Department of Brain and Cognitive Engineering, Korea University, Seoul, Republic of Korea..
Biol Pharm Bull. 2011;34(11):1759-64. doi: 10.1248/bpb.34.1759.
Hippocampus is one of the earliest brain regions that gets affected by ischemia, however, no pharmacological therapy exists yet that can fully counteract the ischemic damage. Here we study the effect of sulbutiamine, a synthetic thiamine analogue that can cross the blood-brain barrier easily, on hippocampal neurons under an in vitro model of ischemia, oxygen-glucose deprivation (OGD). We find that exposure to OGD in the presence of sulbutiamine significantly increases neuronal viability and enhances electrophysiological properties such as excitatory synaptic transmissions and intrinsic neuronal membrane input resistance in a concentration-dependent manner. Overall, here we report, for the first time, the neuroprotective evidence of sulbutiamine on hippocampal CA1 pyramidal neurons under OGD, which may have beneficial implications as a possible therapeutic agent/substance against ischemic insult.
海马体是最早受到缺血影响的大脑区域之一,但目前还没有能够完全对抗缺血损伤的药物治疗方法。在这里,我们研究了一种能够轻易穿过血脑屏障的合成硫胺素类似物——丁硫胺素,对体外缺血模型(氧葡萄糖剥夺,OGD)中海马神经元的影响。我们发现,在存在丁硫胺素的情况下,OGD 暴露会显著增加神经元活力,并以浓度依赖性方式增强电生理特性,如兴奋性突触传递和内在神经元膜输入电阻。总的来说,我们首次报告了丁硫胺素对 OGD 中海马 CA1 锥体神经元的神经保护作用,这可能作为一种对抗缺血损伤的潜在治疗剂/物质具有有益意义。