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Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui

Objective: Homalium letestui Pellegr (Flacourtiaceae) is used in traditional medicine in parts of Nigeria for the treatment of malaria, ulcer, and inflammatory diseases and as an aphrodisiac. This investigation was aimed to evaluate the cytotoxic, immunomodulatory, and antileishmanial properties of...

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Autores principales: Efiom Okokon, Jude, Dar Farooq, Ahsana, Choudhary, Mohammed Iqbal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075688/
https://www.ncbi.nlm.nih.gov/pubmed/25050257
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author Efiom Okokon, Jude
Dar Farooq, Ahsana
Choudhary, Mohammed Iqbal
author_facet Efiom Okokon, Jude
Dar Farooq, Ahsana
Choudhary, Mohammed Iqbal
author_sort Efiom Okokon, Jude
collection PubMed
description Objective: Homalium letestui Pellegr (Flacourtiaceae) is used in traditional medicine in parts of Nigeria for the treatment of malaria, ulcer, and inflammatory diseases and as an aphrodisiac. This investigation was aimed to evaluate the cytotoxic, immunomodulatory, and antileishmanial properties of stem extract and fractions of Homalium letestui (H. letestui). Materials and Methods: Cytotoxic activity against HeLa cells was done using sulphorhodamine (SRB) method and DNA interaction activity using gel electrophoresis. Immunomodulatory activity of the extract in whole blood, neutrophils, and macrophages was also investigated using luminol/lucigenin-based chemiluminescence assay. The extract and fractions were similarly screened for antileishmanial activity against promastigotes of Leishmania major in vitro. The GCMS analysis of the most active fraction against HeLa cells was carried out. Results: The stem extract exerted prominent cytotoxic activity with the dichloromethane fraction exhibiting the most pronounced effect (GI(50 )-5.12±1.45 µg/ml, LC(50)- 57.3±2.33 µg/ml, TGI -12.6±0.87 µg/ml). The crude extract and the fractions did not interact with DNA when investigated using electrophoresis. The extract significantly ((p<0.05 – 0.001) inhibited oxidative burst activity in whole blood (–27.90-66.90%), isolated polymorphonuclear cells (PMNs) (16.50-67.0%), and mononuclear cells (MNCs) (4.31-98.50%) when two different phagocytosis activators (serum opsonizing zymosan-A and PMA) were used. The extract also exhibited moderate antileishmanial activity against promastigotes of Leishmania major in vitro. GCMS analysis of active fraction revealed pharmacologically active compounds. Conclusion: These results suggest that the stem extract/fractions of H. letestui possess cytotoxic, immunomodulatory, and antileishmanial activities.
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spelling pubmed-40756882014-07-21 Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui Efiom Okokon, Jude Dar Farooq, Ahsana Choudhary, Mohammed Iqbal Avicenna J Phytomed Original Article Objective: Homalium letestui Pellegr (Flacourtiaceae) is used in traditional medicine in parts of Nigeria for the treatment of malaria, ulcer, and inflammatory diseases and as an aphrodisiac. This investigation was aimed to evaluate the cytotoxic, immunomodulatory, and antileishmanial properties of stem extract and fractions of Homalium letestui (H. letestui). Materials and Methods: Cytotoxic activity against HeLa cells was done using sulphorhodamine (SRB) method and DNA interaction activity using gel electrophoresis. Immunomodulatory activity of the extract in whole blood, neutrophils, and macrophages was also investigated using luminol/lucigenin-based chemiluminescence assay. The extract and fractions were similarly screened for antileishmanial activity against promastigotes of Leishmania major in vitro. The GCMS analysis of the most active fraction against HeLa cells was carried out. Results: The stem extract exerted prominent cytotoxic activity with the dichloromethane fraction exhibiting the most pronounced effect (GI(50 )-5.12±1.45 µg/ml, LC(50)- 57.3±2.33 µg/ml, TGI -12.6±0.87 µg/ml). The crude extract and the fractions did not interact with DNA when investigated using electrophoresis. The extract significantly ((p<0.05 – 0.001) inhibited oxidative burst activity in whole blood (–27.90-66.90%), isolated polymorphonuclear cells (PMNs) (16.50-67.0%), and mononuclear cells (MNCs) (4.31-98.50%) when two different phagocytosis activators (serum opsonizing zymosan-A and PMA) were used. The extract also exhibited moderate antileishmanial activity against promastigotes of Leishmania major in vitro. GCMS analysis of active fraction revealed pharmacologically active compounds. Conclusion: These results suggest that the stem extract/fractions of H. letestui possess cytotoxic, immunomodulatory, and antileishmanial activities. Mashhad University of Medical Sciences 2013 /pmc/articles/PMC4075688/ /pubmed/25050257 Text en © 2013: Avicenna Journal of Phytomedicine This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Efiom Okokon, Jude
Dar Farooq, Ahsana
Choudhary, Mohammed Iqbal
Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui
title Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui
title_full Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui
title_fullStr Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui
title_full_unstemmed Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui
title_short Cellular antioxidative, cytotoxic, and antileishmanial activities of Homalium letestui
title_sort cellular antioxidative, cytotoxic, and antileishmanial activities of homalium letestui
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075688/
https://www.ncbi.nlm.nih.gov/pubmed/25050257
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