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Exercise training induces several skeletal muscle adaptations. Beta-guanidinopropionic acid (β-GPA) is a creatine analog that simulates the effect of exercise to induce mitochondrial biogenesis. However, the effects of β-GPA on resistance training adaptation, such as muscle hypertrophy and mitochondrial biogenesis, are unclear. Therefore, using a resistance exercise model in rats, the present study was designed to investigate the effects of β-GPA administration on resistance training adaptations. This study was approved by the Ethics Committee for Animal Experiments at Ritsumeikan University (approval number: BKC2022-009). Male Sprague Dawley rats were randomly divided into placebo or β-GPA groups. β-GPA (1000 mg/kg) was orally administered once daily, starting seven days before the initiation of electromyostimulation as a model for resistance exercise, and continued throughout the training period. Electromyostimulation was applied to the right gastrocnemius muscle via electrical stimulation every other day for a total of 12 sessions Peroxisome proliferators-activated receptor-γ co-activator-1α, a regulator of mitochondrial biogenesis, was significantly increased by the combination of training and β-GPA compared to the training leg (p<0.05). Protein expression of Total OXPHOS, a marker of mitochondrial content, was significantly increased by the combination of training and β-GPA compared to the training leg (p<0.05). β-GPA intake reduced muscle mass (main effect of β-GPA, p<0.05) and was associated with muscle protein breakdown-related Fbx32 and LC3-II protein expression levels but did not counteract the increase in muscle mass caused by resistance training. Administration of exogenous β-GPA enhanced resistance training-induced mitochondrial biogenesis. Moreover, β-GPA still permitted resistance electromyostimulation-induced muscle mass gains, but that effect was attenuated as compared to placebo. [ABSTRACT FROM AUTHOR]

Leucine is a branched-chain amino acid that is present in protein, and it is an essential factor in activating the mechanistic target of the rapamycin complex 1 signaling pathway and increasing muscle protein synthesis. However, the loss of digestive function after total gastrectomy leads to impaired protein absorption, potentially failing to stimulate muscle protein synthesis. Therefore, this study aimed to investigate whether muscle protein synthesis is enhanced by oral skim milk administration after total gastrectomy. Male Sprague Dawley rats were divided into total gastrectomy (TG) and sham surgery (S) groups. After five weeks postoperatively, we orally administered skim milk to achieve 3.1 g protein/kg body weight and collected blood and gastrocnemius muscle. The gastrocnemius muscle weight was significantly lower in the TG group than in the S group (p < 0.05). The increase in plasma leucine concentration was significantly lower in the TG group than in the S group (p < 0.05). The skeletal muscle protein synthesis and the phosphorylation of p70S6K and 4E-BP1 showed a similar increase in both groups. Even after TG, muscle protein synthesis was stimulated by consuming skim milk, accompanied by a sufficient rise in plasma leucine concentration. [ABSTRACT FROM AUTHOR]

• Magnetic liposomes enable the efficient magnetization of mesenchymal stem cells. • Magnetized MSCs were much retained in mouse skeletal muscle under a magnetic field. • Magnetized MSCs showed high immunomodulatory effects on inflamed skeletal muscle. Sarcopenia, an age-related reduction in skeletal muscle mass and strength, is mainly caused by chronic inflammation. Because mesenchymal stem cells (MSCs) have the capacity to both promote myogenic cell differentiation and suppress inflammation, they are a promising candidate for sarcopenia treatment. In this study, to achieve the long-term retention of MSCs in skeletal muscle, we prepared magnetized MSCs using magnetic anionic liposome/atelocollagen complexes that we had previously developed, and evaluated their retention efficiency and immunomodulatory effects in mouse inflamed skeletal muscle. Mouse MSCs were efficiently magnetized by incubation with magnetic anionic liposome/atelocollagen complexes for 30 min under a magnetic field. The magnetized MSCs differentiated normally into osteoblasts and adipocytes. Additionally, non-magnetized MSCs and magnetized MSCs increased IL-6 and inducible nitric oxide synthase mRNA expression and decreased TNF-α and IL-1β mRNA expression in C2C12 mouse skeletal muscle myotubes through paracrine effects. Moreover, magnetized MSCs were significantly retained in cell culture plates and mouse skeletal muscle after their local injection in the presence of a magnetic field. Furthermore, magnetized MSCs significantly increased IL-6 and IL-10 mRNA expression and decreased TNF-α and IL-1β mRNA expression in inflamed skeletal muscle. These results suggest that magnetized MSCs may be useful for effective sarcopenia treatment. [ABSTRACT FROM AUTHOR]