Askew E W, Dohm G L, Huston R L
J Nutr. 1975 Nov;105(11):1422-32. doi: 10.1093/jn/105.11.1422.
This study was designed to measure the response of key enzymes of ketone body metabolism in heart, skeletal muscle, and liver to diet and exercise, two conditions known to influence ketone body utilization. A 3 (diet: control, high fat, or high carbohydrate) X 2 (kill condition: rested or exhausted) X 2 (training: trained or untrained) factorial design was used to estimate main experimental effects as well as identify significant interactions of the variables. Physical training (treadmill running) was associated with a doubling of the activity of skeletal muscle 3-oxoacid CoA transferase, a key enzyme in extrahepatic ketone body utilization. The activity of the rate-limiting enzyme of liver ketone body production, hydroxymethylglutaryl CoA synthetase (HMG CoA synthetase), was not greatly influenced by training or exhuastive exercise indicating that the metabolic control of the ketosis of exercise may more likely be a function of the supply of fatty acids to the liver rather than the activity of HMG CoA synthetase. Feeding a high fat diet, on the other hand, significantly increased the activity of liver HMG CoA synthetase, indicating that the ketosis of fat feeding may be of a different nature than that of exercise. The results of this study indicate that physical training is associated with biochemical adaptations in ketone body metabolism as well as fatty acid oxidation, and that trained individuals are metabolically better endowed to benefit from the ketosis of exercise than untrained individuals.
本研究旨在测定心脏、骨骼肌和肝脏中酮体代谢关键酶对饮食和运动的反应,饮食和运动是已知会影响酮体利用的两种情况。采用3(饮食:对照、高脂肪或高碳水化合物)×2(处死条件:休息或疲劳)×2(训练:训练或未训练)析因设计来估计主要实验效应,并确定变量之间的显著相互作用。体育训练(跑步机跑步)与骨骼肌3-氧代酸辅酶A转移酶(肝外酮体利用的关键酶)活性加倍有关。肝脏酮体生成的限速酶羟甲基戊二酰辅酶A合成酶(HMG CoA合成酶)的活性不受训练或力竭运动的显著影响,这表明运动性酮症的代谢控制更可能是肝脏脂肪酸供应的功能,而不是HMG CoA合成酶的活性。另一方面,喂食高脂肪饮食会显著增加肝脏HMG CoA合成酶的活性,这表明高脂肪饮食导致的酮症可能与运动导致的酮症性质不同。本研究结果表明,体育训练与酮体代谢以及脂肪酸氧化的生化适应性有关,并且训练有素的个体比未训练的个体在代谢上更有优势从运动性酮症中获益。