Torre-Fuentes L, Moreno-Jiménez L, Pytel V, Matías-Guiu J A, Gómez-Pinedo U, Matías-Guiu J
Servicio de Neurología, Instituto de Neurociencias, IdISSC, Hospital Clínico San Carlos, Universidad Complutense de Madrid, Madrid, España.
Servicio de Neurología, Instituto de Neurociencias, IdISSC, Hospital Clínico San Carlos, Universidad Complutense de Madrid, Madrid, España.
Neurologia (Engl Ed). 2020 Jan-Feb;35(1):32-39. doi: 10.1016/j.nrl.2017.07.002. Epub 2017 Aug 31.
Experimental animal models constitute a useful tool to deepen our knowledge of central nervous system disorders. In the case of multiple sclerosis, however, there is no such specific model able to provide an overview of the disease; multiple models covering the different pathophysiological features of the disease are therefore necessary.
We reviewed the different in vitro and in vivo experimental models used in multiple sclerosis research. Concerning in vitro models, we analysed cell cultures and slice models. As for in vivo models, we examined such models of autoimmunity and inflammation as experimental allergic encephalitis in different animals and virus-induced demyelinating diseases. Furthermore, we analysed models of demyelination and remyelination, including chemical lesions caused by cuprizone, lysolecithin, and ethidium bromide; zebrafish; and transgenic models.
Experimental models provide a deeper understanding of the different pathogenic mechanisms involved in multiple sclerosis. Choosing one model or another depends on the specific aims of the study.
实验动物模型是深化我们对中枢神经系统疾病认识的有用工具。然而,就多发性硬化症而言,尚无能够全面呈现该疾病的特定模型;因此,需要多种涵盖该疾病不同病理生理特征的模型。
我们回顾了用于多发性硬化症研究的不同体外和体内实验模型。关于体外模型,我们分析了细胞培养和切片模型。至于体内模型,我们研究了自身免疫和炎症模型,如不同动物中的实验性变应性脑脊髓炎以及病毒诱导的脱髓鞘疾病。此外,我们分析了脱髓鞘和髓鞘再生模型,包括由铜螯合剂、溶血卵磷脂和溴化乙锭引起的化学损伤模型、斑马鱼模型以及转基因模型。
实验模型有助于更深入地了解多发性硬化症涉及的不同致病机制。选择何种模型取决于研究的具体目的。