Azain M J, Ontko J A
Oklahoma Medical Research Foundation, Oklahoma City.
Am J Physiol. 1989 Oct;257(4 Pt 2):R822-8. doi: 10.1152/ajpregu.1989.257.4.R822.
These studies were undertaken to further characterize and explain the differences in hepatic fatty acid metabolism between lean and obese Zucker rats. It was shown that the rate of palmitate or octanoate oxidation and the inhibition of palmitate oxidation by malonyl CoA in mitochondria isolated from lean and obese Zucker rats were similar. Cytochrome oxidase activity was similar in lean and obese rat livers. It was found that the addition of cytosol from the obese rat liver inhibited palmitate oxidation by 20-30% in mitochondria isolated from lean or obese rat livers and thus reproduced the conditions observed in the intact cell. Increased concentrations of metabolites such as malonyl CoA and glycerophosphate in the liver of the obese rat are likely contributors to this inhibitory effect. These results are extrapolated to the intact cell and suggest that decreased hepatic fatty acid oxidation in the obese rat can be accounted for by cytosolic influences on the mitochondria. The decreased rate of fatty acid oxidation observed in the intact hepatocyte or perfused liver cannot be explained by a defect in the capacity of mitochondria to oxidize substrate or by a decrease in mitochondrial number in the obese rat liver.
进行这些研究是为了进一步表征和解释瘦型与肥胖型 Zucker 大鼠肝脏脂肪酸代谢的差异。结果表明,从瘦型和肥胖型 Zucker 大鼠分离的线粒体中,棕榈酸或辛酸的氧化速率以及丙二酰辅酶 A 对棕榈酸氧化的抑制作用相似。瘦型和肥胖型大鼠肝脏中的细胞色素氧化酶活性相似。研究发现,添加肥胖大鼠肝脏的胞质溶胶可使从瘦型或肥胖型大鼠肝脏分离的线粒体中棕榈酸氧化受到 20% - 30% 的抑制,从而重现了在完整细胞中观察到的情况。肥胖大鼠肝脏中丙二酰辅酶 A 和甘油磷酸等代谢物浓度的增加可能是这种抑制作用的原因。这些结果外推至完整细胞,表明肥胖大鼠肝脏脂肪酸氧化减少可归因于胞质溶胶对线粒体的影响。在完整肝细胞或灌注肝脏中观察到的脂肪酸氧化速率降低,不能用肥胖大鼠肝脏线粒体氧化底物能力的缺陷或线粒体数量的减少来解释。