Teng Yang D, Choi Howard, Huang Wenzheng, Onario Renna C, Frontera Walter R, Snyder Evan Y, Sabharwal Sunil
Department of Neurosurgery, Harvard Medical School/Children's Hospital Boston, MA, USA.
Neurosci Lett. 2006;397(1-2):155-8. doi: 10.1016/j.neulet.2005.12.007. Epub 2006 Jan 18.
We investigated the effects of clenbuterol, a beta2-adrenoceptor agonist with known anabolic and neuroprotective properties, on G93A-SOD1 mice, a transgenic murine model of familial amyotrophic lateral sclerosis (ALS). Relative to saline-treated vehicle controls (0.2 ml/kg/day; i.p.), early pathologic G93A-SOD1 mice treated with clenbuterol (1.5 mg/kg/day; i.p.) demonstrated a delayed onset of hindlimb signs as measured by rotarod performance, slowed disease progression, as well as trends toward mitigated losses of lumbar motoneurons and body weight. Responses in female G93A-SOD1 mice were favorable to those of males, suggesting synergistic effects between clenbuterol and sex-specific factors. Overall, our data suggest that clenbuterol offers therapeutic effects on ALS-related neuromuscular degeneration.
我们研究了克仑特罗(一种已知具有合成代谢和神经保护特性的β2-肾上腺素能受体激动剂)对G93A-SOD1小鼠(一种家族性肌萎缩侧索硬化症(ALS)的转基因小鼠模型)的影响。相对于生理盐水处理的载体对照(0.2毫升/千克/天;腹腔注射),用克仑特罗(1.5毫克/千克/天;腹腔注射)处理的早期病理G93A-SOD1小鼠,通过转棒试验测量显示后肢症状出现延迟,疾病进展减缓,并且腰椎运动神经元和体重减轻也有减轻趋势。雌性G93A-SOD1小鼠的反应优于雄性,表明克仑特罗与性别特异性因素之间存在协同作用。总体而言,我们的数据表明克仑特罗对ALS相关的神经肌肉变性具有治疗作用。