Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck
ABSTRACT: Background and Objective: Plasmodium resistance to antimalarial drugs has expanded and intensified, making new and effective antimalarial drugs urgently. The objective of this work was the in vitro evaluation of antiplasmodial activity of extracts of different polarity and compounds of the...
- Autores:
-
Mesa Vanegas, Ana María
Toro Suaza, Jhon Fredy
Vásquez Cardona, Ana María
Blair Trujillo, Silvia
Peláez Jaramillo, Carlos
Díaz Oltra, Santiago
Pachón, César Augusto
Carda, Miguel
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2018
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/29711
- Acceso en línea:
- https://hdl.handle.net/10495/29711
- Palabra clave:
- Plasmodium falciparum
Piper pidecuestanum
Antiplasmodial activity
Cytotoxic activity
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by/4.0/
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Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| title |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| spellingShingle |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck Plasmodium falciparum Piper pidecuestanum Antiplasmodial activity Cytotoxic activity |
| title_short |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| title_full |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| title_fullStr |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| title_full_unstemmed |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| title_sort |
Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and Yunck |
| dc.creator.fl_str_mv |
Mesa Vanegas, Ana María Toro Suaza, Jhon Fredy Vásquez Cardona, Ana María Blair Trujillo, Silvia Peláez Jaramillo, Carlos Díaz Oltra, Santiago Pachón, César Augusto Carda, Miguel |
| dc.contributor.author.none.fl_str_mv |
Mesa Vanegas, Ana María Toro Suaza, Jhon Fredy Vásquez Cardona, Ana María Blair Trujillo, Silvia Peláez Jaramillo, Carlos Díaz Oltra, Santiago Pachón, César Augusto Carda, Miguel |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo Interdisciplinario de Estudios Moleculares Grupo Malaria Grupo Interdisciplinario de Estudios Moleculares Grupo Malaria |
| dc.subject.decs.none.fl_str_mv |
Plasmodium falciparum |
| topic |
Plasmodium falciparum Piper pidecuestanum Antiplasmodial activity Cytotoxic activity |
| dc.subject.proposal.spa.fl_str_mv |
Piper pidecuestanum Antiplasmodial activity Cytotoxic activity |
| description |
ABSTRACT: Background and Objective: Plasmodium resistance to antimalarial drugs has expanded and intensified, making new and effective antimalarial drugs urgently. The objective of this work was the in vitro evaluation of antiplasmodial activity of extracts of different polarity and compounds of the species P. piedecuestanum. Materials and Methods: The plant materials were obtained through successive extractions using solvents of different polarity such as hexane (H), dichloromethane (D), ethyl acetate (A) and methanol (M) and separations techniques for fractionation and isolation of compounds. The antiplasmodial activities of the extracts and compounds were evaluated by SYBR Green I® method and evaluated the cytotoxicity in the cell lines U-937, HUVEC by the MTT method. Results: The antiplasmodial and cytotoxic activity of the extracts of dichloromethane (PPD) and ethyl acetate (PPAE) with antiplasmodial activity of IC50 = 17.93 µg mLG1 ; IS = 2.093 and IC50 = 19.5 µg mLG1 ; IS = 0.791, respectively are reported for the first time. In addition, from P. piedecuestanum species were isolation and characterization five metabolites 5,8-Hydroxy-7-methoxyflavone(1), 6,7-dimethoxy-5,8- dihydroxyflavone(2), 6,7-dimethoxy-5-hydroxyflavone (mosloflavone) (3), 5,6-dihydroxy-7-methoxyflavone (negletein) (4), 5-hydroxy-7- methoxyflavone (5) and a brominated derivative from (5) named 6,8 bromo-5-hydroxy-7-methoxyflavone(7). Compound (1) presented promising antiplasmodial activity with an IC50 = 7.325 µg mLG1 (25.69 µM); ISHUVEC =13.65. Conclusion: Chemical analysis of extracts and compounds from P. piedecuestanum spices will play a central role in the development and modernization of an antimalarial herbal traditional in Colombia. |
| publishDate |
2018 |
| dc.date.issued.none.fl_str_mv |
2018 |
| dc.date.accessioned.none.fl_str_mv |
2022-07-13T18:27:54Z |
| dc.date.available.none.fl_str_mv |
2022-07-13T18:27:54Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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Ana María Mesa Vanegas, Jhon Fredy Toro Suaza, Ana María Vásquez Cardona, Silvia Blair Trujillo, Carlos Peláez Jaramill, Santiago Díaz Oltra, César Augusto Pachón, Miguel Carda, 2018. Antiplasmodial and cytotoxic activity of piper piedecuestanum Trel. and Yunck. Res. J. Med. Plants, 12: 57-64 |
