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Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice

BACKGROUND: Malaria remains a major worldwide public health problem leading to death of millions of people. Spread and emergence of antimalarial drug resistance are the major challenge in malaria control. Medicinal plants are the key source of new effective antimalarial agents. Cordia africana (Lam....

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Autores principales: Wondafrash, Dawit Zewdu, Bhoumik, Dayananda, Altaye, Birhanetensay Masresha, Tareke, Helen Bitew, Assefa, Brhane Teklebrhan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721471/
https://www.ncbi.nlm.nih.gov/pubmed/31531119
http://dx.doi.org/10.1155/2019/8324596
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author Wondafrash, Dawit Zewdu
Bhoumik, Dayananda
Altaye, Birhanetensay Masresha
Tareke, Helen Bitew
Assefa, Brhane Teklebrhan
author_facet Wondafrash, Dawit Zewdu
Bhoumik, Dayananda
Altaye, Birhanetensay Masresha
Tareke, Helen Bitew
Assefa, Brhane Teklebrhan
author_sort Wondafrash, Dawit Zewdu
collection PubMed
description BACKGROUND: Malaria remains a major worldwide public health problem leading to death of millions of people. Spread and emergence of antimalarial drug resistance are the major challenge in malaria control. Medicinal plants are the key source of new effective antimalarial agents. Cordia africana (Lam.) is widely used for traditional management of malaria by local people in different parts of Ethiopia. The present study aimed to evaluate in vivo antimalarial effects of leaf extracts and solvent fractions of Cordia africana on Plasmodium berghei-infected mice. METHODS: The leaf extracts were prepared and tested for oral acute toxicity according to the OECD guideline. In vivo antimalarial effects of various doses of C. africana extracts and solvent fractions were determined using the four-day suppression test (both crude and fractions), as well as curative and chemoprophylactic tests (crude extracts). RESULTS: The acute toxicity test of the plant extract revealed that the medium lethal dose is higher than 2000 mg/kg. The crude extract of the plant exhibited significant parasitemia suppression in the four-day suppression (51.19%), curative (57.14%), and prophylactic (46.48%) tests at 600 mg/kg. The n-butanol fraction exhibited the highest chemosuppression (55.62%) at 400 mg/kg, followed by the chloroform fraction (45.04%) at the same dose. CONCLUSION: Our findings indicated that both the crude leaf extracts and fractions of C. africana possess antimalarial effects, supporting the traditional claim of the plant.
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spelling pubmed-67214712019-09-17 Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice Wondafrash, Dawit Zewdu Bhoumik, Dayananda Altaye, Birhanetensay Masresha Tareke, Helen Bitew Assefa, Brhane Teklebrhan Evid Based Complement Alternat Med Research Article BACKGROUND: Malaria remains a major worldwide public health problem leading to death of millions of people. Spread and emergence of antimalarial drug resistance are the major challenge in malaria control. Medicinal plants are the key source of new effective antimalarial agents. Cordia africana (Lam.) is widely used for traditional management of malaria by local people in different parts of Ethiopia. The present study aimed to evaluate in vivo antimalarial effects of leaf extracts and solvent fractions of Cordia africana on Plasmodium berghei-infected mice. METHODS: The leaf extracts were prepared and tested for oral acute toxicity according to the OECD guideline. In vivo antimalarial effects of various doses of C. africana extracts and solvent fractions were determined using the four-day suppression test (both crude and fractions), as well as curative and chemoprophylactic tests (crude extracts). RESULTS: The acute toxicity test of the plant extract revealed that the medium lethal dose is higher than 2000 mg/kg. The crude extract of the plant exhibited significant parasitemia suppression in the four-day suppression (51.19%), curative (57.14%), and prophylactic (46.48%) tests at 600 mg/kg. The n-butanol fraction exhibited the highest chemosuppression (55.62%) at 400 mg/kg, followed by the chloroform fraction (45.04%) at the same dose. CONCLUSION: Our findings indicated that both the crude leaf extracts and fractions of C. africana possess antimalarial effects, supporting the traditional claim of the plant. Hindawi 2019-08-18 /pmc/articles/PMC6721471/ /pubmed/31531119 http://dx.doi.org/10.1155/2019/8324596 Text en Copyright © 2019 Dawit Zewdu Wondafrash et al. http://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
Wondafrash, Dawit Zewdu
Bhoumik, Dayananda
Altaye, Birhanetensay Masresha
Tareke, Helen Bitew
Assefa, Brhane Teklebrhan
Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice
title Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice
title_full Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice
title_fullStr Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice
title_full_unstemmed Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice
title_short Antimalarial Activity of Cordia africana (Lam.) (Boraginaceae) Leaf Extracts and Solvent Fractions in Plasmodium berghei-Infected Mice
title_sort antimalarial activity of cordia africana (lam.) (boraginaceae) leaf extracts and solvent fractions in plasmodium berghei-infected mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721471/
https://www.ncbi.nlm.nih.gov/pubmed/31531119
http://dx.doi.org/10.1155/2019/8324596
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