Pégorier J P, Duée P H, Girard J, Peret J
Biochem J. 1983 Apr 15;212(1):93-7. doi: 10.1042/bj2120093.
In hepatocytes isolated from 48 h-old starved of suckling newborn pigs or from 15-day-old starved piglets, the rate of ketogenesis from oleate or from octanoate is very low. This is not due to an inappropriate fatty acid uptake by the isolated liver cells, but results from a limited capacity for fatty acid oxidation. Some 80-95% of oleate taken up is converted into esterified fats, whatever the age or the nutritional conditions. Three lines of indirect evidences suggest that fatty acid oxidation is not controlled primarily by malonyl-CoA concentration in newborn pig liver. Firstly, the addition of glucagon does not increase fatty acid oxidation or ketogenesis. Secondly, the rate of lipogenesis is very low in isolated hepatocytes from newborn pigs. Thirdly, the rates of oxidation and ketogenesis from octanoate are also decreased in isolated hepatocytes from newborn and young piglets. The huge rate of esterification of fatty acids in the liver of the newborn pigs probably represents a species-specific difference in intrahepatic fatty acid metabolism.
在从48小时未哺乳的新生仔猪或15日龄饥饿仔猪分离出的肝细胞中,油酸或辛酸的生酮速率非常低。这并非由于分离的肝细胞摄取脂肪酸不当,而是脂肪酸氧化能力有限所致。无论年龄或营养状况如何,摄取的油酸中约80 - 95%会转化为酯化脂肪。三条间接证据表明,新生猪肝中脂肪酸氧化并非主要受丙二酰辅酶A浓度控制。首先,添加胰高血糖素并不会增加脂肪酸氧化或生酮作用。其次,新生猪分离肝细胞中的脂肪生成速率非常低。第三,新生和幼龄仔猪分离肝细胞中辛酸的氧化和生酮速率也会降低。新生猪肝中脂肪酸的巨大酯化速率可能代表了肝内脂肪酸代谢的种属特异性差异。