Wang Helen H, Portincasa Piero, Liu Min, Tso Patrick, Samuelson Linda C, Wang David Q-H
Department of Medicine, Liver Center and Gastroenterology Division, Beth Israel Deaconess Medical Center, Harvard Medical School and Harvard Digestive Diseases Center, Boston, MA, USA.
Biochim Biophys Acta. 2010 Feb;1801(2):138-46. doi: 10.1016/j.bbalip.2009.10.003. Epub 2009 Oct 22.
We investigated the effect of gallbladder hypomotility on cholesterol crystallization and growth during the early stage of gallstone formation in CCK knockout mice. Contrary to wild-type mice, fasting gallbladder volumes were enlarged and the response of gallbladder emptying to a high-fat meal was impaired in knockout mice on chow or the lithogenic diet. In the lithogenic state, large amounts of mucin gel and liquid crystals as well as arc-like and tubular crystals formed first, followed by rapid formation of classic parallelogram-shaped cholesterol monohydrate crystals in knockout mice. Furthermore, three patterns of crystal growth habits were observed: proportional enlargement, spiral dislocation growth, and twin crystal growth, all enlarging solid cholesterol crystals. At day 15 on the lithogenic diet, 75% of knockout mice formed gallstones. However, wild-type mice formed very little mucin gel, liquid, and solid crystals, and gallstones were not observed. We conclude that lack of CCK induces gallbladder hypomotility that prolongs the residence time of excess cholesterol in the gallbladder, leading to rapid crystallization and precipitation of solid cholesterol crystals. Moreover, during the early stage of gallstone formation, there are two pathways of liquid and polymorph anhydrous crystals evolving to monohydrate crystals and three modes for cholesterol crystal growth.
我们研究了胆囊运动功能减退对CCK基因敲除小鼠胆结石形成早期胆固醇结晶和生长的影响。与野生型小鼠相反,在给予普通饲料或致石性饲料的基因敲除小鼠中,空腹胆囊体积增大,且胆囊对高脂餐的排空反应受损。在致石状态下,基因敲除小鼠首先形成大量粘蛋白凝胶和液晶以及弧形和管状晶体,随后迅速形成经典的平行四边形单水合胆固醇晶体。此外,观察到三种晶体生长习性模式:比例增大、螺旋位错生长和孪晶生长,所有这些都使固态胆固醇晶体增大。在给予致石性饲料第15天时,75%的基因敲除小鼠形成了胆结石。然而,野生型小鼠形成的粘蛋白凝胶、液体和固态晶体很少,未观察到胆结石。我们得出结论,CCK的缺乏会导致胆囊运动功能减退,从而延长过量胆固醇在胆囊中的停留时间,导致固态胆固醇晶体迅速结晶和沉淀。此外,在胆结石形成的早期阶段,存在液体和多晶型无水晶体演变为单水合晶体的两条途径以及胆固醇晶体生长的三种模式。