Sugden M C, Watts D I, Marshall C E, McCormack J G
Biosci Rep. 1982 May;2(5):289-97. doi: 10.1007/BF01115114.
Glucose or insulin increased lipogenesis (measured in vivo using 3H2O) in brown fat of starved rats. Such increases were associated with activation of pyruvate dehydrogenase and increased use of glucose as a lipogenic precursor (monitored as an increase in the 14C/3H ratio in brown-fat fatty acids in rats injected with both 3H20 and [U-14C]glucose). (-) Hydroxycitrate did not inhibit basal rates of brown-fat lipogenesis in starved rats but suppressed the increases in lipogenesis and glucose utilization observed in response to insulin. (-)Hydroxycitrate did not, however, inhabit the increase in 14C/3H observed after insulin treatment. The results indicate that in brown fat, glucose is utilized for fatty-acid synthesis predominantly via citrate, and that insulin acts to increase lipogenesis at site(s) prior to citrate cleavage. As basal rates of lipogenesis were not inhibited by (-)hydroxycitrate, it is suggested that acetate may be a lipogenic substrate for brown fat in starvation, and experiments are described which support this suggestion.
葡萄糖或胰岛素可增加饥饿大鼠棕色脂肪中的脂肪生成(采用3H2O进行体内测量)。这种增加与丙酮酸脱氢酶的激活以及葡萄糖作为脂肪生成前体的利用率增加有关(通过给同时注射3H2O和[U-14C]葡萄糖的大鼠棕色脂肪脂肪酸中14C/3H比值的增加来监测)。(-)羟基柠檬酸并不抑制饥饿大鼠棕色脂肪脂肪生成的基础速率,但可抑制因胰岛素作用而观察到的脂肪生成和葡萄糖利用的增加。然而,(-)羟基柠檬酸并不抑制胰岛素处理后观察到的14C/3H增加。结果表明,在棕色脂肪中,葡萄糖主要通过柠檬酸用于脂肪酸合成,并且胰岛素在柠檬酸裂解之前的位点起作用以增加脂肪生成。由于(-)羟基柠檬酸并不抑制脂肪生成的基础速率,因此提示乙酸盐可能是饥饿状态下棕色脂肪的脂肪生成底物,并且描述了支持该提示的实验。