Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, São Paulo 05508-220, Brazil.
Divisions of Nephrology and Molecular Medicine, LIM-29, Department of Medicine, University of São Paulo, São Paulo 05508-220, Brazil.
Nutrients. 2023 Nov 7;15(22):4711. doi: 10.3390/nu15224711.
To evaluate the effects of resistance exercise training (RET) and/or glutamine supplementation (GS) on signaling protein synthesis in adult rat skeletal muscles.
The following groups were studied: (1) control, no exercise (C); (2) exercise, hypertrophy resistance exercise training protocol (T); (3) no exercise, supplemented with glutamine (G); and (4) exercise and supplemented with glutamine (GT). The rats performed hypertrophic training, climbing a vertical ladder with a height of 1.1 m at an 80° incline relative to the horizontal with extra weights tied to their tails. The RET was performed three days a week for five weeks. Each training session consisted of six ladder climbs. The extra weight load was progressively increased for each animal during each training session. The G groups received daily L-glutamine by gavage (one g per kilogram of body weight per day) for five weeks. The C group received the same volume of water during the same period. The rats were euthanized, and the extensor digitorum longus (EDL) muscles from both hind limbs were removed and immediately weighed. Glutamine and glutamate concentrations were measured, and histological, signaling protein contents, and mRNA expression analyses were performed.
Supplementation with free L-glutamine increased the glutamine concentration in the EDL muscle in the C group. The glutamate concentration was augmented in the EDL muscles from T rats. The EDL muscle mass did not change, but a significant rise was reported in the cross-sectional area (CSA) of the fibers in the three experimental groups. The levels of the phosphorylated proteins (pAkt/Akt, pp70S6K/p70S6K, p4E-BP1/4E-BP1, and pS6/S6 ratios) were significantly increased in EDL muscles of G rats, and the activation of p4E-BP1 was present in T rats. The fiber CSAs of the EDL muscles in T, G, and GT rats were increased compared to the C group. These changes were accompanied by a reduction in the 26 proteasome activity of EDL muscles from T rats.
Five weeks of GS and/or RET induced muscle hypertrophy, as indicated by the increased CSAs of the EDL muscle fibers. The increase in CSA was mediated via the upregulated phosphorylation of Akt, 4E-BP1, p70S6k, and S6 in G animals and 4E-BP1 in T animals. In the EDL muscles from T animals, a decrease in proteasome activity, favoring a further increase in the CSA of the muscle fibers, was reported.
评估抗阻运动训练(RET)和/或谷氨酰胺补充(GS)对成年大鼠骨骼肌信号蛋白合成的影响。
研究了以下几组:(1)对照组,无运动(C);(2)运动组,进行肥大抗阻运动训练方案(T);(3)无运动,补充谷氨酰胺(G);和(4)运动和补充谷氨酰胺(GT)。大鼠进行肥大训练,爬上一个相对于水平方向倾斜 80°的高度为 1.1 米的垂直梯子,尾巴上绑有额外的重量。RET 每周进行三天,持续五周。每次训练课包括六次爬梯。每个训练课程中,每个动物的额外重量负荷逐渐增加。G 组每天通过管饲给予 L-谷氨酰胺(每天每公斤体重 1 克)五周。C 组在同一时期接受相同体积的水。处死大鼠,从后腿的伸趾长肌(EDL)中取出并立即称重。测量谷氨酰胺和谷氨酸浓度,并进行组织学、信号蛋白含量和 mRNA 表达分析。
补充游离 L-谷氨酰胺可增加 C 组 EDL 肌肉中的谷氨酰胺浓度。T 组大鼠 EDL 肌肉中的谷氨酸浓度增加。EDL 肌肉质量没有变化,但三个实验组的纤维横截面积(CSA)均有显著增加。G 组大鼠 EDL 肌肉中磷酸化蛋白(pAkt/Akt、pp70S6K/p70S6K、p4E-BP1/4E-BP1 和 pS6/S6 比值)水平显著升高,T 组大鼠 p4E-BP1 被激活。T、G 和 GT 组大鼠 EDL 肌肉的纤维 CSA 均高于 C 组。这些变化伴随着 T 组大鼠 EDL 肌肉 26 蛋白酶体活性的降低。
五周的 GS 和/或 RET 诱导肌肉肥大,表现为 EDL 肌肉纤维 CSA 的增加。在 G 动物中,CSA 的增加是通过 Akt、4E-BP1、p70S6k 和 S6 的磷酸化上调介导的,而在 T 动物中则是通过 4E-BP1 介导的。在 T 组动物的 EDL 肌肉中,蛋白酶体活性降低,有利于肌肉纤维 CSA 的进一步增加。