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Effect of mild and moderate hypothermia on hypoxic injury in nearly pure neuronal culture.

机译:在几乎纯净的神经元培养物中,轻度和中度低温对缺氧损伤的影响。

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PURPOSE: The effects of mild and moderate hypothermic therapy on cerebral injury are still controversial. Our hypothesis is that mild and moderate hypothermia should have some effects on neurons themselves if they really have protective effects. By using a nearly pure neuronal culture, we evaluated the effects and mechanism of hypothermia against hypoxic insult. METHODS: A nearly pure neuronal culture from cortices of 18-day-old Wister rats was used. The neurons were exposed to below 1% oxygen at 3 different temperatures (30, 33 and 37 degrees C). First, cell viability was measured by assessing viable neurons with trypan blue. Second, to evaluate the mechanism, the extracellular glutamate concentration was measured by high-performance liquid chromatography after hypoxia; cell viability after exposure to extrinsic glutamate was also evaluated. Next, mitochondrial membrane potential was estimated, by monitoring aggregation of MitoCapture, and the percentage of apoptotic cells was evaluated by staining with Hoechst 33342 and propidium iodide. RESULTS: After 24-h hypoxic insult, cell viability at 30 and 33 degrees C was significantly higher than at 37 degrees C. There was no significant difference between extracellular concentrations of glutamate after hypoxia or cell viability after glutamate exposure among the 3 temperature groups. In moderate hypothermia, the number of neurons with mitochondrial injury and the percentage of apoptotic cells were significantly reduced. CONCLUSION: Mild and moderate hypothermia inhibited hypoxic neuronal cell death. The mechanism of this effect may be related to protection of mitochondrial function, presumably followed by inhibition of apoptosis, at least in moderate hypothermia.
机译:目的:轻度和中度低温治疗对脑损伤的影响仍存在争议。我们的假设是,轻度和中度体温过低如果确实具有保护作用,则应对神经元本身产生一些影响。通过使用近乎纯净的神经元文化,我们评估了针对低氧损伤的低温治疗的作用和机制。方法:使用了来自18日龄Wister大鼠皮层的近乎纯净的神经元培养物。神经元在3个不同的温度(30、33和37摄氏度)下暴露于低于1%的氧气。首先,通过用锥虫蓝评估存活的神经元来测量细胞的存活率。其次,为了评估其机理,在缺氧后通过高效液相色谱法测量细胞外谷氨酸的浓度。还评估了暴露于外源谷氨酸后的细胞存活率。接着,通过监测MitoCapture的聚集来估计线粒体膜电位,并通过用Hoechst 33342和碘化丙啶染色来评估凋亡细胞的百分比。结果:缺氧损伤24小时后,在30和33摄氏度时细胞活力显着高于在37摄氏度。缺氧后谷氨酸的细胞外浓度或暴露于谷氨酸后的细胞活力在3个温度组之间没有显着差异。在中度低温下,线粒体损伤的神经元数量和凋亡细胞的百分比显着减少。结论:轻度和中度低温可抑制缺氧性神经元细胞死亡。这种作用的机制可能与保护线粒体功能有关,至少在中度低温时可能与抑制细胞凋亡有关。

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