Lichtenberg D, Ragimova S, Bor A, Almog S, Vinkler C, Peled Y, Halpern Z
Department of Physiology and Pharmacology, Icholov Hospital, Tel-Aviv Medical Center, Israel.
Hepatology. 1990 Sep;12(3 Pt 2):149S-153S; discussion 153S-154S.
Complete solubilization of phosphatidylcholine and cholesterol by bile salts in the form of stable mixed micelles requires that the effective ratio of bile salt/lipids in the mixed micelles (Re = ([bile salt] - critical micellar concentration)/([phosphatidylcholine] + [cholesterol]) will exceed a critical value. This equilibrium solubilizing ratio is an increasing function of the cholesterol/phosphatidylcholine ratio. In contrast, the concentration of sodium cholate required for solubilization of vesicles made of phosphatidylcholine and cholesterol does not increase by increasing the cholesterol/phosphatidylcholine ratio. Consequently, the latter solubilization procedure yields metastable mixed micelles whenever the cholate concentration is higher than that required for vesicle solubilization but lower than that needed for establishing a micellar equilibrium. These metastable mixed micelles undergo partial revesiculation to form cholesterol-rich vesicles that subsequently aggregate. Cholesterol crystallization appears to occur through its reorganization within these aggregated vesicles. The overall rate of the above series of processes increases sharply with the total lipid concentration and with the cholesterol/phosphatidylcholine ratio. The dependence of the rate on the effective ratio of bile salts/lipids is very complex: at any given ratio of cholesterol/phosphatidylcholine within the range of 0.3 to 0.5, increasing the cholesterol/phosphatidylcholine ratio requires higher cholate concentrations for the formation of stable mixed micelles (higher equilibrium solubilizing ratio). On the other hand, the metastable mixed micellar larsystems are long-lived whenever the effective ratio of cholate/lipids is lower than a critical value.(ABSTRACT TRUNCATED AT 250 WORDS)
胆汁盐以稳定的混合微团形式使磷脂酰胆碱和胆固醇完全溶解,这要求混合微团中胆汁盐/脂质的有效比例(Re = ([胆汁盐] - 临界胶束浓度)/([磷脂酰胆碱] + [胆固醇]))超过一个临界值。这个平衡溶解比例是胆固醇/磷脂酰胆碱比例的增函数。相比之下,溶解由磷脂酰胆碱和胆固醇构成的囊泡所需的胆酸钠浓度不会因胆固醇/磷脂酰胆碱比例的增加而升高。因此,只要胆酸盐浓度高于囊泡溶解所需浓度但低于建立胶束平衡所需浓度,后一种溶解过程就会产生亚稳态混合微团。这些亚稳态混合微团会部分重新形成囊泡,形成富含胆固醇的囊泡,随后这些囊泡聚集。胆固醇结晶似乎是通过其在这些聚集囊泡内的重新组织而发生的。上述一系列过程的总体速率会随着总脂质浓度和胆固醇/磷脂酰胆碱比例的增加而急剧上升。速率对胆汁盐/脂质有效比例的依赖性非常复杂:在胆固醇/磷脂酰胆碱比例为0.3至0.5的任何给定范围内,增加胆固醇/磷脂酰胆碱比例需要更高的胆酸盐浓度来形成稳定的混合微团(更高的平衡溶解比例)。另一方面,只要胆酸盐/脂质的有效比例低于临界值,亚稳态混合微团系统就会长期存在。(摘要截选至250字)