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Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats

The effect of biphenyldimethyldicarboxylate (DDB), a synthetic compound, in use for the treatment of chronic hepatitis was studied on hepatic injury caused in rats by administration of carbon tetrachloride (CCl(4)). Starting at time of administration of the first dose of CCl(4), rats received DDB at...

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Autores principales: Abdel-Salam, Omar M. E., Sleem, Amany A., Morsy, Fatma A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901054/
https://www.ncbi.nlm.nih.gov/pubmed/17721639
http://dx.doi.org/10.1100/tsw.2007.193
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author Abdel-Salam, Omar M. E.
Sleem, Amany A.
Morsy, Fatma A.
author_facet Abdel-Salam, Omar M. E.
Sleem, Amany A.
Morsy, Fatma A.
author_sort Abdel-Salam, Omar M. E.
collection PubMed
description The effect of biphenyldimethyldicarboxylate (DDB), a synthetic compound, in use for the treatment of chronic hepatitis was studied on hepatic injury caused in rats by administration of carbon tetrachloride (CCl(4)). Starting at time of administration of the first dose of CCl(4), rats received DDB at four dose levels (3, 15, 75 or 375 mg/kg), silymarin (22 mg/kg), a combination of DDB (75 mg/kg) and silymarin (22 mg/kg) or saline (control) once orally daily for 30 days. The administration of DDB in CCl(4)-treated rats at 75 or 375 mg/kg resulted in 61.2-76.2% decrease in alanine aminotransferase (ALT) and 46.9-60.8% decrease in aspartate aminotransferase (AST), respectively compared with the CCl(4) control group. Silymarin treatment resulted in 34.6 and 30% decrease in ALT and AST, while DDB (75 mg/kg) combined with silymarin (22 mg/kg) resulted in 58.2 and 31% decrease in ALT and AST, respectively. Serum creatinine increased by 50% by DDB at 375 mg/kg. After treatment with DDB at 75 or 375 mg/kg or DDB combined with silymarin, the development of liver necrosis and fibrosis caused by CCl(4) was markedly reduced, while after DDB combined with silymarin no DNA aneuploid cells could be observed. The decrease in glycogen and protein contents in hepatocytes caused by CCl(4) was markedly prevented by co-treatment with DDB at 75 or 375 mg/kg or DDB combined with silymarin. It is concluded that in the model of hepatic injury caused by chronic administration of CCl(4) in rats, the synthetic compound DDB, limits hepatocellular injury and exerts antifibrotic effect. Better improvement in protein, DNA, mucopolysaccharide content was seen after both DDB and silymarin compared to DDB alone. It is suggested, therefore, that DDB alone or in combination with silymarin might prove of benefit in the therapy of chronic liver disease. Monitoring of kidney functions in patients taking DDB is warranted.
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spelling pubmed-59010542018-06-03 Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats Abdel-Salam, Omar M. E. Sleem, Amany A. Morsy, Fatma A. ScientificWorldJournal Research Article The effect of biphenyldimethyldicarboxylate (DDB), a synthetic compound, in use for the treatment of chronic hepatitis was studied on hepatic injury caused in rats by administration of carbon tetrachloride (CCl(4)). Starting at time of administration of the first dose of CCl(4), rats received DDB at four dose levels (3, 15, 75 or 375 mg/kg), silymarin (22 mg/kg), a combination of DDB (75 mg/kg) and silymarin (22 mg/kg) or saline (control) once orally daily for 30 days. The administration of DDB in CCl(4)-treated rats at 75 or 375 mg/kg resulted in 61.2-76.2% decrease in alanine aminotransferase (ALT) and 46.9-60.8% decrease in aspartate aminotransferase (AST), respectively compared with the CCl(4) control group. Silymarin treatment resulted in 34.6 and 30% decrease in ALT and AST, while DDB (75 mg/kg) combined with silymarin (22 mg/kg) resulted in 58.2 and 31% decrease in ALT and AST, respectively. Serum creatinine increased by 50% by DDB at 375 mg/kg. After treatment with DDB at 75 or 375 mg/kg or DDB combined with silymarin, the development of liver necrosis and fibrosis caused by CCl(4) was markedly reduced, while after DDB combined with silymarin no DNA aneuploid cells could be observed. The decrease in glycogen and protein contents in hepatocytes caused by CCl(4) was markedly prevented by co-treatment with DDB at 75 or 375 mg/kg or DDB combined with silymarin. It is concluded that in the model of hepatic injury caused by chronic administration of CCl(4) in rats, the synthetic compound DDB, limits hepatocellular injury and exerts antifibrotic effect. Better improvement in protein, DNA, mucopolysaccharide content was seen after both DDB and silymarin compared to DDB alone. It is suggested, therefore, that DDB alone or in combination with silymarin might prove of benefit in the therapy of chronic liver disease. Monitoring of kidney functions in patients taking DDB is warranted. TheScientificWorldJOURNAL 2007-08-24 /pmc/articles/PMC5901054/ /pubmed/17721639 http://dx.doi.org/10.1100/tsw.2007.193 Text en Copyright © 2007 Omar M. E. Abdel-Salam et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Abdel-Salam, Omar M. E.
Sleem, Amany A.
Morsy, Fatma A.
Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats
title Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats
title_full Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats
title_fullStr Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats
title_full_unstemmed Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats
title_short Effects of Biphenyldimethyl-dicarboxylate Administration Alone or Combined with Silymarin in the CCL(4) Model of Liver Fibrosis in Rats
title_sort effects of biphenyldimethyl-dicarboxylate administration alone or combined with silymarin in the ccl(4) model of liver fibrosis in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901054/
https://www.ncbi.nlm.nih.gov/pubmed/17721639
http://dx.doi.org/10.1100/tsw.2007.193
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