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Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice
BACKGROUND: Continuous emergence of multi-drug-resistant malaria parasites and their rapid spread across the globe warrant urgent search for new anti-malarial chemotherapeutics. Traditional medicinal plants have been the main sources for screening active phytochemicals against malaria. Accordingly,...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467072/ https://www.ncbi.nlm.nih.gov/pubmed/26077462 http://dx.doi.org/10.1186/s12906-015-0715-3 |
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author | Girma, Senait Giday, Mirutse Erko, Berhanu Mamo, Hassen |
author_facet | Girma, Senait Giday, Mirutse Erko, Berhanu Mamo, Hassen |
author_sort | Girma, Senait |
collection | PubMed |
description | BACKGROUND: Continuous emergence of multi-drug-resistant malaria parasites and their rapid spread across the globe warrant urgent search for new anti-malarial chemotherapeutics. Traditional medicinal plants have been the main sources for screening active phytochemicals against malaria. Accordingly, this study was aimed at evaluating the anti-malarial activity of Osyris quadripartita Salzm. Ex Decne., a plant which is used for traditional malaria treatment by local people in different parts of Ethiopia. METHODS: Aqueous, chloroform and methanol crude leaf extracts of the plant have been prepared and tested for acute toxicity and anti-malarial efficacy in Plasmodium berghei (ANKA strain)-infected Swiss albino mice. RESULTS: At three oral doses of 200, 400 and 600 mg/kg the plant material was safe, chemosuppressive and thus prevented body weight loss, hematological abnormalities and increased mice mean survival time compared to the negative control. The most efficacious extract was that of chloroform which prolonged mean mouse survival past day 11 of infection with all the mice in this group having the highest parasitemia suppression rate (41.3 %, at 600 mg/kg) although parasite clearance was not achieved compared to the standard drug (chloroquine) against the parasite. CONCLUSION: The finding supports the traditional use of the plant for the treatment of malaria. However, further confirmatory studies followed by isolation and characterization of the active anti-malarial compound (s) of the plant that is/are responsible for the observed parasite suppression is needed before it is recommended for malaria drug search and discovery. |
format | Online Article Text |
id | pubmed-4467072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44670722015-06-16 Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice Girma, Senait Giday, Mirutse Erko, Berhanu Mamo, Hassen BMC Complement Altern Med Research Article BACKGROUND: Continuous emergence of multi-drug-resistant malaria parasites and their rapid spread across the globe warrant urgent search for new anti-malarial chemotherapeutics. Traditional medicinal plants have been the main sources for screening active phytochemicals against malaria. Accordingly, this study was aimed at evaluating the anti-malarial activity of Osyris quadripartita Salzm. Ex Decne., a plant which is used for traditional malaria treatment by local people in different parts of Ethiopia. METHODS: Aqueous, chloroform and methanol crude leaf extracts of the plant have been prepared and tested for acute toxicity and anti-malarial efficacy in Plasmodium berghei (ANKA strain)-infected Swiss albino mice. RESULTS: At three oral doses of 200, 400 and 600 mg/kg the plant material was safe, chemosuppressive and thus prevented body weight loss, hematological abnormalities and increased mice mean survival time compared to the negative control. The most efficacious extract was that of chloroform which prolonged mean mouse survival past day 11 of infection with all the mice in this group having the highest parasitemia suppression rate (41.3 %, at 600 mg/kg) although parasite clearance was not achieved compared to the standard drug (chloroquine) against the parasite. CONCLUSION: The finding supports the traditional use of the plant for the treatment of malaria. However, further confirmatory studies followed by isolation and characterization of the active anti-malarial compound (s) of the plant that is/are responsible for the observed parasite suppression is needed before it is recommended for malaria drug search and discovery. BioMed Central 2015-06-16 /pmc/articles/PMC4467072/ /pubmed/26077462 http://dx.doi.org/10.1186/s12906-015-0715-3 Text en © Girma et al. 2015 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Girma, Senait Giday, Mirutse Erko, Berhanu Mamo, Hassen Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice |
title | Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice |
title_full | Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice |
title_fullStr | Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice |
title_full_unstemmed | Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice |
title_short | Effect of crude leaf extract of Osyris quadripartita on Plasmodium berghei in Swiss albino mice |
title_sort | effect of crude leaf extract of osyris quadripartita on plasmodium berghei in swiss albino mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467072/ https://www.ncbi.nlm.nih.gov/pubmed/26077462 http://dx.doi.org/10.1186/s12906-015-0715-3 |
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