Department of Pharmacological Sciences, Molecular and Cellular Pharmacology, Stony Brook University, Stony Brook, NY 11794-8651, USA.
Neurobiol Dis. 2010 Jul;39(1):85-97. doi: 10.1016/j.nbd.2010.04.001. Epub 2010 Apr 9.
Activated microglia have been associated with neurodegeneration in patients and in animal models of Temporal Lobe Epilepsy (TLE), however their precise functions as neurotoxic or neuroprotective is a topic of significant investigation. To explore this, we examined the effects of pilocarpine-induced seizures in transgenic mice where microglia/macrophages were conditionally ablated. We found that unilateral ablation of microglia from the dorsal hippocampus did not alter acute seizure sensitivity. However, when this procedure was coupled with lipopolysaccharide (LPS) preconditioning (1 mg/kg given 24 h prior to acute seizure), we observed a significant pro-convulsant phenomenon. This effect was associated with lower metabolic activation in the ipsilateral hippocampus during acute seizures, and could be attributed to activity in the mossy fiber pathway. These findings reveal that preconditioning with LPS 24 h prior to seizure induction may have a protective effect which is abolished by unilateral hippocampal microglia/macrophage ablation.
活化的小胶质细胞与颞叶癫痫(TLE)患者和动物模型中的神经退行性变有关,但其作为神经毒性或神经保护的确切功能仍是一个重要的研究课题。为了探讨这一问题,我们研究了条件性消融小胶质细胞/巨噬细胞的转基因小鼠中匹鲁卡品诱导的癫痫发作的影响。我们发现,从背侧海马区消融小胶质细胞不会改变急性癫痫发作的敏感性。然而,当将此程序与脂多糖(LPS)预处理(急性癫痫发作前 24 小时给予 1mg/kg)相结合时,我们观察到明显的促惊厥现象。这种效应与急性癫痫发作期间同侧海马体代谢激活降低有关,可能与苔藓纤维通路的活性有关。这些发现表明,在癫痫发作前 24 小时进行 LPS 预处理可能具有保护作用,而这种作用会被单侧海马小胶质细胞/巨噬细胞消融所消除。