Kuo T H, Giacomelli F, Wiener J, Lapanowski-Netzel K
Diabetes. 1985 Nov;34(11):1075-81. doi: 10.2337/diab.34.11.1075.
Pyruvate dehydrogenase (PDH) was studied in isolated heart mitochondria from genetically diabetic mice (C57BL/KsJ db/db) with progressive cardiomyopathy. Both the basal activity (active enzyme) and the total activity (the sum of active and inactive enzyme) were determined. In mitochondrial extracts from 8-18-wk-old db/db mice, there was a 73% decrease of basal activity accompanied by a 38% decrease of total activity as compared with controls. The lower basal activity at 8 wk of age suggests an increased conversion of the enzyme into the phosphorylated (inactive) form. Evidence is also given that the conversion of inactive (phosphorylated) enzyme into active (dephosphorylated) enzyme is inhibited in cardiac mitochondria prepared from 8-wk and older db/db mice. These changes coincide with the onset of defective oxidative metabolism and can explain the depressed pyruvate oxidation reported previously.
对患有进行性心肌病的遗传性糖尿病小鼠(C57BL/KsJ db/db)分离出的心脏线粒体中的丙酮酸脱氢酶(PDH)进行了研究。测定了基础活性(活性酶)和总活性(活性酶与非活性酶之和)。与对照组相比,在8 - 18周龄db/db小鼠的线粒体提取物中,基础活性降低了73%,总活性降低了38%。8周龄时较低的基础活性表明该酶向磷酸化(非活性)形式的转化增加。同时也有证据表明,从8周龄及以上的db/db小鼠制备的心脏线粒体中,非活性(磷酸化)酶向活性(去磷酸化)酶的转化受到抑制。这些变化与氧化代谢缺陷的开始相吻合,并且可以解释先前报道的丙酮酸氧化降低的现象。