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Secondary bile acids and the biliary epithelia: The good and the bad
The biliary tract has been considered for several decades a passive system just leading the hepatic bile to the intestine. Nowadays several researches demonstrated an important role of biliary epithelia (i.e. cholangiocytes) in bile formation. The study of biliary processes therefore maintains a con...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846939/ https://www.ncbi.nlm.nih.gov/pubmed/36687129 http://dx.doi.org/10.3748/wjg.v29.i2.357 |
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author | Lenci, Ilaria Milana, Martina Signorello, Alessandro Grassi, Giuseppe Baiocchi, Leonardo |
author_facet | Lenci, Ilaria Milana, Martina Signorello, Alessandro Grassi, Giuseppe Baiocchi, Leonardo |
author_sort | Lenci, Ilaria |
collection | PubMed |
description | The biliary tract has been considered for several decades a passive system just leading the hepatic bile to the intestine. Nowadays several researches demonstrated an important role of biliary epithelia (i.e. cholangiocytes) in bile formation. The study of biliary processes therefore maintains a continuous interest since the possible important implications regarding chronic cholestatic human diseases, such as primary biliary cholangitis or primary sclerosing cholangitis. Bile acids (BAs), produced by the liver, are the most represented organic molecules in bile. The physiologic importance of BAs was initially attributed to their behavior as natural detergents but several studies now demonstrate they are also important signaling molecules. In this minireview the effect of BAs on the biliary epithelia are reported focusing in particular on secondary (deriving by bacterial manipulation of primary molecules) ones. This class of BAs is demonstrated to have relevant biological effects, ranging from toxic to therapeutic ones. In this family ursodeoxycholic and lithocholic acid present the most interesting features. The molecular mechanisms linking ursodeoxycholic acid to its beneficial effects on the biliary tract are discussed in details as well as data on the processes leading to lithocholic damage. These findings suggest that expansion of research in the field of BAs/cholangiocytes interaction may increase our understanding of cholestatic diseases and should be helpful in designing more effective therapies for biliary disorders. |
format | Online Article Text |
id | pubmed-9846939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-98469392023-01-19 Secondary bile acids and the biliary epithelia: The good and the bad Lenci, Ilaria Milana, Martina Signorello, Alessandro Grassi, Giuseppe Baiocchi, Leonardo World J Gastroenterol Minireviews The biliary tract has been considered for several decades a passive system just leading the hepatic bile to the intestine. Nowadays several researches demonstrated an important role of biliary epithelia (i.e. cholangiocytes) in bile formation. The study of biliary processes therefore maintains a continuous interest since the possible important implications regarding chronic cholestatic human diseases, such as primary biliary cholangitis or primary sclerosing cholangitis. Bile acids (BAs), produced by the liver, are the most represented organic molecules in bile. The physiologic importance of BAs was initially attributed to their behavior as natural detergents but several studies now demonstrate they are also important signaling molecules. In this minireview the effect of BAs on the biliary epithelia are reported focusing in particular on secondary (deriving by bacterial manipulation of primary molecules) ones. This class of BAs is demonstrated to have relevant biological effects, ranging from toxic to therapeutic ones. In this family ursodeoxycholic and lithocholic acid present the most interesting features. The molecular mechanisms linking ursodeoxycholic acid to its beneficial effects on the biliary tract are discussed in details as well as data on the processes leading to lithocholic damage. These findings suggest that expansion of research in the field of BAs/cholangiocytes interaction may increase our understanding of cholestatic diseases and should be helpful in designing more effective therapies for biliary disorders. Baishideng Publishing Group Inc 2023-01-14 2023-01-14 /pmc/articles/PMC9846939/ /pubmed/36687129 http://dx.doi.org/10.3748/wjg.v29.i2.357 Text en ©The Author(s) 2023. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Minireviews Lenci, Ilaria Milana, Martina Signorello, Alessandro Grassi, Giuseppe Baiocchi, Leonardo Secondary bile acids and the biliary epithelia: The good and the bad |
title | Secondary bile acids and the biliary epithelia: The good and the bad |
title_full | Secondary bile acids and the biliary epithelia: The good and the bad |
title_fullStr | Secondary bile acids and the biliary epithelia: The good and the bad |
title_full_unstemmed | Secondary bile acids and the biliary epithelia: The good and the bad |
title_short | Secondary bile acids and the biliary epithelia: The good and the bad |
title_sort | secondary bile acids and the biliary epithelia: the good and the bad |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9846939/ https://www.ncbi.nlm.nih.gov/pubmed/36687129 http://dx.doi.org/10.3748/wjg.v29.i2.357 |
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