Mirrione Martine M, Schiffer Wynne K, Siddiq Mustafa, Dewey Stephen L, Tsirka Stella E
Graduate Program in Molecular and Cellular Pharmacology, State University of New York at Stony Brook, Stony Brook, New York 11794, USA.
Synapse. 2006 Feb;59(2):119-21. doi: 10.1002/syn.20216.
Here we present the first demonstration that 2-deoxy-2[18F]fluoro-D-glucose (18FDG) and micro Positron Emission Tomography (microPET) can be used successfully to monitor regional changes in brain metabolism during acute seizure induction in C57Bl/6 mice. These longitudinal studies show a significant increase in 18FDG uptake in the hippocampus (33.2%) which correlates directly with seizure severity (R2=0.86). 18FDG microPET can potentially be used to monitor the development of TLE in mouse models from the acute phase of status epilepticus to the chronic phase of spontaneous recurrent seizures. These studies provide a foundation upon which we can begin to identify genetic contributions to the metabolic signature of TLE in mice, since many transgenics are in the C57Bl/6 background strain.
在此,我们首次证明2-脱氧-2-[¹⁸F]氟-D-葡萄糖(¹⁸FDG)和微型正电子发射断层扫描(microPET)可成功用于监测C57Bl/6小鼠急性癫痫发作诱导期间脑代谢的区域变化。这些纵向研究表明,海马体中¹⁸FDG摄取量显著增加(33.2%),这与癫痫发作严重程度直接相关(R² = 0.86)。¹⁸FDG microPET有可能用于监测小鼠模型中从癫痫持续状态急性期到自发性反复癫痫发作慢性期的颞叶癫痫(TLE)发展。这些研究提供了一个基础,基于此我们可以开始确定基因对小鼠TLE代谢特征的贡献,因为许多转基因小鼠处于C57Bl/6背景品系。