Cohen D E, Carey M C
Department of Medicine, Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Hepatology. 1990 Sep;12(3 Pt 2):143S-147S; discussion 147S-148S.
Present concepts suggest that the canalicular secretion of bile salts is monomeric, which in turn drives the hepatic secretion of lecithin and cholesterol presumably as unilamellar vesicles into bile. As biliary lipids are concentrated within the biliary tree and gallbladder, bile salts structurally alter lecithin-cholesterol vesicles to form a variety of metastable aggregates whose structures and phase transformations are predicted by phase equilibria considerations. These structural transformations ultimately result in the dispersion of biliary lipids as thermodynamically stable micelles or micelles plus thermodynamically unstable vesicles in common duct and gallbladder biles. The experiments reviewed herein represent experimental simulations of these processes. We used pure aqueous lipid systems to model the putative stages of biliary lipid aggregation on the basis of interactions of small unilamellar vesicles of lecithin-cholesterol with bile salts as the latter's concentrations were varied from below to well above the critical micellar concentration. With submicellar bile salt concentrations likely to be found within hepatocytes, vesicle structures are not appreciably altered. However, perimicellar bile salt concentrations possibly occurring in canaliculi and bile ductules induce the formation of a hexagonal rodlike phase. On further increases in bile salt concentration, the hexagonal rods (formed from lecithin-rich and cholesterol-poor vesicles) are dissolved into mixed micelles as bile salt concentrations exceed their critical micellar concentrations. In slightly cholesterol-"supersaturated" biles, the rapid dissolution of this intermediate phase results in the formation of cholesterol-supersaturated mixed micelles that, in time, give rise to a new population of cholesterol-rich vesicles that coexist with saturated micelles.(ABSTRACT TRUNCATED AT 250 WORDS)
目前的概念表明,胆盐的胆小管分泌是单体形式的,这反过来又促使卵磷脂和胆固醇大概以单层囊泡的形式分泌入胆汁。随着胆汁脂质在胆管树和胆囊中浓缩,胆盐在结构上改变卵磷脂 - 胆固醇囊泡,形成各种亚稳聚集体,其结构和相变可通过相平衡考虑来预测。这些结构转变最终导致胆汁脂质以热力学稳定的微团或微团加上热力学不稳定的囊泡形式分散在胆总管和胆囊胆汁中。本文综述的实验代表了这些过程的实验模拟。我们使用纯水性脂质系统,根据卵磷脂 - 胆固醇小单层囊泡与胆盐的相互作用,模拟胆汁脂质聚集的假定阶段,胆盐浓度从低于临界胶束浓度变化到远高于临界胶束浓度。在肝细胞内可能发现的亚胶束胆盐浓度下,囊泡结构没有明显改变。然而,在胆小管和胆小管中可能出现的近胶束胆盐浓度会诱导形成六方棒状相。随着胆盐浓度进一步增加,当胆盐浓度超过其临界胶束浓度时,由富含卵磷脂和贫胆固醇的囊泡形成的六方棒溶解为混合微团。在轻度胆固醇“过饱和”胆汁中,这个中间相的快速溶解导致形成胆固醇过饱和混合微团,随着时间的推移,会产生与饱和微团共存的新的富含胆固醇的囊泡群体。(摘要截短于250字)