Schiene K, Bruehl C, Zilles K, Qü M, Hagemann G, Kraemer M, Witte O W
Neurologische Klinik, Heinrich Heine Universität, Düsseldorf, Germany.
J Cereb Blood Flow Metab. 1996 Sep;16(5):906-14. doi: 10.1097/00004647-199609000-00014.
Changes of neuronal excitability and gamma-aminobutyric acid (GABAA)-receptor expression were studied in the surround of photothrombotic infarcts, which were produced in the sensorimotor cortex of the rat by using the rose bengal technique. In a first series of experiments, multiunit recordings were performed on anesthetized animals 2-3 mm lateral from the lesion. Mean discharge frequency was considerably higher in recordings from lesioned animals (> 100 Hz in the first postlesional week) compared with control animals (mean, 15 Hz). These alterations were already present after 1 day but were most pronounced 3 to 7 days after lesion induction. Thereafter the hyperexcitability declined again, although it remained visible up to 4 months. In a second series of experiments, the GABAA-receptor expression was studied autoradiographically. This revealed a reduction of GABAA receptors in widespread brain areas ipsilateral to the lesion. The reduction was most pronounced in the first days after lesion induction and declined with longer intervals. It is concluded that cortical infarction due to photothrombosis leads to a long-lasting and widespread reduction of GABAA-receptor expression in the surround of the lesion, which is associated with an increased neuronal excitability. Such alterations may be responsible for epileptic seizures that can be observed in some patients after stroke and may contribute to neurologic deficits after stroke.
利用孟加拉玫瑰红技术在大鼠感觉运动皮层制造光血栓性梗死灶,研究梗死灶周围神经元兴奋性和γ-氨基丁酸(GABAA)受体表达的变化。在第一组实验中,对麻醉动物在距病灶外侧2 - 3毫米处进行多单位记录。与对照动物(平均15赫兹)相比,损伤动物记录中的平均放电频率显著更高(损伤后第一周>100赫兹)。这些改变在1天后就已出现,但在损伤诱导后3至7天最为明显。此后,过度兴奋性再次下降,尽管在长达4个月时仍可见。在第二组实验中,通过放射自显影研究GABAA受体表达。这显示在病灶同侧广泛脑区GABAA受体减少。减少在损伤诱导后的头几天最为明显,并随时间间隔延长而下降。得出的结论是,光血栓形成导致的皮质梗死会使病灶周围GABAA受体表达长期且广泛减少,这与神经元兴奋性增加有关。此类改变可能是部分中风患者出现癫痫发作的原因,也可能导致中风后的神经功能缺损。