Decaux J F, Ferré P, Robin D, Robin P, Girard J
Centre de Recherches sur la Nutrition, Centre National de la Recherche Scientifique, Meudon-Bellevue, France.
J Biol Chem. 1988 Mar 5;263(7):3284-9.
In rats weaned on a high-carbohydrate diet, hepatic fatty acid oxidation capacity is decreased when compared to suckling rats. Previous studies (Benito et al., 1979) suggested that a malonyl-CoA-dependent mechanism could be at the origin of this decrease. Studies on isolated hepatocytes show that despite, respectively, a low and a high lipogenic rate in suckling and weaned rats, malonyl-CoA concentrations are similar in the two groups. This might be due to the lower ratio fatty acid synthetase/acetyl-CoA carboxylase (EC 6.4.1.2) activities during suckling than after weaning. Different rates of hepatic fatty acid oxidation despite similar malonyl-CoA concentrations can be explained by the 2.5-fold higher carnitine palmitoyltransferase I (EC 2.3.1.21) activity in suckling rats together with a 7-fold higher Ki for malonyl-CoA. This precludes a tight control of fatty acid oxidation by [malonyl-CoA] in suckling rats. Weaning on a high-fat carbohydrate-free diet abolishes the changes previously described for the kinetic characteristics of carnitine palmitoyltransferase I suggesting that nutritional modifications rather than a developmental stage are involved. Thus, during the suckling-weaning transition, a variation of [malonyl-CoA] is not responsible for the decrease in hepatic fatty acid oxidation. It involves, in addition, a decrease in carnitine palmitoyltransferase I activity and an increase of the sensitivity of this enzyme to malonyl-CoA.
在以高碳水化合物饮食断奶的大鼠中,与哺乳大鼠相比,肝脏脂肪酸氧化能力降低。先前的研究(贝尼托等人,1979年)表明,丙二酰辅酶A依赖性机制可能是这种降低的原因。对分离的肝细胞的研究表明,尽管哺乳和断奶大鼠的生脂率分别较低和较高,但两组中的丙二酰辅酶A浓度相似。这可能是由于哺乳期间脂肪酸合成酶/乙酰辅酶A羧化酶(EC 6.4.1.2)活性的比率低于断奶后。尽管丙二酰辅酶A浓度相似,但肝脏脂肪酸氧化速率不同可以通过哺乳大鼠中肉碱棕榈酰转移酶I(EC 2.3.1.21)活性高2.5倍以及丙二酰辅酶A的Ki高7倍来解释。这排除了哺乳大鼠中[丙二酰辅酶A]对脂肪酸氧化的严格控制。以高脂肪无碳水化合物饮食断奶消除了先前描述的肉碱棕榈酰转移酶I动力学特征的变化,这表明涉及的是营养改变而非发育阶段。因此,在哺乳-断奶过渡期间,[丙二酰辅酶A]的变化不是肝脏脂肪酸氧化降低的原因。此外,它还涉及肉碱棕榈酰转移酶I活性的降低以及该酶对丙二酰辅酶A敏感性的增加。