Hwang Jieun, Kim Mi-Bo, Lee Sanggil, Hwang Jae-Kwan
Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul 03722, Republic of Korea.
Department of Food Science and Nutrition, Pukyong National University, Busan 48513, Republic of Korea.
Mar Drugs. 2024 Dec 12;22(12):557. doi: 10.3390/md22120557.
The objective of this study was to examine whether fucosterol, a phytosterol of marine algae, could ameliorate skeletal muscle atrophy in tumor necrosis factor-alpha (TNF-α)-treated C2C12 myotubes and in immobilization-induced C57BL/6J mice. Male C57BL6J mice were immobilized for 1 week to induce skeletal muscle atrophy. Following immobilization, the mice were administrated orally with saline or fucosterol (10 or 30 mg/kg/day) for 1 week. Fucosterol significantly attenuated immobilization-induced muscle atrophy by enhancing muscle strength, with a concomitant increase in muscle volume, mass, and myofiber cross-sectional area in the tibialis anterior (TA) muscle in mice. In both the TNF-α-treated C2C12 myotubes and the TA muscle of immobilized mice, fucosterol significantly prevented muscle protein degradation, which was attributed to a reduction in atrogin-1 and muscle ring finger 1 gene expression through an increase in forkhead box O3α (FoxO3α) phosphorylation. Continuously, fucosterol stimulated muscle protein synthesis by increasing the phosphorylation of the mammalian target of the rapamycin (mTOR), 70 kDa ribosomal protein S6 kinase, and 4E binding protein 1, which was mediated through the stimulation of the phosphatidylinositol 3-kinase (PI3K)/Akt signaling pathway. Thus, fucosterol alleviated skeletal muscle atrophy in TNF-α-treated C2C12 myotubes and immobilized C57BL/6J mice through the regulation of the Akt/mTOR/FoxO3α signaling pathway.
本研究的目的是检验岩藻甾醇(一种海藻植物甾醇)是否能改善经肿瘤坏死因子-α(TNF-α)处理的C2C12肌管以及固定诱导的C57BL/6J小鼠的骨骼肌萎缩。将雄性C57BL6J小鼠固定1周以诱导骨骼肌萎缩。固定后,给小鼠口服生理盐水或岩藻甾醇(10或30毫克/千克/天),持续1周。岩藻甾醇通过增强肌肉力量显著减轻了固定诱导的肌肉萎缩,同时小鼠胫骨前肌(TA)的肌肉体积、质量和肌纤维横截面积增加。在经TNF-α处理的C2C12肌管和固定小鼠的TA肌肉中,岩藻甾醇均显著抑制了肌肉蛋白质降解,这归因于通过增加叉头框O3α(FoxO3α)磷酸化,atrogin-1和肌肉环指蛋白1基因表达降低。持续地,岩藻甾醇通过刺激磷脂酰肌醇3激酶(PI3K)/Akt信号通路,增加雷帕霉素靶蛋白(mTOR)、70 kDa核糖体蛋白S6激酶和4E结合蛋白1的磷酸化,从而刺激肌肉蛋白质合成。因此,岩藻甾醇通过调节Akt/mTOR/FoxO3α信号通路,减轻了经TNF-α处理的C2C12肌管和固定的C57BL/6J小鼠的骨骼肌萎缩。