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PMID: 8498510 Published · ppublish English Comparative Study Journal Article

Protection against hydrophobic bile salt-induced cell membrane damage by liposomes and hydrophilic bile salts.

The American journal of physiology ·Vol. 264 ·No. 5 Pt 1 ·1993-05-00 ·Pages G835-9

Sagawa H, Tazuma S, Kajiyama G

Abstract

Under physiological circumstances, cell membrane damage is not evident in biliary systems, despite the fact that hydrophobic bile salts are known to induce such damage by their detergent effects. The aim of this study was to determine the cytoprotective effects of liposomes and hydrophilic bile salts against hydrophobic bile salt-induced cell membrane damage, with the use of hemolysis of erythrocytes as a model of cytotoxicity. Washed human erythrocytes were incubated for 10, 30, 60, 90, and 120 min in buffered media (pH 7.45) containing increasing concentrations of different bile salts (1, 2.5, 5, 25, 50 mM). The cytotoxicity of the bile salts was found to be dose and time dependent and was correlated to the degree of the hydrophobicity of the bile salts as determined by the retention factor in reversed-phase high-performance liquid chromatography. Hydrophobic bile salt-induced hemolysis was reduced by liposomes and hydrophilic bile salts. Cytoprotection by liposomes was related to the degree of saturation of the fatty acyl chains, and cytoprotection by hydrophilic bile salts was related to their hydrophilicity. These in vitro findings indicate that vesicles may play a role in protection against cell membrane damage by hydrophobic bile salts in biliary systems and that such damage may be caused by an imbalance between hydrophobic and hydrophilic bile salts.

MeSH Terms
Bile Acids and Salts/pharmacology,toxicity Cell Membrane/drug effects,ultrastructure Cell Survival/drug effects Chromatography, High Pressure Liquid Dose-Response Relationship, Drug Erythrocytes/cytology,drug effects Hemolysis/drug effects Humans Kinetics Liposomes/pharmacology Phosphatidylcholines/pharmacology Structure-Activity Relationship Time Factors
Chemicals
Bile Acids and Salts Liposomes Phosphatidylcholines
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Sagawa H
First Department of Internal Medicine, Hiroshima University School of Medicine, Japan.
Tazuma S
Kajiyama G
Article Info
Journal
The American journal of physiology
Abbr.
Am J Physiol
ISSN
0002-9513
Published
1993-05-00
Pages
G835-9
Language
English
Region
United States
NLM ID
0370511
Subset
IM
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