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Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model
BACKGROUND: Rumex hastatus leaves have been widely used as food additive and for the treatment of various liver ailments. According to our previous studies, ethyle acetate (ERL) and methanolic (MRL) fractions of R. hastatus leaves are an accessible source of natural antioxidants. In the present rese...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577788/ https://www.ncbi.nlm.nih.gov/pubmed/28854968 http://dx.doi.org/10.1186/s12906-017-1943-5 |
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author | Sahreen, Sumaira Khan, Muhammad Rashid Khan, Rahmat Ali |
author_facet | Sahreen, Sumaira Khan, Muhammad Rashid Khan, Rahmat Ali |
author_sort | Sahreen, Sumaira |
collection | PubMed |
description | BACKGROUND: Rumex hastatus leaves have been widely used as food additive and for the treatment of various liver ailments. According to our previous studies, ethyle acetate (ERL) and methanolic (MRL) fractions of R. hastatus leaves are an accessible source of natural antioxidants. In the present research work we arranged to investigate the R. hastatus leaves as hepaptoprotective agent verse hepatic damages caused by CCl(4). METHODS: During this project we divided 48 rats into eight groups randomly. CCl(4)-induced damages were assessed through liver function markers viz.; alkaline phosphatase (ALP), alanine transaminase (ALT), aspartate transaminase (AST), γ-glutamyltransferase (γ-GT) and lactate dehydrogenase (LDH). Changes in lipid profile were checked by measuring serum total cholesterol (TC), triglycerides (Tg), high density lipoproteins (HDL) and low density lipoproteins (LDL). Antioxidant status was checked by the activities of antioxidant enzymes, DNA damages and cellular abnormalities at histo level. RESULTS: Administration of CCl(4) in rats caused significant increase in liver function and lipid profile indicating hepatic damages which were restored by co-administration of R. hastatus extracts. Cellular and DNA damages in hepatic tissues were caused by CCl(4) which shown clear hepatic fibrosis in addition to disturb antioxidant enzyme level. Co-treatment with various fractions of R. hastatus leaves regulated these markers of oxidative dysfunctions. CONCLUSION: From the present report it was inferred that R. hastatus leaves have the ability to reverse CCl(4 -) induced hepatic damages. |
format | Online Article Text |
id | pubmed-5577788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55777882017-08-31 Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model Sahreen, Sumaira Khan, Muhammad Rashid Khan, Rahmat Ali BMC Complement Altern Med Research Article BACKGROUND: Rumex hastatus leaves have been widely used as food additive and for the treatment of various liver ailments. According to our previous studies, ethyle acetate (ERL) and methanolic (MRL) fractions of R. hastatus leaves are an accessible source of natural antioxidants. In the present research work we arranged to investigate the R. hastatus leaves as hepaptoprotective agent verse hepatic damages caused by CCl(4). METHODS: During this project we divided 48 rats into eight groups randomly. CCl(4)-induced damages were assessed through liver function markers viz.; alkaline phosphatase (ALP), alanine transaminase (ALT), aspartate transaminase (AST), γ-glutamyltransferase (γ-GT) and lactate dehydrogenase (LDH). Changes in lipid profile were checked by measuring serum total cholesterol (TC), triglycerides (Tg), high density lipoproteins (HDL) and low density lipoproteins (LDL). Antioxidant status was checked by the activities of antioxidant enzymes, DNA damages and cellular abnormalities at histo level. RESULTS: Administration of CCl(4) in rats caused significant increase in liver function and lipid profile indicating hepatic damages which were restored by co-administration of R. hastatus extracts. Cellular and DNA damages in hepatic tissues were caused by CCl(4) which shown clear hepatic fibrosis in addition to disturb antioxidant enzyme level. Co-treatment with various fractions of R. hastatus leaves regulated these markers of oxidative dysfunctions. CONCLUSION: From the present report it was inferred that R. hastatus leaves have the ability to reverse CCl(4 -) induced hepatic damages. BioMed Central 2017-08-30 /pmc/articles/PMC5577788/ /pubmed/28854968 http://dx.doi.org/10.1186/s12906-017-1943-5 Text en © The Author(s). 2017 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 Sahreen, Sumaira Khan, Muhammad Rashid Khan, Rahmat Ali Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model |
title | Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model |
title_full | Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model |
title_fullStr | Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model |
title_full_unstemmed | Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model |
title_short | Evaluation of Rumex hastatus leaves against hepatic fibrosis: a rat model |
title_sort | evaluation of rumex hastatus leaves against hepatic fibrosis: a rat model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577788/ https://www.ncbi.nlm.nih.gov/pubmed/28854968 http://dx.doi.org/10.1186/s12906-017-1943-5 |
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