Wu Li-ying, Ding Ai-shi, Zhao Tong, Ma Zi-min, Wang Fu-zhuang, Fan Ming
Department of Neurobiology, Institute of Basic Medical Sciences, Beijing, PR China.
Neurosignals. 2005;14(3):109-16. doi: 10.1159/000086293.
It is known that hypoxic preconditioning (HP, a brief period of sublethal hypoxia) provides neuroprotection against subsequent severe anoxia, but the mechanisms of this increased tolerance have not been fully elucidated. A hypoxic preconditioning model was established by exposing a 4-day hippocampal culture to 1% O(2) for 20 min/day for 8 days. The preconditioning significantly decreased the number of apoptotic neurons at reoxygenation 24 h after 4 h of severe anoxia (0% O(2)). Further study demonstrated that the degradation of mitochondrial membrane potential (MMP) was greatly inhibited and the expression of B-cell lymphoma protein-2 (Bcl-2) was increased considerably after severe anoxia in the HP groups. These results indicate that the increased anoxic tolerance, which is induced by HP in cultured hippocampal cells, may be correlated with Bcl-2 overexpression and enhanced stability of MMP, which ultimately reduces apoptosis 24 h after reoxygenation.
已知低氧预处理(HP,一段短暂的亚致死性低氧)可提供针对后续严重缺氧的神经保护作用,但这种耐受性增加的机制尚未完全阐明。通过将4天龄的海马培养物每天暴露于1% O₂ 20分钟,持续8天,建立了低氧预处理模型。预处理显著减少了在严重缺氧(0% O₂)4小时后再给氧24小时时凋亡神经元的数量。进一步研究表明,在低氧预处理组中,严重缺氧后线粒体膜电位(MMP)的降解受到极大抑制,且B细胞淋巴瘤-2(Bcl-2)蛋白的表达显著增加。这些结果表明,低氧预处理在培养的海马细胞中诱导的缺氧耐受性增加,可能与Bcl-2过表达和MMP稳定性增强相关,这最终减少了再给氧24小时后的细胞凋亡。