title.alternative.eng.fl_str_mv |
Study of interactions of Miltefosine with membranes of L. (Leishmania) amazonensis and peritoneal macrophages |
title |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
spellingShingle |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais Fernandes, Kelly de Souza Miltefosina L. (L.) amazonensis Macrófagos peritoneais RPE Marcador de spin Miltefosine L. (L.) amazonensis Peritoneal macrophages EPR Spin label FISICA::FISICA GERAL |
title_short |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
title_full |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
title_fullStr |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
title_full_unstemmed |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
title_sort |
Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais |
author |
Fernandes, Kelly de Souza |
author_facet |
Fernandes, Kelly de Souza |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Alonso, Antonio |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/5013069863616789 |
dc.contributor.advisor-co1.fl_str_mv |
Dorta, Miriam Cristina Leandro |
dc.contributor.advisor-co1Lattes.fl_str_mv |
ttp://lattes.cnpq.br/3933395097851681 |
dc.contributor.referee1.fl_str_mv |
Alonso, Antonio |
dc.contributor.referee2.fl_str_mv |
Dorta, Miriam Cristina Leandro |
dc.contributor.referee3.fl_str_mv |
Izumi, Erika |
dc.contributor.referee4.fl_str_mv |
Souza, Paulo Eduardo Narcizo de |
dc.contributor.referee5.fl_str_mv |
Oliveira, Valéria de |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/5214388420773954 |
dc.contributor.author.fl_str_mv |
Fernandes, Kelly de Souza |
contributor_str_mv |
Alonso, Antonio Dorta, Miriam Cristina Leandro Alonso, Antonio Dorta, Miriam Cristina Leandro Izumi, Erika Souza, Paulo Eduardo Narcizo de Oliveira, Valéria de |
dc.subject.por.fl_str_mv |
Miltefosina L. (L.) amazonensis Macrófagos peritoneais RPE Marcador de spin |
topic |
Miltefosina L. (L.) amazonensis Macrófagos peritoneais RPE Marcador de spin Miltefosine L. (L.) amazonensis Peritoneal macrophages EPR Spin label FISICA::FISICA GERAL |
dc.subject.eng.fl_str_mv |
Miltefosine L. (L.) amazonensis Peritoneal macrophages EPR Spin label |
dc.subject.cnpq.fl_str_mv |
FISICA::FISICA GERAL |
description |
Miltefosine (MT) is a alkylphospholipid originally developed for treatment of breast cancer and other solid tumors. It is currently used in the treatment of leishmaniasis, an infectious parasitic disease caused by protozoa of the genus Leishmania, being the first oral drug adopted for this purpose. However, its mechanism of action remains unclear. Electron paramagnetic resonance (EPR) spectroscopy of a spin-labeled lipid (5-DOXIL stearate) and a thiol-specific spin label (4-maleimido-TEMPO) in the membrane of axenic amastigotes of L.(Leishmania) amazonensis and peritoneal macrophages from Balb/c mice showed that MT causes significant increase in membrane dynamics at similar concentrations that inhibit parasite growth or are cytotoxic to macrophage. Although these alterations can be detected using a spin-labeled lipid, our experimental results indicated that MT interacts predominantly with the protein component of the membrane. Using a method for the rapid incorporation of MT into the membrane, these effects were measured immediately after treatment. Cytotoxicity, estimated via microscopic counting of living and dead cells, indicated ~80% parasites and macrophages death at the concentration of MT at which EPR spectroscopy detected a significant change in membrane dynamics. Cell viability, analyzed using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5- diphenyltetrazolium bromide tetrazolium) reduction assay, showed that 50% inhibitory concentration (IC50) of MT depends on the cell concentration used in the assay. This dependence was analyzed using a theoretical equation involving biophysical parameters such as the partition coefficient of watermembrane and MT concentrations on the membrane and in the aqueous medium. The data showed that cells more sensitive to MT are respectively: erythrocytes, Leishmania promastigotes and Leishmania amastigotes and macrophage. The IC50 value of MT for 4 x 107 parasites/mL was 24,35 M. For the same cell concentration, a significant alteration was detected in the membrane lipid fluidity of parasites to 15 M of MT. The EPR spectra of spinlabeled membrane-bound proteins were consistent with more expanded and solvent exposed protein conformations, suggesting a detergent-like action, with a possible formation of micelle-like structures around polypeptide chains. |
publishDate |
2016 |
dc.date.accessioned.fl_str_mv |
2016-06-10T13:24:18Z |
dc.date.issued.fl_str_mv |
2016-02-15 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
FERNANDES, K. S. Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais. 2016. 146 f. Tese (Doutorado em Física) - Universidade Federal de Goiás, Goiânia, 2016. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/5684 |
identifier_str_mv |
FERNANDES, K. S. Estudo das interações da miltefosina com membranas de L. (Leishmania) amazonensis e macrófagos peritoneais. 2016. 146 f. Tese (Doutorado em Física) - Universidade Federal de Goiás, Goiânia, 2016. |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/5684 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.program.fl_str_mv |
3162138865744262028 |
dc.relation.confidence.fl_str_mv |
600 600 600 600 |
dc.relation.department.fl_str_mv |
-4029658853652049306 |
dc.relation.cnpq.fl_str_mv |
4652787352762697830 |
dc.relation.sponsorship.fl_str_mv |
2075167498588264571 |
dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Fisica (IF) |
dc.publisher.initials.fl_str_mv |
UFG |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Instituto de Física - IF (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFG instname:Universidade Federal de Goiás (UFG) instacron:UFG |
instname_str |
Universidade Federal de Goiás (UFG) |
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UFG |
institution |
UFG |
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Repositório Institucional da UFG |
collection |
Repositório Institucional da UFG |
bitstream.url.fl_str_mv |
http://repositorio.bc.ufg.br/tede/bitstreams/6114ca55-b51c-4bbd-b229-1bdb84ce499a/download http://repositorio.bc.ufg.br/tede/bitstreams/97a7762f-a78b-4756-a34a-5a12914e92f1/download http://repositorio.bc.ufg.br/tede/bitstreams/90747a89-3222-4ccb-b495-8c87cd05c3e4/download http://repositorio.bc.ufg.br/tede/bitstreams/8b8027fc-0f7c-4812-b2e7-58f8078230bc/download http://repositorio.bc.ufg.br/tede/bitstreams/52febf49-108a-4083-aa52-3b20dbf2fc51/download |
bitstream.checksum.fl_str_mv |
4afdbb8c545fd630ea7db775da747b2f ef48816a10f2d45f2e2fee2f478e2faf 9da0b6dfac957114c6a7714714b86306 bd3efa91386c1718a7f26a329fdcb468 a2c065301e1443bb424fa23c738e43d2 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
repository.mail.fl_str_mv |
tasesdissertacoes.bc@ufg.br |
_version_ |
1798044375693918208 |