Bile salt sequestration induces hepatic de novo lipogenesis through farnesoid X receptor– and liver X receptora–controlled metabolic pathways in mice

H.J. Herrema, M. Meissner, Th. van Dijk, G. Brufau, R. Boverhof, M.H. Oosterveer, D.J. Reijngoud, M.R. Müller, F. Stellaard, A.K. Groen, F. Kuipers

Research output: Contribution to journalArticleAcademicpeer-review

67 Citations (Scopus)

Abstract

Diabetes is characterized by high blood glucose levels and dyslipidemia. Bile salt sequestration has been found to improve both plasma glycemic control and cholesterol profiles in diabetic patients. Yet bile salt sequestration is also known to affect triglyceride (TG) metabolism, possibly through signaling pathways involving farnesoid X receptor (FXR) and liver X receptor a (LXRa). We quantitatively assessed kinetic parameters of bile salt metabolism in lean C57Bl/6J and in obese, diabetic db/db mice upon bile salt sequestration using colesevelam HCl (2% wt/wt in diet) and related these to quantitative changes in hepatic lipid metabolism. As expected, bile salt sequestration reduced intestinal bile salt reabsorption. Importantly, bile salt pool size and biliary bile salt secretion remained unchanged upon sequestrant treatment due to compensation by de novo bile salt synthesis in both models. Nevertheless, lean and db/db mice showed increased, mainly periportally confined, hepatic TG contents, increased expression of lipogenic genes, and increased fractional contributions of newly synthesized fatty acids. Lipogenic gene expression was not induced in sequestrant-treated Fxr-/- and Lxra-/- mice compared with wild-type littermates, in line with reports indicating a regulatory role of FXR and LXRa in bile salt–mediated regulation of hepatic lipid metabolism. Conclusion: Bile salt sequestration by colesevelam induces the lipogenic pathway in an FXR- and LXRa-dependent manner without affecting the total pool size of bile salts in mice. We speculate that a shift from intestinal reabsorption to de novo synthesis as source of bile salts upon bile salt sequestration affects zonation of metabolic processes within the liver acinus
Original languageEnglish
Pages (from-to)806-816
JournalHepatology
Volume51
Issue number3
DOIs
Publication statusPublished - 2010

Keywords

  • peripheral insulin sensitivity
  • type-2 diabetes-mellitus
  • cholesterol 7-alpha-hydroxylase
  • colesevelam hydrochloride
  • enterohepatic circulation
  • chenodeoxycholic acid
  • glycemic control
  • deficient mice
  • double-blind
  • ob/ob mice

Fingerprint Dive into the research topics of 'Bile salt sequestration induces hepatic de novo lipogenesis through farnesoid X receptor– and liver X receptora–controlled metabolic pathways in mice'. Together they form a unique fingerprint.

  • Cite this

    Herrema, H. J., Meissner, M., van Dijk, T., Brufau, G., Boverhof, R., Oosterveer, M. H., Reijngoud, D. J., Müller, M. R., Stellaard, F., Groen, A. K., & Kuipers, F. (2010). Bile salt sequestration induces hepatic de novo lipogenesis through farnesoid X receptor– and liver X receptora–controlled metabolic pathways in mice. Hepatology, 51(3), 806-816. https://doi.org/10.1002/hep.23408