McGarry J D, Foster D W
Diabetes. 1980 Mar;29(3):236-40. doi: 10.2337/diab.29.3.236.
Studies were conducted to clarify the relationship between the external fatty acid concentration and glucagon in the regulation of hepatic fatty acid metabolism. Hepatocytes from fed rats were incubated with increasing concentrations of oleate (up to 1 mM) in the presence and absence of glucagon and the time sequence of changes in cellular malonyl-CoA levels, fatty acid synthesis, fatty acid oxidation, and ketogenesis were measured. At low concentrations of fatty acid the effect of glucagon was to abolish malonyl-CoA synthesis and lipogenesis and to produce a marked stimulation of fatty acid oxidation and ketogenesis. Similar effects were obtained with high concentrations of fatty acid in the absence of glucagon and, under these conditions, the additional presence of the hormone produced little further response. The results are consistent with the concept that the rate of fatty acid oxidation in liver is dictated largely by the relative concentrations of long-chain acyl-CoA (substrate for carnitine acyltransferase I) and malonyl-CoA (inhibitor of the transferase). They also indicate that the preemptive effect of fatty acids on glucagon-induced changes in fatty acid metabolism stems from their ability to reduce the tissue malonyl-CoA content, probably through long-chain acyl-CoA suppression of acetyl-CoA carboxylase.
开展了多项研究以阐明在肝脏脂肪酸代谢调节过程中,细胞外脂肪酸浓度与胰高血糖素之间的关系。将喂食后的大鼠的肝细胞在有和没有胰高血糖素的情况下,与浓度不断增加的油酸(高达1 mM)一起孵育,并测定细胞丙二酰辅酶A水平、脂肪酸合成、脂肪酸氧化和生酮作用变化的时间顺序。在低脂肪酸浓度下,胰高血糖素的作用是消除丙二酰辅酶A合成和脂肪生成,并显著刺激脂肪酸氧化和生酮作用。在没有胰高血糖素的情况下,高浓度脂肪酸也得到了类似的效果,在这些条件下,额外添加该激素几乎没有产生进一步的反应。这些结果与以下概念一致,即肝脏中脂肪酸氧化的速率很大程度上取决于长链酰基辅酶A(肉碱酰基转移酶I的底物)和丙二酰辅酶A(该转移酶的抑制剂)的相对浓度。它们还表明,脂肪酸对胰高血糖素诱导的脂肪酸代谢变化的抢先作用源于其降低组织丙二酰辅酶A含量的能力,可能是通过长链酰基辅酶A对乙酰辅酶A羧化酶的抑制作用实现的。