β-Muricholic acid; potentiometric and cholesterol-dissolving properties

Some physicochemical properties of β-niuricholic acid (3α,6β,7β-trihydroxyβ-cholanic acid), a major bile acid biosynthesized by rat liver, were determined and compared to those of ursodeoxycholic and chenodeoxycholic acids. From potentiometric studies, the following characteristics of β-muricholic a...

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Published inBiochimica et biophysica acta Vol. 918; no. 1; pp. 1 - 10
Main Authors Montet, Jean-Claude, Parquet, Michel, Sacquet, Edmond, Montet, Anne-Marie, Infante, Recaredo, Amic, Jean
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 13.03.1987
Elsevier
North-Holland
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Summary:Some physicochemical properties of β-niuricholic acid (3α,6β,7β-trihydroxyβ-cholanic acid), a major bile acid biosynthesized by rat liver, were determined and compared to those of ursodeoxycholic and chenodeoxycholic acids. From potentiometric studies, the following characteristics of β-muricholic acid were shown: a low monomer solubility (13 μM), a high equilibrium precipitation pH (7.92 for 30 mM solution), an apparent critical micellar concentration of 4 mM, and a very low micellar capacity of the bile salt to dissolve the protonated bile acid. Sodium β-muricholate solution (30 mM) poorly solubilized cholesterol, as indicated by a bile salt/cholesterol molar ratio of 1430, whereas saturation ratios obtained with chenodeoxycholate and ursoseoxycholate were 24 and 384, respectively. Sodium β-muricholate (30 mM)/phosphatidylcholine/cholesterol mixtures contained non-micellar aggregates from very low cholesterol concentrations. At physiological phosphatidylcholine concentrations, sodium β-muricholate (100 mM) dissolved cholesterol crystals via essentially lamellar liquid-crystal formation. These solubilizing properties might have important physiological relevance to the dissolution of cholesterol gallstones in man.
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ISSN:0005-2760
0006-3002
1879-145X
1878-2434
DOI:10.1016/0005-2760(87)90002-6