Focal BOLD fMRI changes in bicuculline-induced tonic-clonic seizures in the rat

被引:49
|
作者
DeSalvo, Matthew N. [1 ]
Schridde, Ulrich [1 ]
Mishra, Asht M. [1 ,4 ]
Motelow, Joshua E. [1 ]
Purcaro, Michael J. [1 ]
Danielson, Nathan [1 ]
Bai, Xiaoxiao [1 ]
Hyder, Fahmeed [2 ,3 ,4 ]
Blumenfeld, Hal [1 ,4 ,5 ,6 ]
机构
[1] Yale Univ, Sch Med, Dept Neurol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Diagnost Radiol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Biomed Engn, New Haven, CT 06520 USA
[4] Yale Univ, Sch Med, Core Ctr Quantitat Neurosci Magnet Resonance, New Haven, CT 06520 USA
[5] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06520 USA
[6] Yale Univ, Sch Med, Dept Neurosurg, New Haven, CT 06520 USA
关键词
Tonic-clonic seizure; fMRI; Cortex; Thalamus; Bicuculline; Cortical focus theory; CEREBRAL-BLOOD-FLOW; ABSENCE SEIZURES; FOCUS; NETWORKS; ADJUSTMENT; DRIFT;
D O I
10.1016/j.neuroimage.2010.01.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Generalized tonic-clonic seizures cause widespread physiological changes throughout the cerebral cortex and subcortical structures in the brain. Using combined blood oxygen level dependent (BOLD) functional magnetic resonance imaging (fMRI) at 9.4 T and electroencephalography (EEG), these changes can be characterized with high spatiotemporal resolution. We studied BOLD changes in anesthetized Wistar rats during bicuculline-induced tonic-clonic seizures. Bicuculline, a GABA(A) receptor antagonist, was injected systemically and seizure activity was observed on EEG as high-amplitude, high-frequency polyspike discharges followed by clonic paroxysmal activity of lower frequency, with mean electrographic seizure duration of 349 s. Our aim was to characterize the spatial localization, direction, and timing of BOLD signal changes during the pre-ictal, ictal and post-ictal periods. Group analysis was performed across seizures using paired t-maps of BOLD signal superimposed on high-resolution anatomical images. Regional analysis was then performed using volumes of interest to quantify BOLD timecourses. In the pre-ictal period we found focal BOLD increases in specific areas of somatosensory cortex (S1, S2) and thalamus several seconds before seizure onset. During seizures we observed BOLD increases in cortex, brainstem and thalamus and BOLD decreases in the hippocampus. The largest ictal BOLD increases remained in the focal regions of somatosensory cortex showing pre-ictal increases. During the post-ictal period we observed widespread BOLD decreases. These findings support a model in which "generalized" tonic-clonic seizures begin with focal changes before electrographic seizure onset, which progress to non-uniform changes during seizures, possibly shedding light on the etiology and pathophysiology of similar seizures in humans. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:902 / 909
页数:8
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