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连续的电刺激诱发收缩会改变大鼠骨骼肌中的核糖体生物合成。

Consecutive bouts of electrical stimulation-induced contractions alter ribosome biogenesis in rat skeletal muscle.

作者信息

Kotani Takaya, Takegaki Junya, Takagi Ryo, Nakazato Koichi, Ishii Naokata

机构信息

Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo , Tokyo , Japan.

Ritsumeikan Global Innovation Research Organization, Ritsumeikan University , Shiga , Japan.

出版信息

J Appl Physiol (1985). 2019 Jun 1;126(6):1673-1680. doi: 10.1152/japplphysiol.00665.2018. Epub 2019 Apr 18.

Abstract

Ribosome biogenesis has been implicated in resistance exercise training (RET)-induced skeletal muscle hypertrophy. However, it is unclear how increasing bouts of RET affects ribosome content and biogenesis. This was investigated in the present study using simulated RET where rat skeletal muscle is subjected to increasing bouts of electrical stimulation. Sprague-Dawley rats were randomly assigned to the following seven groups: sedentary for 5 days (SED) or 6 wk (SED_6w), resistance-exercise trained with 1 bout (1B), 2 bouts (2B), 3 bouts (3B), 6 bouts (6B), and 18 bouts (18B). RET was simulated on the right gastrocnemius muscle by transcutaneous electric stimulation under isoflurane anesthesia, and a RET bout was given 3 times a week. Rats in 1B, 2B, and 3B groups showed increased 45S precursor (pre-) rRNA and 18S+28S rRNA content per muscle weight and elevated mRNA levels of c- and upstream binding factor (UBF). Increases in phosphorylated UBF and total cyclin D1 protein level were observed 48 h after RET; the former increased as a function of RET duration. In 3B, 6B, and 18B groups, the 18S+28S rRNA content per muscle weight was kept unchanged, and 45S pre-rRNA, cyclin D1, and phosphorylated UBF levels in 18B were lower than those in 3B. These results suggest that RET activates ribosome biogenesis and increases ribosome content through modulation of UBF and cyclin D1 activity at its early phase. Additional bouts of RET may not lead to a further increase in ribosome content per muscle weight through possibly the attenuation of transcription process. Ribosome biogenesis has been implicated in resistance exercise training-induced skeletal muscle hypertrophy. However, it remains unclear how this is influenced by the volume of repeated bouts of resistance exercise training. Using resistance exercise training model with rat skeletal muscle, we provide evidence that ribosome biogenesis is stimulated by the initial few bouts of resistance exercise training with no additional effect of further increase in the exercise bout.

摘要

核糖体生物合成与抗阻运动训练(RET)诱导的骨骼肌肥大有关。然而,尚不清楚增加RET的次数如何影响核糖体含量和生物合成。在本研究中,使用模拟RET的方法对此进行了研究,即将大鼠骨骼肌置于递增次数的电刺激下。将Sprague-Dawley大鼠随机分为以下七组:久坐5天(SED)或6周(SED_6w),接受1次(1B)、2次(2B)、3次(3B)、6次(6B)和18次(18B)抗阻运动训练。在异氟烷麻醉下通过经皮电刺激对右侧腓肠肌进行RET模拟,每周进行3次RET训练。1B、2B和3B组大鼠每肌肉重量的45S前体(pre-)rRNA和18S+28S rRNA含量增加,c-myc和上游结合因子(UBF)的mRNA水平升高。RET后48小时观察到磷酸化UBF和总细胞周期蛋白D1蛋白水平增加;前者随RET持续时间而增加。在3B、6B和18B组中,每肌肉重量的18S+28S rRNA含量保持不变,18B组中的45S pre-rRNA、细胞周期蛋白D1和磷酸化UBF水平低于3B组。这些结果表明,RET在早期阶段通过调节UBF和细胞周期蛋白D1的活性激活核糖体生物合成并增加核糖体含量。额外的RET训练可能不会导致每肌肉重量的核糖体含量进一步增加,这可能是由于转录过程的减弱。核糖体生物合成与抗阻运动训练诱导的骨骼肌肥大有关。然而,尚不清楚这如何受到重复抗阻运动训练次数的影响。使用大鼠骨骼肌抗阻运动训练模型,我们提供证据表明,核糖体生物合成受到最初几次抗阻运动训练的刺激,增加训练次数没有额外效果。

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