首页> 外文期刊>Frontiers in Cellular Neuroscience >Perspectives on Cannabis-Based Therapy of Multiple Sclerosis: A Mini-Review
【24h】

Perspectives on Cannabis-Based Therapy of Multiple Sclerosis: A Mini-Review

机译:关于大麻的多发性硬化症治疗的观点:迷你审查

获取原文
           

摘要

The consistency, efficacy, and safety of cannabis-based medicines have been demonstrated in humans, leading to the approval of the first cannabis-based therapy to alleviate spasticity and pain associated with multiple sclerosis (MS). Indeed, the evidence supporting the therapeutic potential of cannabinoids for the management of pathological events related to this disease is ever increasing. Different mechanisms of action have been proposed for cannabis-based treatments in mouse models of demyelination, such as Experimental Autoimmune Encephalomyelitis (EAE) and Theiler’s Murine Encephalomyelitis Virus-Induced Demyelinating Disease (TMEV-IDD). Cells in the immune and nervous system express the machinery to synthesize and degrade endocannabinoids, as well as their CB1 and CB2 receptors, each mediating different intracellular pathways upon activation. Hence, the effects of cannabinoids on cells of the immune system, on the blood-brain barrier (BBB), microglia, astrocytes, oligodendrocytes and neurons, potentially open the way for a plethora of therapeutic actions on different targets that could aid the management of MS. As such, cannabinoids could have an important impact on the outcome of MS in terms of the resolution of inflammation or the potentiation of endogenous repair in the central nervous system (CNS), as witnessed in the EAE, TMEV-IDD and toxic demyelination models, and through other in vitro approaches. In this mini review article, we summarize what is currently known about the peripheral and central effects of cannabinoids in relation to the neuroinflammation coupled to MS. We pay special attention to their effects on remyelination and axon preservation within the CNS, considering the major questions raised in the field and future research directions.
机译:在人类中证明了大麻药物的一致性,疗效和安全性,从而批准了第一个基于大麻的疗法,以减轻与多发性硬化症(MS)相关的痉挛和疼痛。实际上,支持大麻素治疗潜力为涉及这种疾病的病理事件的治疗潜力的证据永远在增加。已经提出了不同的作用机制,用于脱髓鞘小鼠模型中的大麻类药物,例如实验性自身免疫性脑脊髓炎(EAE)和Therer的鼠脑脑炎病毒诱导的脱髓鞘疾病(TMEV-IDD)。免疫和神经系统中的细胞表达机器以合成和降解内胆碱,以及它们的CB1和CB2受体,各自在激活时介导不同的细胞内途径。因此,大麻素对免疫系统细胞的影响,对血脑屏障(BBB),小胶质细胞,星形胶质细胞,少突胶质细胞和神经元的影响,可能对不同目标的过多治疗行动开放方式可以帮助管理小姐。因此,根据EAE,TMEV-IDD和有毒的脱髓鞘模型,大麻管蛋白在炎症或内源性修复的增强方面可能对MS的结果产生重要影响。并通过其他体外方法。在这个迷你评论文章中,我们总结了关于大麻素与耦合到MS的神经炎性的外周和核心效应所知的内容。考虑到在现场和未来的研究方向上提出的主要问题,我们特别注意其对CNS内的重新选择和轴突保护的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号