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肝硬化中的胆汁酸代谢。IV. 脱氧胆酸代谢异常的特征

Bile acid metabolism in cirrhosis. IV. Characterization of the abnormality in deoxycholic acid metabolism.

作者信息

Yoshida T, McCormick W C, Swell L, Vlahcevic Z R

出版信息

Gastroenterology. 1975 Feb;68(2):335-41.

PMID:1116679
Abstract

Several recent studies have demonstrated that patients with cirrhosis frequently lack deoxycholic acid in bile and plasma. In order to explain this observation, comparative experiments on the colonic absorption of deoxycholic acid and on the colonic conversion of cholic to deoxycholic acid were carried out in the cirrhotic patients with normal and very low percentages of deoxycholic acid. Deoxycholic or cholic acid (100 mg) plus 5 muc of each [14C] bile acid were administered by enema to 8 patients with and 5 without liver disease. Deoxycholic acid produced a significant increase in the percentage of biliary deoxycholic acid in patients with cirrhosis. However, the rate of appearance of 14C-deoxycholic acid in patients with cirrhosis was slower than in normal control subjects. Distribution of the 14C activity among the bile acids indicated that rehydroxylation of deoxycholic to cholic acid did not occur. The distribution of 14C activity in biliary bile acids after the rectal administration of [14C]cholic acid showed that patients with severe cirrhosis converted [14C]cholic to [14C]deoxycholic acid at a much slower rate than did cirrhotic patients with normal percentages of biliary deoxycholic acid. Feeding of cholic acid (450 mg per day) for 3 days to 4 cirrhotic patients resulted in a 2-fold increase in the percentage of biliary cholic acid, but only a small increase in the percentage of deoxycholic acid. In a separate group of 9 cirrhotic patients, fecal bile acid analysis indicated that cirrhotic patients had a significantly lower percentage of deoxycholic acid than 12 patients without liver disease; there was no significant difference in fecal lithocholic acid. The data suggest that alteration of bacterial flora and/or altered conditions for bacterial 7alpha-dehydroxylase enzyme activity in the colon could account for the virtual absence of biliary deoxycholic acid in severely cirrhotic patients.

摘要

最近的几项研究表明,肝硬化患者的胆汁和血浆中常常缺乏脱氧胆酸。为了解释这一现象,对脱氧胆酸结肠吸收及胆酸向脱氧胆酸结肠转化进行了对比实验,实验对象为脱氧胆酸百分比正常和极低的肝硬化患者。将脱氧胆酸或胆酸(100毫克)加5微升每种[¹⁴C]胆汁酸通过灌肠给予8例有肝病和5例无肝病的患者。脱氧胆酸使肝硬化患者胆汁中脱氧胆酸的百分比显著增加。然而,肝硬化患者中¹⁴C - 脱氧胆酸的出现速率比正常对照受试者慢。¹⁴C活性在胆汁酸中的分布表明,脱氧胆酸不会再羟基化为胆酸。直肠给予[¹⁴C]胆酸后,胆汁中胆汁酸的¹⁴C活性分布显示,重度肝硬化患者将[¹⁴C]胆酸转化为[¹⁴C]脱氧胆酸的速率比胆汁中脱氧胆酸百分比正常的肝硬化患者慢得多。给4例肝硬化患者连续3天每天喂食胆酸(450毫克),导致胆汁中胆酸百分比增加了2倍,但脱氧胆酸百分比仅略有增加。在另一组9例肝硬化患者中,粪便胆汁酸分析表明,肝硬化患者的脱氧胆酸百分比显著低于12例无肝病的患者;粪便中石胆酸无显著差异。数据表明,结肠中细菌菌群的改变和/或细菌7α - 脱氢酶活性条件的改变可能是重度肝硬化患者胆汁中几乎不存在脱氧胆酸的原因。

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