Triscari J, Greenwood M R, Sullivan A C
Metabolism. 1982 Mar;31(3):223-8. doi: 10.1016/0026-0495(82)90057-9.
Ketone body production and oxidation of 14C fatty acids to CO2 were measured in hepatocytes isolated from lean and obese Zucker rats. The oxidation of [1-14C]octanoate, [1-14C]palmitate and [1-14C]palmitoyl carnitine to 14CO2 was 50%--70% less in obese than in lean rats. Although ketone body production in hepatocytes from both lean and obese rats was increased by fasting, there was a significantly lower rate of ketone body production in hepatocytes from obese rats. Ketone body production was reduced to a comparable extent by increasing the glucose concentration in the incubation media of hepatocytes from both lean and obese rats. Glucagon and carnitine increased ketogenesis and the effect were additive and similar in lean and obese rats. These data suggest that beta-oxidation and ketogenesis are suppressed in the obese Zucker rat, and further that ketone bodies can be modulated similarly in hepatocytes from lean and obese rats by nutritional and hormonal intervention. It is postulated that the decreased beta-oxidation and ketone body production may play a role in the development or maintenance of obesity in the Zucker rat.
在从瘦型和肥胖型 Zucker 大鼠分离出的肝细胞中,测定了酮体生成以及 14C 脂肪酸氧化为二氧化碳的情况。肥胖大鼠肝细胞中,[1-14C]辛酸、[1-14C]棕榈酸和[1-14C]棕榈酰肉碱氧化为 14CO2 的量比瘦型大鼠低 50% - 70%。尽管禁食会使瘦型和肥胖型大鼠肝细胞中的酮体生成增加,但肥胖大鼠肝细胞中酮体生成的速率明显更低。通过提高瘦型和肥胖型大鼠肝细胞孵育培养基中的葡萄糖浓度,酮体生成降低到了相当的程度。胰高血糖素和肉碱增加了酮体生成,且在瘦型和肥胖型大鼠中的作用具有相加性且相似。这些数据表明,肥胖型 Zucker 大鼠的β-氧化和酮体生成受到抑制,而且通过营养和激素干预,瘦型和肥胖型大鼠肝细胞中的酮体可以受到类似的调节。据推测,β-氧化和酮体生成的减少可能在 Zucker 大鼠肥胖的发生或维持中起作用。