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Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats
This study was undertaken to evaluate the protective effect of aqueous extract of Psidium guajava leaves against sodium arsenite-induced toxicity in experimental rats. Animals were divided into four groups. Control group received arsenic free distilled water and three treatment groups (II, III, and...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532768/ https://www.ncbi.nlm.nih.gov/pubmed/23293461 http://dx.doi.org/10.4103/0971-6580.103658 |
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author | Tandon, Neeraj Roy, Manju Roy, Sushovan Gupta, Neelu |
author_facet | Tandon, Neeraj Roy, Manju Roy, Sushovan Gupta, Neelu |
author_sort | Tandon, Neeraj |
collection | PubMed |
description | This study was undertaken to evaluate the protective effect of aqueous extract of Psidium guajava leaves against sodium arsenite-induced toxicity in experimental rats. Animals were divided into four groups. Control group received arsenic free distilled water and three treatment groups (II, III, and IV) exposed to the arsenic (NaAsO(2)) (20 mg/kg b.wt) through drinking water. Group III and IV were administered a daily oral dose of P. guajava leaf extract 50 and 100 mg/kg b.wt. (AEPG(50) and AEPG(100)) for the period of 6 weeks. Blood samples and organs were collected at the end of the experiment. Arsenic exposure resulted in significant rise in lipid peroxidation (LPO) levels in erythrocyte, liver, kidney, and brain. In addition toxin decreased (P<0.05) the level of reduced glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) activities in the studied tissues. Residual effect of arsenic in various tissues was also observed. Histopathological results revealed mild to severe type of necrosis and degenerative changes in kidney and liver of arsenic intoxicated animals. Cytological alteration in brain tissue was also observed. Treatment with AEPG(100) (aqueous extract of P. guajava) @100 mg/kg body weight) significantly restored activities of oxidative stress markers like LPO levels, GSH levels, SOD, and CAT activities but having the limited protective activity of the herbal extract was observed on tissues architecture. It is therefore concluded that prophylactic co-administration of AEPG could provide specific protection from oxidative injury and to some extent on tissue damage. |
format | Online Article Text |
id | pubmed-3532768 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35327682013-01-04 Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats Tandon, Neeraj Roy, Manju Roy, Sushovan Gupta, Neelu Toxicol Int Original Article This study was undertaken to evaluate the protective effect of aqueous extract of Psidium guajava leaves against sodium arsenite-induced toxicity in experimental rats. Animals were divided into four groups. Control group received arsenic free distilled water and three treatment groups (II, III, and IV) exposed to the arsenic (NaAsO(2)) (20 mg/kg b.wt) through drinking water. Group III and IV were administered a daily oral dose of P. guajava leaf extract 50 and 100 mg/kg b.wt. (AEPG(50) and AEPG(100)) for the period of 6 weeks. Blood samples and organs were collected at the end of the experiment. Arsenic exposure resulted in significant rise in lipid peroxidation (LPO) levels in erythrocyte, liver, kidney, and brain. In addition toxin decreased (P<0.05) the level of reduced glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) activities in the studied tissues. Residual effect of arsenic in various tissues was also observed. Histopathological results revealed mild to severe type of necrosis and degenerative changes in kidney and liver of arsenic intoxicated animals. Cytological alteration in brain tissue was also observed. Treatment with AEPG(100) (aqueous extract of P. guajava) @100 mg/kg body weight) significantly restored activities of oxidative stress markers like LPO levels, GSH levels, SOD, and CAT activities but having the limited protective activity of the herbal extract was observed on tissues architecture. It is therefore concluded that prophylactic co-administration of AEPG could provide specific protection from oxidative injury and to some extent on tissue damage. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3532768/ /pubmed/23293461 http://dx.doi.org/10.4103/0971-6580.103658 Text en Copyright: © Toxicology International http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Tandon, Neeraj Roy, Manju Roy, Sushovan Gupta, Neelu Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats |
title | Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats |
title_full | Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats |
title_fullStr | Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats |
title_full_unstemmed | Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats |
title_short | Protective Effect of Psidium guajava in Arsenic-induced Oxidative Stress and Cytological Damage in Rats |
title_sort | protective effect of psidium guajava in arsenic-induced oxidative stress and cytological damage in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3532768/ https://www.ncbi.nlm.nih.gov/pubmed/23293461 http://dx.doi.org/10.4103/0971-6580.103658 |
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