Sevoflurane Affects Memory Through Impairing Insulin-Like Growth Factor Receptor Signaling

被引:4
作者
Tian, Yuan [1 ]
Song, Mingrui [2 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Dept Anesthesiol, Sch Med, 100 Haining Rd, Shanghai 200080, Peoples R China
[2] Second Mil Med Univ, Shanghai Changzheng Hosp, Dept Neurol, Shanghai, Peoples R China
关键词
Alzheimer's disease; IGF1R; miR-223-3p; sevoflurane; PREGNANT MICE; FACTOR-I; RATS; HIPPOCAMPUS; NEURODEGENERATION; EXPOSURE; TARGET; IGF-1; NEUROGENESIS; ANESTHESIA;
D O I
10.3233/JAD-190596
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Administration of sevoflurane (SEVO) may induce learning and memory deficits, which increases the chances of developing Alzheimer's disease. Here, we studied the effects of SEVO exposure on rats with a focus on the role of insulin-like growth factor (IGF) signaling. SEVO exposure significantly increased neuron cell apoptosis, and caused poor performance of the rats in behavior tests, by suppressing IGF-1 receptor (IGF1R). Bioinformatic analysis predicted microRNA(miR)-223-3p as an IGF1R-binding miRNA, the level of which increased in neurons after exposure to SEVO. In vitro, miR-223-3p suppressed the translation of IGF1R in neural cells. Moreover, transfection with antisense of miR-223-3p significantly attenuated SEVO exposure-induced neuron cell apoptosis. Taken together, these data suggest that SEVO-induced miR-223-3p upregulation suppresses IGF1R to impair IGF signaling, which subsequently leads to learning and memory impairments.
引用
收藏
页码:825 / 832
页数:8
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