Kołosowska Karolina, Maciejak Piotr, Szyndler Janusz, Turzyńska Danuta, Sobolewska Alicja, Płaźnik Adam
Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology CePT, Medical University of Warsaw, Banacha 1B, 02-097 Warsaw, Poland.
Department of Experimental and Clinical Pharmacology, Centre for Preclinical Research and Technology CePT, Medical University of Warsaw, Banacha 1B, 02-097 Warsaw, Poland; Department of Neurochemistry, Institute of Psychiatry and Neurology, Sobieskiego Street 9, 02-957 Warsaw, Poland.
J Neuroimmunol. 2016 Sep 15;298:146-52. doi: 10.1016/j.jneuroim.2016.07.018. Epub 2016 Jul 21.
In our study, we used rapid electrical hippocampal kindling and in vivo microdialysis methods to assess the involvement of inflammatory mediators: lipopolysaccharide (LPS) and proinflammatory interleukin-1β (IL-1β) in mechanisms of epileptogenesis. We observed, that both, LPS and IL-1β, administered into stimulated hippocampus, accelerated kindling process. LPS also increased the expression of IL-1β in stimulated hippocampus in kindled rats. In vivo acute LPS perfusion, via a microdialysis cannula implanted into the naïve rat's hippocampus, produced an increase in extracellular glutamate release. We suppose, that particularly IL-1β action and increased glutamate concentration may significantly contribute to LPS effects on kindling development.
在我们的研究中,我们使用快速电刺激海马体点燃和体内微透析方法,来评估炎症介质:脂多糖(LPS)和促炎白细胞介素-1β(IL-1β)在癫痫发生机制中的作用。我们观察到,将LPS和IL-1β注入受刺激的海马体中,均可加速点燃过程。LPS还增加了点燃大鼠受刺激海马体中IL-1β的表达。通过植入未点燃大鼠海马体的微透析套管进行体内急性LPS灌注,可使细胞外谷氨酸释放增加。我们推测,特别是IL-1β的作用和谷氨酸浓度的增加,可能对LPS对点燃发展的影响有显著贡献。