Cargando…

In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack

BACKGROUND: Toxoplasma gondii infection causes toxoplasmosis, an infectious disease with worldwide prevalence. The limited efficiency of drugs against this infection, their side effects and the potential appearance of resistant strains make the search of novel drugs an essential need. We examined Eu...

Descripción completa

Detalles Bibliográficos
Autores principales: Kavitha, Nowroji, Noordin, Rahmah, Chan, Kit-Lam, Sasidharan, Sreenivasan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488307/
https://www.ncbi.nlm.nih.gov/pubmed/22781137
http://dx.doi.org/10.1186/1472-6882-12-91
_version_ 1782248597742419968
author Kavitha, Nowroji
Noordin, Rahmah
Chan, Kit-Lam
Sasidharan, Sreenivasan
author_facet Kavitha, Nowroji
Noordin, Rahmah
Chan, Kit-Lam
Sasidharan, Sreenivasan
author_sort Kavitha, Nowroji
collection PubMed
description BACKGROUND: Toxoplasma gondii infection causes toxoplasmosis, an infectious disease with worldwide prevalence. The limited efficiency of drugs against this infection, their side effects and the potential appearance of resistant strains make the search of novel drugs an essential need. We examined Eurycoma longifolia root extract and fractions as potential sources of new compounds with high activity and low toxicity. The main goal of this study was to investigate the anti-T. gondii activity of crude extract (TACME) and four fractions (TAF 273, TAF 355, TAF 191 and TAF 401) from E. longifolia, with clindamycin as the positive control. METHODS: In vitro toxoplasmacidal evaluation was performed using Vero cells as host for T. gondii. Light microscopy technique was used to study in situ antiparasitic activity. RESULTS: Significant anti-T. gondii activity was observed with clindamycin (EC50 = 0.016 μg/ml), follow by TAF 355 (EC50 = 0.369 μg/ml) and TAF 401 (EC50 = 0.882 μg/ml). Light microscopy revealed that most Vero cells were infected after 3 h of exposure to T. gondii. After 36 h of exposure to the E. longifolia fraction, the host Vero cells showed no visible intracellular parasite and no remarkable morphological changes. CONCLUSIONS: Our study demonstrated that TAF 355 and TAF401 fractions may be the sources of new anti-T. gondii compounds.
format Online
Article
Text
id pubmed-3488307
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-34883072012-11-04 In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack Kavitha, Nowroji Noordin, Rahmah Chan, Kit-Lam Sasidharan, Sreenivasan BMC Complement Altern Med Research Article BACKGROUND: Toxoplasma gondii infection causes toxoplasmosis, an infectious disease with worldwide prevalence. The limited efficiency of drugs against this infection, their side effects and the potential appearance of resistant strains make the search of novel drugs an essential need. We examined Eurycoma longifolia root extract and fractions as potential sources of new compounds with high activity and low toxicity. The main goal of this study was to investigate the anti-T. gondii activity of crude extract (TACME) and four fractions (TAF 273, TAF 355, TAF 191 and TAF 401) from E. longifolia, with clindamycin as the positive control. METHODS: In vitro toxoplasmacidal evaluation was performed using Vero cells as host for T. gondii. Light microscopy technique was used to study in situ antiparasitic activity. RESULTS: Significant anti-T. gondii activity was observed with clindamycin (EC50 = 0.016 μg/ml), follow by TAF 355 (EC50 = 0.369 μg/ml) and TAF 401 (EC50 = 0.882 μg/ml). Light microscopy revealed that most Vero cells were infected after 3 h of exposure to T. gondii. After 36 h of exposure to the E. longifolia fraction, the host Vero cells showed no visible intracellular parasite and no remarkable morphological changes. CONCLUSIONS: Our study demonstrated that TAF 355 and TAF401 fractions may be the sources of new anti-T. gondii compounds. BioMed Central 2012-07-10 /pmc/articles/PMC3488307/ /pubmed/22781137 http://dx.doi.org/10.1186/1472-6882-12-91 Text en Copyright ©2012 Kavitha et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kavitha, Nowroji
Noordin, Rahmah
Chan, Kit-Lam
Sasidharan, Sreenivasan
In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack
title In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack
title_full In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack
title_fullStr In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack
title_full_unstemmed In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack
title_short In vitro Anti-Toxoplasma gondii Activity of Root Extract/Fractions of Eurycoma longifolia Jack
title_sort in vitro anti-toxoplasma gondii activity of root extract/fractions of eurycoma longifolia jack
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488307/
https://www.ncbi.nlm.nih.gov/pubmed/22781137
http://dx.doi.org/10.1186/1472-6882-12-91
work_keys_str_mv AT kavithanowroji invitroantitoxoplasmagondiiactivityofrootextractfractionsofeurycomalongifoliajack
AT noordinrahmah invitroantitoxoplasmagondiiactivityofrootextractfractionsofeurycomalongifoliajack
AT chankitlam invitroantitoxoplasmagondiiactivityofrootextractfractionsofeurycomalongifoliajack
AT sasidharansreenivasan invitroantitoxoplasmagondiiactivityofrootextractfractionsofeurycomalongifoliajack