Kern F, Everson G T, DeMark B, McKinley C, Showalter R, Braverman D Z, Szczepanik-Van Leeuwen P, Klein P D
J Lab Clin Med. 1982 Jun;99(6):798-805.
Individuals who take contraceptive steroids or estrogens are at increased risk of developing cholesterol gallstones. The mechanisms of the increased stone formation are incompletely understood. In this study we report biliary lipid composition and secretion, bile acid composition and kinetics, and gallbladder function in a group of healthy, nonobese women taking a contraceptive steroid preparation. A comparable group of healthy women served as controls. Bile-rich duodenal fluid was obtained after stimulation of gallbladder contraction; bile acid, phospholipid, and cholesterol concentrations were determined. Biliary lipid secretion rate was measured by the marker perfusion technique. Bile acid distribution was determined by gas-liquid chromatography. The pool size, FTR, and synthesis rate of each bile acid were measured by using CA and CDCA labeled with the stable isotope of carbon, 13C. In some of the subjects gallbladder storage and emptying were measured during the kinetic study, by real-time ultrasonography. Contraceptive steroid use was associated with a significant increase in biliary cholesterol saturation and in the lithogenic index of bile. The rate of cholesterol secretion in the contraceptive steroid group was 50% greater than in the control (p much less than 0.001) and the rate of bile acid secretion was reduced (p less than 0.02). The total bile acid pool size was significantly increased by contraceptive steroids. The major increase occurred in the CA pool (p less than 0.04). The daily rate of enterohepatic cycles of the bile acid pool was decreased by contraceptive steroids from 6.6 to 4.3 (p less than 0.01). The only effect of contraceptive steroids on gallbladder function was a slower emptying rate in response to intraduodenal amino acid infusion. No index of gallbladder function correlated significantly with any parameter of bile acid kinetics in this small group of subjects. The findings confirm the lithogenic effect of contraceptive steroids and indicate that its causes are an increase in cholesterol secretion and a decrease in bile acid secretion.
服用避孕类固醇或雌激素的个体患胆固醇胆结石的风险会增加。结石形成增加的机制尚未完全明确。在本研究中,我们报告了一组服用避孕类固醇制剂的健康、非肥胖女性的胆汁脂质成分与分泌、胆汁酸成分与动力学以及胆囊功能。一组健康女性作为对照组。在刺激胆囊收缩后获取富含胆汁的十二指肠液;测定胆汁酸、磷脂和胆固醇浓度。通过标记灌注技术测量胆汁脂质分泌率。通过气液色谱法测定胆汁酸分布。使用标记有碳的稳定同位素(^{13}C)的胆酸(CA)和鹅去氧胆酸(CDCA)测量每种胆汁酸的池大小、肠肝循环率(FTR)和合成率。在一些受试者中,在动力学研究期间通过实时超声检查测量胆囊的储存和排空情况。使用避孕类固醇与胆汁胆固醇饱和度和胆汁成石指数显著增加有关。避孕类固醇组的胆固醇分泌率比对照组高50%((p\lt0.001)),胆汁酸分泌率降低((p\lt0.02))。避孕类固醇使总胆汁酸池大小显著增加。主要增加发生在胆酸池((p\lt0.04))。避孕类固醇使胆汁酸池的每日肠肝循环率从6.6降至4.3((p\lt0.01))。避孕类固醇对胆囊功能的唯一影响是对十二指肠内输注氨基酸的排空率减慢。在这一小群受试者中,没有胆囊功能指标与胆汁酸动力学的任何参数显著相关。这些发现证实了避孕类固醇的致石作用,并表明其原因是胆固醇分泌增加和胆汁酸分泌减少。