Poorman J A, Buck R A, Smith S A, Overturf M L, Loose-Mitchell D S
Department of Pharmacology, University of Texas Medical School at Houston 77225.
J Lipid Res. 1993 Oct;34(10):1675-85.
We have developed a partially inbred substrain of New Zealand white rabbits (CRT/mlo) that are resistant to the hypercholesterolemia that accompanies cholesterol feeding to normal rabbits. The plasma cholesterol concentration of normal rabbits increases dramatically from about 30 mg/dl to > 300 mg/dl after they are fed a 0.1% cholesterol-enriched diet for 3-4 months. Cholesterol-fed CRT/mlo animals, however, maintain a cholesterol level of about 30 mg/dl during the entire cholesterol feeding period. In addition to the low plasma cholesterol level, measurements of cellular cholesterol indicate that the hepatic cholesterol content of the cholesterol-fed resistant rabbit remains markedly lower than it does in normal animals fed the same diet. The only mechanism for removal of significant quantities of cholesterol carbon from the body is via the fecal excretion of cholesterol, neutral sterol metabolites, and bile acids. In comparison to the basal, low-cholesterol diet, we observed that cholesterol-fed resistant rabbits had increased excretion of lithocholic acid, while excretion of this bile acid by cholesterol-fed normal rabbit remained similar to basal diet levels. Deoxycholic acid excretion, the other main bile acid excreted in the feces of rabbits, was decreased in response to cholesterol challenge in animals with either resistant or normal phenotypes, but the decrease was significantly less in the resistant rabbits. Thus, the resistant rabbits excreted relatively more lithocholic and deoxycholic acid than did the cholesterol-fed normal rabbit. The difference in bile acid excretion was also manifest by a higher than normal level of cholesterol 7 alpha-hydroxylase activity and cholesterol 7 alpha-hydroxylase mRNA in the livers from resistant versus normal rabbits. As cholesterol 7 alpha-hydroxylase is the putative rate-limiting step of bile acid synthesis, we believe that the increased excretion of bile acids by resistant animals is due, at least in part, to increased levels of cholesterol 7 alpha-hydroxylase expression.
我们培育出了一种新西兰白兔的部分近交亚系(CRT/mlo),该亚系对正常兔子喂食胆固醇后所伴随的高胆固醇血症具有抗性。正常兔子在喂食0.1%胆固醇丰富饮食3 - 4个月后,血浆胆固醇浓度会从约30毫克/分升急剧增加至>300毫克/分升。然而,喂食胆固醇的CRT/mlo动物在整个胆固醇喂食期间,胆固醇水平维持在约30毫克/分升。除了血浆胆固醇水平较低外,细胞胆固醇的测量表明,喂食胆固醇的抗性兔子肝脏中的胆固醇含量仍明显低于喂食相同饮食的正常动物。从体内清除大量胆固醇碳的唯一机制是通过粪便排泄胆固醇、中性固醇代谢物和胆汁酸。与基础低胆固醇饮食相比,我们观察到喂食胆固醇的抗性兔子石胆酸排泄增加,而喂食胆固醇的正常兔子这种胆汁酸的排泄仍与基础饮食水平相似。脱氧胆酸排泄是兔子粪便中排泄的另一种主要胆汁酸,在具有抗性或正常表型的动物中,其排泄量因胆固醇刺激而减少,但抗性兔子的减少幅度明显较小。因此,抗性兔子排泄的石胆酸和脱氧胆酸相对比喂食胆固醇的正常兔子更多。胆汁酸排泄的差异还表现为抗性兔子肝脏中胆固醇7α - 羟化酶活性和胆固醇7α - 羟化酶mRNA水平高于正常水平。由于胆固醇7α - 羟化酶是胆汁酸合成的假定限速步骤,我们认为抗性动物胆汁酸排泄增加至少部分是由于胆固醇7α - 羟化酶表达水平升高所致。