Opinion - Pathologically activated therapeutics for neuroprotection

被引:213
作者
Lipton, Stuart A.
机构
[1] Burnham Inst Med Res, Salk Inst Biol Studies, Scripps Res Inst, La Jolla, CA USA
[2] Univ Calif San Diego, La Jolla, CA 29037 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrn2229
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Many drugs that have been developed to treat neurodegenerative diseases fail to gain approval for clinical use because they are not well tolerated in humans. In this article, I describe a series of strategies for the development of neuroprotective therapeutics that are both effective and well tolerated. These strategies are based on the principle that drugs should be activated by the pathological state that they are intended to inhibit. This approach has already met with success, and has led to the development of the potentially neuroprotective drug memantine, an N-methyl-Da-spartate (NMDA)-type and glutamate receptor antagonist.
引用
收藏
页码:803 / 808
页数:6
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