Yan Y Q, Zhou Z H, Ji P, Gu J F
Shanghai Institute of Physiology, Academia Sinica.
Sheng Li Xue Bao. 1992 Oct;44(5):524-7.
Pure neurons from embryonic day 8 chick forebrain were cultured under anoxic condition (95% N2 and 5% CO2). After 24, 48 and 72 h in culture, MTT colorimetric microassay showed a reduced production of formazan, indicating that the neurons were seriously damaged. In addition, the glucose of the cultured media was significantly depleted. Even when glucose concentration was increased to 800-1,200 mg/100 ml, anoxia still caused neurons to die. The results indicate that brain neurons in embryo are sensitive to anoxia, and any protective influence of glia on anoxic neurons could not be mediated by supplying the latter with glycogen.
将来自胚胎第8天鸡前脑的纯神经元在缺氧条件(95% N₂和5% CO₂)下培养。培养24、48和72小时后,MTT比色微量测定法显示甲臜生成减少,表明神经元受到严重损伤。此外,培养基中的葡萄糖显著耗尽。即使将葡萄糖浓度提高到800 - 1200 mg/100 ml,缺氧仍会导致神经元死亡。结果表明胚胎期脑神经元对缺氧敏感,神经胶质细胞对缺氧神经元的任何保护作用都不能通过为后者提供糖原介导。