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多发性硬化症神经保护疗法的进展

Advancement of therapies for neuroprotection in multiple sclerosis.

作者信息

Lo Albert

机构信息

Department of Clinical Neurosciences, Brown University, Providence, RI, USA.

出版信息

Expert Rev Neurother. 2008 Sep;8(9):1355-66. doi: 10.1586/14737175.8.9.1355.

Abstract

There is increased awareness and interest in the neurodegenerative component of multiple sclerosis. Available disease-modifying agents, primarily developed to suppress inflammation and modulate the immune system, have not been effective at halting neurodegeneration. Although understanding of the inter-relationship between the autoimmune and neurodegenerative processes continues to evolve, at a minimum, both elements are present in the disease. Accordingly, a more balanced treatment strategy should be directed at both processes, and it is necessary to introduce agents with prominent neuroprotective properties to augment immunomodulatory therapies. Potential agents reviewed include sodium channel-blocking drugs, glutamate antagonists, hormones, tetracyclines, polyphenolic compounds, cannabinoids and serotonin reuptake inhibitors. As putative neuroprotective agents are being investigated, it is being recognized that most agents are not exclusively neuroprotective or immunomodulatory, and mechanisms of action can inhibit toxic pathways or activate trophic pathways. Critical to establishing new agents is the concomitant development of outcomes specific to neuroprotective change. Human studies have been initiated to test the most promising agents for feasibility, safety and efficacy.

摘要

人们对多发性硬化的神经退行性成分的认识和兴趣日益增加。现有的疾病修正药物主要是为了抑制炎症和调节免疫系统而开发的,但在阻止神经退行性变方面并未取得成效。尽管对自身免疫和神经退行性过程之间的相互关系的理解仍在不断发展,但至少这两个因素都存在于该疾病中。因此,更平衡的治疗策略应针对这两个过程,有必要引入具有显著神经保护特性的药物来增强免疫调节治疗。所审查的潜在药物包括钠通道阻断药物、谷氨酸拮抗剂、激素、四环素、多酚化合物、大麻素和5-羟色胺再摄取抑制剂。随着对假定神经保护药物的研究,人们认识到大多数药物并非单纯具有神经保护或免疫调节作用,其作用机制可能是抑制毒性途径或激活营养途径。确定新药物的关键在于同时开发针对神经保护变化的特定结果。已经启动了人体研究,以测试最有前景的药物的可行性、安全性和有效性。

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