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Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis

This study was to evaluate the effects of thalidomide on expression of adhesion molecules in liver cirrhosis. The cirrhosis was induced in Wistar rats by intraperitoneal injection of CCl(4), and thalidomide (10 mg/kg/day or 100 mg/kg/day) was given by intragastric administration for 8 weeks. Liver h...

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Detalles Bibliográficos
Autores principales: Lv, Peng, Paul, Shelley Chireyath, Xiao, Yanjv, Liu, Shiquan, Luo, Hesheng
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1618940/
https://www.ncbi.nlm.nih.gov/pubmed/17047296
http://dx.doi.org/10.1155/MI/2006/93253
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author Lv, Peng
Paul, Shelley Chireyath
Xiao, Yanjv
Liu, Shiquan
Luo, Hesheng
author_facet Lv, Peng
Paul, Shelley Chireyath
Xiao, Yanjv
Liu, Shiquan
Luo, Hesheng
author_sort Lv, Peng
collection PubMed
description This study was to evaluate the effects of thalidomide on expression of adhesion molecules in liver cirrhosis. The cirrhosis was induced in Wistar rats by intraperitoneal injection of CCl(4), and thalidomide (10 mg/kg/day or 100 mg/kg/day) was given by intragastric administration for 8 weeks. Liver histopathology and immunohistochemistry were significantly improved and the expressions of ICAM-1, VCAM-1, E-selectin, and TNF-α mRNA and protein were decreased significantly in rats treated with a high dose of thalidomide. Close positive correlation was observed in the expression of the TNF-α mRNA and that of ICAM-1, VCAM-1, and E-selectin mRNA, respectively. These results indicate that thalidomide exerts its effect on the downregulation of adhesion molecules via TNF-α signaling pathway to inhibit liver fibrosis.
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spelling pubmed-16189402006-11-15 Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis Lv, Peng Paul, Shelley Chireyath Xiao, Yanjv Liu, Shiquan Luo, Hesheng Mediators Inflamm Research Communication This study was to evaluate the effects of thalidomide on expression of adhesion molecules in liver cirrhosis. The cirrhosis was induced in Wistar rats by intraperitoneal injection of CCl(4), and thalidomide (10 mg/kg/day or 100 mg/kg/day) was given by intragastric administration for 8 weeks. Liver histopathology and immunohistochemistry were significantly improved and the expressions of ICAM-1, VCAM-1, E-selectin, and TNF-α mRNA and protein were decreased significantly in rats treated with a high dose of thalidomide. Close positive correlation was observed in the expression of the TNF-α mRNA and that of ICAM-1, VCAM-1, and E-selectin mRNA, respectively. These results indicate that thalidomide exerts its effect on the downregulation of adhesion molecules via TNF-α signaling pathway to inhibit liver fibrosis. Hindawi Publishing Corporation 2006 2006-05-11 /pmc/articles/PMC1618940/ /pubmed/17047296 http://dx.doi.org/10.1155/MI/2006/93253 Text en Copyright © 2006 Peng Lv et al. 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 Communication
Lv, Peng
Paul, Shelley Chireyath
Xiao, Yanjv
Liu, Shiquan
Luo, Hesheng
Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis
title Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis
title_full Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis
title_fullStr Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis
title_full_unstemmed Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis
title_short Effects of Thalidomide on the Expression of Adhesion Molecules in Rat Liver Cirrhosis
title_sort effects of thalidomide on the expression of adhesion molecules in rat liver cirrhosis
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1618940/
https://www.ncbi.nlm.nih.gov/pubmed/17047296
http://dx.doi.org/10.1155/MI/2006/93253
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