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Neuroprotective Effects of α-Tocotrienol on Kainic Acid-Induced Neurotoxicity in Organotypic Hippocampal Slice Cultures

机译:α-生育三烯酚对海藻酸诱导的器官型海马切片培养物中神经毒性的神经保护作用。

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摘要

Vitamin E, such as alpha-tocopherol (ATPH) and alpha-tocotrienol (ATTN), is a chain-breaking antioxidant that prevents the chain propagation step during lipid peroxidation. In the present study, we investigated the effects of ATTN on KA-induced neuronal death using organotypic hippocampal slice culture (OHSC) and compared the neuroprotective effects of ATTN and ATPH. After 15 h KA (5 μM) treatment, delayed neuronal death was detected in the CA3 region and reactive oxygen species (ROS) formation and lipid peroxidation were also increased. Both co-treatment and post-treatment of ATPH (100 μM) or ATTN (100 μM) significantly increased the cell survival and reduced the number of TUNEL-positive cells in the CA3 region. Increased dichlorofluorescein (DCF) fluorescence and levels of thiobarbiturate reactive substances (TBARS) were decreased by ATPH and ATTN treatment. These data suggest that ATPH and ATTN treatment have protective effects on KA-induced cell death in OHSC. ATTN treatment tended to be more effective than ATPH treatment, even though there was no significant difference between ATPH and ATTN in co-treatment or post-treatment.
机译:维生素E,例如α-生育酚(ATPH)和α-生育三烯酚(ATTN),是一种断链抗氧化剂,可防止脂质过氧化过程中的链增长步骤。在本研究中,我们使用器官型海马切片培养物(OHSC)研究了ATTN对KA诱导的神经元死亡的影响,并比较了ATTN和ATPH的神经保护作用。进行15 h KA(5μM)处理后,在CA3区检测到延迟的神经元死亡,并且活性氧(ROS)的形成和脂质过氧化也增加了。 ATPH(100μM)或ATTN(100μM)的共同处理和后处理均显着提高了细胞存活率,并减少了CA3区中TUNEL阳性细胞的数量。通过ATPH和ATTN处理,增加的二氯荧光素(DCF)荧光和硫代巴比妥酸酯反应性物质(TBARS)的水平降低。这些数据表明,ATPH和ATTN处理对OHSC中KA诱导的细胞死亡具有保护作用。尽管ATPH和ATTN之间的联合治疗或后处理之间无显着差异,但ATTN治疗往往比ATPH治疗更有效。

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