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Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun
BACKGROUND: Hydnora abyssinica (HA) A. Braun is an endemic Sudanese medicinal plant traditionally used as anti-inflammatory and against many infectious diseases. However, it proved to be very rich in phenols and tannins, so the present study was undertaken to investigate the immunomodulatory potenti...
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/PMC4638089/ https://www.ncbi.nlm.nih.gov/pubmed/26553149 http://dx.doi.org/10.1186/s12906-015-0931-x |
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author | Koko, Waleed S. Mesaik, Mohamed A. Ranjitt, Rosa Galal, Mohamed Choudhary, Muhammad I. |
author_facet | Koko, Waleed S. Mesaik, Mohamed A. Ranjitt, Rosa Galal, Mohamed Choudhary, Muhammad I. |
author_sort | Koko, Waleed S. |
collection | PubMed |
description | BACKGROUND: Hydnora abyssinica (HA) A. Braun is an endemic Sudanese medicinal plant traditionally used as anti-inflammatory and against many infectious diseases. However, it proved to be very rich in phenols and tannins, so the present study was undertaken to investigate the immunomodulatory potential of the whole plant ethanolic extract and its isolated compounds. METHODS: Lymphocyte proliferation, chemiluminescence and superoxide reduction assays were used for immunomodulatory evaluation. While, MTT (3–(4, 5-dimethylthazol-2-yl)-2, 5-diphenyl tetrazonium bromide) test was performed on 3 T3 cell line clone in order to evaluate the cytoxicity effect of the extracts and isolated compounds of phenolic derivatives which were carried out by chromotographic techniques. RESULTS: Catechin, (1), tyrosol (2) and benzoic acid, 3, 4, dihydroxy-, ethyl ester (3) compounds were isolated from HA ethanolic extract which revealed potent immunosuppressive activity against reactive oxygen species from both polymorph nuclear cells (PMNs) (45–90 % inhibition) and mononuclear cells (MNCs) (30 -65 % inhibition), T lymphocyte proliferation assay (70–93 % inhibition) as well as potent inhibitory effect against superoxide production (42–71 % inhibition) at concentrations of 6.25–100 μg/mL. Catechin (1) was found the most potent immunosuppressive agent among all constituents examined. CONCLUSION: These results can support the traditional uses of H. abyssinica extracts as anti-inflammatory and immunosuppressive and further investigations of the mode of action and other pharmacological studies are highly desirable. |
format | Online Article Text |
id | pubmed-4638089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46380892015-11-10 Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun Koko, Waleed S. Mesaik, Mohamed A. Ranjitt, Rosa Galal, Mohamed Choudhary, Muhammad I. BMC Complement Altern Med Research Article BACKGROUND: Hydnora abyssinica (HA) A. Braun is an endemic Sudanese medicinal plant traditionally used as anti-inflammatory and against many infectious diseases. However, it proved to be very rich in phenols and tannins, so the present study was undertaken to investigate the immunomodulatory potential of the whole plant ethanolic extract and its isolated compounds. METHODS: Lymphocyte proliferation, chemiluminescence and superoxide reduction assays were used for immunomodulatory evaluation. While, MTT (3–(4, 5-dimethylthazol-2-yl)-2, 5-diphenyl tetrazonium bromide) test was performed on 3 T3 cell line clone in order to evaluate the cytoxicity effect of the extracts and isolated compounds of phenolic derivatives which were carried out by chromotographic techniques. RESULTS: Catechin, (1), tyrosol (2) and benzoic acid, 3, 4, dihydroxy-, ethyl ester (3) compounds were isolated from HA ethanolic extract which revealed potent immunosuppressive activity against reactive oxygen species from both polymorph nuclear cells (PMNs) (45–90 % inhibition) and mononuclear cells (MNCs) (30 -65 % inhibition), T lymphocyte proliferation assay (70–93 % inhibition) as well as potent inhibitory effect against superoxide production (42–71 % inhibition) at concentrations of 6.25–100 μg/mL. Catechin (1) was found the most potent immunosuppressive agent among all constituents examined. CONCLUSION: These results can support the traditional uses of H. abyssinica extracts as anti-inflammatory and immunosuppressive and further investigations of the mode of action and other pharmacological studies are highly desirable. BioMed Central 2015-11-09 /pmc/articles/PMC4638089/ /pubmed/26553149 http://dx.doi.org/10.1186/s12906-015-0931-x Text en © Koko et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Koko, Waleed S. Mesaik, Mohamed A. Ranjitt, Rosa Galal, Mohamed Choudhary, Muhammad I. Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun |
title | Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun |
title_full | Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun |
title_fullStr | Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun |
title_full_unstemmed | Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun |
title_short | Immunosuppressive phenolic compounds from Hydnora abyssinica A. Braun |
title_sort | immunosuppressive phenolic compounds from hydnora abyssinica a. braun |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4638089/ https://www.ncbi.nlm.nih.gov/pubmed/26553149 http://dx.doi.org/10.1186/s12906-015-0931-x |
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