Chow J C, Jesse B W
Department of Animal Sciences, Rutgers, State University, New Brunswick, NJ 08903.
J Dairy Sci. 1992 Aug;75(8):2142-8. doi: 10.3168/jds.S0022-0302(92)77974-0.
The interaction of gluconeogenesis and fatty acid oxidation in isolated sheep hepatocytes was studied. Addition of tetradecylglycidic acid, an inhibitor of carnitine palmitoyltransferase I (EC 2.3.1.21), to isolated hepatocytes inhibited gluconeogenesis from a mixture of pyruvate plus lactate and from propionate alone. Inhibition constants for tetradecylglycidic acid on gluconeogenesis were 4.77 +/- 1.00 microM and 7.25 +/- 1.52 microM, respectively, for pyruvate plus lactate and for propionate as gluconeogenic substrates. The inhibition constants were not different. At the highest substrate concentrations examined, gluconeogenesis from pyruvate plus lactate and from propionate in the presence of 10 microM tetradecylglycidic acid was 47.3 and 41.4% of their respective controls. Similar to previous observations with butyrate, caproate addition inhibited gluconeogenesis from propionate by isolated hepatocytes and was unable to prevent inhibition of gluconeogenesis induced by tetradecylglycidic acid. Carnitine palmitoyltransferase I activity was lower in mitochondria isolated from hepatocytes preincubated with insulin than in control hepatocytes. The data suggest 1) that maximum rates of gluconeogenesis in isolated sheep hepatocytes from either pyruvate plus lactate or from propionate as gluconeogenic substrates require beta-oxidation, 2) that intermediates common to the metabolism of butyrate and caproate may be involved in the inhibition of propionate conversion to glucose by isolated sheep hepatocytes, and 3) that carnitine palmitoyltransferase I activity in isolated sheep hepatocytes can be modulated by insulin treatment.
研究了分离的绵羊肝细胞中糖异生作用与脂肪酸氧化之间的相互作用。向分离的肝细胞中添加肉碱棕榈酰转移酶I(EC 2.3.1.21)的抑制剂十四烷基缩水甘油酸,可抑制丙酮酸加乳酸混合物以及单独丙酸的糖异生作用。十四烷基缩水甘油酸对以丙酮酸加乳酸和丙酸作为糖异生底物的糖异生作用的抑制常数分别为4.77±1.00微摩尔和7.25±1.52微摩尔。这两个抑制常数没有差异。在检测的最高底物浓度下,存在10微摩尔十四烷基缩水甘油酸时,由丙酮酸加乳酸和丙酸生成的糖异生作用分别为各自对照的47.3%和41.4%。与先前对丁酸的观察结果相似,添加己酸可抑制分离的肝细胞由丙酸进行的糖异生作用,并且无法阻止十四烷基缩水甘油酸诱导的糖异生作用抑制。与对照肝细胞相比,用胰岛素预孵育的肝细胞分离出的线粒体中肉碱棕榈酰转移酶I活性较低。数据表明:1)以丙酮酸加乳酸或丙酸作为糖异生底物时,分离的绵羊肝细胞中糖异生的最大速率需要β氧化;2)丁酸和己酸代谢的共同中间产物可能参与了分离的绵羊肝细胞中丙酸向葡萄糖转化的抑制过程;3)胰岛素处理可调节分离的绵羊肝细胞中肉碱棕榈酰转移酶I的活性。