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首页> 外文期刊>Nutrients >Post-Meal Responses of Elongation Factor 2 (eEF2) and Adenosine Monophosphate-Activated Protein Kinase (AMPK) to Leucine and Carbohydrate Supplements for Regulating Protein Synthesis Duration and Energy Homeostasis in Rat Skeletal Muscle
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Post-Meal Responses of Elongation Factor 2 (eEF2) and Adenosine Monophosphate-Activated Protein Kinase (AMPK) to Leucine and Carbohydrate Supplements for Regulating Protein Synthesis Duration and Energy Homeostasis in Rat Skeletal Muscle

机译:餐后伸长因子2(eEF2)和单磷酸腺苷激活的蛋白激酶(AMPK)对亮氨酸和糖补充剂的调节,以调节大鼠骨骼肌的蛋白合成持续时间和能量稳态

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Previous research demonstrates that the anabolic response of muscle protein synthesis (MPS) to a meal is regulated at the level of translation initiation with signals derived from leucine (Leu) and insulin to activate mTORC1 signaling. Recent evidence suggests that the duration of the meal response is limited by energy status of the cell and inhibition of translation elongation factor 2 (eEF2). This study evaluates the potential to extend the anabolic meal response with post-meal supplements of Leu or carbohydrates. Adult (~256 g) male Sprague-Dawley rats were food deprived for 12 h, then either euthanized before a standard meal (time 0) or at 90 or 180 min post-meal. At 135 min post-meal, rats received one of five oral supplements: 270 mg leucine (Leu270), 80:40:40 mg leucine, isoleucine, and valine (Leu80), 2.63 g carbohydrates (CHO2.6), 1 g carbohydrates (CHO1.0), or water (Sham control). Following the standard meal, MPS increased at 90 min then declined to pre-meal baseline at 180 min. Rats administered Leu270, Leu80, CHO2.6, or CHO1.0 maintained elevated rates of MPS at 180 min, while Sham controls declined from peak values. Leu80 and CHO1.0 treatments maintained MPS, but with values intermediate between Sham controls and Leu270 and CHO2.6 supplements. Consistent with MPS findings, the supplements maintained elongation activity and cellular energy status by preventing increases in AMP/ATP and phosphorylation of adenosine monophosphate-activated protein kinase (AMPK), acetyl-CoA carboxylase ACC and eEF2. The impact of the supplements on MPS and cellular energy status was in proportion to the energy content within the individual treatments (i.e., Leu270 Leu80; CHO2.6 CHO1.0), but the Leu supplements produced a disproportionate anabolic stimulation of MPS, eEF2 and energy status with significantly lower energy content. In summary, the incongruity between MPS and translation initiation at 180 min reflects a block in translation elongation due to reduced cellular energy, and the extent to which Leu or carbohydrate supplements are able to enhance energy status and prolong the period of muscle anabolism are dose and time-dependent.
机译:先前的研究表明,肌肉蛋白合成(MPS)对一餐的合成代谢反应在翻译起始水平受到亮氨酸(Leu)和胰岛素信号的激活,从而激活mTORC1信号。最近的证据表明,进餐反应的持续时间受到细胞能量状态和翻译延伸因子2(eEF2)抑制的限制。这项研究评估了用餐后补充Leu或碳水化合物来延长合成代谢餐响应的潜力。成年(约256 g)雄性Sprague-Dawley大鼠被禁食12小时,然后在标准餐前(时间0)或餐后90或180分钟处以安乐死。餐后135分钟,大鼠接受以下五种口服补充剂之一:270 mg亮氨酸(Leu270),80:40:40 mg亮氨酸,异亮氨酸和缬氨酸(Leu80),2.63 g碳水化合物(CHO2.6),1 g碳水化合物(CHO1.0)或水(假控制)。标准餐后,MPS在90分钟时增加,然后在180分钟时下降到餐前基线。施用Leu270,Leu80,CHO2.6或CHO1.0的大鼠在180分钟时MPS速率保持升高,而假手术对照组从峰值下降。 Leu80和CHO1.0处理维持MPS,但介于假对照和Leu270和CHO2.6补充剂之间。与MPS的发现一致,这些补品通过防止AMP / ATP的增加以及单磷酸腺苷激活的蛋白激酶(AMPK),乙酰辅酶A羧化酶ACC和eEF2的磷酸化来维持延伸活性和细胞能量状态。补品对MPS和细胞能量状态的影响与各个治疗中的能量含量成正比(即Leu270> Leu80; CHO2.6> CHO1.0),但Leu补品对MPS产生了不成比例的合成代谢刺激, eEF2和能量状态的能量含量大大降低。总而言之,MPS与180分钟翻译起始之间的不一致性反映了由于细胞能量降低导致翻译延伸受阻,并且Leu或碳水化合物补充剂能够增强能量状态并延长肌肉合成代谢时间的程度是剂量和与时间相关。

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