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The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation.
To determine whether oxygen free radicals are responsible for the pathogenesis of the cholestasis induced by ligation of common bile duct (CBD) variables which reflect the hepatic function in the serum, the amount of superoxide radical production, and xanthine oxidase(XO) activity were studied. The...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Medical Sciences
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054052/ https://www.ncbi.nlm.nih.gov/pubmed/8843006 |
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author | Mun, K. C. Kwak, C. S. Kwon, K. Y. |
author_facet | Mun, K. C. Kwak, C. S. Kwon, K. Y. |
author_sort | Mun, K. C. |
collection | PubMed |
description | To determine whether oxygen free radicals are responsible for the pathogenesis of the cholestasis induced by ligation of common bile duct (CBD) variables which reflect the hepatic function in the serum, the amount of superoxide radical production, and xanthine oxidase(XO) activity were studied. The activity of serum alanine aminotransferase, bilirubin level in the serum and the amount of superoxide radical production were lower in a CBD ligation with allopurinol treated group than in a CBD ligation without allopurinol treated group. Abnormalities of the microscopic structures were reduced in a CBD ligation with allopurinol treated group than in a CBD ligation without allopurinol treated group. Allopurinol, an inhibitor of XO, prevented the hepatic damage induced by CBD ligation through the inhibition of XO. These experiments demonstrate that oxygen free radicals are responsible for the pathogenesis of the cholestatic liver. |
format | Text |
id | pubmed-3054052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-30540522011-03-15 The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. Mun, K. C. Kwak, C. S. Kwon, K. Y. J Korean Med Sci Research Article To determine whether oxygen free radicals are responsible for the pathogenesis of the cholestasis induced by ligation of common bile duct (CBD) variables which reflect the hepatic function in the serum, the amount of superoxide radical production, and xanthine oxidase(XO) activity were studied. The activity of serum alanine aminotransferase, bilirubin level in the serum and the amount of superoxide radical production were lower in a CBD ligation with allopurinol treated group than in a CBD ligation without allopurinol treated group. Abnormalities of the microscopic structures were reduced in a CBD ligation with allopurinol treated group than in a CBD ligation without allopurinol treated group. Allopurinol, an inhibitor of XO, prevented the hepatic damage induced by CBD ligation through the inhibition of XO. These experiments demonstrate that oxygen free radicals are responsible for the pathogenesis of the cholestatic liver. Korean Academy of Medical Sciences 1996-06 /pmc/articles/PMC3054052/ /pubmed/8843006 Text en |
spellingShingle | Research Article Mun, K. C. Kwak, C. S. Kwon, K. Y. The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
title | The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
title_full | The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
title_fullStr | The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
title_full_unstemmed | The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
title_short | The protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
title_sort | protective effect of allopurinol on cholestatic liver injury induced by bile duct ligation. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054052/ https://www.ncbi.nlm.nih.gov/pubmed/8843006 |
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