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Three-Dimensional Culture Model of Skeletal Muscle Tissue with Atrophy Induced by Dexamethasone

机译:地塞米松致骨骼肌萎缩的三维培养模型

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摘要

Drug screening systems for muscle atrophy based on the contractile force of cultured skeletal muscle tissues are required for the development of preventive or therapeutic drugs for atrophy. This study aims to develop a muscle atrophy model by inducing atrophy in normal muscle tissues constructed on microdevices capable of measuring the contractile force and to verify if this model is suitable for drug screening using the contractile force as an index. Tissue engineered skeletal muscles containing striated myotubes were prepared on the microdevices for the study. The addition of 100 µM dexamethasone (Dex), which is used as a muscle atrophy inducer, for 24 h reduced the contractile force significantly. An increase in the expression of Atrogin-1 and MuRF-1 in the tissues treated with Dex was established. A decrease in the number of striated myotubes was also observed in the tissues treated with Dex. Treatment with 8 ng/mL Insulin-like Growth Factor (IGF-I) for 24 h significantly increased the contractile force of the Dex-induced atrophic tissues. The same treatment, though, had no impact on the force of the normal tissues. Thus, it is envisaged that the atrophic skeletal muscle tissues induced by Dex can be used for drug screening against atrophy.
机译:为了开发用于萎缩的预防或治疗药物,需要基于培养的骨骼肌组织的收缩力的用于肌肉萎缩的药物筛选系统。这项研究旨在通过在能够测量收缩力的微型设备上构造的正常肌肉组织中诱导萎缩来开发肌肉萎缩模型,并验证该模型是否适合以收缩力为指标进行药物筛选。在用于研究的微型设备上准备了包含横纹肌管的组织工程骨骼肌。加入100 µM地塞米松(Dex)用作肌肉萎缩诱导剂,持续24 h可显着降低收缩力。建立在用Dex处理的组织中Atrogin-1和MuRF-1的表达增加。在用Dex处理的组织中也观察到横纹肌管数量的减少。用8 ng / mL胰岛素样生长因子(IGF-1)处理24小时可显着增加Dex诱导的萎缩组织的收缩力。但是,相同的处理对正常组织的力量没有影响。因此,设想由Dex诱导的萎缩性骨骼肌组织可用于针对萎缩的药物筛选。

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