Holzbach R T
Hepatology. 1984 Sep-Oct;4(5 Suppl):173S-176S. doi: 10.1002/hep.1840040833.
Dilution induces structural alterations (i.e., vesicle formation) in the lipid particles of supersaturated human hepatic bile and in dilute model bile systems of comparable composition. These alterations strikingly increase both the degree and duration of metastable supersaturation. Concentrated normal human gallbladder bile also shows an increased but less striking degree and duration of metastability compared to comparable model biles. These differences, particularly with respect to gallbladder bile, cannot be attributed solely to compositional or lipid structural differences between native and model systems. They imply that additional factors are responsible for metastability. Furthermore, recent data suggest that biliary proteins may be involved. A limited number of these unidentified proteins have been shown to have the capacity to prolong metastability in supersaturated in vitro model systems. Thus, these recombined systems more nearly resemble the behavior of native bile. The mechanism of the nucleation inhibitory effect of these proteins is not clearly established.
稀释会导致过饱和人肝胆汁的脂质颗粒以及成分相当的稀释模型胆汁系统中出现结构改变(即囊泡形成)。这些改变显著增加了亚稳过饱和度的程度和持续时间。与相当的模型胆汁相比,浓缩的正常人胆囊胆汁也显示出亚稳性增加,但程度和持续时间不那么显著。这些差异,特别是关于胆囊胆汁的差异,不能仅仅归因于天然系统和模型系统之间的成分或脂质结构差异。这意味着还有其他因素导致亚稳性。此外,最近的数据表明胆汁蛋白可能参与其中。已表明少数这些未鉴定的蛋白质能够在过饱和体外模型系统中延长亚稳性。因此,这些重组系统更接近天然胆汁的行为。这些蛋白质的成核抑制作用机制尚未明确确立。