Ulla Anayt, Rahman Md Mizanur, Uchida Takayuki, Kayaki Hiroyuki, Nishitani Yosuke, Yoshino Susumu, Kuwahara Hiroshige, Nikawa Takeshi
Department of Nutritional Physiology, Institute of Biomedical Sciences, Tokushima University Graduate School, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.
Research Center, Maruzen Pharmaceuticals Co., Ltd., 1089-8 Sagata, Shinichi-cho, Fukuyama, Hiroshima 729-3102, Japan.
J Clin Biochem Nutr. 2025 Jan;76(1):16-24. doi: 10.3164/jcbn.23-70. Epub 2024 Jul 25.
3-(4-Hydroxy-3-methoxyphenyl) propionic acid is an metabolite of 4-hydroxy-3-methoxycinnamic acid which is abundantly found in coffee bean, rice bran, fruits, and vegetables. Previous studies reported that polyphenols and their metabolites exhibit positive effects on muscle health. Thus, the effect of 3-(4-hydroxy-3-methoxyphenyl) propionic acid on muscle atrophy induced by dexamethasone was investigated using mouse C2C12 skeletal myotubes. Dexamethasone treatment (10 μM) reduced the diameter and myosin heavy chain protein expression in C2C12 myotubes; it also increased muscle atrophy-associated ubiquitin ligases, such as muscle atrophy F-box protein 1/Atrogin-1 and muscle ring finger protein-1, along with their upstream regulator Krüppel-like factor 15. Dexamethasone dephosphorylated FoxO3a transcription factor and increased total FoxO3a expression. Interestingly, 10 μM 3-(4-hydroxy-3-methoxyphenyl) propionic acid treatment significantly attenuated dexamethasone-induced reduction in myotube thickness and muscle protein degradation and suppressed muscle atrophy-associated ubiquitin ligases. 3-(4-Hydroxy-3-methoxyphenyl) propionic acid also prevented dexamethasone-induced Krüppel-like factor 15 and FoxO3a expression. In conclusion, these results suggest that metabolite of polyphenols per se could be the real origin of the anti-muscular atrophy activity, as 3-(4-hydroxy-3-methoxyphenyl) propionic acid ameliorated glucocorticoid-induced muscle atrophy by suppressing Atrogin-1 and MuRF-1.
3-(4-羟基-3-甲氧基苯基)丙酸是4-羟基-3-甲氧基肉桂酸的一种代谢产物,在咖啡豆、米糠、水果和蔬菜中大量存在。先前的研究报道,多酚及其代谢产物对肌肉健康具有积极作用。因此,本研究使用小鼠C2C12骨骼肌肌管,探究了3-(4-羟基-3-甲氧基苯基)丙酸对由地塞米松诱导的肌肉萎缩的影响。地塞米松处理(10 μM)可减小C2C12肌管的直径并降低肌球蛋白重链蛋白的表达;还可增加与肌肉萎缩相关的泛素连接酶,如肌肉萎缩F盒蛋白1/Atrogin-1和肌肉环指蛋白-1,以及它们的上游调节因子Krüppel样因子15的表达。地塞米松使FoxO3a转录因子去磷酸化并增加了FoxO3a的总表达。有趣的是,10 μM 3-(4-羟基-3-甲氧基苯基)丙酸处理可显著减轻地塞米松诱导的肌管厚度减小和肌肉蛋白降解,并抑制与肌肉萎缩相关的泛素连接酶。3-(4-羟基-3-甲氧基苯基)丙酸还可阻止地塞米松诱导的Krüppel样因子15和FoxO3a的表达。总之,这些结果表明,多酚的代谢产物本身可能是抗肌肉萎缩活性的真正来源,因为3-(4-羟基-3-甲氧基苯基)丙酸通过抑制Atrogin-1和MuRF-1改善了糖皮质激素诱导的肌肉萎缩。