Nishida Ryoichi, Nukaga Shota, Kawahara Isao, Miyagawa Yoshihiro, Goto Kei, Nakashima Chie, Luo Yi, Sasaki Takamitsu, Fujii Kiyomu, Ohmori Hitoshi, Ogata Ruiko, Mori Shiori, Fujiwara-Tani Rina, Kuniyasu Hiroki
Department of Molecular Pathology, Nara Medical University, 840 Shijo-cho, Kashihara 634-8521, Japan.
Antioxidants (Basel). 2024 Jul 9;13(7):821. doi: 10.3390/antiox13070821.
Nutritional interventions are one focus of sarcopenia treatment. As medium-chain fatty acids (MCFAs) are oxidized in the mitochondria and produce energy through oxidative phosphorylation (OXPHOS), they are key parts of nutritional interventions. We investigated the in vitro effects of three types of MCFA, caprylic acid (C8), capric acid (C10), and lauric acid (C12), in skeletal muscle cells. Compared with C10 and C12, C8 promoted mitophagy through the phosphatase and tensin homolog (PTEN)-induced kinase 1-Parkin pathway and increased the expression of peroxisome proliferator-activated receptor gamma coactivator 1-α and dynamin-related protein 1 to reduce mitochondrial oxidative stress and promote OXPHOS. Furthermore, the expression of myogenic differentiation 1 and myosin heavy chain increased in myotubes, thus promoting muscle differentiation and maturation. These results suggest that C8 improves mitochondrial quality and promotes skeletal muscle maturation; in contrast, C10 and C12 poorly promoted mitochondrial quality control and oxidative stress and suppressed energy production. Future animal experiments are required to establish the usefulness of C8 for nutritional interventions for sarcopenia.
营养干预是肌肉减少症治疗的一个重点。由于中链脂肪酸(MCFAs)在线粒体中被氧化并通过氧化磷酸化(OXPHOS)产生能量,它们是营养干预的关键部分。我们研究了三种类型的MCFA,即辛酸(C8)、癸酸(C10)和月桂酸(C12)对骨骼肌细胞的体外影响。与C10和C12相比,C8通过磷酸酶和张力蛋白同源物(PTEN)诱导激酶1-帕金途径促进线粒体自噬,并增加过氧化物酶体增殖物激活受体γ共激活因子1-α和动力蛋白相关蛋白1的表达,以降低线粒体氧化应激并促进氧化磷酸化。此外,肌管中肌源性分化1和肌球蛋白重链的表达增加,从而促进肌肉分化和成熟。这些结果表明,C8可改善线粒体质量并促进骨骼肌成熟;相比之下,C10和C12对线粒体质量控制和氧化应激的促进作用较差,并抑制能量产生。未来需要进行动物实验,以确定C8在肌肉减少症营养干预中的有效性。