Flavie Ouali Boimpoundi Eunice, Wang Hao-Ven
Department of Life Sciences, College of Biosciences and Biotechnology, National Cheng Kung University, Tainan City, 701, Taiwan, ROC.
Center for Bioscience and Biotechnology, National Cheng Kung University, Tainan City, 701, Taiwan, ROC.
Biochem Biophys Rep. 2021 May 18;26:101019. doi: 10.1016/j.bbrep.2021.101019. eCollection 2021 Jul.
Essentially employed for the treatment of airway obstructions in humans, β-agonists are also known to have an anabolic effect in animals' skeletal muscle. and studies have attested the increase in animal body mass and the hypertrophy of muscle cells following the administration of specific β-agonists. However, the contribution of β-agonists to C2C12 myoblasts growth remains obscure. We therefore aimed to investigate the impact of β1-and β2-agonist drugs on the proliferation and differentiation of skeletal muscle cells. Direct observations and cytotoxicity assay showed that clenbuterol, salbutamol, cimaterol and ractopamine enhanced muscle cell growth and viability during the proliferation stage. Structural examinations coupled to Western blot analysis indicated that salbutamol and cimaterol triggered a decrease in myotube formation. A better comprehension of the effect of β-agonists on myogenic regulatory genes in the muscle cells is crucial to establish a specific role of β-agonists in muscle development, growth, and regeneration.
β-激动剂主要用于治疗人类气道阻塞,已知其对动物骨骼肌也有合成代谢作用。研究证实,给予特定的β-激动剂后,动物体重增加,肌肉细胞肥大。然而,β-激动剂对C2C12成肌细胞生长的作用仍不清楚。因此,我们旨在研究β1和β2激动剂药物对骨骼肌细胞增殖和分化的影响。直接观察和细胞毒性试验表明,克伦特罗、沙丁胺醇、西马特罗和莱克多巴胺在增殖阶段可促进肌肉细胞生长和活力。结合蛋白质免疫印迹分析的结构检查表明,沙丁胺醇和西马特罗可导致肌管形成减少。更好地理解β-激动剂对肌肉细胞中肌源性调节基因的作用,对于确定β-激动剂在肌肉发育、生长和再生中的特定作用至关重要。