Sauter Gerd H, Thiessen Kai, Parhofer Klaus G, Jüngst Christoph, Fischer Sven, Jüngst Dieter
Department of Medicine II, Klinikum Grosshadern, Ludwig Maximilians University, Munich, Germany.
Digestion. 2004;70(2):79-83. doi: 10.1159/000080925. Epub 2004 Sep 16.
BACKGROUND/AIMS: Ursodeoxycholic acid (UDCA) decreases biliary secretion of cholesterol and is therefore used for the dissolution of cholesterol gallstones. It remains unclear whether these changes in biliary cholesterol excretion are associated with changes in cholesterol synthesis and bile acid synthesis. We therefore studied the activities of rate-limiting enzymes of cholesterol synthesis and bile acid synthesis, 3-hydroxy-3-methylglutaryl-coenzyme A reductase and cholesterol 7alpha-hydroxylase, respectively, in normal subjects during UDCA feeding.
UDCA was given to 8 healthy volunteers (5 men, 3 women; age 24-44 years) in a single dose of 10-15 mg/kg body weight for 40 days. Before and during (days 3, 5, 10, 20, 30 and 40) UDCA treatment, urinary excretion of mevalonic acid and serum concentrations of 7alpha-hydroxy-4-cholesten-3-one (7alpha-HCO) were determined as markers of cholesterol and bile acid synthesis, respectively. The Wilcoxon signed rank test and Spearman's rank correlation coefficient were used for statistical analysis.
Cholesterol synthesis and serum lipid concentrations remained unchanged during UDCA treatment for 40 days. However, synthesis of bile acids increased during long-term treatment with UDCA as reflected by an increase in 7alpha-HCO serum concentrations from 39.7 +/- 21.3 ng/ml (median 32.8 ng/ml) before treatment to 64.0 +/- 30.4 ng/ml (median 77.5 ng/ml) at days 30-40 of UDCA treatment (p < 0.05).
UDCA treatment does not affect cholesterol synthesis in the liver, but does increase bile acid synthesis after prolonged treatment. This may represent a compensatory change following decreased absorption of endogenous bile acids as observed with UDCA therapy.
背景/目的:熊去氧胆酸(UDCA)可减少胆固醇的胆汁分泌,因此用于溶解胆固醇性胆结石。目前尚不清楚胆汁胆固醇排泄的这些变化是否与胆固醇合成和胆汁酸合成的变化有关。因此,我们研究了正常受试者在服用UDCA期间胆固醇合成和胆汁酸合成的限速酶,即3-羟基-3-甲基戊二酰辅酶A还原酶和胆固醇7α-羟化酶的活性。
8名健康志愿者(5名男性,3名女性;年龄24 - 44岁)接受UDCA,单剂量为10 - 15 mg/kg体重,持续40天。在UDCA治疗前及治疗期间(第3、5、10、20、30和40天),分别测定甲羟戊酸的尿排泄量和7α-羟基-4-胆甾烯-3-酮(7α-HCO)的血清浓度,作为胆固醇和胆汁酸合成的标志物。采用Wilcoxon符号秩检验和Spearman秩相关系数进行统计分析。
在UDCA治疗40天期间,胆固醇合成和血脂浓度保持不变。然而,长期使用UDCA治疗期间胆汁酸合成增加,这表现为UDCA治疗第30 - 40天时7α-HCO血清浓度从治疗前的39.7±21.3 ng/ml(中位数32.8 ng/ml)增加到64.0±30.4 ng/ml(中位数77.5 ng/ml)(p < 0.05)。
UDCA治疗不影响肝脏中的胆固醇合成,但长期治疗后会增加胆汁酸合成。这可能是UDCA治疗中观察到内源性胆汁酸吸收减少后的一种代偿性变化。