| dc.identifier.issn.none.fl_str_mv |
1819-3455 |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/29711 |
| dc.identifier.doi.none.fl_str_mv |
10.3923/rjmp.2018.57.64 |
| dc.identifier.eissn.none.fl_str_mv |
2151-7924 |
| identifier_str_mv |
Ana María Mesa Vanegas, Jhon Fredy Toro Suaza, Ana María Vásquez Cardona, Silvia Blair Trujillo, Carlos Peláez Jaramill, Santiago Díaz Oltra, César Augusto Pachón, Miguel Carda, 2018. Antiplasmodial and cytotoxic activity of piper piedecuestanum Trel. and Yunck. Res. J. Med. Plants, 12: 57-64 1819-3455 10.3923/rjmp.2018.57.64 2151-7924 |
| url |
https://hdl.handle.net/10495/29711 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Res. J. Med. Plants |
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64 |
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2 |
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57 |
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12 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Research Journal of Medicinal Plants |
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https://creativecommons.org/licenses/by/4.0/ |
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http://creativecommons.org/licenses/by/2.5/co/ |
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openAccess |
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New York, Estados Unidos |
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Universidad de Antioquia |
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Mesa Vanegas, Ana MaríaToro Suaza, Jhon FredyVásquez Cardona, Ana MaríaBlair Trujillo, SilviaPeláez Jaramillo, CarlosDíaz Oltra, SantiagoPachón, César AugustoCarda, MiguelGrupo Interdisciplinario de Estudios MolecularesGrupo MalariaGrupo Interdisciplinario de Estudios MolecularesGrupo Malaria2022-07-13T18:27:54Z2022-07-13T18:27:54Z2018Ana María Mesa Vanegas, Jhon Fredy Toro Suaza, Ana María Vásquez Cardona, Silvia Blair Trujillo, Carlos Peláez Jaramill, Santiago Díaz Oltra, César Augusto Pachón, Miguel Carda, 2018. Antiplasmodial and cytotoxic activity of piper piedecuestanum Trel. and Yunck. Res. J. Med. Plants, 12: 57-641819-3455https://hdl.handle.net/10495/2971110.3923/rjmp.2018.57.642151-7924ABSTRACT: Background and Objective: Plasmodium resistance to antimalarial drugs has expanded and intensified, making new and effective antimalarial drugs urgently. The objective of this work was the in vitro evaluation of antiplasmodial activity of extracts of different polarity and compounds of the species P. piedecuestanum. Materials and Methods: The plant materials were obtained through successive extractions using solvents of different polarity such as hexane (H), dichloromethane (D), ethyl acetate (A) and methanol (M) and separations techniques for fractionation and isolation of compounds. The antiplasmodial activities of the extracts and compounds were evaluated by SYBR Green I® method and evaluated the cytotoxicity in the cell lines U-937, HUVEC by the MTT method. Results: The antiplasmodial and cytotoxic activity of the extracts of dichloromethane (PPD) and ethyl acetate (PPAE) with antiplasmodial activity of IC50 = 17.93 µg mLG1 ; IS = 2.093 and IC50 = 19.5 µg mLG1 ; IS = 0.791, respectively are reported for the first time. In addition, from P. piedecuestanum species were isolation and characterization five metabolites 5,8-Hydroxy-7-methoxyflavone(1), 6,7-dimethoxy-5,8- dihydroxyflavone(2), 6,7-dimethoxy-5-hydroxyflavone (mosloflavone) (3), 5,6-dihydroxy-7-methoxyflavone (negletein) (4), 5-hydroxy-7- methoxyflavone (5) and a brominated derivative from (5) named 6,8 bromo-5-hydroxy-7-methoxyflavone(7). Compound (1) presented promising antiplasmodial activity with an IC50 = 7.325 µg mLG1 (25.69 µM); ISHUVEC =13.65. Conclusion: Chemical analysis of extracts and compounds from P. piedecuestanum spices will play a central role in the development and modernization of an antimalarial herbal traditional in Colombia.COL0007524COL0007462COL0007462COL00075248application/pdfengAcademic JournalsNew York, Estados Unidoshttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Antiplasmodial and Cytotoxic Activity of Piper Piedecuestanum Trel. and YunckArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPlasmodium falciparumPiper pidecuestanumAntiplasmodial activityCytotoxic activityRes. J. Med. 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