Zhang Gan, Liu Rong, Sheng Zhaofu, Zhang Yonghe, Fan Dongsheng
Department of Neurology, Peking University Third Hospital, Beijing 100191, China.
Beijing Municipal Key Laboratory of Biomarker and Translational Research in Neurodegenerative Disease, Beijing 100191, China.
Brain Sci. 2022 Apr 11;12(4):490. doi: 10.3390/brainsci12040490.
The participation of silent mating type information regulation 2 homolog 1 (SIRT1) in amyotrophic lateral sclerosis (ALS) has been reported in many studies. However, the role of the expression and function of SIRT1 in the hypothalamus in ALS remains unknown. In the current study, we performed western blot, co-immunoprecipitation and immunofluorescence analyses to determine the expression and in-depth mechanism of SIRT1 in the hypothalamus in SOD1G93A transgenic mice. We found that SIRT1 was overexpressed in the hypothalamus after motor symptom onset. In addition, SIRT1 interacted with prepro-orexin, a molecule involved in energy balance and the sleep/wake cycle, in both preclinical and clinical ALS regardless of whether SIRT1 levels were elevated. These findings indicate that SIRT1 might participate in sleep and metabolic changes in ALS, suggesting that SIRT1 is a new target for ALS treatment.
许多研究已报道沉默信息调节因子2同源蛋白1(SIRT1)参与肌萎缩侧索硬化症(ALS)。然而,SIRT1在下丘脑中的表达及功能在ALS中的作用仍不清楚。在本研究中,我们进行了蛋白质免疫印迹、免疫共沉淀和免疫荧光分析,以确定SOD1G93A转基因小鼠下丘脑中SIRT1的表达及深入机制。我们发现运动症状出现后,下丘脑中SIRT1过表达。此外,在临床前和临床ALS中,无论SIRT1水平是否升高,SIRT1都与前阿片黑素细胞皮质素原相互作用,前阿片黑素细胞皮质素原是一种参与能量平衡和睡眠/觉醒周期的分子。这些发现表明,SIRT1可能参与ALS的睡眠和代谢变化,提示SIRT1是ALS治疗的一个新靶点。