东桂柏根肌切片简单配方对C2C12细胞成肌调节因子及IGF-1表达的影响

In-Jun Yang, C. Tettey, H. Shin
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引用次数: 7

摘要

长期以来,东桂伯梗肌节的简单配方一直被用于增强肌肉和/或预防与年龄相关的肌肉损失。然而,它们影响成肌细胞分化的生物活性和机制尚未得到研究。因此,本研究评估了14种简单配方在无细胞毒(0.5 mg / ml)条件下对C2C12成肌细胞分化的影响。用简单配方水提液处理C2C12细胞72 h, RT-PCR检测myoD、myogenin、MRF4、myf5、胰岛素样生长因子-1 (IGF-1)等肌生成调节因子(MRFs)的基因表达水平。大肠根茎(CR)、松子(PS)和芝麻子(SS)处理后,C2C12细胞中肌原素的表达显著增加。大茎葱(Allii Macrostemi Bulbus, AM)、大枣根(Colocasiae Rhizoma, CR)和松子(Pini Semen, PS)处理也能增加C2C12细胞中MRF4的表达。此外,在C2C12细胞中,杜仲皮质(EC)、薯蓣根茎(DR)、山茱萸根茎(CR)、Pini Semen (PS)和Sesami Semen (SS)处理后,IGF-1的表达增强。这些结果表明,东桂波根肌切片的简单配方可能至少部分通过增加肌原素和/或MRF4和/或IGF-1的表达来促进成肌细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Simple Formulas of Muscle Section in Donguibogam on Myogenic Regulatory Factors and IGF-1 Expression in C2C12 Cells
Simple formulas (單方) of muscle section in Donguibogam (東醫寶鑑) have long been prescribed for strengthening muscle and/or prevention of age-related muscle loss. However, biological activity and mechanisms by which they influence myoblast differentiation have not been studied. Therefore, in this study, we evaluated the effects of 14 simple formulas on myoblast differentiation in C2C12 myoblast cells under non-cytotoxic (0.5 ㎎/㎖) conditions. C2C12 cells were treated with water extracts of simple formulas for 72 h, and RT-PCR was performed to determine the gene expression levels of myogenic regulatory factors (MRFs), including myoD, myogenin, MRF4, myf5, and insulin like growth factor-1 (IGF-1). Treatment with Colocasiae Rhizoma (CR), Pini Semen (PS), and Sesami Semen (SS) resulted in a significant increase in expression of myogenin in C2C12 cells. Treatment with Allii Macrostemi Bulbus (AM), Colocasiae Rhizoma (CR), and Pini Semen (PS) also resulted in increased expression of MRF4 in C2C12 cells. In addition, enhanced expression of IGF-1 was observed in treatment with Eucommiae cortex (EC), Dioscoreae Rhizoma (DR), Colocasiae Rhizoma (CR), Pini Semen (PS), and Sesami Semen (SS) in C2C12 cells. These results indicate that simple formulas of muscle section in Donguibogam could potentially enhance myoblast differentiation at least in part via increasing expression of myogenin, and/or MRF4 and/or IGF-1.
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