Holness M J, Kraus A, Harris R A, Sugden M C
Department of Diabetes and Metabolic Medicine, St. Bartholomew's and the Royal London School of Medicine and Dentistry, Queen Mary and Westfield College, University of London, UK.
Diabetes. 2000 May;49(5):775-81. doi: 10.2337/diabetes.49.5.775.
In using Western blot analysis with antibodies raised against recombinant pyruvate dehydrogenase kinase (PDK) isoforms PDK2 and PDK4, this study demonstrates selective PDK isoform switching in specific skeletal muscle types in response to high-fat feeding that is associated with altered regulation of PDK activity by pyruvate. The administration of a diet high in saturated fats led to stable (approximately 2-fold) increases in PDK activities in both a typical slow-twitch (soleus [SOL]) muscle and a typical fast-twitch (anterior tibialis [AT]) muscle. Western blot analysis revealed that high-fat feeding significantly increased (approximately 2-fold; P < 0.001) PDK4 protein expression in SOL, with a modest (1.3-fold) increase in PDK2 protein expression. The relative increase in PDK4 protein expression in SOL was associated with a 7.6-fold increase in the pyruvate concentration that was required to elicit a 50% active pyruvate dehydrogenase complex, which indicates a marked decrease in the sensitivity of PDK to inhibition by pyruvate. In AT muscle, high-fat feeding elicited comparable (1.5- to 1.7-fold) increases (P < 0.05) in PDK4 and PDK2 protein expression. Loss of sensitivity of PDK to inhibition by pyruvate was less marked. The data suggest that a positive correlation exists between increases in PDK4 expression and the propensity with which muscles use lipid-derived fuels as respiratory substrates rather than with the degree of insulin resistance induced in skeletal muscles by high-fat feeding. In conclusion, high-fat feeding leads to selective upregulation of PDK4 expression in slow-twitch muscle in response to high-fat feeding in vivo, which is associated with a pronounced loss of sensitivity of PDK activity to acute inhibition by pyruvate. Thus, increased PDK4 expression may underlie the stable modification of the regulatory characteristics of PDK observed in slow-twitch muscle in response to high-fat feeding.
在使用针对重组丙酮酸脱氢酶激酶(PDK)亚型PDK2和PDK4产生的抗体进行蛋白质印迹分析时,本研究表明,在高脂喂养的情况下,特定骨骼肌类型中会发生选择性的PDK亚型转换,这与丙酮酸对PDK活性的调节改变有关。给予富含饱和脂肪的饮食会导致典型的慢肌(比目鱼肌[SOL])和典型的快肌(胫前肌[AT])中的PDK活性稳定增加(约2倍)。蛋白质印迹分析显示,高脂喂养显著增加了SOL中PDK4蛋白的表达(约2倍;P<0.001),PDK2蛋白表达有适度增加(1.3倍)。SOL中PDK4蛋白表达的相对增加与使丙酮酸脱氢酶复合体50%激活所需的丙酮酸浓度增加7.6倍有关,这表明PDK对丙酮酸抑制的敏感性显著降低。在AT肌中,高脂喂养使PDK4和PDK2蛋白表达有相当程度的增加(1.5至1.7倍)(P<0.05)。PDK对丙酮酸抑制的敏感性丧失不太明显。数据表明,PDK4表达的增加与肌肉将脂质衍生燃料用作呼吸底物的倾向之间存在正相关,而与高脂喂养在骨骼肌中诱导的胰岛素抵抗程度无关。总之,高脂喂养导致体内慢肌中PDK4表达选择性上调,这与PDK活性对丙酮酸急性抑制的敏感性明显丧失有关。因此,PDK4表达增加可能是慢肌中观察到的PDK调节特性因高脂喂养而发生稳定改变的基础。