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载脂蛋白在过饱和模型胆汁中对胆固醇晶体形成的抑制作用。

Inhibition of cholesterol crystal formation by apolipoproteins in supersaturated model bile.

作者信息

Kibe A, Holzbach R T, LaRusso N F, Mao S J

出版信息

Science. 1984 Aug 3;225(4661):514-6. doi: 10.1126/science.6429856.

Abstract

Apolipoproteins A-1 and A-2 were purified from human plasma. At concentrations present in human bile these proteins prolonged the nucleation time of cholesterol monohydrate crystals when added to model systems of supersaturated bile. In contrast, apolipoprotein C-3 and other serum proteins did not have this effect. Also, when human gallbladder bile was fractionated by gel filtration chromatography, apolipoproteins A-1 and A-2 were among the proteins present in a fraction of bile enriched in potent inhibitors of cholesterol crystal nucleation. These findings suggest that apolipoproteins A-1 and A-2 in supersaturated human gallbladder bile could inhibit the rate of formation of solid cholesterol crystals and thus help to prevent spontaneous cholesterol gallstone formation in humans.

摘要

载脂蛋白A-1和A-2从人血浆中纯化得到。当添加到过饱和胆汁的模型系统中时,在人胆汁中存在的浓度下,这些蛋白质延长了一水合胆固醇晶体的成核时间。相比之下,载脂蛋白C-3和其他血清蛋白没有这种作用。此外,当用人胆囊胆汁进行凝胶过滤层析分离时,载脂蛋白A-1和A-2存在于富含胆固醇晶体成核强效抑制剂的胆汁组分中。这些发现表明,过饱和人胆囊胆汁中的载脂蛋白A-1和A-2可以抑制固体胆固醇晶体的形成速率,从而有助于预防人类自发性胆固醇胆结石的形成。

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