Lyn D, Coore H G
Biochem Biophys Res Commun. 1985 Feb 15;126(3):992-8. doi: 10.1016/0006-291x(85)90283-9.
Pyruvate inhibited pyruvate dehydrogenase kinase activity in mitochondria from adipose tissue, heart, brain and kidney of fed rats. Starvation for 24 h led to increased kinase activity in mitochondria from adipose tissue and heart but not from brain or kidney and to reduction of pyruvate inhibition of the enzyme from adipose tissue, heart and brain. Insulin injection into starved animals rapidly restored pyruvate inhibition without alteration of kinase activity in adipose tissue and heart mitochondria. Induction of streptozotocin diabetes resulted in loss of pyruvate inhibition of the kinase in heart mitochondria at 48 h but not at 24 h whereas a significant increase of kinase activity was seen at 24 h. It is concluded that the mechanisms which control fluctuations of pyruvate sensitivity of the kinase are different from the mechanisms which control fluctuations of the uninhibited kinase activity.
丙酮酸可抑制喂食大鼠脂肪组织、心脏、大脑和肾脏线粒体中的丙酮酸脱氢酶激酶活性。饥饿24小时会导致脂肪组织和心脏线粒体中的激酶活性增加,但大脑和肾脏线粒体中的激酶活性未增加,同时脂肪组织、心脏和大脑中该酶受到的丙酮酸抑制作用减弱。给饥饿动物注射胰岛素可迅速恢复丙酮酸抑制作用,而脂肪组织和心脏线粒体中的激酶活性未发生改变。链脲佐菌素诱导糖尿病,在48小时时心脏线粒体中丙酮酸对激酶的抑制作用丧失,但在24小时时未丧失,而在24小时时激酶活性显著增加。结论是,控制激酶丙酮酸敏感性波动的机制与控制未受抑制的激酶活性波动的机制不同。