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影响过饱和胆汁模型系统中胆固醇一水合物晶体成核时间的因素。

Factors affecting cholesterol monohydrate crystal nucleation time in model systems of supersaturated bile.

作者信息

Kibe A, Dudley M A, Halpern Z, Lynn M P, Breuer A C, Holzbach R T

出版信息

J Lipid Res. 1985 Sep;26(9):1102-11.

PMID:4067431
Abstract

We explored the influence of several compositional factors considered capable of influencing the nucleation time of model biles supersaturated in cholesterol. In addition to the classical techniques, e.g., electron microscopy and quasielastic light scattering, employed for size measurement and structural assessment, we employed a novel technique, i.e., video-enhanced microscopy, for particle evaluation in these polydisperse systems which often may simultaneously contain isolated small vesicles, their complex aggregates, and small cholesterol monohydrate crystals. The factors we studied included dilution, degree of cholesterol supersaturation, bile salt/lecithin molar ratio, and Ca2+ concentration. Dilution markedly raised the degree of cholesterol saturation, prolonged nucleation time for cholesterol monohydrate crystals, and favored formation of metastable small unilamellar vesicles. Increasing the degree of cholesterol supersaturation as an independent variable in more concentrated systems both shortened the nucleation time and favored spontaneous formation of a relatively small number of isolated vesicles. A decrease in bile salt/lecithin molar ratio within the physiologically relevant range was accompanied by a prolonged nucleation time and favored spontaneous vesicle formation. Large numbers of small unilamellar vesicles were observed even in concentrated model bile solutions (total lipids: 20 g/dl) when the bile salt/lecithin molar ratio was 1.9 or less. At physiological concentrations, Ca2+ promoted nucleation of cholesterol monohydrate crystals only in vesicle-containing solutions. Taken together, the following conclusions can be drawn. First, spontaneous vesicle formation in dilute systems prolongs solid cholesterol crystal nucleation. It can thus provide a supplementary non-micellar mode of cholesterol transport in micellar systems of supersaturated human bile. Second, dilution, degree of cholesterol supersaturation, and a decrease in bile salt/lecithin ratio prolong cholesterol crystal nucleation time and favor spontaneous vesicle formation. With increasing calcium concentrations, opposite effects are observed. Third, the presence of vesicles may help to account for the frequently observed and otherwise unexplained remarkable degree of metastable supersaturation and prolonged metastability (delayed nucleation time) for cholesterol in human bile.

摘要

我们探究了几种被认为能够影响胆固醇过饱和模型胆汁成核时间的成分因素的影响。除了用于尺寸测量和结构评估的经典技术,如电子显微镜和准弹性光散射外,我们还采用了一种新技术,即视频增强显微镜,用于在这些多分散系统中评估颗粒,这些系统通常可能同时包含孤立的小囊泡、它们的复杂聚集体以及小的胆固醇一水合物晶体。我们研究的因素包括稀释、胆固醇过饱和度、胆盐/卵磷脂摩尔比和Ca2+浓度。稀释显著提高了胆固醇饱和度,延长了胆固醇一水合物晶体的成核时间,并有利于亚稳小单层囊泡的形成。在更浓缩的系统中,将胆固醇过饱和度作为一个独立变量增加,既缩短了成核时间,又有利于自发形成相对少量的孤立囊泡。在生理相关范围内,胆盐/卵磷脂摩尔比的降低伴随着成核时间的延长,并有利于囊泡的自发形成。当胆盐/卵磷脂摩尔比为1.9或更低时,即使在浓缩的模型胆汁溶液(总脂质:20 g/dl)中也观察到大量的小单层囊泡。在生理浓度下,Ca2+仅在含囊泡的溶液中促进胆固醇一水合物晶体的成核。综上所述,可以得出以下结论。首先,稀释系统中的自发囊泡形成延长了固体胆固醇晶体的成核。因此,它可以在过饱和人胆汁的胶束系统中提供一种补充性的非胶束胆固醇转运模式。其次,稀释、胆固醇过饱和度以及胆盐/卵磷脂比例的降低延长了胆固醇晶体的成核时间,并有利于自发囊泡形成。随着钙浓度的增加,观察到相反的效果。第三,囊泡的存在可能有助于解释人胆汁中胆固醇经常观察到的、否则无法解释的显著亚稳过饱和度和延长的亚稳性(延迟成核时间)。

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