Carter T C, Coore H G
Department of Biochemistry, Faculty of Medical Sciences, University of the West Indies, St. Augustine, Trinidad, West Indies.
Mol Cell Biochem. 1995 Aug-Sep;149-150:71-5. doi: 10.1007/BF01076565.
Sensitivity of rat heart pyruvate dehydrogenase kinase (PDHK) to pyruvate inhibition was tested under various conditions using pyruvate dehydrogenase complex (PDC) in mitochondria (mPDC) and in a high speed precipitate of whole tissue homogenates (hPDC). In the latter preparation pyruvate in the range of concentration 1-10 mM caused increasing inhibition of PDHK when the enzyme was prepared from animals fed ad libitum but had no effect when the enzyme was prepared from 48 h starved animals. Similar behaviour was observed in mPDC from fed and starved animals when rotenone was present, pyruvate at 1 mM concentration stimulated PDHK from hearts of fed animals but was without effect at 10 mM. When mPDC or hPDC from hearts of starved animals was incubated at 30 degrees C for 30 min, inhibition of PDHK by pyruvate was restored.
在各种条件下,利用线粒体中的丙酮酸脱氢酶复合物(mPDC)和全组织匀浆高速沉淀物中的丙酮酸脱氢酶复合物(hPDC),测试了大鼠心脏丙酮酸脱氢酶激酶(PDHK)对丙酮酸抑制的敏感性。在后者的制备中,当酶从自由进食的动物中制备时,浓度范围为1-10 mM的丙酮酸对PDHK的抑制作用增强,但当酶从饥饿48小时的动物中制备时则没有作用。当存在鱼藤酮时,在喂食和饥饿动物的mPDC中观察到类似的行为,1 mM浓度的丙酮酸刺激喂食动物心脏中的PDHK,但在10 mM时没有作用。当饥饿动物心脏的mPDC或hPDC在30℃孵育30分钟时,丙酮酸对PDHK的抑制作用得以恢复。