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Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats

BACKGROUND: Carissa opaca is a Pakistani fruit, traditionally used in the treatment of various human ailments including asthma and pulmonary damage. The present study investigated the protective effects of Carissa opaca against CCl(4)-induced oxidative stress in rat lungs. METHODS: To assess the pro...

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Autores principales: Sahreen, Sumaira, Khan, Muhammad Rashid, Khan, Rahmat Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916826/
https://www.ncbi.nlm.nih.gov/pubmed/24479952
http://dx.doi.org/10.1186/1472-6882-14-40
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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: Carissa opaca is a Pakistani fruit, traditionally used in the treatment of various human ailments including asthma and pulmonary damage. The present study investigated the protective effects of Carissa opaca against CCl(4)-induced oxidative stress in rat lungs. METHODS: To assess the protective effects of Carissa opaca, 42 Sprague–Dawley male rats (170–180 g) were randomly divided into 7 groups. Group I was untreated and group II received olive oil intraperitoneally (i.p.) and dimethyl sulfoxide orally. Groups III, IV, V, VI and VII were administered CCl(4), 3 ml/kg bodyweight (30% in olive oil i.p.). Group IV was administered 50 mg/kg bodyweight silymarin whereas groups V, VI and VII were treated with 200 mg/kg of various fractions of Carissa opaca after 48 h of CCl(4) treatment for eight weeks. Antioxidant profiles in lungs were evaluated by estimating the activities of antioxidant enzymes: catalase, peroxidase, superoxide dismutase, glutathione-S-transferase, glutathione reductase, glutathione peroxidase, quinone reductase and reduced glutathione. CCl(4)-induced lipid peroxidation was determined by measuring the level of thiobarbituric acid reactive substances (TBARS) with conjugation of DNA damage and histopathology. RESULTS: Administration of CCl(4) for 8 weeks significantly reduced (p < 0.05) the activities of antioxidant enzymes and GSH concentration while increasing TBARS content and DNA damage. Co-treatment of various fractions of Carissa opaca and silymarin restored the activities of antioxidant enzymes and glutathione content. Changes in TBARS concentration and DNA fragmentation was significantly decreased (p < 0.05) following Carissa opaca and silymarin treatment in lung. CONCLUSIONS: Histopathological changes in rat lungs induced by CCl(4) were significantly restored by co-treatment with Carissa opaca and silymarin.
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spelling pubmed-39168262014-02-08 Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats Sahreen, Sumaira Khan, Muhammad Rashid Khan, Rahmat Ali BMC Complement Altern Med Research Article BACKGROUND: Carissa opaca is a Pakistani fruit, traditionally used in the treatment of various human ailments including asthma and pulmonary damage. The present study investigated the protective effects of Carissa opaca against CCl(4)-induced oxidative stress in rat lungs. METHODS: To assess the protective effects of Carissa opaca, 42 Sprague–Dawley male rats (170–180 g) were randomly divided into 7 groups. Group I was untreated and group II received olive oil intraperitoneally (i.p.) and dimethyl sulfoxide orally. Groups III, IV, V, VI and VII were administered CCl(4), 3 ml/kg bodyweight (30% in olive oil i.p.). Group IV was administered 50 mg/kg bodyweight silymarin whereas groups V, VI and VII were treated with 200 mg/kg of various fractions of Carissa opaca after 48 h of CCl(4) treatment for eight weeks. Antioxidant profiles in lungs were evaluated by estimating the activities of antioxidant enzymes: catalase, peroxidase, superoxide dismutase, glutathione-S-transferase, glutathione reductase, glutathione peroxidase, quinone reductase and reduced glutathione. CCl(4)-induced lipid peroxidation was determined by measuring the level of thiobarbituric acid reactive substances (TBARS) with conjugation of DNA damage and histopathology. RESULTS: Administration of CCl(4) for 8 weeks significantly reduced (p < 0.05) the activities of antioxidant enzymes and GSH concentration while increasing TBARS content and DNA damage. Co-treatment of various fractions of Carissa opaca and silymarin restored the activities of antioxidant enzymes and glutathione content. Changes in TBARS concentration and DNA fragmentation was significantly decreased (p < 0.05) following Carissa opaca and silymarin treatment in lung. CONCLUSIONS: Histopathological changes in rat lungs induced by CCl(4) were significantly restored by co-treatment with Carissa opaca and silymarin. BioMed Central 2014-01-30 /pmc/articles/PMC3916826/ /pubmed/24479952 http://dx.doi.org/10.1186/1472-6882-14-40 Text en Copyright © 2014 sahreen et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Sahreen, Sumaira
Khan, Muhammad Rashid
Khan, Rahmat Ali
Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
title Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
title_full Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
title_fullStr Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
title_full_unstemmed Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
title_short Effects of Carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
title_sort effects of carissa opaca fruits extracts on oxidative pulmonary damages and fibrosis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3916826/
https://www.ncbi.nlm.nih.gov/pubmed/24479952
http://dx.doi.org/10.1186/1472-6882-14-40
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