Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species
ABSTRACT: Background: The challenge in anti-malarial chemotherapy is based on the emergence of resistance to drugs and the search for medicines against all stages of the life cycle of Plasmodium spp. as a therapeutic target. Nowadays, many molecules with anti-malarial activity are reported. However,...
- Autores:
-
Bonilla Ramírez, Leonardo
Galiano, Silvia
Quiliano, Miguel
Aldana, Ignacio
Pabón Vidal, Adriana Lucía
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2019
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/42301
- Acceso en línea:
- https://hdl.handle.net/10495/42301
- Palabra clave:
- Antimaláricos
Antimalarials
Eritrocitos
Erythrocytes
Células Hep G2
Hep G2 Cells
Plasmodium yoelii
Primaquina
Primaquine
Quinoxalinas
Quinoxalines
Esporozoítos
Sporozoites
https://id.nlm.nih.gov/mesh/D056945
https://id.nlm.nih.gov/mesh/D010600
https://id.nlm.nih.gov/mesh/D004912
https://id.nlm.nih.gov/mesh/D010967
https://id.nlm.nih.gov/mesh/D011319
https://id.nlm.nih.gov/mesh/D011810
https://id.nlm.nih.gov/mesh/D034101
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by/2.5/co/
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Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| title |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| spellingShingle |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species Antimaláricos Antimalarials Eritrocitos Erythrocytes Células Hep G2 Hep G2 Cells Plasmodium yoelii Primaquina Primaquine Quinoxalinas Quinoxalines Esporozoítos Sporozoites https://id.nlm.nih.gov/mesh/D056945 https://id.nlm.nih.gov/mesh/D010600 https://id.nlm.nih.gov/mesh/D004912 https://id.nlm.nih.gov/mesh/D010967 https://id.nlm.nih.gov/mesh/D011319 https://id.nlm.nih.gov/mesh/D011810 https://id.nlm.nih.gov/mesh/D034101 |
| title_short |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| title_full |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| title_fullStr |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| title_full_unstemmed |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| title_sort |
Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species |
| dc.creator.fl_str_mv |
Bonilla Ramírez, Leonardo Galiano, Silvia Quiliano, Miguel Aldana, Ignacio Pabón Vidal, Adriana Lucía |
| dc.contributor.author.none.fl_str_mv |
Bonilla Ramírez, Leonardo Galiano, Silvia Quiliano, Miguel Aldana, Ignacio Pabón Vidal, Adriana Lucía |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo Malaria |
| dc.subject.decs.none.fl_str_mv |
Antimaláricos Antimalarials Eritrocitos Erythrocytes Células Hep G2 Hep G2 Cells Plasmodium yoelii Primaquina Primaquine Quinoxalinas Quinoxalines Esporozoítos Sporozoites |
| topic |
Antimaláricos Antimalarials Eritrocitos Erythrocytes Células Hep G2 Hep G2 Cells Plasmodium yoelii Primaquina Primaquine Quinoxalinas Quinoxalines Esporozoítos Sporozoites https://id.nlm.nih.gov/mesh/D056945 https://id.nlm.nih.gov/mesh/D010600 https://id.nlm.nih.gov/mesh/D004912 https://id.nlm.nih.gov/mesh/D010967 https://id.nlm.nih.gov/mesh/D011319 https://id.nlm.nih.gov/mesh/D011810 https://id.nlm.nih.gov/mesh/D034101 |
| dc.subject.meshuri.none.fl_str_mv |
https://id.nlm.nih.gov/mesh/D056945 https://id.nlm.nih.gov/mesh/D010600 https://id.nlm.nih.gov/mesh/D004912 https://id.nlm.nih.gov/mesh/D010967 https://id.nlm.nih.gov/mesh/D011319 https://id.nlm.nih.gov/mesh/D011810 https://id.nlm.nih.gov/mesh/D034101 |
| description |
ABSTRACT: Background: The challenge in anti-malarial chemotherapy is based on the emergence of resistance to drugs and the search for medicines against all stages of the life cycle of Plasmodium spp. as a therapeutic target. Nowadays, many molecules with anti-malarial activity are reported. However, few studies about the cellular and molecular mechanisms to understand their mode of action have been explored. Recently, new primaquine-based hybrids as new molecules with potential multi-acting anti-malarial activity were reported and two hybrids of primaquine linked to quinoxaline 1,4-di-N-oxide (PQ-QdNO) were identified as the most active against erythrocytic, exoerythrocytic and sporogonic stages. Methods: To further understand the anti-malarial mode of action (MA) of these hybrids, hepg2-CD81 were infected with Plasmodium yoelii 17XNL and treated with PQ-QdNO hybrids during 48 h. After were evaluated the production of ROS, the mitochondrial depolarization, the total glutathione content, the DNA damage and proteins related to oxidative stress and death cell. Results: In a preliminary analysis as tissue schizonticidals, these hybrids showed a mode of action dependent on peroxides production, but independent of the activation of transcription factor p53, mitochondrial depolarization and arrest cell cycle. Conclusions: Primaquine-quinoxaline 1,4-di-N-oxide hybrids exert their antiplasmodial activity in the exoerythrocytic phase by generating high levels of oxidative stress which promotes the increase of total glutathione levels, through oxidation stress sensor protein DJ-1. In addition, the role of HIF1a in the mode of action of quinoxaline 1,4-di-N-oxide is independent of biological activity. Keywords: 4-Di-N-oxide; Cell death; Exoerythrocytic stage; Malaria; Oxidative stress; Plasmodium; Quinoxaline 1. |
