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Journal of Lipid Research, Vol 37, 562-573, Copyright © 1996 by Lipid Research, Inc.
DM Heuman, RS Bajaj and Q Lin
Tauroursodeoxycholate (TUDC), a relatively hydrophilic bile salt, reduces
disruption of cholesterol-rich membranes by more hydrophobic bile salts
such as taurocholate (TC), taurochenodeoxycholate (TCDC), or
taurodeoxycholate (TDC). We examined the interactions of these bile salts
in adsorption to large unilamellar vesicles to determine whether TUDC may
stabilize membranes by preventing adsorption of more toxic bile salts.
Fractional adsorption was quantified by rapid ultrafiltration. Adsorption
coefficient Ai was defined for each bile salt i as ([bound i]/[free
i])/[lecithin]. Affinity of different bile salts for lecithin vesicles
varied with their relative hydrophobicity, increasing in the order TUDC
< TC << TCDC < or = TDC. Ai of each bile salt fell with its
accumulation on membranes, reaching a minimum at bound bile salt/lecithin
mole ratio (B:L) between 0.05 and 0.1, then increasing with formation of
higher-affinity mixed micelles. Inclusion of cholesterol in vesicles
reduced Ai of all bile salts. In heterologous binding studies at
submicellar concentrations, Ai of each bile salt varied with total B:L but
was independent of the specific bile salts present on the membrane.
Addition of TUDC to TDC reduced binding of TDC to membranes only slightly
and lowered the threshold TDC concentration associated with transition to
mixed micelles. However, above this threshold, TUDC markedly altered the
adsorption of TDC to lecithin-containing phases. We conclude that TUDC does
not directly stabilize membranes; rather, reduced permeabilization and
dissolution of cholesterol-rich membranes after addition of TUDC to TDC may
result from effects on the formation and structure of simple and mixed
micelles.
ARTICLES
Adsorption of mixtures of bile salt taurine conjugates to lecithin- cholesterol membranes: implications for bile salt toxicity and cytoprotection
Medical College of Virginia, Richmond, USA.
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