二甲双胍
SH-SY5Y型
自噬
细胞内
细胞凋亡
程序性细胞死亡
神经毒性
细胞外
神经保护
细胞生物学
药理学
化学
细胞培养
生物
医学
内分泌学
内科学
生物化学
糖尿病
毒性
遗传学
神经母细胞瘤
作者
Lixia Li,Mengyu Liu,Xue Jiang,Zhen‐hong Xia,Yuxiang Wang,Di An,Hong‐Gang Wang,Bin Heng,Yan‐qiang Liu
摘要
Metformin, a first-line drug for type-2 diabetes, plays a potentially protective role in preventing Alzheimer's disease (AD), but its underlying mechanism is unclear. In this study, Aβ25-35 -treated SH-SY5Y cells were used as a cell model of AD to investigate the neuroprotective effect of metformin, as well as its underlying mechanisms. We found that metformin decreased the cell apoptosis rate and death, ratio of Bcl-2/Bax, and expression of NR2A and NR2B, and increased the expression of LC3 in Aβ25-35 -treated SH-SY5Y cells. Metformin also reduced intracellular and extracellular Glu concentrations, as well as the intracellular concentration of Ca2+ and ROS in Aβ25-35 -treated SH-SY5Y cells. These findings suggest that metformin inhibits Aβ25-35 -treated SH-SY5Y cell death by inhibiting apoptosis, decreasing intracellular Ca2+ and ROS by reducing neurotoxicity of excitatory amino acids, and by possibly reversing autophagy disorder via regulating autophagy process.
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