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Effect of beta-muricholic acid on the prevention and dissolution of cholesterol gallstones in C57L/J mice.

Abstract
This study investigated whether beta-muricholic acid, a natural trihydroxy hydrophilic bile acid of rodents, acts as a biliary cholesterol-desaturating agent to prevent cholesterol gallstones and if it facilitates the dissolution of gallstones compared with ursodeoxycholic acid (UDCA). For gallstone prevention study, gallstone-susceptible male C57L mice were fed 8 weeks with a lithogenic diet (2% cholesterol and 0.5% cholic acid) with or without 0.5% UDCA or beta-muricholic acid. For gallstone dissolution study, additional groups of mice that have formed gallstones were fed chow with or without 0.5% beta-muricholic acid or UDCA for 8 weeks. One hundred percent of mice fed the lithogenic diet formed cholesterol gallstones. Addition of beta-muricholic acid and UDCA decreased gallstone prevalence to 20% and 50% through significantly reducing biliary secretion rate, saturation index, and intestinal absorption of cholesterol, as well as inducing phase boundary shift and an enlarged Region E that prevented the transition of cholesterol from its liquid crystalline phase to solid crystals and stones. Eight weeks of beta-muricholic acid and UDCA administration produced complete gallstone dissolution rates of 100% and 60% compared with the chow (10%). We conclude that beta-muricholic acid is more effective than UDCA in treating or preventing diet-induced or experimental cholesterol gallstones in mice.
AuthorsDavid Q-H Wang, Susumu Tazuma
JournalJournal of lipid research (J Lipid Res) Vol. 43 Issue 11 Pg. 1960-8 (Nov 2002) ISSN: 0022-2275 [Print] United States
PMID12401895 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Bile Acids and Salts
  • Cholic Acids
  • muricholic acid
  • Cholesterol
Topics
  • Animals
  • Bile Acids and Salts (chemistry, metabolism)
  • Bile Ducts (physiopathology)
  • Cholelithiasis (metabolism, prevention & control)
  • Cholesterol (metabolism)
  • Cholic Acids (pharmacology)
  • Disease Models, Animal
  • Intestinal Absorption
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Particle Size

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