Chen Yi-Wen, Li Tsung-Ju, Wang Li-Ching, Yang Bi-Hua, Chen Yen-Lien, Chen Chin-Chu, Lin Hsin-Tang
Biotech Research Institute, Grape King Bio Ltd., Taoyuan City 325, Taiwan.
Department of Food Safety, National Chung Hsing University, Taichung City 402, Taiwan.
Curr Issues Mol Biol. 2024 Dec 12;46(12):14033-14044. doi: 10.3390/cimb46120839.
Muscle atrophy, an age-related condition, presents a growing healthcare concern within the context of global population aging. While studies have investigated for its potential antifatigue properties, reports on its active components remain limited. This study evaluated the efficacy of mycelium extract on muscle health, utilizing a 1:1 water-ethanol preparation administered to C57BL/6 mice exhibiting acute hind leg atrophy. The results indicated no adverse effects, with significant improvements in muscle endurance and soleus muscle mass observed over a 14-day period. To further elucidate the mechanisms and effects of mycelium on dexamethasone-induced muscle atrophy, the water extract was fractionated into components of <3.5 kDa, 3.5-10 kDa, and >10 kDa using dialysis membranes. The investigation utilized a C2C12 cell atrophy model, induced by dexamethasone, to analyze the expression of relevant genes via qPCR. The results demonstrated that the <3.5 kDa and >10 kDa fractions significantly upregulated the expression of and genes while simultaneously downregulating the expression of and . It is noteworthy that the <3.5 kDa fraction exclusively enhanced MYHC protein expression and suppressed AMPK expression, as confirmed by Western blot analysis. This comprehensive pilot study suggests that the low-molecular-weight fraction of mycelium exhibits considerable potential for muscle mass preservation and atrophy mitigation. As a result, it offers a promising direction for the development of supplements aimed at addressing fatigue and preventing muscle atrophy.
肌肉萎缩是一种与年龄相关的病症,在全球人口老龄化的背景下,它引发了越来越多的医疗保健关注。虽然已有研究调查了其潜在的抗疲劳特性,但其活性成分的相关报道仍然有限。本研究评估了菌丝体提取物对肌肉健康的功效,采用1:1水 - 乙醇制剂对表现出急性后腿萎缩的C57BL/6小鼠进行给药。结果表明没有不良反应,在14天的时间里观察到肌肉耐力和比目鱼肌质量有显著改善。为了进一步阐明菌丝体对地塞米松诱导的肌肉萎缩的作用机制和效果,使用透析膜将水提取物分离成分子量小于3.5 kDa、3.5 - 10 kDa和大于10 kDa的组分。该研究利用地塞米松诱导的C2C12细胞萎缩模型,通过qPCR分析相关基因的表达。结果表明,分子量小于3.5 kDa和大于10 kDa的组分显著上调了[基因名称1]和[基因名称2]基因的表达,同时下调了[基因名称3]和[基因名称4]的表达。值得注意的是,经蛋白质免疫印迹分析证实,分子量小于3.5 kDa的组分专门增强了肌球蛋白重链(MYHC)蛋白的表达并抑制了腺苷酸活化蛋白激酶(AMPK)的表达。这项全面的初步研究表明,菌丝体的低分子量组分在保留肌肉质量和减轻萎缩方面具有相当大的潜力。因此,它为开发旨在解决疲劳和预防肌肉萎缩的补充剂提供了一个有前景的方向。