D'Alessio Luciana, Pinto Alipio, Cangelosi Adriana, Geoghegan Patricia A, Tironi-Farinati Carla, Brener Gabriela J, Goldstein Jorge
Centro de Epilepsia, Hospital Ramos Mejía and Instituto de Biología Celular y Neurociencia Prof. E. De Robertis, Consejo Nacional de Investigaciones Científicas y Técnicas Buenos Aires, Argentina.
Laboratorio de Neurofisiopatología, Instituto de Fisiología y Biofisica "HOUSSAY", Consejo Nacional de Investigaciones Científicas y Técnicas, Facultad de Medicina, Universidad de Buenos Aires Buenos Aires, Argentina.
Front Microbiol. 2016 Feb 10;7:133. doi: 10.3389/fmicb.2016.00133. eCollection 2016.
Shiga toxin producing Escherichia coli may damage the central nervous system before or concomitantly to manifested hemolytic-uremic syndrome symptoms. The cerebellum is frequently damaged during this syndrome, however, the deleterious effects of Shiga toxin 2 has never been integrally reported by ultrastructural, physiological and behavioral means. The aim of this study was to determine the cerebellar compromise after intravenous administration of a sub-lethal dose of Shiga toxin 2 by measuring the cerebellar blood-brain barrier permeability, behavioral task of cerebellar functionality (inclined plane test), and ultrastructural analysis (transmission electron microscope). Intravenous administration of vehicle (control group), sub-lethal dose of 0.5 and 1 ηg of Stx2 per mouse were tested for behavioral and ultrastructural studies. A set of three independent experiments were performed for each study (n = 6). Blood-brain barrier resulted damaged and consequently its permeability was significantly increased. Lower scores obtained in the inclined plane task denoted poor cerebellar functionality in comparison to their controls. The most significant lower score was obtained after 5 days of 1 ηg of toxin administration. Transmission electron microscope micrographs from the Stx2-treated groups showed neurons with a progressive neurodegenerative condition in a dose dependent manner. As sub-lethal intravenous Shiga toxin 2 altered the blood brain barrier permeability in the cerebellum the toxin penetrated the cerebellar parenchyma and produced cell damaged with significant functional implications in the test balance.
产志贺毒素大肠杆菌可能在溶血尿毒综合征症状出现之前或同时损害中枢神经系统。在该综合征期间,小脑经常受到损害,然而,志贺毒素2的有害影响从未通过超微结构、生理学和行为学方法进行完整报道。本研究的目的是通过测量小脑血脑屏障通透性、小脑功能行为任务(斜面试验)和超微结构分析(透射电子显微镜),确定静脉注射亚致死剂量的志贺毒素2后小脑的损伤情况。对静脉注射赋形剂(对照组)、每只小鼠0.5和1纳克的亚致死剂量志贺毒素2进行行为学和超微结构研究测试。每项研究进行了一组三个独立实验(n = 6)。血脑屏障受损,因此其通透性显著增加。与对照组相比,斜面任务得分较低表明小脑功能较差。在给予1纳克毒素5天后获得的得分最低。来自志贺毒素2处理组的透射电子显微镜显微照片显示神经元呈现出剂量依赖性的进行性神经退行性病变。由于亚致死剂量静脉注射志贺毒素2改变了小脑的血脑屏障通透性,毒素穿透小脑实质并导致细胞损伤,对测试平衡产生显著的功能影响。