Instituto Teófilo Hernando and Departamento de Farmacología y Terapéutica, Universidad Autónoma de Madrid, Madrid, Spain.
Brain Res. 2011 Nov 14;1423:77-86. doi: 10.1016/j.brainres.2011.09.025. Epub 2011 Sep 19.
The neurotoxic effects of cerebrospinal fluid (CSF) from patients suffering amyotrophic lateral sclerosis (ALS), have been reported by various authors. However, variable results have been communicated and the mechanism of such neurotoxicity has been attributed to excess glutamate concentrations in ALS/CSF. We have studied here the properties of 14 CSFs from control patients and 29 CSFs from patients of ALS. We found that while ALS/CSF impairs the viability of rat brain cortical motoneurons maintained in primary cultures, this effect seemed to be exerted through a glutamate-independent mechanism. Resveratrol protected against such neurotoxic effects and antagonized the Ca(+2) elevation produced by ALS/CSF. However, riluzole did not afford protection and antagonized the resveratrol-elicited neuroprotective effects. We conclude that ALS/CSF elicited neurotoxicity on in vitro cultures of rat brain cortical motor neurons may become a sound microassay to test available novel multitargeted neuroprotective compounds with potential therapeutic application in ALS patients.
各种作者已经报道了患有肌萎缩性侧索硬化症(ALS)的患者的脑脊液(CSF)的神经毒性作用。然而,已经传达了不同的结果,并且这种神经毒性的机制归因于 ALS/CSF 中谷氨酸浓度过高。我们在这里研究了 14 例对照患者的 CSF 和 29 例 ALS 患者的 CSF 的特性。我们发现,虽然 ALS/CSF 会损害原代培养的大鼠大脑皮质运动神经元的活力,但这种作用似乎是通过谷氨酸非依赖性机制发挥的。白藜芦醇可以预防这种神经毒性作用,并拮抗 ALS/CSF 引起的 Ca(+2)升高。然而,利鲁唑不能提供保护作用,并拮抗白藜芦醇引起的神经保护作用。我们得出结论,ALS/CSF 对体外培养的大鼠大脑皮质运动神经元的神经毒性作用可能成为一种可靠的微测定方法,用于测试具有潜在治疗应用于 ALS 患者的新型多靶点神经保护化合物。