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Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition
Aframomum melegueta is a commonly used African spice. Through a hepatoprotective bioassay-guided isolation, the chloroform fraction of A.melegueta seeds yielded one new diarylheptanoid named 3-(S)-acetyl-1-(4′-hydroxy-3′, 5′-di methoxyphenyl)-7-(3″,4″, 5″-trihydroxyphenyl)heptane (1), and two new hy...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376205/ https://www.ncbi.nlm.nih.gov/pubmed/25077538 http://dx.doi.org/10.1038/srep05880 |
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author | El-Halawany, Ali M. Dine, Riham Salah El El Sayed, Nesrine S. Hattori, Masao |
author_facet | El-Halawany, Ali M. Dine, Riham Salah El El Sayed, Nesrine S. Hattori, Masao |
author_sort | El-Halawany, Ali M. |
collection | PubMed |
description | Aframomum melegueta is a commonly used African spice. Through a hepatoprotective bioassay-guided isolation, the chloroform fraction of A.melegueta seeds yielded one new diarylheptanoid named 3-(S)-acetyl-1-(4′-hydroxy-3′, 5′-di methoxyphenyl)-7-(3″,4″, 5″-trihydroxyphenyl)heptane (1), and two new hydroxyphenylalkanones, [8]-dehydrogingerdione (2) and [6]-dehydroparadol (3), in addition to six known compounds (4–9). The hepatoprotective effect of A. melegueta methanol extract, sub-fractions and isolated compounds was investigated using carbon tetrachloride (CCl(4))-induced liver injury in a rat hepatocytes model. The methanol, chloroform extracts and compounds 1, 5, 8 and 9 of A. melegueta significantly inhibited the elevated serum alanine aminotransferase (ALT), thiobarbituric acid reactive substances (TBARS), tumor necrosis factor (TNFα), interleukin-1beta (Il-1β), caspase3 and 9 and enhanced the reduced liver glutathione (GSH) level caused by CCl(4) intoxication. These results indicate that A.melegueta extracts, and isolated compounds play a protective role in CCl(4) induced acute liver injury which might be due to elevated antioxidative defense potentials, suppressed inflammatory responses and apoptosis of liver tissue. |
format | Online Article Text |
id | pubmed-5376205 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53762052017-04-03 Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition El-Halawany, Ali M. Dine, Riham Salah El El Sayed, Nesrine S. Hattori, Masao Sci Rep Article Aframomum melegueta is a commonly used African spice. Through a hepatoprotective bioassay-guided isolation, the chloroform fraction of A.melegueta seeds yielded one new diarylheptanoid named 3-(S)-acetyl-1-(4′-hydroxy-3′, 5′-di methoxyphenyl)-7-(3″,4″, 5″-trihydroxyphenyl)heptane (1), and two new hydroxyphenylalkanones, [8]-dehydrogingerdione (2) and [6]-dehydroparadol (3), in addition to six known compounds (4–9). The hepatoprotective effect of A. melegueta methanol extract, sub-fractions and isolated compounds was investigated using carbon tetrachloride (CCl(4))-induced liver injury in a rat hepatocytes model. The methanol, chloroform extracts and compounds 1, 5, 8 and 9 of A. melegueta significantly inhibited the elevated serum alanine aminotransferase (ALT), thiobarbituric acid reactive substances (TBARS), tumor necrosis factor (TNFα), interleukin-1beta (Il-1β), caspase3 and 9 and enhanced the reduced liver glutathione (GSH) level caused by CCl(4) intoxication. These results indicate that A.melegueta extracts, and isolated compounds play a protective role in CCl(4) induced acute liver injury which might be due to elevated antioxidative defense potentials, suppressed inflammatory responses and apoptosis of liver tissue. Nature Publishing Group 2014-07-30 /pmc/articles/PMC5376205/ /pubmed/25077538 http://dx.doi.org/10.1038/srep05880 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Article El-Halawany, Ali M. Dine, Riham Salah El El Sayed, Nesrine S. Hattori, Masao Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition |
title | Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition |
title_full | Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition |
title_fullStr | Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition |
title_full_unstemmed | Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition |
title_short | Protective Effect of Aframomum melegueta phenolics Against CCl(4)-Induced Rat Hepatocytes Damage; Role of Apoptosis and Pro-inflammatory Cytokines inhibition |
title_sort | protective effect of aframomum melegueta phenolics against ccl(4)-induced rat hepatocytes damage; role of apoptosis and pro-inflammatory cytokines inhibition |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5376205/ https://www.ncbi.nlm.nih.gov/pubmed/25077538 http://dx.doi.org/10.1038/srep05880 |
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