Wu P, Sato J, Zhao Y, Jaskiewicz J, Popov K M, Harris R A
Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, 635 Barnhill Drive, Indianapolis, IN 46202-5122, USA.
Biochem J. 1998 Jan 1;329 ( Pt 1)(Pt 1):197-201. doi: 10.1042/bj3290197.
This study investigated whether conditions known to alter the activity and phosphorylation state of the pyruvate dehydrogenase complex have specific effects on the levels of isoenzymes of pyruvate dehydrogenase kinase (PDK) in rat heart. Immunoblot analysis revealed a remarkable increase in the amount of PDK4 in the hearts of rats that had been starved or rendered diabetic with streptozotocin. Re-feeding of starved rats and insulin treatment of diabetic rats very effectively reversed the increase in PDK4 protein and restored PDK enzyme activity to levels of chow-fed control rats. Starvation and diabetes also markedly increased the abundance of PDK4 mRNA, and re-feeding and insulin treatment reduced levels of the message to that of controls. In contrast with the findings for PDK4, little or no changes in the amounts of PDK1 and PDK2 protein and the abundance of their messages occurred in response to starvation and diabetes. The observed shift in the relative abundance of PDK isoenzymes probably explains previous studies of the effects of starvation and diabetes on heart PDK activity. The results indicate that control of the amount of PDK4 is important in long-term regulation of the activity of the pyruvate dehydrogenase complex in rat heart.
本研究调查了已知可改变丙酮酸脱氢酶复合体活性和磷酸化状态的条件是否对大鼠心脏中丙酮酸脱氢酶激酶(PDK)同工酶水平有特定影响。免疫印迹分析显示,饥饿或用链脲佐菌素诱导糖尿病的大鼠心脏中PDK4的量显著增加。饥饿大鼠重新喂食以及糖尿病大鼠接受胰岛素治疗非常有效地逆转了PDK4蛋白的增加,并将PDK酶活性恢复到正常饮食对照大鼠的水平。饥饿和糖尿病也显著增加了PDK4 mRNA的丰度,重新喂食和胰岛素治疗将该信使RNA的水平降低至对照水平。与PDK4的研究结果相反,饥饿和糖尿病对PDK1和PDK2蛋白的量及其信使RNA的丰度几乎没有影响。观察到的PDK同工酶相对丰度的变化可能解释了先前关于饥饿和糖尿病对心脏PDK活性影响的研究。结果表明,控制PDK4的量对大鼠心脏中丙酮酸脱氢酶复合体活性的长期调节很重要。