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Short-term effects of simvastatin on bile acid synthesis and bile lipid secretion in human subjects

โœ Scribed by Paola Loria; Marco Bertolotti; M. Teresa Cassinadri; Michele A. Dilengite; Mara Bozzoli; Francesca Carubbi; Mauro Concari; M. Eugenia Guicciardi; Nicola Carulli


Publisher
John Wiley and Sons
Year
1994
Tongue
English
Weight
778 KB
Volume
19
Category
Article
ISSN
0270-9139

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โœฆ Synopsis


To test whether de nouo synthesis of cholesterol is a limiting factor for bile acid synthesis, we studied the acute effect of simvastatin, an inhibitor of HMGcoenzyme A reductase (the limiting step of cholesterol synthesis) on bile acid synthesis and biliary lipid secretion in subjects with interrupted enterohepatic circulation. In these conditions bile acid synthesis is derepressed and is assumed to equal biliary bile acid secretion. Five cholecystectomized patients fitted with T-tubes were studied. All subjects were administered simvastatin (80 mg as a single dose) 5 days after surgery. Bile was collected in 3-hr intervals for 15 hr before and 30 hr after the administration of the drug. During the experiment we kept the enterohepatic circulation of bile acid interrupted by Mating an occludable balloon inserted, during cholecystectomy, in the common bile duct. Simvastatin induced significant decreases of plasma total and low density lipoprotein cholesterol concentrations, from 163 2 29 mg/dl and 97 f 24 mg/d of the pretreatment value to 144 f 30 mg/d and 82 f 22 mg/dl 18 hr after simvastatin administration, respectively. Bile flow tended to increase after simvastatin, and the mean values from the third to the 15th hour after simvastatin administration (22.1 2 1.9 ml/hr) were significantly greater than the mean values of the pretreatment period (19.9 f 2.8 ml/hr). Concomitantly biliary bile acid, cholesterol and phospholipid concentrations fell from basal values of 15.9 f 5.1, 2.3 f 0.3 and 5.5 f 0.3 mmoUL to mean values, after treatment, of 9.0 f 3.5, 1.9 f 0.5 and 3.0 f 0.9 mmoUL, respectively. Cholesterol saturation index increased from a mean value of 1.51 f 0.31 in the pretreatment period to 1.98 f 0.52 after simvastatin. Bile acid output decreased from a mean pretreatment value of 308.0 f 79.1 pmol/hr to 191.9 f 69.2 pmol/hr after simvastatin administration. Secretion rates of phospholipids decreased to a lesser extent, whereas cholesterol output remained constant.


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