Departamento de Neurobiologia Conductual y Cognitiva, Instituto de Neurobiologia, Universidad Nacional Autonoma de Mexico, Campus UNAM-Juriquilla, 76230, Queretaro, Mexico.
Departamento de Neurobiologia Conductual y Cognitiva, Instituto de Neurobiologia, Universidad Nacional Autonoma de Mexico, Campus UNAM-Juriquilla, 76230, Queretaro, Mexico.
Seizure. 2021 Aug;90:130-140. doi: 10.1016/j.seizure.2021.02.011. Epub 2021 Feb 13.
Temporal lobe epilepsy is associated with tissue abnormalities of several gray and white matter structures that are reproduced in animal models. Few longitudinal studies have focused on the identification of structural differences during epileptogenesis. The diffusion tensor model is a useful tool for evaluating cell death, gliosis, and axonal plasticity in epileptic subjects. This study aimed to evaluate temporal tissue changes after experimental status epilepticus in an animal model of chronic temporal lobe epilepsy.
Systemic pilocarpine-induced status epilepticus in adult Sprague-Dawley rats. Animals were scanned using diffusion tensor imaging (DTI) at three time points: prior to status epilepticus, and 24 and 64 days post-induction (early and late chronic, respectively). Fractional anisotropy, apparent diffusion coefficient, axial diffusivity (D), and radial diffusivity (D) were evaluated in white (fimbria, cingulum, corpus callosum, and internal capsule) and gray (dorsal hippocampus, dentate gyrus, and CA3) matter regions for the three time points. Histological assessment of neurodegeneration in Klüver-Barrera preparations from the same animals was performed.
Significantly reduced volume of dorsal hippocampus and fimbria of the epileptic animals was observed already at 24 days post-status epilepticus. Progressive changes of DTI parameters in both the white and gray matter structures of the experimental group were also observed. Stained sections confirmed such alterations.
Our study revealed time-dependent diffusion changes in gray and white matter structures after pilocarpine-induced status epilepticus. The characterization of these alterations over time may be potential imaging markers for epileptogenesis.
颞叶癫痫与几种灰质和白质结构的组织异常有关,这些异常在动物模型中得到重现。少数纵向研究集中在癫痫发生过程中识别结构差异。扩散张量模型是评估癫痫患者细胞死亡、神经胶质增生和轴突可塑性的有用工具。本研究旨在评估实验性癫痫持续状态后慢性颞叶癫痫动物模型中的颞叶组织变化。
在成年 Sprague-Dawley 大鼠中采用全身匹鲁卡品诱导癫痫持续状态。动物在癫痫持续状态前、诱导后 24 天和 64 天(分别为早期和晚期慢性)使用扩散张量成像(DTI)进行扫描。在三个时间点评估白质(内囊、穹窿、胼胝体和内囊)和灰质(背侧海马、齿状回和 CA3)区域的各向异性分数、表观扩散系数、轴突弥散度(D)和径向弥散度(D)。对来自相同动物的 Klüver-Barrera 制剂进行神经退行性变的组织学评估。
在癫痫动物中,癫痫持续状态后 24 天即观察到背侧海马和穹窿体积明显减小。实验组的白质和灰质结构的 DTI 参数也观察到进行性变化。染色切片证实了这些改变。
我们的研究揭示了匹鲁卡品诱导癫痫持续状态后灰、白质结构的时间依赖性扩散变化。这些变化的时间特征可能是癫痫发生的潜在影像学标志物。