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评估神经元生物能量状态。

Assessing neuronal bioenergetic status.

作者信息

Zeiger Stephanie L H, Stankowski Jeannette N, McLaughlin BethAnn

机构信息

Department of Medicine, Vanderbilt Kennedy Center on Human Development, Vanderbilt University, Nashville, TN, USA.

出版信息

Methods Mol Biol. 2011;758:215-35. doi: 10.1007/978-1-61779-170-3_15.

Abstract

Drug discovery and therapeutic development for disorders of the central nervous system (CNS) represents one of the largest unmet markets in modern medicine. We have increasingly recognized that the lack of stringent assessment of mitochondrial function during the discovery process has resulted in drug recalls, black box warnings, and an urgent need to understand the metabolic liability of small molecules in neural systems. Given that the brain is the most energetically demanding organ, even modest perturbations in neuronal energetic pathways have been shown to impact growth, signaling, connectivity, and the restorative capacity of the CNS. In this work, we describe several tools to assess metabolic activity of primary neuronal cultures and neural cell lines using an acute model of injury induced by oxygen glucose deprivation. Methods include the measurement of total ATP and NADH, enzymatic assessment of lactate production by anaerobic respiration, as well as viability assays. We also present a modified screening method for assessing aerobic respiration of immortalized cell lines using galactose challenge.

摘要

中枢神经系统(CNS)疾病的药物发现和治疗开发是现代医学中最大的未满足市场之一。我们越来越认识到,在发现过程中缺乏对线粒体功能的严格评估已导致药物召回、黑框警告,以及迫切需要了解小分子在神经系统中的代谢负担。鉴于大脑是能量需求最高的器官,即使神经元能量途径的适度扰动也已显示会影响中枢神经系统的生长、信号传导、连接性和恢复能力。在这项工作中,我们描述了几种使用氧糖剥夺诱导的急性损伤模型来评估原代神经元培养物和神经细胞系代谢活性的工具。方法包括总ATP和NADH的测量、无氧呼吸产生乳酸的酶促评估以及活力测定。我们还提出了一种改良的筛选方法,用于使用半乳糖激发来评估永生化细胞系的有氧呼吸。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afa5/3678904/576764ef6664/nihms464629f1.jpg

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