Tomas-Roig J, Torrente M, Cabré M, Vilella E, Colomina M T
Girona Neuroimmunology and Multiple Sclerosis Unit (UNIEMTG), Dr. Josep Trueta University Hospital and Neurodegeneration and Neuroinflammation Research Group, Girona Biomedical Research Institute (IDIBGI), Spain.
Dept. of Psychology, Universitat Rovira i Virgili, Tarragona, Spain; Research Center for Behavior Assessment (CRAMC), Universitat Rovira i Virgili, Tarragona, Spain; Laboratory of Toxicology and Environmental Health, School of Medicine, Reus, Spain; Institut d'Investigació Sanitària Pere Virgili (IISPV), Universitat Rovira i Virgili, Tarragona, Spain.
Behav Brain Res. 2019 May 2;363:38-44. doi: 10.1016/j.bbr.2019.01.036. Epub 2019 Jan 28.
Destruction of the myelin sheath in the central nervous system (CNS) is prominent in many clinico-pathologic conditions. Among animal models that reproduce the pathological features of de- and remyelination processes, the mouse model of cuprizone administration is widely used. Both hyperactivity and motor impairment have been reported upon cuprizone exposure. The aim of the present study was to assess behaviour in mice after CPZ withdrawal.To summarize, animals showed hypo-activity and deficits in motor coordination when they were subjected to acute demyelinating insult while minor exploratory activity, impairment in motor coordination and lower anxiety levels emerged when remyelination was reached following cuprizone withdrawal. A recovery period of 6 weeks after removal of CPZ was not accompanied by a similar return of normal activity indicating long lasting behavioural effects caused by this neurotoxicant. Specifically, the recovery group showed impairments in neurological functions involved in sensorimotor, neuromuscular, motor coordination and the capacity to cope with a stress-inducing event.
在许多临床病理情况下,中枢神经系统(CNS)的髓鞘破坏都很显著。在重现脱髓鞘和再髓鞘化过程病理特征的动物模型中,铜离子螯合剂(cuprizone)给药的小鼠模型被广泛使用。据报道,接触铜离子螯合剂后会出现多动和运动障碍。本研究的目的是评估停用铜离子螯合剂后小鼠的行为。总之,动物在遭受急性脱髓鞘损伤时表现出活动减少和运动协调缺陷,而在停用铜离子螯合剂后达到再髓鞘化时,出现轻微的探索活动、运动协调受损和较低的焦虑水平。停用铜离子螯合剂后6周的恢复期并没有伴随着类似的正常活动恢复,这表明这种神经毒素会产生持久的行为影响。具体而言,恢复组在涉及感觉运动、神经肌肉、运动协调以及应对应激诱导事件能力的神经功能方面存在损伤。