Wallis R A, Panizzon K L
Neuronal Injury Laboratory, Sepulveda VAMC, Sepulveda, CA 90024, USA.
Eur J Pharmacol. 1995 Dec 29;294(2-3):475-82. doi: 10.1016/0014-2999(95)00568-4.
Traumatic brain injury is a leading cause of disability and death. Since the anticonvulsant felbamate provides hypoxic neuroprotection, we investigated whether felbamate would provide protection against traumatic neuronal injury as well. Traumatic injury to CA1 neurons in hippocampal slices was induced by fluid percussion, and CA1 evoked response was monitored. Pre-treatment with felbamate was strongly protective against neuronal injury, and permitted CA1 antidromic population spike recovery to a mean 94 +/- 1% (S.E.M.) of initial amplitude, compared to unmedicated slices which regained only 15 +/- 6%. The felbamate EC50 for this protection was 136 mg/1, and significant protection was found at felbamate concentrations similar to those reported in felbamate monotherapy for seizures. Significant protection was also detected when felbamate was initiated 15 min after trauma. Slices given brief post-trauma felbamate treatment could demonstrate long-term potentiation when assessed 8 h after trauma. These studies indicate that felbamate is neuroprotective against CA1 traumatic neuronal injury.
创伤性脑损伤是致残和致死的主要原因。由于抗惊厥药非氨酯具有缺氧神经保护作用,我们研究了非氨酯是否也能预防创伤性神经元损伤。通过液压冲击诱导海马切片中CA1神经元的创伤性损伤,并监测CA1诱发反应。非氨酯预处理对神经元损伤具有很强的保护作用,与未用药切片相比,未用药切片仅恢复到初始幅度的15±6%,而使用非氨酯预处理可使CA1逆向群体峰电位恢复到平均94±1%(标准误)。非氨酯对这种保护作用的半数有效浓度(EC50)为136mg/L,在与非氨酯单药治疗癫痫时报道的浓度相似的非氨酯浓度下发现了显著的保护作用。在创伤后15分钟开始使用非氨酯时也检测到了显著的保护作用。创伤后给予非氨酯短暂治疗的切片在创伤后8小时评估时可表现出长时程增强。这些研究表明,非氨酯对CA1创伤性神经元损伤具有神经保护作用。