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Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats

Citrus maxima peel is rich in natural phenolic compounds and has a long use in the traditional medicine. HPLC-DAD analysis on Citrus maxima peel powder exhibited the presence of various phenolic compounds such as caffeic acid and (−)-epicatechin. To determine the plausible hepatoprotective activity...

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Autores principales: Chowdhury, Mohammed Riaz Hasan, Sagor, Md Abu Taher, Tabassum, Nabila, Potol, Md Abdullah, Hossain, Hemayet, Alam, Md Ashraful
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464682/
https://www.ncbi.nlm.nih.gov/pubmed/26106435
http://dx.doi.org/10.1155/2015/598179
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author Chowdhury, Mohammed Riaz Hasan
Sagor, Md Abu Taher
Tabassum, Nabila
Potol, Md Abdullah
Hossain, Hemayet
Alam, Md Ashraful
author_facet Chowdhury, Mohammed Riaz Hasan
Sagor, Md Abu Taher
Tabassum, Nabila
Potol, Md Abdullah
Hossain, Hemayet
Alam, Md Ashraful
author_sort Chowdhury, Mohammed Riaz Hasan
collection PubMed
description Citrus maxima peel is rich in natural phenolic compounds and has a long use in the traditional medicine. HPLC-DAD analysis on Citrus maxima peel powder exhibited the presence of various phenolic compounds such as caffeic acid and (−)-epicatechin. To determine the plausible hepatoprotective activity of Citrus maxima peel powder, we used carbon tetrachloride (CCl(4)) treated rat model. Liver damage in rats was confirmed by measuring the AST, ALT, and ALP enzyme activities. In addition, lipid peroxidation products (MDA), nitric oxide, advanced protein oxidation products level (APOP), and catalase activities were also analyzed along with the histological profiling for the inflammatory cell infiltration, collagen, and iron deposition in liver. Dietary supplementation of Citrus maxima peel powder exhibited significant reduction of serum AST, ALT, and ALP activities in carbon tetrachloride treated rats. Moreover, Citrus maxima peel powder also showed a significant reduction of the oxidative stress markers (MDA, NO, and APOP level) and restored the catalase activity in CCl(4) treated rats. Histological examination of the liver section revealed reduced inflammatory cells infiltration, collagen, and iron deposition in CCl(4) treated rats. The results from this study demonstrated that Citrus maxima peel powder produced significant hepatoprotective action in CCl(4) administered rats.
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spelling pubmed-44646822015-06-23 Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats Chowdhury, Mohammed Riaz Hasan Sagor, Md Abu Taher Tabassum, Nabila Potol, Md Abdullah Hossain, Hemayet Alam, Md Ashraful Evid Based Complement Alternat Med Research Article Citrus maxima peel is rich in natural phenolic compounds and has a long use in the traditional medicine. HPLC-DAD analysis on Citrus maxima peel powder exhibited the presence of various phenolic compounds such as caffeic acid and (−)-epicatechin. To determine the plausible hepatoprotective activity of Citrus maxima peel powder, we used carbon tetrachloride (CCl(4)) treated rat model. Liver damage in rats was confirmed by measuring the AST, ALT, and ALP enzyme activities. In addition, lipid peroxidation products (MDA), nitric oxide, advanced protein oxidation products level (APOP), and catalase activities were also analyzed along with the histological profiling for the inflammatory cell infiltration, collagen, and iron deposition in liver. Dietary supplementation of Citrus maxima peel powder exhibited significant reduction of serum AST, ALT, and ALP activities in carbon tetrachloride treated rats. Moreover, Citrus maxima peel powder also showed a significant reduction of the oxidative stress markers (MDA, NO, and APOP level) and restored the catalase activity in CCl(4) treated rats. Histological examination of the liver section revealed reduced inflammatory cells infiltration, collagen, and iron deposition in CCl(4) treated rats. The results from this study demonstrated that Citrus maxima peel powder produced significant hepatoprotective action in CCl(4) administered rats. Hindawi Publishing Corporation 2015 2015-05-28 /pmc/articles/PMC4464682/ /pubmed/26106435 http://dx.doi.org/10.1155/2015/598179 Text en Copyright © 2015 Mohammed Riaz Hasan Chowdhury et al. https://creativecommons.org/licenses/by/3.0/ 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
Chowdhury, Mohammed Riaz Hasan
Sagor, Md Abu Taher
Tabassum, Nabila
Potol, Md Abdullah
Hossain, Hemayet
Alam, Md Ashraful
Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats
title Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats
title_full Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats
title_fullStr Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats
title_full_unstemmed Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats
title_short Supplementation of Citrus maxima Peel Powder Prevented Oxidative Stress, Fibrosis, and Hepatic Damage in Carbon Tetrachloride (CCl(4)) Treated Rats
title_sort supplementation of citrus maxima peel powder prevented oxidative stress, fibrosis, and hepatic damage in carbon tetrachloride (ccl(4)) treated rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464682/
https://www.ncbi.nlm.nih.gov/pubmed/26106435
http://dx.doi.org/10.1155/2015/598179
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