Cerebrospinal fluid from rats given hypoxic preconditioning protects neurons from oxygen-glucose deprivation-induced injury

被引:4
|
作者
Zhang, Yan-bo [1 ]
Guo, Zheng-dong [2 ]
Li, Mei-yi [3 ]
Li, Si-jie [4 ]
Niu, Jing-zhong [1 ]
Yang, Ming-feng [1 ]
Ji, Xun-ming [4 ]
Lv, Guo-wei [4 ]
机构
[1] Taishan Med Univ, Dept Neurol, Affiliated Hosp, Tai An, Shandong, Peoples R China
[2] Taishan Med Univ, Dept Endocrinol, Affiliated Hosp, Tai An, Shandong, Peoples R China
[3] Shandong Taishan Chron Dis Hosp, Dept Neurol, Tai An, Shandong, Peoples R China
[4] Capital Med Univ, Hypoxia Med Inst, Xuanwu Hosp, Beijing, Peoples R China
关键词
nerve regeneration; hypoxic preconditioning; cerebrospinal fluid; cerebral cortex; oxygen-glucose deprivation; neurons; apoptosis; Bcl-2/Bax; neural regeneration; VASCULAR DEMENTIA; APOPTOSIS; BRAIN; MODEL; CASPASE-3; CELLS; MICE; EXPRESSION; INHIBITOR; BAX/BCL-2;
D O I
10.4103/1673-5374.165519
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hypoxic preconditioning activates endogenous mechanisms that protect against cerebral ischemic and hypoxic injury. To better understand these protective mechanisms, adult rats were housed in a hypoxic environment (8% O-2/92% N-2) for 3 hours, and then in a normal oxygen environment for 12 hours. Their cerebrospinal fluid was obtained to culture cortical neurons from newborn rats for 1 day, and then the neurons were exposed to oxygen-glucose deprivation for 1.5 hours. The cerebrospinal fluid from rats subjected to hypoxic preconditioning reduced oxygen-glucose deprivation-induced injury, increased survival rate, upregulated Bcl-2 expression and downregulated Box expression in the cultured cortical neurons, compared with control. These results indicate that cerebrospinal fluid from rats given hypoxic preconditioning protects against oxygen-glucose deprivation-induced injury by affecting apoptosis-related protein expression in neurons from newborn rats.
引用
收藏
页码:1471 / 1476
页数:6
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