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在大鼠中,抵抗训练和肌酸补充对 UPR-PERK 通路和肌肉肥大的影响。

Changes in UPR-PERK pathway and muscle hypertrophy following resistance training and creatine supplementation in rats.

机构信息

Department of Physical Education and Sport Sciences, University of Kurdistan, Sanandaj, Iran.

Liver and Digestive Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.

出版信息

J Physiol Biochem. 2021 May;77(2):331-339. doi: 10.1007/s13105-021-00801-4. Epub 2021 Feb 26.


DOI:10.1007/s13105-021-00801-4
PMID:33635524
Abstract

The unfolded protein response (UPR) plays a pivotal role in some exercise training-induced physiological adaptation. Our aim was to evaluate the changes in the protein kinase R-like endoplasmic reticulum kinase (PERK) arm of the UPR and hypertrophy signaling pathway following 8 weeks of resistance training and creatine (Cr) supplementation in rats. Thirty-two adult male Wistar rats (8 weeks old) were randomly divided into 4 groups of 8: untrained + placebo (UN+P), resistance training + placebo (RT+P), untrained + Cr (UN+Cr), and resistance training + Cr (RT+Cr). Trained animals were submitted to the ladder-climbing exercise training 5 days per week for a total of 8 weeks. Cr supplementation groups received creatine diluted with 1.5 ml of 5% dextrose orally. The flexor hallucis longus (FHL) muscle was extracted 48 h after the last training session and used for western blotting. After training period, the RT+Cr and RT+P groups presented a significant increase in phosphorylated and phosphorylated/total ratio hypertrophy indices, phosphorylated and phosphorylated/total ratio PERK pathway proteins, and other downstream proteins of the PERK cascade compared with their untrained counterparts (P < 0.05). The increase in hypertrophy indices were higher but PERK pathway proteins were lower in the RT-Cr group than in the RT+P group (P < 0.05). There was no significant difference between the untrained groups (P > 0.05). Our study suggests that resistance training in addition to Cr supplementation modifies PERK pathway response and improves skeletal muscle hypertrophy.

摘要

未折叠蛋白反应(UPR)在某些运动训练引起的生理适应中起着关键作用。我们的目的是评估大鼠 8 周抗阻训练和肌酸(Cr)补充后 UPR 和肥大信号通路中蛋白激酶 R 样内质网激酶(PERK)臂的变化。32 只成年雄性 Wistar 大鼠(8 周龄)随机分为 4 组,每组 8 只:未训练+安慰剂(UN+P)、抗阻训练+安慰剂(RT+P)、未训练+Cr(UN+Cr)和抗阻训练+Cr(RT+Cr)。训练动物每周进行 5 天的爬梯运动训练,共 8 周。Cr 补充组口服 1.5ml5%葡萄糖稀释的肌酸。最后一次训练结束后 48 小时提取屈肌趾长肌(FHL),用于 Western 印迹分析。经过训练期后,与未训练组相比,RT+Cr 和 RT+P 组的磷酸化和磷酸化/总比值肥大指数、磷酸化和磷酸化/总比值 PERK 通路蛋白以及 PERK 级联的其他下游蛋白均显著增加(P<0.05)。与 RT+P 组相比,RT-Cr 组的肥大指数增加更高,但 PERK 通路蛋白降低(P<0.05)。未训练组之间无显著差异(P>0.05)。我们的研究表明,抗阻训练加 Cr 补充可改变 PERK 通路反应,改善骨骼肌肥大。

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Changes in UPR-PERK pathway and muscle hypertrophy following resistance training and creatine supplementation in rats.

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[2]
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本文引用的文献

[1]
Effects of a resistance-training programme on endoplasmic reticulum unfolded protein response and mitochondrial functions in PBMCs from elderly subjects.

Eur J Sport Sci. 2019-1-7

[2]
Mutual interaction between oxidative stress and endoplasmic reticulum stress in the pathogenesis of diseases specifically focusing on non-alcoholic fatty liver disease.

World J Biol Chem. 2018-10-18

[3]
High-fat diet suppresses the positive effect of creatine supplementation on skeletal muscle function by reducing protein expression of IGF-PI3K-AKT-mTOR pathway.

PLoS One. 2018-10-4

[4]
PERK regulates skeletal muscle mass and contractile function in adult mice.

FASEB J. 2018-9-11

[5]
The PERK arm of the unfolded protein response regulates satellite cell-mediated skeletal muscle regeneration.

Elife. 2017-3-23

[6]
Long-term resistance exercise-induced muscular hypertrophy is associated with autophagy modulation in rats.

J Physiol Sci. 2018-5

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The role of mTOR signalling in the regulation of skeletal muscle mass in a rodent model of resistance exercise.

Sci Rep. 2016-8-9

[8]
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J Exp Biol. 2016-1

[9]
Excessive eccentric exercise-induced overtraining model leads to endoplasmic reticulum stress in mice skeletal muscles.

Life Sci. 2016-1-15

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Skeletal muscle-specific eukaryotic translation initiation factor 2α phosphorylation controls amino acid metabolism and fibroblast growth factor 21-mediated non-cell-autonomous energy metabolism.

FASEB J. 2016-2

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