Roberts Michael D, Holland A Maleah, Kephart Wesley C, Mobley C Brooks, Mumford Petey W, Lowery Ryan P, Fox Carlton D, McCloskey Anna E, Shake Joshua J, Mesquita Paulo, Patel Romil K, Martin Jeffrey S, Young Kaelin C, Kavazis Andreas N, Wilson Jacob M
Department of Kinesiology, Auburn University, Auburn, Alabama; Edward Via College of Osteopathic Medicine, Auburn Campus, Auburn, Alabama; and.
Department of Kinesiology, Auburn University, Auburn, Alabama;
J Appl Physiol (1985). 2016 May 15;120(10):1173-85. doi: 10.1152/japplphysiol.00837.2015. Epub 2015 Dec 30.
We examined whether acute and/or chronic skeletal muscle anabolism is impaired with a low-carbohydrate diet formulated to elicit ketosis (LCKD) vs. a mixed macronutrient Western diet (WD). Male Sprague-Dawley rats (9-10 wk of age, 300-325 g) were provided isoenergetic amounts of a LCKD or a WD for 6 wk. In AIM 1, basal serum and gastrocnemius assessments were performed. In AIM 2, rats were resistance exercised for one bout and were euthanized 90-270 min following exercise for gastrocnemius analyses. In AIM 3, rats voluntarily exercised daily with resistance-loaded running wheels, and hind limb muscles were analyzed for hypertrophy markers at the end of the 6-wk protocol. In AIM 1, basal levels of gastrocnemius phosphorylated (p)-rps6, p-4EBP1, and p-AMPKα were similar between diets, although serum insulin (P < 0.01), serum glucose (P < 0.001), and several essential amino acid levels (P < 0.05) were lower in LCKD-fed rats. In AIM 2, LCKD- and WD-fed rats exhibited increased postexercise muscle protein synthesis levels (P < 0.0125), but no diet effect was observed (P = 0.59). In AIM 3, chronically exercise-trained LCKD- and WD-fed rats presented similar increases in relative hind limb muscle masses compared with their sedentary counterparts (12-24%, P < 0.05), but there was no between-diet effects. Importantly, the LCKD induced "mild" nutritional ketosis, as the LCKD-fed rats in AIM 2 exhibited ∼1.5-fold greater serum β-hydroxybutyrate levels relative to WD-fed rats (diet effect P = 0.003). This study demonstrates that the tested LCKD in rodents, while only eliciting mild nutritional ketosis, does not impair the acute or chronic skeletal muscle hypertrophic responses to resistance exercise.
我们研究了与混合宏量营养素的西方饮食(WD)相比,旨在引发酮症的低碳水化合物饮食(LCKD)是否会损害急性和/或慢性骨骼肌合成代谢。给雄性斯普拉格-道利大鼠(9 - 10周龄,300 - 325克)提供等能量的LCKD或WD,持续6周。在目标1中,进行了基础血清和腓肠肌评估。在目标2中,大鼠进行一次抗阻运动,并在运动后90 - 270分钟处死,用于腓肠肌分析。在目标3中,大鼠每天使用带阻力的跑步轮进行自主运动,在6周实验方案结束时分析后肢肌肉的肥大标志物。在目标1中,尽管LCKD喂养的大鼠血清胰岛素(P < 0.01)、血清葡萄糖(P < 0.001)和几种必需氨基酸水平(P < 0.05)较低,但两种饮食之间腓肠肌磷酸化(p)-rps6、p-4EBP1和p-AMPKα的基础水平相似。在目标2中,LCKD和WD喂养的大鼠运动后肌肉蛋白质合成水平均升高(P < 0.0125),但未观察到饮食效应(P = 0.59)。在目标3中,与久坐的对照组相比,长期进行运动训练的LCKD和WD喂养的大鼠相对后肢肌肉质量有相似的增加(12 - 24%,P < 0.05),但饮食之间没有差异。重要的是,LCKD诱导了“轻度”营养性酮症,因为目标2中LCKD喂养的大鼠血清β-羟基丁酸水平比WD喂养的大鼠高约1.5倍(饮食效应P = 0.003)。这项研究表明,在啮齿动物中测试的LCKD虽然仅引发轻度营养性酮症,但不会损害对抗阻运动的急性或慢性骨骼肌肥大反应。