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Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora

Context:Alchornea laxiflora (Benth.) Pax. & Hoffman (Euphorbiaceae) root decoctions are traditionally used in the treatment of malaria and pain in Nigeria. Objective: To assess the antimalarial, antiplasmodial and analgesic potentials of root extract and fractions against malarial infections and...

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Autores principales: Okokon, Jude E., Augustine, Nkemnele Bensella, Mohanakrishnan, Dinesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130711/
https://www.ncbi.nlm.nih.gov/pubmed/28183236
http://dx.doi.org/10.1080/13880209.2017.1285947
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author Okokon, Jude E.
Augustine, Nkemnele Bensella
Mohanakrishnan, Dinesh
author_facet Okokon, Jude E.
Augustine, Nkemnele Bensella
Mohanakrishnan, Dinesh
author_sort Okokon, Jude E.
collection PubMed
description Context:Alchornea laxiflora (Benth.) Pax. & Hoffman (Euphorbiaceae) root decoctions are traditionally used in the treatment of malaria and pain in Nigeria. Objective: To assess the antimalarial, antiplasmodial and analgesic potentials of root extract and fractions against malarial infections and chemically-induced pains. Material and methods: The root extract and fractions of Alchornea laxiflora were investigated for antimalarial activity against Plasmodium berghei infection in mice, antiplasmodial activity against chloroquine sensitive (Pf 3D7) and resistant (Pf INDO) strains of Plasmodium falciparum using SYBR green assay method and analgesic activity against experimentally-induced pain models. Acute toxicity study of the extract, cytotoxic activity against HeLa cells and GCMS analysis of the active fraction were carried out. Results: The root extract (75–225 mg/kg, p.o.) with LD(50) of 748.33 mg/kg exerted significant (p < 0.05–0.001) antimalarial activity against P. berghei infection in suppressive, prophylactive and curative tests. The root extract and fractions also exerted moderate activity against chloroquine sensitive (Pf 3D7) and resistant (Pf INDO) strains of P. falciparum with the ethyl acetate fraction exerting the highest activity with IC(50) value of 38.44 ± 0.89 μg/mL (Pf 3D7) and 40.17 ± 0.78 μg/mL (Pf INDO). The crude extract was not cytotoxic to HeLa cells with LC(50) value >100 μg/mL. The crude extract and ethyl acetate fraction exerted significant (p < 0.05–0.001) analgesic activity in all pain models used. Discussion and conclusions: These results suggest that the root extract/fractions of A. laxiflora possess antimalarial, antiplasmodial and analgesic potentials and these justify its use in ethnomedicine to treat malaria and pain.
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spelling pubmed-61307112018-09-27 Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora Okokon, Jude E. Augustine, Nkemnele Bensella Mohanakrishnan, Dinesh Pharm Biol Research Article Context:Alchornea laxiflora (Benth.) Pax. & Hoffman (Euphorbiaceae) root decoctions are traditionally used in the treatment of malaria and pain in Nigeria. Objective: To assess the antimalarial, antiplasmodial and analgesic potentials of root extract and fractions against malarial infections and chemically-induced pains. Material and methods: The root extract and fractions of Alchornea laxiflora were investigated for antimalarial activity against Plasmodium berghei infection in mice, antiplasmodial activity against chloroquine sensitive (Pf 3D7) and resistant (Pf INDO) strains of Plasmodium falciparum using SYBR green assay method and analgesic activity against experimentally-induced pain models. Acute toxicity study of the extract, cytotoxic activity against HeLa cells and GCMS analysis of the active fraction were carried out. Results: The root extract (75–225 mg/kg, p.o.) with LD(50) of 748.33 mg/kg exerted significant (p < 0.05–0.001) antimalarial activity against P. berghei infection in suppressive, prophylactive and curative tests. The root extract and fractions also exerted moderate activity against chloroquine sensitive (Pf 3D7) and resistant (Pf INDO) strains of P. falciparum with the ethyl acetate fraction exerting the highest activity with IC(50) value of 38.44 ± 0.89 μg/mL (Pf 3D7) and 40.17 ± 0.78 μg/mL (Pf INDO). The crude extract was not cytotoxic to HeLa cells with LC(50) value >100 μg/mL. The crude extract and ethyl acetate fraction exerted significant (p < 0.05–0.001) analgesic activity in all pain models used. Discussion and conclusions: These results suggest that the root extract/fractions of A. laxiflora possess antimalarial, antiplasmodial and analgesic potentials and these justify its use in ethnomedicine to treat malaria and pain. Taylor & Francis 2017-02-09 /pmc/articles/PMC6130711/ /pubmed/28183236 http://dx.doi.org/10.1080/13880209.2017.1285947 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Okokon, Jude E.
Augustine, Nkemnele Bensella
Mohanakrishnan, Dinesh
Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora
title Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora
title_full Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora
title_fullStr Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora
title_full_unstemmed Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora
title_short Antimalarial, antiplasmodial and analgesic activities of root extract of Alchornea laxiflora
title_sort antimalarial, antiplasmodial and analgesic activities of root extract of alchornea laxiflora
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130711/
https://www.ncbi.nlm.nih.gov/pubmed/28183236
http://dx.doi.org/10.1080/13880209.2017.1285947
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