| publishDate |
2019 |
| dc.date.issued.none.fl_str_mv |
2019 |
| dc.date.accessioned.none.fl_str_mv |
2024-09-20T15:48:11Z |
| dc.date.available.none.fl_str_mv |
2024-09-20T15:48:11Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
| dc.type.redcol.spa.fl_str_mv |
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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info:eu-repo/semantics/publishedVersion |
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Bonilla-Ramírez L, Galiano S, Quiliano M, Aldana I, Pabón A. Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species. Malar J. 2019 Jun 19;18(1):201. doi: 10.1186/s12936-019-2825-8. |
| dc.identifier.uri.none.fl_str_mv |
https://hdl.handle.net/10495/42301 |
| dc.identifier.doi.none.fl_str_mv |
10.1186/s12936-019-2825-8. |
| dc.identifier.eissn.none.fl_str_mv |
1475-2875 |
| identifier_str_mv |
Bonilla-Ramírez L, Galiano S, Quiliano M, Aldana I, Pabón A. Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species. Malar J. 2019 Jun 19;18(1):201. doi: 10.1186/s12936-019-2825-8. 10.1186/s12936-019-2825-8. 1475-2875 |
| url |
https://hdl.handle.net/10495/42301 |
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eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Malar. J. |
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13 |
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1 |
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1 |
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18 |
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Malaria Journal |
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http://creativecommons.org/licenses/by/2.5/co/ |
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Bonilla Ramírez, LeonardoGaliano, SilviaQuiliano, MiguelAldana, IgnacioPabón Vidal, Adriana LucíaGrupo Malaria2024-09-20T15:48:11Z2024-09-20T15:48:11Z2019Bonilla-Ramírez L, Galiano S, Quiliano M, Aldana I, Pabón A. Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen species. Malar J. 2019 Jun 19;18(1):201. doi: 10.1186/s12936-019-2825-8.https://hdl.handle.net/10495/4230110.1186/s12936-019-2825-8.1475-2875ABSTRACT: Background: The challenge in anti-malarial chemotherapy is based on the emergence of resistance to drugs and the search for medicines against all stages of the life cycle of Plasmodium spp. as a therapeutic target. Nowadays, many molecules with anti-malarial activity are reported. However, few studies about the cellular and molecular mechanisms to understand their mode of action have been explored. Recently, new primaquine-based hybrids as new molecules with potential multi-acting anti-malarial activity were reported and two hybrids of primaquine linked to quinoxaline 1,4-di-N-oxide (PQ-QdNO) were identified as the most active against erythrocytic, exoerythrocytic and sporogonic stages. Methods: To further understand the anti-malarial mode of action (MA) of these hybrids, hepg2-CD81 were infected with Plasmodium yoelii 17XNL and treated with PQ-QdNO hybrids during 48 h. After were evaluated the production of ROS, the mitochondrial depolarization, the total glutathione content, the DNA damage and proteins related to oxidative stress and death cell. Results: In a preliminary analysis as tissue schizonticidals, these hybrids showed a mode of action dependent on peroxides production, but independent of the activation of transcription factor p53, mitochondrial depolarization and arrest cell cycle. Conclusions: Primaquine-quinoxaline 1,4-di-N-oxide hybrids exert their antiplasmodial activity in the exoerythrocytic phase by generating high levels of oxidative stress which promotes the increase of total glutathione levels, through oxidation stress sensor protein DJ-1. In addition, the role of HIF1a in the mode of action of quinoxaline 1,4-di-N-oxide is independent of biological activity. Keywords: 4-Di-N-oxide; Cell death; Exoerythrocytic stage; Malaria; Oxidative stress; Plasmodium; Quinoxaline 1.Colombia. Ministerio de Ciencia, Tecnología e Innovación - MinCienciasUniversidad de NavarraCOL002415913 páginasapplication/pdfengBMC (BioMed Central)Londres, Inglaterrahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Primaquine-quinoxaline 1,4-di-N-oxide hybrids with action on the exo-erythrocytic forms of Plasmodium induce their effect by the production of reactive oxygen speciesArtículo 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/publishedVersionAntimaláricosAntimalarialsEritrocitosErythrocytesCélulas Hep G2Hep G2 CellsPlasmodium yoeliiPrimaquinaPrimaquineQuinoxalinasQuinoxalinesEsporozoítosSporozoiteshttps://id.nlm.nih.gov/mesh/D056945https://id.nlm.nih.gov/mesh/D010600https://id.nlm.nih.gov/mesh/D004912https://id.nlm.nih.gov/mesh/D010967https://id.nlm.nih.gov/mesh/D011319https://id.nlm.nih.gov/mesh/D011810https://id.nlm.nih.gov/mesh/D034101Malar. 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