DECREASED BILIARY GLUTATHIONE CONTENT IS RESPONSIBLE FOR THE DECLINE IN BILE SALT-INDEPENDENT FLOW-INDUCED BY ETHINYL ESTRADIOL IN RATS

Citation
G. Bouchard et al., DECREASED BILIARY GLUTATHIONE CONTENT IS RESPONSIBLE FOR THE DECLINE IN BILE SALT-INDEPENDENT FLOW-INDUCED BY ETHINYL ESTRADIOL IN RATS, Toxicology letters, 74(3), 1994, pp. 221-233
Citations number
35
Categorie Soggetti
Toxicology
Journal title
ISSN journal
03784274
Volume
74
Issue
3
Year of publication
1994
Pages
221 - 233
Database
ISI
SICI code
0378-4274(1994)74:3<221:DBGCIR>2.0.ZU;2-#
Abstract
Glutathione appears to be a major osmotic factor in the generation of bile salt-independent flow (BSIF), This study was designed to investig ate its importance in the pathology of 17-alpha-ethinyl estradiol (EE) -induced cholestasis. Five-day EE treatment at the dose level of 5 mg/ kg/day significantly decreased bile flow (57% of controls) and biliary glutathione secretion. Evaluation of the contribution of bile salt de pendent flow (BSDF), glutathione dependent flow (GSDF) and the bile fl ow generated independently of both bile salts and glutathione (BS-GSIF ) revealed that EE decreased all portions of the flow (63, 44 and 52% of control values, respectively). At 4 and 20 h after a single adminis tration of the same EE dose, a significant diminution of bile flow was noted (decreases of 17 and 29%, respectively) in association with a s ignificant fall in biliary glutathione content. Under these conditions , BSDF and BS-GSIF were not modified (98 and 112% of control BSDF valu es, respectively; 96 and 99% of control BS-GSIF values, respectively) while GSDF was decreased markedly, representing 65 and 50% of control values. Biliary glutathione secretion was diminished without modificat ion of liver and blood glutathione concentration or redox status follo wing single EE dose whereas, after 5 days of EE treatment, a significa nt increase in liver glutathione was observed, suggesting that EE may interfere with the glutathione secretory process. This study demonstra tes that EE rapidly alters biliary glutathione content, leading to a m arked decline in GSDF. This reduction may explain the decrease in BSIF produced by EE at the outset of cholestasis.