†CNRS, UMR-5203, Institut de Génomique Fonctionnelle, F-34000 Montpellier, France.
‡Inserm, U1191, F-34000 Montpellier, France.
ACS Chem Neurosci. 2015 Jul 15;6(7):940-3. doi: 10.1021/acschemneuro.5b00135. Epub 2015 May 26.
Alzheimer's disease (AD) is the most common form of dementia affecting 35 million individuals worldwide. Current AD treatments provide only brief symptomatic relief. It is therefore urgent to replace this symptomatic approach with a curative one. Increasing serotonin signaling as well as developing molecules that enhance serotonin concentration in the synaptic cleft have been debated as possible therapeutic strategies to slow the progression of AD. In this Viewpoint, we discuss exciting new insights regarding the modulation of serotonin signaling for AD prevention and therapy.
阿尔茨海默病(AD)是最常见的痴呆症,影响着全球 3500 万人。目前的 AD 治疗方法只能提供短暂的症状缓解。因此,急需用一种更具疗效的方法来替代这种对症治疗。增加 5-羟色胺信号传递,以及开发能够提高突触间隙 5-羟色胺浓度的分子,一直被认为是减缓 AD 进展的可能治疗策略。在本观点中,我们讨论了关于调节 5-羟色胺信号传递以预防和治疗 AD 的令人兴奋的新见解。