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Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats
BACKGROUND: In Pakistan numerous medicinal floras has used in the treatment of various human ailments. Among them Trifolium alexandrinum L. is traditionally used in the curing of disease. Presently we designed to ascertain the protective role of Trifolium alexandrinum methanolic extracts (TAME) agai...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Co-Action Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102104/ https://www.ncbi.nlm.nih.gov/pubmed/27834184 http://dx.doi.org/10.3402/fnr.v60.30433 |
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author | Khan, Rahmat Ali Alkreathy, Huda Mohammad Saboorshah, Abdus Ahmed, Mushtaq Khan, Samiullah |
author_facet | Khan, Rahmat Ali Alkreathy, Huda Mohammad Saboorshah, Abdus Ahmed, Mushtaq Khan, Samiullah |
author_sort | Khan, Rahmat Ali |
collection | PubMed |
description | BACKGROUND: In Pakistan numerous medicinal floras has used in the treatment of various human ailments. Among them Trifolium alexandrinum L. is traditionally used in the curing of disease. Presently we designed to ascertain the protective role of Trifolium alexandrinum methanolic extracts (TAME) against carbon tetrachloride (CCl(4))-induced lung injury and oxidative stress in rats. METHODS: Exposure to CCl(4) induces oxidative stress and causes tissue damage by the induction of CCl(4) free radicals. Twenty-four male albino rats were divided equally into four groups. Rats in group I had free access to drinking water and laboratory food. Group II was treated with 1 ml/kg body weight (b.w.) CCl(4) (30% in olive oil). Groups III and IV rats were fed (p.o.) 200 mg/kg b.w. TAME and 50 mg/kg b.w. silymarin after 24 h of CCl(4) treatment for 2 weeks. RESULTS: Administration of CCl(4) caused a significant (p<0.01) decrease in the activities of antioxidant enzymes (catalase, peroxidase, glutathione peroxidase, glutathione-S-transferase), and glutathione contents were decreased; however, thiobarbituric acid-reactive substances were increased (p<0.01). The alterations caused by CCl(4) were significantly (p<0.01) reversed toward control levels by supplementation of TAME and silymarin. CONCLUSION: These results suggest that in rats TAME and silymarin could protect the lungs against CCl(4)-induced oxidative damage. |
format | Online Article Text |
id | pubmed-5102104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Co-Action Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-51021042016-11-18 Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats Khan, Rahmat Ali Alkreathy, Huda Mohammad Saboorshah, Abdus Ahmed, Mushtaq Khan, Samiullah Food Nutr Res Original Article BACKGROUND: In Pakistan numerous medicinal floras has used in the treatment of various human ailments. Among them Trifolium alexandrinum L. is traditionally used in the curing of disease. Presently we designed to ascertain the protective role of Trifolium alexandrinum methanolic extracts (TAME) against carbon tetrachloride (CCl(4))-induced lung injury and oxidative stress in rats. METHODS: Exposure to CCl(4) induces oxidative stress and causes tissue damage by the induction of CCl(4) free radicals. Twenty-four male albino rats were divided equally into four groups. Rats in group I had free access to drinking water and laboratory food. Group II was treated with 1 ml/kg body weight (b.w.) CCl(4) (30% in olive oil). Groups III and IV rats were fed (p.o.) 200 mg/kg b.w. TAME and 50 mg/kg b.w. silymarin after 24 h of CCl(4) treatment for 2 weeks. RESULTS: Administration of CCl(4) caused a significant (p<0.01) decrease in the activities of antioxidant enzymes (catalase, peroxidase, glutathione peroxidase, glutathione-S-transferase), and glutathione contents were decreased; however, thiobarbituric acid-reactive substances were increased (p<0.01). The alterations caused by CCl(4) were significantly (p<0.01) reversed toward control levels by supplementation of TAME and silymarin. CONCLUSION: These results suggest that in rats TAME and silymarin could protect the lungs against CCl(4)-induced oxidative damage. Co-Action Publishing 2016-11-07 /pmc/articles/PMC5102104/ /pubmed/27834184 http://dx.doi.org/10.3402/fnr.v60.30433 Text en © 2016 Rahmat Ali Khan et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license. |
spellingShingle | Original Article Khan, Rahmat Ali Alkreathy, Huda Mohammad Saboorshah, Abdus Ahmed, Mushtaq Khan, Samiullah Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats |
title | Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats |
title_full | Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats |
title_fullStr | Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats |
title_full_unstemmed | Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats |
title_short | Protective effects of Trifolium alexandrinum L. against lung injury induced by environmental toxin CCl(4) in experimental rats |
title_sort | protective effects of trifolium alexandrinum l. against lung injury induced by environmental toxin ccl(4) in experimental rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5102104/ https://www.ncbi.nlm.nih.gov/pubmed/27834184 http://dx.doi.org/10.3402/fnr.v60.30433 |
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