Horie S, Isobe M, Suga T
J Biochem. 1986 May;99(5):1345-52. doi: 10.1093/oxfordjournals.jbchem.a135602.
Changes in peroxisomal CoA pools in the liver of fasted, diabetic, high-fat diet-fed and clofibrate-treated rats were studied. Total-CoA increased slightly in the fasted group and markedly in the diabetic, high-fat and clofibrate-treated groups. Fractionation studies showed that changes in free CoA levels were much greater in peroxisomes than in mitochondria. The concentrations of CoAs were calculated from the contents of CoAs in organelles and the changes in volume of organelles under these conditions; the concentration of total CoA in peroxisomes was higher than that in cytosol, but lower than that in mitochondria. These changes were accompanied by an increase in the activity of peroxisomal beta-oxidation. The results obtained from these experiments indicate that the peroxisomal beta-oxidation system is controlled not only at the enzyme level but also at the substrate or co-factor level.
研究了禁食、糖尿病、高脂饮食喂养和氯贝丁酯处理的大鼠肝脏中过氧化物酶体辅酶A池的变化。禁食组总辅酶A略有增加,而糖尿病组、高脂组和氯贝丁酯处理组则显著增加。分级分离研究表明,过氧化物酶体中游离辅酶A水平的变化比线粒体中的变化大得多。根据细胞器中辅酶A的含量以及这些条件下细胞器体积的变化计算辅酶A的浓度;过氧化物酶体中总辅酶A的浓度高于细胞质,但低于线粒体。这些变化伴随着过氧化物酶体β-氧化活性的增加。这些实验结果表明,过氧化物酶体β-氧化系统不仅在酶水平受到控制,而且在底物或辅因子水平也受到控制。