Arévalo-Martín Angel, Vela José Miguel, Molina-Holgado Eduardo, Borrell José, Guaza Carmen
Neuroimmunology Group, Neural Plasticity Department, Cajal Institute, Consejo Superior de Investigaciones Científicas, 28002 Madrid, Spain.
J Neurosci. 2003 Apr 1;23(7):2511-6. doi: 10.1523/JNEUROSCI.23-07-02511.2003.
Theiler's virus infection of the CNS induces an immune-mediated demyelinating disease in susceptible mouse strains and serves as a relevant infection model for human multiple sclerosis (MS). Cannabinoids may act as immunosuppressive compounds that have shown therapeutic potential in chronic inflammatory disorders. Using the Theiler's murine encephalomyelitis virus model, we report here that treatment with the synthetic cannabinoids WIN 55,212-2, ACEA, and JWH-015 during established disease significantly improved the neurological deficits in a long-lasting way. At a histological level, cannabinoids reduced microglial activation, abrogated major histocompatibility complex class II antigen expression, and decreased the number of CD4+ infiltrating T cells in the spinal cord. Both recovery of motor function and diminution of inflammation paralleled extensive remyelination. Overall, the data presented may have potential therapeutic implications in demyelinating pathologies such as MS; in particular, the possible involvement of cannabinoid receptor CB2 would enable nonpsychoactive therapy suitable for long-term use.
中枢神经系统感染泰勒氏病毒会在易感小鼠品系中引发免疫介导的脱髓鞘疾病,并作为人类多发性硬化症(MS)的相关感染模型。大麻素可能作为免疫抑制化合物,已在慢性炎症性疾病中显示出治疗潜力。利用泰勒氏鼠脑脊髓炎病毒模型,我们在此报告,在疾病已确立期间用合成大麻素WIN 55,212-2、ACEA和JWH-015进行治疗可长期显著改善神经功能缺损。在组织学水平上,大麻素减少了小胶质细胞的激活,消除了主要组织相容性复合体II类抗原的表达,并减少了脊髓中浸润的CD4+ T细胞数量。运动功能的恢复和炎症的减轻与广泛的髓鞘再生同时发生。总体而言,所呈现的数据可能对MS等脱髓鞘疾病具有潜在的治疗意义;特别是,大麻素受体CB2的可能参与将使适合长期使用的非精神活性疗法成为可能。