Kuan S I, Stewart J, Dowd M K, Patterson L, Dupont J, Seagrave R C
Department of Chemical Engineering, Iowa State University, Ames 50011.
J Lipid Res. 1992 Nov;33(11):1619-28.
Differences in dietary fats cause differences in cholesterol metabolism in mice. CBA/J mice are resistant to diet-induced hypercholesterolemia and atherosclerosis; they adjust hepatic hydroxymethyl-glutaryl-CoA reductase activity (HMGR) to maintain homeostasis; C57BR/cdJ mice are susceptible, but young animals are thought to maintain homeostasis by changing fecal excretion of sterols. Compartmental modelling of movement of [4-14C]cholesterol was used to analyze movement of cholesterol between serum and liver, heart, and carcass in mice fed 40 en% fat, polyunsaturated to saturated fatty acid ratio (P/S) = 0.24 (US74) or 30 en% fat, P/S = 1 (MOD). Dietary effects were quite pronounced, while strain effects were more subdued. The C57/cdJ animals appear to regulate the overall cholesterol balance by reducing synthesis, as do the CBA/J animals, even though synthesis is not reduced to the same degree as in the CBA/J animals. Both diet and strain influence the whole-animal turnover rate, with slower turnover occurring for C57BR/cdJ animals and animals fed the US74 diet.
饮食脂肪的差异会导致小鼠胆固醇代谢的差异。CBA/J小鼠对饮食诱导的高胆固醇血症和动脉粥样硬化具有抗性;它们会调节肝脏羟甲基戊二酰辅酶A还原酶活性(HMGR)以维持体内平衡;C57BR/cdJ小鼠易感,但幼龄动物被认为通过改变粪便中固醇的排泄来维持体内平衡。采用[4-14C]胆固醇转运的房室模型来分析喂食40能量%脂肪、多不饱和脂肪酸与饱和脂肪酸比例(P/S)=0.24(US74)或30能量%脂肪、P/S = 1(MOD)的小鼠血清与肝脏、心脏和胴体之间胆固醇的转运情况。饮食效应相当显著,而品系效应则较为微弱。C57/cdJ动物似乎像CBA/J动物一样通过减少合成来调节整体胆固醇平衡,尽管其合成减少的程度与CBA/J动物不同。饮食和品系都会影响全动物的周转率,C57BR/cdJ动物和喂食US74饮食的动物周转率较慢。