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Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model
The initial success of any adopted anti-infective strategy to malaria is followed by a descent due to the emergence of resistance to it. The search for new drugs and drug targets is a consistent demand in this disease. Eosin B, a common laboratory dye, is reported to have good antiparasitic properti...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533449/ https://www.ncbi.nlm.nih.gov/pubmed/23365788 http://dx.doi.org/10.1155/2012/381724 |
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author | Zamani, Zahra Tafreshi, Alireza Sadeghi Nahrevanian, Hossein Lame-Rad, Behzad Pourfallah, Fatemeh Eslamifar, Hossein Sadeghi, Sedigheh Vahabi, Farideh Iravani, Ayda Arjmand, Mohammad |
author_facet | Zamani, Zahra Tafreshi, Alireza Sadeghi Nahrevanian, Hossein Lame-Rad, Behzad Pourfallah, Fatemeh Eslamifar, Hossein Sadeghi, Sedigheh Vahabi, Farideh Iravani, Ayda Arjmand, Mohammad |
author_sort | Zamani, Zahra |
collection | PubMed |
description | The initial success of any adopted anti-infective strategy to malaria is followed by a descent due to the emergence of resistance to it. The search for new drugs and drug targets is a consistent demand in this disease. Eosin B, a common laboratory dye, is reported to have good antiparasitic properties in vitro. It was studied for its antiparasitic effect in vivo on chloroquine-sensitive Plasmodium berghei murine malaria. Eosin B was administered in 2 different doses by either the oral or parenteral route, once or twice daily to mice infected with Plasmodium berghei. Both the doses of eosin B 400 mg/kg and 800 mg/kg gave better results than the controls which were 40 mg/kg chloroquine and 100 mg/kg of arteether with P < 0.005 significance. Percentage suppressive activity by Peter's test of eosin B was better, though at a higher dose than both the controls. Survival rate of mice receiving the higher dose of eosin B was longer than that of the controls. When administered twice daily, the mice were fully cured after 4 days. Eosin B seems to be a promising drug exhibiting good antimalarial effects in the murine model of the disease. |
format | Online Article Text |
id | pubmed-3533449 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-35334492013-01-30 Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model Zamani, Zahra Tafreshi, Alireza Sadeghi Nahrevanian, Hossein Lame-Rad, Behzad Pourfallah, Fatemeh Eslamifar, Hossein Sadeghi, Sedigheh Vahabi, Farideh Iravani, Ayda Arjmand, Mohammad Malar Res Treat Research Article The initial success of any adopted anti-infective strategy to malaria is followed by a descent due to the emergence of resistance to it. The search for new drugs and drug targets is a consistent demand in this disease. Eosin B, a common laboratory dye, is reported to have good antiparasitic properties in vitro. It was studied for its antiparasitic effect in vivo on chloroquine-sensitive Plasmodium berghei murine malaria. Eosin B was administered in 2 different doses by either the oral or parenteral route, once or twice daily to mice infected with Plasmodium berghei. Both the doses of eosin B 400 mg/kg and 800 mg/kg gave better results than the controls which were 40 mg/kg chloroquine and 100 mg/kg of arteether with P < 0.005 significance. Percentage suppressive activity by Peter's test of eosin B was better, though at a higher dose than both the controls. Survival rate of mice receiving the higher dose of eosin B was longer than that of the controls. When administered twice daily, the mice were fully cured after 4 days. Eosin B seems to be a promising drug exhibiting good antimalarial effects in the murine model of the disease. Hindawi Publishing Corporation 2012 2012-12-16 /pmc/articles/PMC3533449/ /pubmed/23365788 http://dx.doi.org/10.1155/2012/381724 Text en Copyright © 2012 Zahra Zamani et al. 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 Zamani, Zahra Tafreshi, Alireza Sadeghi Nahrevanian, Hossein Lame-Rad, Behzad Pourfallah, Fatemeh Eslamifar, Hossein Sadeghi, Sedigheh Vahabi, Farideh Iravani, Ayda Arjmand, Mohammad Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model |
title | Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model |
title_full | Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model |
title_fullStr | Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model |
title_full_unstemmed | Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model |
title_short | Efficacy of Eosin B as a New Antimalarial Drug in a Murine Model |
title_sort | efficacy of eosin b as a new antimalarial drug in a murine model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3533449/ https://www.ncbi.nlm.nih.gov/pubmed/23365788 http://dx.doi.org/10.1155/2012/381724 |
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