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Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid
In a previous study, obeticholic acid (OCA) increased liver growth before partial hepatectomy (PHx) in rats through the bile acid receptor farnesoid X-receptor (FXR). In that model, OCA was administered during obstructive cholestasis. However, patients normally undergo PHx several days after biliary...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916678/ https://www.ncbi.nlm.nih.gov/pubmed/33578971 http://dx.doi.org/10.3390/biom11020260 |
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author | de Haan, Lianne R. Verheij, Joanne van Golen, Rowan F. Horneffer-van der Sluis, Verena Lewis, Matthew R. Beuers, Ulrich H. W. van Gulik, Thomas M. Olde Damink, Steven W. M. Schaap, Frank G. Heger, Michal Olthof, Pim B. |
author_facet | de Haan, Lianne R. Verheij, Joanne van Golen, Rowan F. Horneffer-van der Sluis, Verena Lewis, Matthew R. Beuers, Ulrich H. W. van Gulik, Thomas M. Olde Damink, Steven W. M. Schaap, Frank G. Heger, Michal Olthof, Pim B. |
author_sort | de Haan, Lianne R. |
collection | PubMed |
description | In a previous study, obeticholic acid (OCA) increased liver growth before partial hepatectomy (PHx) in rats through the bile acid receptor farnesoid X-receptor (FXR). In that model, OCA was administered during obstructive cholestasis. However, patients normally undergo PHx several days after biliary drainage. The effects of OCA on liver regeneration were therefore studied in post-cholestatic Wistar rats. Rats underwent sham surgery or reversible bile duct ligation (rBDL), which was relieved after 7 days. PHx was performed one day after restoration of bile flow. Rats received 10 mg/kg OCA per day or were fed vehicle from restoration of bile flow until sacrifice 5 days after PHx. Liver regeneration was comparable between cholestatic and non-cholestatic livers in PHx-subjected rats, which paralleled liver regeneration a human validation cohort. OCA treatment induced ileal Fgf15 mRNA expression but did not enhance post-PHx hepatocyte proliferation through FXR/SHP signaling. OCA treatment neither increased mitosis rates nor recovery of liver weight after PHx but accelerated liver regrowth in rats that had not been subjected to rBDL. OCA did not increase biliary injury. Conclusively, OCA does not induce liver regeneration in post-cholestatic rats and does not exacerbate biliary damage that results from cholestasis. This study challenges the previously reported beneficial effects of OCA in liver regeneration in cholestatic rats. |
format | Online Article Text |
id | pubmed-7916678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79166782021-03-01 Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid de Haan, Lianne R. Verheij, Joanne van Golen, Rowan F. Horneffer-van der Sluis, Verena Lewis, Matthew R. Beuers, Ulrich H. W. van Gulik, Thomas M. Olde Damink, Steven W. M. Schaap, Frank G. Heger, Michal Olthof, Pim B. Biomolecules Article In a previous study, obeticholic acid (OCA) increased liver growth before partial hepatectomy (PHx) in rats through the bile acid receptor farnesoid X-receptor (FXR). In that model, OCA was administered during obstructive cholestasis. However, patients normally undergo PHx several days after biliary drainage. The effects of OCA on liver regeneration were therefore studied in post-cholestatic Wistar rats. Rats underwent sham surgery or reversible bile duct ligation (rBDL), which was relieved after 7 days. PHx was performed one day after restoration of bile flow. Rats received 10 mg/kg OCA per day or were fed vehicle from restoration of bile flow until sacrifice 5 days after PHx. Liver regeneration was comparable between cholestatic and non-cholestatic livers in PHx-subjected rats, which paralleled liver regeneration a human validation cohort. OCA treatment induced ileal Fgf15 mRNA expression but did not enhance post-PHx hepatocyte proliferation through FXR/SHP signaling. OCA treatment neither increased mitosis rates nor recovery of liver weight after PHx but accelerated liver regrowth in rats that had not been subjected to rBDL. OCA did not increase biliary injury. Conclusively, OCA does not induce liver regeneration in post-cholestatic rats and does not exacerbate biliary damage that results from cholestasis. This study challenges the previously reported beneficial effects of OCA in liver regeneration in cholestatic rats. MDPI 2021-02-10 /pmc/articles/PMC7916678/ /pubmed/33578971 http://dx.doi.org/10.3390/biom11020260 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article de Haan, Lianne R. Verheij, Joanne van Golen, Rowan F. Horneffer-van der Sluis, Verena Lewis, Matthew R. Beuers, Ulrich H. W. van Gulik, Thomas M. Olde Damink, Steven W. M. Schaap, Frank G. Heger, Michal Olthof, Pim B. Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid |
title | Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid |
title_full | Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid |
title_fullStr | Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid |
title_full_unstemmed | Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid |
title_short | Unaltered Liver Regeneration in Post-Cholestatic Rats Treated with the FXR Agonist Obeticholic Acid |
title_sort | unaltered liver regeneration in post-cholestatic rats treated with the fxr agonist obeticholic acid |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7916678/ https://www.ncbi.nlm.nih.gov/pubmed/33578971 http://dx.doi.org/10.3390/biom11020260 |
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