Vaithilingam D S, Antao V, Kakis G
Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Ontario, Canada.
Mol Cell Biochem. 1994 Jan 12;130(1):67-74. doi: 10.1007/BF01084269.
Inbred mouse strains vary in susceptibility or resistance to dietary induced atherosclerosis. To investigate the effect of polyunsaturated fat feeding on postprandial serum cholesterol levels, in C57BL/67 (B6) and BALB/cJ inbred mice, we fed by stomach gavage previously fasted mice, a mixture containing 30% sunflower oil, 5% cholesterol, 2% sodium cholate and 0.5% choline chloride. The most significant difference in serum cholesterol levels between B6 and BALB/cJ mouse strains was observed at 2 h postfeeding. Susceptible B6 strain mice had a 41% postprandial increment in serum cholesterol. The resistant BALB/cJ strain had an insignificant 16% rise in serum cholesterol, at 2 h. We next examined eight other inbred mouse strains, to identify the gene(s) that regulate the observed 2 h postprandial hypercholesterolemia response, in the susceptible B6 mouse strain. Only the C57BR/cdJ and C57L/J strains developed postprandial hypercholesterolemia, at 2 h. The C57BR/cdJ strain had a 20% increase and the C57L/J strain a 62% increase in postprandial serum cholesterol levels. From this result, we found that the postprandial hypercholesterolemic response to an acute polyunsaturated fat-cholesterol feed, cosegregated with the a allele at the Gpd-1 and Ahd-1 loci, on mouse chromosome 4. In this study, non-responsiveness cosegregated with the b allele at the Gpd-1 and Ahd-1 loci. Thus polyunsaturated fat-cholesterol induced postprandial hypercholesterolemia appeared to be genetically determined by a gene located between the Gpd-1 and Ahd-1 loci, in mice. The putative gene regulating polyunsaturated fat-cholesterol induced post-absorptive hypercholesterolemia was designated Phc-2.(ABSTRACT TRUNCATED AT 250 WORDS)
近交系小鼠品系对饮食诱导的动脉粥样硬化的易感性或抗性各不相同。为了研究多不饱和脂肪喂养对餐后血清胆固醇水平的影响,我们对C57BL/67(B6)和BALB/cJ近交系小鼠进行胃内灌喂,给先前禁食的小鼠喂一种含有30%向日葵油、5%胆固醇、2%胆酸钠和0.5%氯化胆碱的混合物。在喂食后2小时观察到B6和BALB/cJ小鼠品系之间血清胆固醇水平的最显著差异。易感的B6品系小鼠餐后血清胆固醇增加了41%。抗性的BALB/cJ品系在2小时时血清胆固醇仅无显著意义地升高了16%。接下来,我们检查了其他八个近交系小鼠品系,以确定调控易感B6小鼠品系中观察到的喂食后2小时高胆固醇血症反应的基因。只有C57BR/cdJ和C57L/J品系在2小时时出现餐后高胆固醇血症。C57BR/cdJ品系餐后血清胆固醇水平增加了20%,C57L/J品系增加了62%。从这个结果,我们发现对急性多不饱和脂肪-胆固醇喂养的餐后高胆固醇血症反应与小鼠4号染色体上Gpd-1和Ahd-1位点的a等位基因共分离遗传。在本研究中,无反应性与Gpd-1和Ahd-1位点的b等位基因共分离遗传。因此,多不饱和脂肪-胆固醇诱导的餐后高胆固醇血症在小鼠中似乎由位于Gpd-1和Ahd-1位点之间的一个基因遗传决定。调控多不饱和脂肪-胆固醇诱导的吸收后高胆固醇血症的假定基因被命名为Phc-2。(摘要截短于250词)