Witters L A, Gao G, Kemp B E, Quistorff B
Department of Medicine, Dartmouth Medical School, Hanover, New Hampshire 03755.
Arch Biochem Biophys. 1994 Feb 1;308(2):413-9. doi: 10.1006/abbi.1994.1058.
Acetyl-CoA carboxylase (ACC) activity in the liver varies markedly as a function of the nutritional state and is subject to complex regulation involving variable enzyme content, enzyme specific activity due to variable phosphorylation, and zonation within the hepatic lobule. A 5'-AMP-activated protein kinase (AMPK) has been identified as the major regulatory kinase active on ACC. Employing dual-digitonin pulse perfusion, the effect of varying nutrition on periportal and perivenous zonation of ACC and AMPK activity within the liver has been characterized. During the transition from fasting to refeeding with high-carbohydrate chow, total ACC activity is increased 11- to 17-fold. This induction of total ACC activity is accounted for by a 4.5- to 6-fold increase in the content of the two major ACC isoforms and by a 2.5-to 3-fold increase in enzyme specific activity (units per mg ACC). Despite a small perivenous preponderance of ACC protein, a gradient of activity to the periportal side, due to this increase in specific activity, is observed in fasted rats and during early refeeding. After 24-48 h of refeeding, maximal induction of both ACC protein and specific activity is observed with obliteration of this total activity gradient. 5'-AMP-activated protein kinase activity is maximal in the fasted rat and is zonated to the perivenous side. During refeeding, this activity is rapidly markedly diminished with abolition of this gradient, correlating inversely with the activation of ACC over a narrow range of kinase activity. Activities of casein kinase II, myelin basic protein kinase(s), and ribosomal S6 kinase(s) show no zonation. These data suggest that the zonal activity of the 5'-AMP-activated protein kinase is responsible, in part, for the intrahepatic gradient in ACC activity and that the regulation of this kinase is responsible for the variations in ACC-specific activity that occur during varying nutrition.
肝脏中的乙酰辅酶A羧化酶(ACC)活性会随着营养状态的变化而显著改变,并且受到复杂的调控,包括酶含量的变化、因磷酸化程度不同导致的酶比活性变化以及肝小叶内的区域化分布。5'-AMP激活的蛋白激酶(AMPK)已被确定为作用于ACC的主要调节激酶。利用双洋地黄皂苷脉冲灌注技术,研究了不同营养状态对肝脏内门周和中央静脉区域ACC及AMPK活性的影响。在从禁食过渡到用高碳水化合物食物重新喂食的过程中,总ACC活性增加了11至17倍。总ACC活性的这种诱导是由两种主要ACC同工型含量增加4.5至6倍以及酶比活性(每毫克ACC的单位数)增加2.5至3倍所导致的。尽管ACC蛋白在中央静脉侧略有优势,但由于比活性的增加,在禁食大鼠和重新喂食早期,可观察到向门周侧的活性梯度。重新喂食24 - 48小时后,观察到ACC蛋白和比活性的最大诱导,且这种总活性梯度消失。5'-AMP激活的蛋白激酶活性在禁食大鼠中最高,且分布于中央静脉侧。在重新喂食期间,这种活性迅速显著降低,梯度消失,在狭窄的激酶活性范围内与ACC的激活呈负相关。酪蛋白激酶II、髓鞘碱性蛋白激酶和核糖体S6激酶的活性没有区域化分布。这些数据表明,5'-AMP激活的蛋白激酶的区域活性部分负责ACC活性的肝内梯度,并且该激酶的调节负责不同营养状态期间ACC比活性的变化。