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克伦特罗在肌萎缩侧索硬化小鼠模型中的治疗作用。

Therapeutic effects of clenbuterol in a murine model of amyotrophic lateral sclerosis.

作者信息

Teng Yang D, Choi Howard, Huang Wenzheng, Onario Renna C, Frontera Walter R, Snyder Evan Y, Sabharwal Sunil

机构信息

Department of Neurosurgery, Harvard Medical School/Children's Hospital Boston, MA, USA.

出版信息

Neurosci Lett. 2006;397(1-2):155-8. doi: 10.1016/j.neulet.2005.12.007. Epub 2006 Jan 18.

Abstract

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.

摘要

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。

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