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Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei

BACKGROUND: Reduction of oxidative stress during malaria infection is considered as being of great benefit so long as treatment and drug development approaches are concerned. This study had the aim of evaluating the antimalarial and antioxidant activities of the ethanolic extract of Terminalia macro...

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Autores principales: Sidiki, Ngouyamsa Nsapkain Aboubakar, Nadia, Noumedem Anangmo Christelle, Cedric, Yamssi, Guy-Armand, Gamago Nkadeu, Sandra, Tientcheu Noutong Jemimah, Kevin, Tako Djimefo Alex, Azizi, Mounvera Abdel, Payne, Vincent Khan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332924/
https://www.ncbi.nlm.nih.gov/pubmed/37435530
http://dx.doi.org/10.1155/2023/3350293
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author Sidiki, Ngouyamsa Nsapkain Aboubakar
Nadia, Noumedem Anangmo Christelle
Cedric, Yamssi
Guy-Armand, Gamago Nkadeu
Sandra, Tientcheu Noutong Jemimah
Kevin, Tako Djimefo Alex
Azizi, Mounvera Abdel
Payne, Vincent Khan
author_facet Sidiki, Ngouyamsa Nsapkain Aboubakar
Nadia, Noumedem Anangmo Christelle
Cedric, Yamssi
Guy-Armand, Gamago Nkadeu
Sandra, Tientcheu Noutong Jemimah
Kevin, Tako Djimefo Alex
Azizi, Mounvera Abdel
Payne, Vincent Khan
author_sort Sidiki, Ngouyamsa Nsapkain Aboubakar
collection PubMed
description BACKGROUND: Reduction of oxidative stress during malaria infection is considered as being of great benefit so long as treatment and drug development approaches are concerned. This study had the aim of evaluating the antimalarial and antioxidant activities of the ethanolic extract of Terminalia macroptera in Swiss albino mice infected with the Plasmodium berghei NK65 strain. METHODS: In vivo, the antiplasmodial activity of the plant ethanolic extract was tested in a four-day suppressive and curative assay using P. berghei in Swiss albino mice. The extract was administered to the mice at doses of 125, 250, and 500 mg/kg per day. Then, parameters, such as parasite suppression and survival time of the mice, were evaluated. Furthermore, the effect of plant extract on liver damage, oxidative stress indicators, and lipid profile changes in P. berghei-infected mice were studied. RESULTS: Administration of T. macroptera significantly suppressed P. berghei infection by 55.17%, 70.69%, and 71.10% at doses of 125, 250, and 500 mg/kg, respectively, whereas chloroquine had 84.64% suppression relative to the untreated group 1% Dimethyl sulfoxide (1% DMSO) at day 4 (post-infection) in the four-day suppressive test. This suppression activity rate was dose-dependent. The curative test also presented a significant reduction in parasitemia and an extension of the survival time of the treated groups. Treatment of infected parasitized mice with the extract of T. macroptera had a significant (p < 0.05) reduction in parameters, such as total protein, aspartate aminotransferase, and alanine aminotransferase. Infection may also lead to a significant increase in the enzymatic activity of liver catalase and superoxide dismutase compared with the normal control group. The non-enzymatic antioxidant activity in parasitized mice was significantly reduced in malondialdehyde and increased in glutathione and nitric oxide when compared with the normal control group. CONCLUSIONS: These findings support the ethnobotanical use of T. macroptera stem bark as an antimalarial remedy coupled with antioxidant activity. However, further in vivo toxicity tests are required to ascertain its safety.
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spelling pubmed-103329242023-07-11 Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei Sidiki, Ngouyamsa Nsapkain Aboubakar Nadia, Noumedem Anangmo Christelle Cedric, Yamssi Guy-Armand, Gamago Nkadeu Sandra, Tientcheu Noutong Jemimah Kevin, Tako Djimefo Alex Azizi, Mounvera Abdel Payne, Vincent Khan J Parasitol Res Research Article BACKGROUND: Reduction of oxidative stress during malaria infection is considered as being of great benefit so long as treatment and drug development approaches are concerned. This study had the aim of evaluating the antimalarial and antioxidant activities of the ethanolic extract of Terminalia macroptera in Swiss albino mice infected with the Plasmodium berghei NK65 strain. METHODS: In vivo, the antiplasmodial activity of the plant ethanolic extract was tested in a four-day suppressive and curative assay using P. berghei in Swiss albino mice. The extract was administered to the mice at doses of 125, 250, and 500 mg/kg per day. Then, parameters, such as parasite suppression and survival time of the mice, were evaluated. Furthermore, the effect of plant extract on liver damage, oxidative stress indicators, and lipid profile changes in P. berghei-infected mice were studied. RESULTS: Administration of T. macroptera significantly suppressed P. berghei infection by 55.17%, 70.69%, and 71.10% at doses of 125, 250, and 500 mg/kg, respectively, whereas chloroquine had 84.64% suppression relative to the untreated group 1% Dimethyl sulfoxide (1% DMSO) at day 4 (post-infection) in the four-day suppressive test. This suppression activity rate was dose-dependent. The curative test also presented a significant reduction in parasitemia and an extension of the survival time of the treated groups. Treatment of infected parasitized mice with the extract of T. macroptera had a significant (p < 0.05) reduction in parameters, such as total protein, aspartate aminotransferase, and alanine aminotransferase. Infection may also lead to a significant increase in the enzymatic activity of liver catalase and superoxide dismutase compared with the normal control group. The non-enzymatic antioxidant activity in parasitized mice was significantly reduced in malondialdehyde and increased in glutathione and nitric oxide when compared with the normal control group. CONCLUSIONS: These findings support the ethnobotanical use of T. macroptera stem bark as an antimalarial remedy coupled with antioxidant activity. However, further in vivo toxicity tests are required to ascertain its safety. Hindawi 2023-07-03 /pmc/articles/PMC10332924/ /pubmed/37435530 http://dx.doi.org/10.1155/2023/3350293 Text en Copyright © 2023 Ngouyamsa Nsapkain Aboubakar Sidiki et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sidiki, Ngouyamsa Nsapkain Aboubakar
Nadia, Noumedem Anangmo Christelle
Cedric, Yamssi
Guy-Armand, Gamago Nkadeu
Sandra, Tientcheu Noutong Jemimah
Kevin, Tako Djimefo Alex
Azizi, Mounvera Abdel
Payne, Vincent Khan
Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei
title Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei
title_full Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei
title_fullStr Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei
title_full_unstemmed Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei
title_short Antimalarial and Antioxidant Activities of Ethanolic Stem Bark Extract of Terminalia macroptera in Swiss Albino Mice Infected with Plasmodium berghei
title_sort antimalarial and antioxidant activities of ethanolic stem bark extract of terminalia macroptera in swiss albino mice infected with plasmodium berghei
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10332924/
https://www.ncbi.nlm.nih.gov/pubmed/37435530
http://dx.doi.org/10.1155/2023/3350293
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