van de Heijning B J, Stolk M F, van Erpecum K J, Renooij W, van Berge Henegouwen G P
Department of Gastroenterology, Utrecht University Hospital, The Netherlands.
Biochim Biophys Acta. 1994 May 13;1212(2):203-10. doi: 10.1016/0005-2760(94)90254-2.
The addition of bile salts to vesicles supersaturated with cholesterol induces cholesterol precipitation, an important step in the formation of cholesterol gallstones. To investigate the effects of bile salt hydrophobicity on vesicle morphology, vesicles obtained from supersaturated model bile by density gradient ultracentrifugation, were incubated with mixtures of deoxycholate (DC) and ursodeoxycholate (UDC) with a constant total bile salt concentration of 30 mM but with a varying hydrophobicity index ranging from -0.31 (UDC alone) up to +0.72 (DC alone) depending on the composition of the mixture. Five days after addition of bile salts to vesicles, cholesterol precipitation was determined microscopically and incubation samples were again subjected to ultracentrifugation to assess the lipid distribution among residual vesicles, mixed micelles, and cholesterol crystals. Structure and size of the isolated residual vesicles were studied by freeze fracture electron microscopy. The control, and samples exposed to hydrophilic bile salt mixtures, consisted of unilamellar vesicles of which more than 75% had a diameter of 50-80 nm. After addition of increasingly hydrophobic bile salt mixtures, multilamellar vesicles with progressively greater diameters (up to 1300 nm) were found, suggesting that vesicle fusion and aggregation took place and might hence be important in the cholesterol precipitation process. Accordingly, crystallization was positively correlated with bile salt hydrophobicity. We conclude that cholesterol crystallization from vesicles depends on the hydrophobicity of the bile salts added, and apparently occurs from fused or aggregated vesicles of extended magnitude and with a multilamellar constitution.
向胆固醇过饱和的囊泡中添加胆汁盐会诱导胆固醇沉淀,这是胆固醇胆结石形成过程中的一个重要步骤。为了研究胆汁盐疏水性对囊泡形态的影响,通过密度梯度超速离心从过饱和模型胆汁中获得的囊泡,与脱氧胆酸盐(DC)和熊去氧胆酸盐(UDC)的混合物一起孵育,总胆汁盐浓度恒定为30 mM,但根据混合物的组成,疏水性指数范围从-0.31(仅UDC)到+0.72(仅DC)。向囊泡中添加胆汁盐五天后,通过显微镜测定胆固醇沉淀,并将孵育样品再次进行超速离心,以评估脂质在残留囊泡、混合微团和胆固醇晶体之间的分布。通过冷冻断裂电子显微镜研究分离出的残留囊泡的结构和大小。对照组以及暴露于亲水性胆汁盐混合物的样品由单层囊泡组成,其中超过75%的囊泡直径为50-80 nm。添加疏水性越来越强的胆汁盐混合物后,发现了直径逐渐增大(高达1300 nm)的多层囊泡,这表明囊泡发生了融合和聚集,因此可能在胆固醇沉淀过程中起重要作用。相应地,结晶与胆汁盐疏水性呈正相关。我们得出结论,囊泡中的胆固醇结晶取决于添加的胆汁盐的疏水性,并且显然发生在大小扩展且具有多层结构的融合或聚集囊泡中。