Biochemistry Department, Faculty of Pharmacy, Delta University, P.O. Box: +11152, Gamasa, Egypt.
Pathology Department, Faculty of Veterinary Medicine, Kafrelsheik University, Kafrelsheik, Egypt.
Mol Cell Biochem. 2018 Jul;444(1-2):161-168. doi: 10.1007/s11010-017-3240-5. Epub 2017 Dec 2.
Skeletal muscle atrophy occurs in different catabolic conditions and mostly accompanied with upregulation of Muscle ring finger 1 (MuRF1) gene which is one of the master regulatory genes in muscle atrophy. Taurine amino acid is widely distributed in different tissues and has anti-inflammatory and antioxidant effects. This study aimed to investigate the potential influence of taurine on muscle atrophy induced by reduced mechanical loading. Twenty-eight Albino mice were used, and divided equally into four groups: group I (control); group II (immobilization); group III (immobilization + taurine); and group IV (taurine). Quadriceps muscle sections were taken for histopathology, immunohistochemical analysis of caspase 3 expression, and qRT-PCR of MuRF1 gene. Our data revealed Zenker necrosis associated with axonal injury of the nerve trunk of the immobilized muscle together with increase of caspase 3 expression and upregulation of MuRF1 gene. While, taurine supplementation alleviated the muscular and neural tissues damage associated with disuse skeletal muscle atrophy through downregulation of MuRF1 gene and decrease of tissue caspase 3 expression. In conclusion, taurine may be helpful to counteract apoptosis and up-regulated MuRF1 gene expression related to muscle atrophy, which might be hopeful for a large number of patients.
骨骼肌萎缩发生在不同的分解代谢状态下,大多伴随着肌肉环指 1(MuRF1)基因的上调,该基因是肌肉萎缩的主要调节基因之一。牛磺酸氨基酸广泛分布于不同组织中,具有抗炎和抗氧化作用。本研究旨在探讨牛磺酸对减少机械负荷引起的肌肉萎缩的潜在影响。使用 28 只白化小鼠,并将其平均分为四组:第 I 组(对照组);第 II 组(固定组);第 III 组(固定+牛磺酸组);和第 IV 组(牛磺酸组)。取股四头肌切片进行组织病理学检查、半胱天冬酶 3 表达的免疫组织化学分析以及 MuRF1 基因的 qRT-PCR。我们的数据显示,与固定肌肉的轴突损伤相关的 Zenker 坏死,以及 caspase 3 表达的增加和 MuRF1 基因的上调。然而,牛磺酸补充通过下调 MuRF1 基因和减少组织 caspase 3 表达,缓解了与废用性骨骼肌萎缩相关的肌肉和神经组织损伤。总之,牛磺酸可能有助于对抗与肌肉萎缩相关的细胞凋亡和上调的 MuRF1 基因表达,这可能对大量患者有帮助。