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Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice

BACKGROUND: Malaria is a leading cause of death in Nigeria. AIM: Antimalarial activity of Stemonocoleus micranthus stem bark was evaluated in mice with an objective to finding scientific evidence for its use as antimalarial remedy in South-east Nigeria. METHODS: Antiplasmodial activities of hydro-me...

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Autores principales: Orabueze, Celestina I., Ota, Duncan A., Coker, Herbert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957798/
https://www.ncbi.nlm.nih.gov/pubmed/31956560
http://dx.doi.org/10.1016/j.jtcme.2019.03.001
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author Orabueze, Celestina I.
Ota, Duncan A.
Coker, Herbert A.
author_facet Orabueze, Celestina I.
Ota, Duncan A.
Coker, Herbert A.
author_sort Orabueze, Celestina I.
collection PubMed
description BACKGROUND: Malaria is a leading cause of death in Nigeria. AIM: Antimalarial activity of Stemonocoleus micranthus stem bark was evaluated in mice with an objective to finding scientific evidence for its use as antimalarial remedy in South-east Nigeria. METHODS: Antiplasmodial activities of hydro-methanolic extract and solvent fractions (hexane, chloroform, ethyl acetate and aqueous) of S. micranthus stem bark against chloroquine-sensitive Plasmodium berghei infected mice were determined using suppressive and curative procedures. Chloroquine was used as positive control. In vitro models, DPPH (1, 1-diphenyl-2- picrylhydrazyl) radical scavenging, FRAP (ferric reducing antioxidant power) and TPC (total phenolic content) were used to assay antioxidant activity of the test samples. Phytoconstituents of the active fractions were analysed by GC-MS. RESULTS: Chemosuppressive effect exerted by extract (50, 100, 200, 400 mg kg(−1)) and fractions (20, 40, 80 mg kg(−1)) ranged between 54.14 – 67.73% and 59.41–94.51% respectively. Curative effects was also dose dependent. In both models, ethyl acetate was the active fraction. At low doses the animals lived longer but not protected (D(0) – D(29)). At high doses, extract (400 mg kg(−1)), active fractions (80 mg kg(−1)) and chloroquine (5 mg kg(−1)) the animals were fully protected. The extract and fractions exhibited antioxidant potentials which could have contributed individually or synergistically to antimalarial activities reported in this study. Oral LD(50) was estimated to be greater than 4000 mg kg(−1), in mice. CONCLUSION: The results of this study may have provided support on traditional therapeutic use of the plant in treatment of malaria.
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spelling pubmed-69577982020-01-17 Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice Orabueze, Celestina I. Ota, Duncan A. Coker, Herbert A. J Tradit Complement Med Original Article BACKGROUND: Malaria is a leading cause of death in Nigeria. AIM: Antimalarial activity of Stemonocoleus micranthus stem bark was evaluated in mice with an objective to finding scientific evidence for its use as antimalarial remedy in South-east Nigeria. METHODS: Antiplasmodial activities of hydro-methanolic extract and solvent fractions (hexane, chloroform, ethyl acetate and aqueous) of S. micranthus stem bark against chloroquine-sensitive Plasmodium berghei infected mice were determined using suppressive and curative procedures. Chloroquine was used as positive control. In vitro models, DPPH (1, 1-diphenyl-2- picrylhydrazyl) radical scavenging, FRAP (ferric reducing antioxidant power) and TPC (total phenolic content) were used to assay antioxidant activity of the test samples. Phytoconstituents of the active fractions were analysed by GC-MS. RESULTS: Chemosuppressive effect exerted by extract (50, 100, 200, 400 mg kg(−1)) and fractions (20, 40, 80 mg kg(−1)) ranged between 54.14 – 67.73% and 59.41–94.51% respectively. Curative effects was also dose dependent. In both models, ethyl acetate was the active fraction. At low doses the animals lived longer but not protected (D(0) – D(29)). At high doses, extract (400 mg kg(−1)), active fractions (80 mg kg(−1)) and chloroquine (5 mg kg(−1)) the animals were fully protected. The extract and fractions exhibited antioxidant potentials which could have contributed individually or synergistically to antimalarial activities reported in this study. Oral LD(50) was estimated to be greater than 4000 mg kg(−1), in mice. CONCLUSION: The results of this study may have provided support on traditional therapeutic use of the plant in treatment of malaria. Elsevier 2019-03-07 /pmc/articles/PMC6957798/ /pubmed/31956560 http://dx.doi.org/10.1016/j.jtcme.2019.03.001 Text en © 2019 Center for Food and Biomolecules, National Taiwan University. Production and hosting by Elsevier Taiwan LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Orabueze, Celestina I.
Ota, Duncan A.
Coker, Herbert A.
Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice
title Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice
title_full Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice
title_fullStr Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice
title_full_unstemmed Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice
title_short Antimalarial potentials of Stemonocoleus micranthus Harms (leguminoseae) stem bark in Plasmodium berghei infected mice
title_sort antimalarial potentials of stemonocoleus micranthus harms (leguminoseae) stem bark in plasmodium berghei infected mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6957798/
https://www.ncbi.nlm.nih.gov/pubmed/31956560
http://dx.doi.org/10.1016/j.jtcme.2019.03.001
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