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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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