Holzbach R T, Kibe A, Thiel E, Howell J H, Marsh M, Hermann R E
J Clin Invest. 1984 Jan;73(1):35-45. doi: 10.1172/JCI111204.
The onset time for cholesterol crystal nucleation of supersaturated normal human gallbladder biles is consistently prolonged when compared with biles from patients with cholesterol gallstone disease. Investigation of the factor(s) responsible for the suspended supersaturation (metastability) of normal human biles revealed that model bile solutions of cholesterol saturation index (CSI) and molar lipid composition identical to individual gallbladder bile specimens had much shorter crystal nucleation times, i.e., exhibited decreased metastability. Unsaturated normal biles, after supplementation with lecithin, cholesterol, and sodium taurocholate to a 'standard' supersaturated lipid composition, also demonstrated nucleation times three- to 15-fold longer than the comparable standard model bile. Total lipid extracts of normal biles, however, when similarly supplemented, did not differ in nucleation time from the control model solution. Gallbladder biles were fractionated by gel chromatography and the eluted fractions were pooled into two fractions. The fractions eluting in about the first 25% of the included volume when mixed with the supersaturated standard model bile induced a modest increase in nucleation time of approximately 1.5 times the control value. The fractions eluting in the second 25% of the included volume and which contained all of the bile lipids, were concentrated and supplemented with lipids to the standard composition. The nucleation times of these supplements were 3-10 times longer than the control nucleation times. Delipidated bile protein mixtures, purified by discontinuous sucrose gradient centrifugation, were recombined with purified lipids at the standard composition used previously. The nucleation times of these mixtures were significantly prolonged to the same extent as those associated with the second chromatographic fraction. These observations demonstrate that the delayed onset (inhibition) of cholesterol crystal nucleation observed in normal human gallbladder bile is produced by a factor(s) present in the biliary protein fraction.
与胆固醇结石病患者的胆汁相比,正常人胆囊过饱和胆汁中胆固醇晶体成核的起始时间持续延长。对导致正常人胆汁中过饱和状态(亚稳性)得以维持的因素进行研究后发现,胆固醇饱和指数(CSI)和摩尔脂质组成与个体胆囊胆汁标本相同的模型胆汁溶液,其晶体成核时间要短得多,即表现出亚稳性降低。不饱和的正常人胆汁在补充卵磷脂、胆固醇和牛磺胆酸钠至“标准”过饱和脂质组成后,其成核时间也比相应的标准模型胆汁长3至15倍。然而,正常人胆汁的总脂质提取物在进行类似补充后,其成核时间与对照模型溶液并无差异。通过凝胶色谱法对胆囊胆汁进行分离,并将洗脱组分合并为两个部分。当与过饱和标准模型胆汁混合时,在约第一个25%的包含体积内洗脱的组分使成核时间适度增加,约为对照值的1.5倍。在第二个25%的包含体积内洗脱且含有所有胆汁脂质的组分被浓缩,并补充脂质至标准组成。这些补充物的成核时间比对照成核时间长3至10倍。通过不连续蔗糖梯度离心纯化的脱脂胆汁蛋白混合物,与先前使用的标准组成的纯化脂质重新组合。这些混合物的成核时间显著延长至与第二个色谱组分相同的程度。这些观察结果表明,正常人胆囊胆汁中观察到的胆固醇晶体成核延迟(抑制)是由胆汁蛋白组分中存在的一种或多种因素引起的。