Long W, Saffer L, Wei L, Barrett E J
Department of Internal Medicine, University of Virginia Health Sciences Center, Charlottesville, Virginia 22908, USA.
Am J Physiol Endocrinol Metab. 2000 Aug;279(2):E301-6. doi: 10.1152/ajpendo.2000.279.2.E301.
Refeeding reverses the muscle protein loss seen with fasting. The physiological regulators and cellular control sites responsible for this reversal are incompletely defined. Phosphorylation of phosphorylated heat-acid stabled protein (PHAS-I) frees eukaryotic initiation factor 4E (eIF4E) and stimulates protein synthesis by accelerating translation initiation. Phosphorylation of p70 S6-kinase (p70(S6k)) is thought to be involved in the regulation of the synthesis of some ribosomsal proteins and other selected proteins with polypyrimidine clusters near the transcription start site. We examined whether phosphorylation of PHAS-I and p70(S6k) was increased by feeding and determined the separate effects of insulin and amino acids on PHAS-I and p70(S6k) phosphorylation in rat skeletal muscle in vivo. Muscle was obtained from rats fed ad libitum or fasted overnight (n = 5 each). Other fasted rats were infused with insulin (3 microU x min(-1) x kg(-1), euglycemic clamp), amino acids, or the two combined. Gastrocnemius was freeze-clamped, and PHAS-I and p70(S6k) phosphorylation was measured by quantifying the several phosphorylated forms of these proteins seen on Western blots. We observed that feeding increased phosphorylation of both PHAS-I and p70(S6k) (P < 0.05). Infusion of amino acids alone reproduced the effect of feeding. Physiological hyperinsulinemia increased p70(S6K) (P < 0.05) but not PHAS-I phosphorylation (P = 0.98). Addition of insulin to amino acid infusion was no more effective than amino acids alone in promoting PHAS-I and p70(S6k) phosphorylation. We conclude that amino acid infusion alone enhances the activation of the protein synthetic pathways in vivo in rat skeletal muscle. This effect is not dependent on increases in plasma insulin and simulates the activation of protein synthesis that accompanies normal feeding.
再喂养可逆转禁食时出现的肌肉蛋白质流失。导致这种逆转的生理调节因子和细胞控制位点尚未完全明确。磷酸化的热酸稳定蛋白(PHAS-I)的磷酸化会释放真核起始因子4E(eIF4E),并通过加速翻译起始来刺激蛋白质合成。p70 S6激酶(p70(S6k))的磷酸化被认为参与了一些核糖体蛋白以及转录起始位点附近带有多嘧啶簇的其他特定蛋白合成的调节。我们研究了喂养是否会增加PHAS-I和p70(S6k)的磷酸化,并确定了胰岛素和氨基酸对大鼠体内骨骼肌中PHAS-I和p70(S6k)磷酸化的单独影响。从自由进食或禁食过夜的大鼠(每组n = 5)获取肌肉。其他禁食大鼠分别输注胰岛素(3微单位×分钟(-1)×千克(-1),正常血糖钳夹)、氨基酸或两者组合。对腓肠肌进行冷冻钳夹,通过定量蛋白质印迹上这些蛋白质的几种磷酸化形式来测量PHAS-I和p70(S6k)的磷酸化。我们观察到喂养增加了PHAS-I和p70(S6k)的磷酸化(P < 0.05)。单独输注氨基酸重现了喂养的效果。生理性高胰岛素血症增加了p70(S6K)(P < 0.05),但未增加PHAS-I的磷酸化(P = 0.98)。在氨基酸输注中添加胰岛素在促进PHAS-I和p70(S6k)磷酸化方面并不比单独输注氨基酸更有效。我们得出结论,单独输注氨基酸可增强大鼠骨骼肌体内蛋白质合成途径的激活。这种作用不依赖于血浆胰岛素的增加,并模拟了正常喂养时伴随的蛋白质合成激活。