Raley-Susman K M, Miller K R, Owicki J C, Sapolsky R M
Department of Biological Sciences, Stanford University, California 94305.
J Neurosci. 1992 Mar;12(3):773-80. doi: 10.1523/JNEUROSCI.12-03-00773.1992.
Increasing evidence implicates glutamate receptor over-stimulation in the neurotoxicity associated with a host of metabolic insults, including seizures and hypoxia-ischemia. To begin to understand more completely the role of energy metabolism in the mechanism of neuron death following excitatory amino acid exposure, we investigated the effects of kainic acid exposure on metabolic rate in cultured hippocampal cells using a recently developed silicon microphysiometer. The device gives a continual real-time measure of metabolism in relatively small numbers of cells, as assessed by efflux of protons generated at least in part by ATP hydrolysis and lactic acid production. In the first half of this report, we characterize the feasibility of using this device for measuring cellular metabolism in hippocampal cultures. Metabolic rate in both astrocytes and neurons was readily detectable, with a high signal-to-noise ratio. The rate was proportional to the number of cells and was sensitive to metabolic enhancement or depression. We then utilized this device to study metabolic responses to the excitotoxin kainic acid. We observed a receptor-mediated, dose-dependent increase in metabolic rate upon stimulation by kainic acid, with an EC50 of approximately 100 microM. Exposure to toxic levels of kainic acid for 10 min produced an initial elevation (for 2 hr) in metabolic rate and then a gradual decline in metabolism over the next 8 hr that preceded a measurable loss of cell viability. This study further delineates a time window for the onset of kainic acid-induced damage. The results clearly show the feasibility of using silicon microphysiometry for assessing metabolism of brain cultures and for exploring the relationship between metabolism and synaptic activation.
越来越多的证据表明,谷氨酸受体过度刺激与一系列代谢损伤相关的神经毒性有关,包括癫痫发作和缺氧缺血。为了更全面地了解能量代谢在兴奋性氨基酸暴露后神经元死亡机制中的作用,我们使用最近开发的硅微生理仪研究了海藻酸暴露对培养的海马细胞代谢率的影响。该设备通过至少部分由ATP水解和乳酸产生所生成的质子外流来评估,能够对相对少量细胞的代谢进行连续实时测量。在本报告的前半部分,我们描述了使用该设备测量海马培养物中细胞代谢的可行性。星形胶质细胞和神经元中的代谢率都很容易检测到,信噪比很高。该速率与细胞数量成正比,并且对代谢增强或抑制敏感。然后,我们利用该设备研究对兴奋性毒素海藻酸的代谢反应。我们观察到,在海藻酸刺激后,代谢率呈受体介导的剂量依赖性增加,EC50约为100 microM。暴露于毒性水平的海藻酸10分钟会使代谢率最初升高(持续2小时),然后在接下来的8小时内代谢逐渐下降,这在可测量的细胞活力丧失之前发生。这项研究进一步划定了海藻酸诱导损伤开始的时间窗口。结果清楚地表明了使用硅微生理测量法评估脑培养物代谢以及探索代谢与突触激活之间关系的可行性。