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Biliary excretory function is regulated by canalicular membrane fluidity associated with phospholipid fatty acyl chains in the bilayer: Implications for the pathophysiology of cholestasis
Author(s) -
Hyogo Hideyuki,
Tazuma Susumu,
Kajiyama Goro
Publication year - 2000
Publication title -
journal of gastroenterology and hepatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.214
H-Index - 130
eISSN - 1440-1746
pISSN - 0815-9319
DOI - 10.1046/j.1440-1746.2000.02221.x
Subject(s) - phospholipid , sphingomyelin , phosphatidylcholine , membrane fluidity , cholestasis , phosphatidylethanolamine , phalloidin , biochemistry , cholesterol , medicine , endocrinology , chemistry , biology , membrane , cytoskeleton , cell
Background and Aims: Bile canalicular membrane fluidity is modulated by phospholipid molecular species within membrane lipid bilayers. Thus, organellar membrane lipid composition is a determinant of canalicular function. In this study, the effect of phalloidin‐induced cholestasis on bile lipid composition and liver subcellular membrane fraction composition in rats was examined to clarify the relationship between cholestasis and hepatic lipid metabolism.Methods and Results: Each rat received one phalloidin dose (400 μg/kg, i.v.). After the bile was collected, liver microsomes and canalicular membranes were analysed. The bile flow rate decreased by 50% 3.5 h after phalloidin administration. Although the bile acid output remained almost the same, the phospholipid and cholesterol output were significantly decreased (by 40.3 ± 5.97% and 76.9 ± 5.56%, respectively). Thus, the cholesterol : phospholipid (C : P) ratio in bile was significantly decreased by 80.4 ± 10.1%. Phalloidin administration also increased the saturated : unsaturated fatty acid ratio (S : U) in bile for phosphatidylcholine by 25.5 ± 3.2%. In the canalicular membrane, the C : P and S : U ratios for phosphatidylcholine were increased (24.8 ± 4.2% and 34.4 ± 6.9%, respectively), while the S : U for sphingomyelin was decreased by 61.0 ± 6.2%. In microsomes, the C : P was decreased by 41.0 ± 6.0%, but the S : U for both phosphatidylcholine and sphingomyelin were unaffected. Canalicular membrane fluidity, assayed by 1,6‐diphenyl‐1,3,5‐hexatriene fluorescence depolarization, decreased significantly. Therefore, increased secretion of hydrophobic phosphatidylcholine into bile was associated with more hydrophobic canalicular membrane phosphatidylcholine, while sphingomyelin in the canalicular membrane was less hydrophobic.Conclusions: These results indicate that phalloidin uncouples secretion of cholesterol and phospholipids, which causes a redistribution of fatty acyl chain species among canalicular membrane phospholipids that alters membrane fluidity. These changes may be a homeostatic response mediated by the phospholipid translocator in the canalicular membrane, although direct evidence for this is unavailable.