Singhal A K, Cohen B I, Mosbach E H, Une M, Stenger R J, McSherry C K, May-Donath P, Palaia T
J Lipid Res. 1984 Jun;25(6):539-49.
Prairie dogs of both sexes were fed a semisynthetic diet containing 0.35% cholesterol for a period of 8 weeks. This lithogenic diet induced cholesterol gallstones in ten "lithogenic control animals", five males and five females. Three animals maintained with a high glucose, fat-free diet did not develop gallstones although the cholesterol saturation of their bile approached unity. The formation of gallstones was prevented in four out of five males and all five females fed the lithogenic diet plus 0.1% hyodeoxycholic acid (30 mg per kg body weight per day). The biles of the prairie dogs receiving hyodeoxycholic acid were abnormally colored, cloudy, and highly saturated with cholesterol but contained neither cholesterol crystals nor gallstones (with the exception of one male). Feeding the relatively hydrophilic bile acid, hyodeoxycholic acid, was associated with an increase in hepatic microsomal HMG-CoA reductase activity. Cholesterol 7 alpha-hydroxylase, on the other hand, was inhibited by the administered bile acid. The dietary hyodeoxycholic acid was transformed, in part, to 3 alpha, 6 beta-dihydroxy-5-beta-cholanoic acid and hyocholic acid. It is concluded that hyodeoxycholic acid and its metabolites did not prevent the induced cholelithiasis by causing a decrease in the concentration of biliary cholesterol. Instead, this hydrophilic bile acid apparently increases the amount of cholesterol in the bile, probably in the form of a liquid crystalline mesophase. Hyodeoxycholic acid apparently prevents gallstones by preventing the nucleation and aggregation of cholesterol crystals. The lithogenic diet induced moderate to marked bile duct proliferation together with portal fibrosis and inflammatory infiltration. The addition of hyodeoxycholic acid to the lithogenic diet reduced all of the portal tract changes.
给雌雄草原犬鼠喂食含0.35%胆固醇的半合成饲料,持续8周。这种致石性饲料在10只“致石对照动物”(5只雄性和5只雌性)中诱发了胆固醇性胆结石。3只维持高糖、无脂饮食的动物未形成胆结石,尽管它们胆汁的胆固醇饱和度接近1。在喂食致石性饲料加0.1%猪去氧胆酸(每天每千克体重30毫克)的5只雄性动物中的4只以及所有5只雌性动物中,胆结石的形成得到了预防。接受猪去氧胆酸的草原犬鼠的胆汁颜色异常、浑浊,胆固醇高度饱和,但除一只雄性外均未含胆固醇晶体或胆结石。喂食相对亲水性胆汁酸猪去氧胆酸与肝微粒体HMG - CoA还原酶活性增加有关。另一方面,胆固醇7α - 羟化酶受到所给予胆汁酸的抑制。膳食中的猪去氧胆酸部分转化为3α, 6β - 二羟基 - 5 - β - 胆烷酸和猪胆酸。结论是,猪去氧胆酸及其代谢产物并非通过降低胆汁胆固醇浓度来预防诱发的胆石症。相反,这种亲水性胆汁酸显然增加了胆汁中胆固醇的量,可能是以液晶中间相的形式。猪去氧胆酸显然是通过防止胆固醇晶体的成核和聚集来预防胆结石的。致石性饲料诱发了中度至明显的胆管增生以及门静脉纤维化和炎症浸润。在致石性饲料中添加猪去氧胆酸减少了所有门静脉区域的变化。