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Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk

The unique characters of camel’s milk make it used extensively in the field of medicine as anti-microbial, anti-diabetic and hepatoprotective agent. The lack of studies demonstrating the protective effect of camel’s milk against hepatotoxic compound was the main reason beyond the conduction of the c...

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Autores principales: Althnaian, Thnaian, Albokhadaim, Ibrahim, El-Bahr, Sabry M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing AG 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593006/
https://www.ncbi.nlm.nih.gov/pubmed/23487568
http://dx.doi.org/10.1186/2193-1801-2-57
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author Althnaian, Thnaian
Albokhadaim, Ibrahim
El-Bahr, Sabry M
author_facet Althnaian, Thnaian
Albokhadaim, Ibrahim
El-Bahr, Sabry M
author_sort Althnaian, Thnaian
collection PubMed
description The unique characters of camel’s milk make it used extensively in the field of medicine as anti-microbial, anti-diabetic and hepatoprotective agent. The lack of studies demonstrating the protective effect of camel’s milk against hepatotoxic compound was the main reason beyond the conduction of the current experiment which aimed to investigate the protective effects of camel’s milk against carbontetrachloride (CCl(4)) induced hepatotoxicity. Therefore, 24 rats were fed on standard diet and divided into four groups. Rats of the first group and second groups were injected i/p with paraffin oil and received either tap water (control 1) or camel’s milk (control 2), respectively. Rats of the third and fourth groups were injected i/p with CCl(4) and received either tap water or camel’s milk, respectively. At the end of the experiment (5 weeks), blood and liver samples were collected for biochemical and histopathological analysis. The present findings revealed that, CCl(4) elevated serum enzyme activities of liver and some biochemical parameters, but these effects were prevented by the treatment of rats with camel milk. Histopathologically, a great amount of mononuclear cells infiltration, necrotic cells and few fibroblasts were observed in liver of CCl(4) treated group. The present study concluded that camel milk treatment may play a protective role against CCl(4)-induced liver damages in rats. These protective effects were in the form of improving of liver enzyme activities, blood biochemical parameters and histological picture of liver of intoxicated rats. In the future, examination of the liver protective effect of camel milk against CCl(4) in dose dependant manner could be investigated.
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spelling pubmed-35930062013-03-11 Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk Althnaian, Thnaian Albokhadaim, Ibrahim El-Bahr, Sabry M Springerplus Research The unique characters of camel’s milk make it used extensively in the field of medicine as anti-microbial, anti-diabetic and hepatoprotective agent. The lack of studies demonstrating the protective effect of camel’s milk against hepatotoxic compound was the main reason beyond the conduction of the current experiment which aimed to investigate the protective effects of camel’s milk against carbontetrachloride (CCl(4)) induced hepatotoxicity. Therefore, 24 rats were fed on standard diet and divided into four groups. Rats of the first group and second groups were injected i/p with paraffin oil and received either tap water (control 1) or camel’s milk (control 2), respectively. Rats of the third and fourth groups were injected i/p with CCl(4) and received either tap water or camel’s milk, respectively. At the end of the experiment (5 weeks), blood and liver samples were collected for biochemical and histopathological analysis. The present findings revealed that, CCl(4) elevated serum enzyme activities of liver and some biochemical parameters, but these effects were prevented by the treatment of rats with camel milk. Histopathologically, a great amount of mononuclear cells infiltration, necrotic cells and few fibroblasts were observed in liver of CCl(4) treated group. The present study concluded that camel milk treatment may play a protective role against CCl(4)-induced liver damages in rats. These protective effects were in the form of improving of liver enzyme activities, blood biochemical parameters and histological picture of liver of intoxicated rats. In the future, examination of the liver protective effect of camel milk against CCl(4) in dose dependant manner could be investigated. Springer International Publishing AG 2013-02-18 /pmc/articles/PMC3593006/ /pubmed/23487568 http://dx.doi.org/10.1186/2193-1801-2-57 Text en © Althnaian et al; licensee Springer. 2013 This article is published under license to BioMed Central Ltd. 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
Althnaian, Thnaian
Albokhadaim, Ibrahim
El-Bahr, Sabry M
Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
title Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
title_full Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
title_fullStr Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
title_full_unstemmed Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
title_short Biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
title_sort biochemical and histopathological study in rats intoxicated with carbontetrachloride and treated with camel milk
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3593006/
https://www.ncbi.nlm.nih.gov/pubmed/23487568
http://dx.doi.org/10.1186/2193-1801-2-57
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