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鹅去氧胆酸和熊去氧胆酸对草原犬鼠脂质代谢及胆结石形成的影响

Effects of chenodeoxycholic and ursodeoxycholic acids on lipid metabolism and gallstone formation in the prairie dog.

作者信息

Cohen B I, Singhal A K, Stenger R J, May-Donath P, Finver-Sadowsky J, McSherry C K, Mosbach E H

出版信息

Hepatology. 1984 Mar-Apr;4(2):300-7. doi: 10.1002/hep.1840040221.

Abstract

The prevention of cholesterol cholelithiasis by dietary chenodeoxycholic and ursodeoxycholic acids was studied in the male prairie dog (Cynomys ludovicianus). Gallstones were induced by administration of a semisynthetic diet containing 0.4% cholesterol for a period of 8 weeks. Groups of 5 or 6 animals received the lithogenic diet with added chenodeoxycholic or ursodeoxycholic acid (0.03% "low dose" or 0.06% "high dose"). Under the conditions used, the incidence of gallstones was reduced with the high dose of chenodeoxycholic acid and the low dose of ursodeoxycholic acid, but cholesterol crystals were detected in the biles of 20 of the 22 animals fed these bile acids. A control group maintained on a low (0.08%) cholesterol semisynthetic diet exhibited neither crystals nor stones and was the only group with a lithogenic index below 1.0. The administered bile acids tended to reduce the accumulation of cholesterol in liver and plasma. The activity of hepatic HMG-CoA reductase was significantly inhibited with all cholesterol-supplemented diets. Cholesterol 7 alpha-hydroxylase activity was elevated 83% in prairie dogs fed 0.4% cholesterol, but tended to return to normal levels when bile acids were added to this diet. Histologically, the livers of all animals on the semisynthetic (cholesterol-supplemented) diet exhibited bile duct proliferation, as well as portal fibrosis and inflammatory infiltration. These morphologic alterations were ameliorated by low dose supplementation with either chenodeoxycholic or ursodeoxycholic acid, but high dose bile acid supplementation failed to reduce these pathologic changes.

摘要

在雄性草原犬鼠(Cynomys ludovicianus)中研究了膳食中鹅去氧胆酸和熊去氧胆酸对胆固醇性胆结石的预防作用。通过给予含0.4%胆固醇的半合成饮食8周来诱发胆结石。每组5或6只动物接受添加了鹅去氧胆酸或熊去氧胆酸(0.03%“低剂量”或0.06%“高剂量”)的致石性饮食。在所采用的条件下,高剂量鹅去氧胆酸和低剂量熊去氧胆酸可降低胆结石的发生率,但在喂食这些胆汁酸的22只动物中的20只动物的胆汁中检测到了胆固醇晶体。维持在低(0.08%)胆固醇半合成饮食的对照组既没有晶体也没有结石,是唯一结石形成指数低于1.0的组。给予的胆汁酸倾向于减少肝脏和血浆中胆固醇的积累。所有补充胆固醇的饮食均显著抑制肝HMG-CoA还原酶的活性。喂食0.4%胆固醇的草原犬鼠中胆固醇7α-羟化酶活性升高了83%,但当在该饮食中添加胆汁酸时,该活性倾向于恢复到正常水平。组织学上,所有接受半合成(补充胆固醇)饮食的动物的肝脏均表现出胆管增生,以及门脉纤维化和炎症浸润。低剂量补充鹅去氧胆酸或熊去氧胆酸可改善这些形态学改变,但高剂量补充胆汁酸未能减轻这些病理变化。

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