Jin Eunsook S, Sherry A Dean, Malloy Craig R
From the Advanced Imaging Research Center, Department of Internal Medicine, and
From the Advanced Imaging Research Center, Radiology, University of Texas Southwestern Medical Center, Dallas, Texas 75390, Department of Chemistry, University of Texas at Dallas, Richardson, Texas 75080, and.
J Biol Chem. 2015 Dec 18;290(51):30486-97. doi: 10.1074/jbc.M115.689174. Epub 2015 Oct 21.
Phosphoenolpyruvate (PEP) generated from pyruvate is required for de novo synthesis of glycerol and glycogen in skeletal muscle. One possible pathway involves synthesis of PEP from the citric acid cycle intermediates via PEP carboxykinase, whereas another could involve reversal of pyruvate kinase (PK). Earlier studies have reported that reverse flux through PK can contribute carbon precursors for glycogen synthesis in muscle, but the physiological importance of this pathway remains uncertain especially in the setting of high plasma glucose. In addition, although PEP is a common intermediate for both glyconeogenesis and glyceroneogenesis, the importance of reverse PK in de novo glycerol synthesis has not been examined. Here we studied the contribution of reverse PK to synthesis of glycogen and the glycerol moiety of acylglycerols in skeletal muscle of animals with high plasma glucose. Rats received a single intraperitoneal bolus of glucose, glycerol, and lactate under a fed or fasted state. Only one of the three substrates was (13)C-labeled in each experiment. After 3 h of normal awake activity, the animals were sacrificed, and the contribution from each substrate to glycogen and the glycerol moiety of acylglycerols was evaluated. The fraction of (13)C labeling in glycogen and the glycerol moiety exceeded the possible contribution from either plasma glucose or muscle oxaloacetate. The reverse PK served as a common route for both glyconeogenesis and glyceroneogenesis in the skeletal muscle of rats with high plasma glucose. The activity of pyruvate carboxylase was low in muscle, and no PEP carboxykinase activity was detected.
丙酮酸生成的磷酸烯醇式丙酮酸(PEP)是骨骼肌中甘油和糖原从头合成所必需的。一种可能的途径涉及通过磷酸烯醇式丙酮酸羧激酶从柠檬酸循环中间体合成PEP,而另一种途径可能涉及丙酮酸激酶(PK)的逆向反应。早期研究报道,PK的逆向通量可为肌肉中的糖原合成提供碳前体,但该途径的生理重要性仍不确定,尤其是在高血糖情况下。此外,虽然PEP是糖异生和甘油生成的共同中间体,但逆向PK在甘油从头合成中的重要性尚未得到研究。在这里,我们研究了逆向PK对高血糖动物骨骼肌中糖原和酰基甘油甘油部分合成的贡献。大鼠在进食或禁食状态下接受单次腹腔注射葡萄糖、甘油和乳酸。在每个实验中,三种底物中只有一种用(13)C标记。正常清醒活动3小时后,处死动物,并评估每种底物对糖原和酰基甘油甘油部分的贡献。糖原和甘油部分中(13)C标记的比例超过了血浆葡萄糖或肌肉草酰乙酸可能的贡献。逆向PK是高血糖大鼠骨骼肌中糖异生和甘油生成的共同途径。肌肉中丙酮酸羧化酶的活性较低,未检测到磷酸烯醇式丙酮酸羧激酶活性。