The role of bile salt composition in liver pathology of mdr2 (-/-) mice: Differences between males and females

Carin M J Van Nieuwerk, Albert K. Groen, Roelof Ottenhoff, Michael Van Wijland, Marius A. Van Den Bergh Weerman, Guido N J Tytgat, Johan J A Offerhaus, Ronald P J Oude Elferink

Research output: Contribution to journalArticle

Abstract

Background/Aims: The mouse mdr2 gene encodes a P-glycoprotein expressed in the canalicular membrane of the hepatocyte. Mice in which this gene has been inactivated (mdr2 -/-) show a defect in biliary phospholipid and cholesterol secretion and develop non-suppurative cholangitis. We hypothesized that secretion of bile salts without lipids initiates this liver disease. Methods: To delineate the pathologic process, mdr2 (-/-) mice were fed different bile salt-supplemented diets for 22 weeks after weaning. Aspects of liver pathology including eosinophilic bodies, portal inflammation, ductular proliferation, mitotic activity and fibrosis were semi-quantitatively scored. Results: It was observed that liver pathology was more severe in female than in male mice when fed a purified control diet. This correlated with a more hydrophohic bile salt composition of female vs. male bile. When increasing amounts of cholate were added to the diet (0.01% and 0.1%), the secretion of taurocholate increased and this was accompanied by a more severe liver pathology. At the high dose of cholate (0.1%), the bile salt compositions of male and female mice became similar, as did the severity of the histological score. Addition of cholate to the diet did not induce liver pathology in (+/+) mice. Addition of ursodeoxycholate to the diet (0.5%) led to a near complete replacement of biliary bile salts by tauroursodeoxycholate and this reduced pathology and dissipated the difference between males and females. Conclusions: These ohservations support our hypothesis that liver pathology in the mdr2 (-/-) mouse is caused by bile salts and depends on the hydrophobicity c.q. cytotoxicity of biliary bile salts.

Original languageEnglish (US)
Pages (from-to)138-145
Number of pages8
JournalJournal of Hepatology
Volume26
Issue number1
DOIs
StatePublished - Jan 1997
Externally publishedYes

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Bile Acids and Salts
Pathology
Cholates
Liver
Diet
Taurocholic Acid
Cholangitis
P-Glycoprotein
Pathologic Processes
Weaning
Hydrophobic and Hydrophilic Interactions
Bile
Genes
Liver Diseases
Hepatocytes
Phospholipids
Fibrosis
Cholesterol
Inflammation
Lipids

Keywords

  • bile constituents
  • bile salt hydrophobicity
  • gender difference
  • mdr2 knockout mice

ASJC Scopus subject areas

  • Gastroenterology

Cite this

Van Nieuwerk, C. M. J., Groen, A. K., Ottenhoff, R., Van Wijland, M., Van Den Bergh Weerman, M. A., Tytgat, G. N. J., ... Oude Elferink, R. P. J. (1997). The role of bile salt composition in liver pathology of mdr2 (-/-) mice: Differences between males and females. Journal of Hepatology, 26(1), 138-145. https://doi.org/10.1016/S0168-8278(97)80020-7

The role of bile salt composition in liver pathology of mdr2 (-/-) mice : Differences between males and females. / Van Nieuwerk, Carin M J; Groen, Albert K.; Ottenhoff, Roelof; Van Wijland, Michael; Van Den Bergh Weerman, Marius A.; Tytgat, Guido N J; Offerhaus, Johan J A; Oude Elferink, Ronald P J.

In: Journal of Hepatology, Vol. 26, No. 1, 01.1997, p. 138-145.

Research output: Contribution to journalArticle

Van Nieuwerk, CMJ, Groen, AK, Ottenhoff, R, Van Wijland, M, Van Den Bergh Weerman, MA, Tytgat, GNJ, Offerhaus, JJA & Oude Elferink, RPJ 1997, 'The role of bile salt composition in liver pathology of mdr2 (-/-) mice: Differences between males and females', Journal of Hepatology, vol. 26, no. 1, pp. 138-145. https://doi.org/10.1016/S0168-8278(97)80020-7
Van Nieuwerk CMJ, Groen AK, Ottenhoff R, Van Wijland M, Van Den Bergh Weerman MA, Tytgat GNJ et al. The role of bile salt composition in liver pathology of mdr2 (-/-) mice: Differences between males and females. Journal of Hepatology. 1997 Jan;26(1):138-145. https://doi.org/10.1016/S0168-8278(97)80020-7
Van Nieuwerk, Carin M J ; Groen, Albert K. ; Ottenhoff, Roelof ; Van Wijland, Michael ; Van Den Bergh Weerman, Marius A. ; Tytgat, Guido N J ; Offerhaus, Johan J A ; Oude Elferink, Ronald P J. / The role of bile salt composition in liver pathology of mdr2 (-/-) mice : Differences between males and females. In: Journal of Hepatology. 1997 ; Vol. 26, No. 1. pp. 138-145.
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abstract = "Background/Aims: The mouse mdr2 gene encodes a P-glycoprotein expressed in the canalicular membrane of the hepatocyte. Mice in which this gene has been inactivated (mdr2 -/-) show a defect in biliary phospholipid and cholesterol secretion and develop non-suppurative cholangitis. We hypothesized that secretion of bile salts without lipids initiates this liver disease. Methods: To delineate the pathologic process, mdr2 (-/-) mice were fed different bile salt-supplemented diets for 22 weeks after weaning. Aspects of liver pathology including eosinophilic bodies, portal inflammation, ductular proliferation, mitotic activity and fibrosis were semi-quantitatively scored. Results: It was observed that liver pathology was more severe in female than in male mice when fed a purified control diet. This correlated with a more hydrophohic bile salt composition of female vs. male bile. When increasing amounts of cholate were added to the diet (0.01{\%} and 0.1{\%}), the secretion of taurocholate increased and this was accompanied by a more severe liver pathology. At the high dose of cholate (0.1{\%}), the bile salt compositions of male and female mice became similar, as did the severity of the histological score. Addition of cholate to the diet did not induce liver pathology in (+/+) mice. Addition of ursodeoxycholate to the diet (0.5{\%}) led to a near complete replacement of biliary bile salts by tauroursodeoxycholate and this reduced pathology and dissipated the difference between males and females. Conclusions: These ohservations support our hypothesis that liver pathology in the mdr2 (-/-) mouse is caused by bile salts and depends on the hydrophobicity c.q. cytotoxicity of biliary bile salts.",
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AU - Van Nieuwerk, Carin M J

AU - Groen, Albert K.

AU - Ottenhoff, Roelof

AU - Van Wijland, Michael

AU - Van Den Bergh Weerman, Marius A.

AU - Tytgat, Guido N J

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