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Bile salt secretion by hepatocytes incubated with bile salts and liposomes or low density lipoproteins

Identifieur interne : 000146 ( France/Analysis ); précédent : 000145; suivant : 000147

Bile salt secretion by hepatocytes incubated with bile salts and liposomes or low density lipoproteins

Auteurs : Thierry Clerc [France] ; Véronique Sbarra [France] ; Danielle Botta-Fridlund [France] ; Huguette Lafont [France] ; Paul Pak-Leung [France] ; André Gauthier [France] ; Françoise Chanussot [France]

Source :

RBID : ISTEX:6C66E86C059AE59B58614075FF71E52F33316114

Abstract

The purpose of this work was to determine the effect of exogenous unesterified cholesterol provided in either artificial liposomes or LDL on bile salt synthesis by isolated rat hepatocytes. Rates of de novo synthesis were determined in the presence of 300 or 600 μM taurocholate, 600 μM taurodehydrocholate, cholate, deoxycholate or chenodeoxycholate. There was no significant difference between the cholesterol uptake by hepatocytes when the degree of hydrophobicity of the bile salts changed (cholate vs deoxycholate or chenodeoxycholate). Compared to taurocholate, taurodehydrocholate lowered the hepatic incorporation of unesterified cholesterol for the first 60 minutes; compared to control, taurocholate stimulated the cholesterol incorporation for the first 20 minutes. A possible explanation for this finding would be an interaction between bile salts and exogenous cholesterol, depending on the kind of conjugated bile salt. Taurocholate increased the exchange of cholesterol between liposomes or LDL and hepatocyte membranes. It resulted in a significant increase of bile salt synthesis and secretion. This phenomenon was not observed with taurodehydrocholate.

Url:
DOI: 10.1016/0024-3205(94)00922-8


Affiliations:


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ISTEX:6C66E86C059AE59B58614075FF71E52F33316114

Le document en format XML

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<div type="abstract" xml:lang="en">The purpose of this work was to determine the effect of exogenous unesterified cholesterol provided in either artificial liposomes or LDL on bile salt synthesis by isolated rat hepatocytes. Rates of de novo synthesis were determined in the presence of 300 or 600 μM taurocholate, 600 μM taurodehydrocholate, cholate, deoxycholate or chenodeoxycholate. There was no significant difference between the cholesterol uptake by hepatocytes when the degree of hydrophobicity of the bile salts changed (cholate vs deoxycholate or chenodeoxycholate). Compared to taurocholate, taurodehydrocholate lowered the hepatic incorporation of unesterified cholesterol for the first 60 minutes; compared to control, taurocholate stimulated the cholesterol incorporation for the first 20 minutes. A possible explanation for this finding would be an interaction between bile salts and exogenous cholesterol, depending on the kind of conjugated bile salt. Taurocholate increased the exchange of cholesterol between liposomes or LDL and hepatocyte membranes. It resulted in a significant increase of bile salt synthesis and secretion. This phenomenon was not observed with taurodehydrocholate.</div>
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