Sendrowski Krzysztof, Boćkowski Leszek, Sobaniec Wojciech, Iłendo Elżbieta, Jaworowska Barbara, Smigielska-Kuzia Joanna
Department of Pediatric Neurology and Rehabilitation, Medical University of Bialystok, Poland.
Folia Histochem Cytobiol. 2011;49(1):148-52. doi: 10.5603/fhc.2011.0021.
Many experimental studies indicate that some antiepileptic drugs possess neuroprotective properties in varied models of neuronal injury. Levetiracetam is a second-generation antiepileptic drug with a novel mechanism of action. In the present study, we evaluated the putative neuroprotective effect of levetiracetam on primary hippocampal cultures at seven day in vitro. Cell death was induced by incubation of neural cultures in hypoxic conditions over 24 hours. Neuronal injury was assessed by morphometric investigation of death/total ratio of neurons in light microscopy using Trypan blue staining and by evaluation of lactate dehydrogenase (LDH) release in the culture medium. Our results indicate that pre-conditioning of hippocampal cultures with high concentrations of levetiracetam (100 μM and 300 μM) protects neurons against hypoxia-induced death. Two-fold higher number of neurons remained viable as compared to control cultures without drug. Lack of neuroprotective action of the drug on hippocampal neural cultures was observed, when a low concentration (10 μM) of levetiracetam was used.
许多实验研究表明,一些抗癫痫药物在多种神经元损伤模型中具有神经保护特性。左乙拉西坦是一种具有新型作用机制的第二代抗癫痫药物。在本研究中,我们评估了左乙拉西坦在体外培养7天时对原代海马培养物的假定神经保护作用。通过将神经培养物在缺氧条件下孵育24小时来诱导细胞死亡。使用台盼蓝染色通过光学显微镜对神经元的死亡/总数比例进行形态计量学研究,并通过评估培养基中乳酸脱氢酶(LDH)的释放来评估神经元损伤。我们的结果表明,用高浓度的左乙拉西坦(100μM和300μM)对海马培养物进行预处理可保护神经元免受缺氧诱导的死亡。与未使用药物的对照培养物相比,存活的神经元数量增加了两倍。当使用低浓度(10μM)的左乙拉西坦时,未观察到该药物对海马神经培养物的神经保护作用。