Gustafsson B E, Angelin B, Einarsson K, Gustafsson J A
J Lipid Res. 1977 Nov;18(6):717-21.
The aim of the present investigation was to study the influence of cholesterol feeding on cholesterol synthesis and fecal excretion of bile acids in germfree rats. Four germfree rats were fed a basal diet containing 0.004% cholesterol and four germfree rats received the same diet supplemented with 0.4% cholesterol for 2 weeks. Cholesterol synthesis was studied by assaying the HMG CoA reductase activity in the liver microsomal fraction. Cholesterol feeding decreased the HMG CoA reductase activity from 28.5 +/- 6.6 (mean +/- SEM) to 9.1 +/- 0.7 pmol/mg protein per min. In another experiment four germfree rats received the basal diet and four germfree rats the cholesterol-enriched diet. After 6 weeks feces were collected in two 4-day pools for analysis of bile acids. The main fecal bile acids were cholic acid and beta-muricholic acid (a metabolite of chenodeoxycholic acid), comprising more than 95% of total bile acids. Cholic acid was increased from 3.9 +/- 0.2 to 9.9 +/- 1.2 mg/kg body weight per day and beta-muricholic acid from 6.6 +/- 0.5 to 21.8 +/- 3.1 mg/kg body weight per day. The percentage of cholic acid decreased from 37.1 +/- 1.1 to 31.2 +/- 1.0%. In conclusion, germfree rats like conventional rats have the ability to compensate for an increased input of dietary cholesterol by inhibition of cholesterol synthesis and stimulation of bile acid synthesis. The synthesis of chenodeoxycholic acid (implied from the fecal excretion of beta-muricholic acid) is stimulated to a greater extent than that of cholic acid.
本研究的目的是探讨在无菌大鼠中,喂食胆固醇对胆固醇合成及胆汁酸粪便排泄的影响。四只无菌大鼠喂食含0.004%胆固醇的基础日粮,另外四只无菌大鼠喂食添加了0.4%胆固醇的相同日粮,持续2周。通过测定肝微粒体部分的HMG CoA还原酶活性来研究胆固醇合成。喂食胆固醇使HMG CoA还原酶活性从28.5±6.6(平均值±标准误)降至9.1±0.7 pmol/mg蛋白每分钟。在另一项实验中,四只无菌大鼠喂食基础日粮,四只无菌大鼠喂食富含胆固醇的日粮。6周后,收集粪便,分两个4天的样本池进行胆汁酸分析。主要的粪便胆汁酸为胆酸和β-鼠胆酸(鹅去氧胆酸的代谢产物),占总胆汁酸的95%以上。胆酸从3.9±0.2增加到9.9±1.2 mg/kg体重每天,β-鼠胆酸从6.6±0.5增加到21.8±3.1 mg/kg体重每天。胆酸的百分比从37.1±1.1降至31.2±1.0%。总之,无菌大鼠与普通大鼠一样,有能力通过抑制胆固醇合成和刺激胆汁酸合成来补偿饮食中胆固醇输入的增加。鹅去氧胆酸的合成(由β-鼠胆酸的粪便排泄推断)比胆酸的合成受到更大程度的刺激。