Williams Brice J, Eriksdotter-Jonhagen Maria, Granholm Ann-Charlotte
Department of Neurosciences and the Center on Aging, Medical University of South Carolina, 173 Ashley Ave BSB 403, Charleston, SC 29425, United States.
Prog Neurobiol. 2006 Oct;80(3):114-28. doi: 10.1016/j.pneurobio.2006.09.001. Epub 2006 Nov 2.
The etiology of Alzheimer's disease (AD) is still unknown. In addition, this terrible neurodegenerative disease will increase exponentially over the next two decades due to longer lifespan and an aging "baby-boomer" generation. All treatments currently approved for AD have moderate efficacy in slowing the rate of cognitive decline in patients, and no efficacy in halting progression of the disease. Hence, there is an urgent need for new drug targets and delivery methods to slow or reverse the progression of AD. One molecule that has received much attention in its potential therapeutic role in AD is nerve growth factor (NGF). This review will demonstrate data from humans and animals which promote NGF as a potential therapeutic target by (1) outlining the hypothesis behind using NGF for the treatment of AD, (2) reviewing both the normal and AD altered signaling pathways and effects of NGF in the central nervous system (CNS), and (3) examining the results of NGF treatment obtained from animal models of AD and AD patients.
阿尔茨海默病(AD)的病因仍然不明。此外,由于寿命延长和“婴儿潮”一代的老龄化,这种可怕的神经退行性疾病在未来二十年将呈指数级增长。目前所有获批用于治疗AD的药物在减缓患者认知衰退速度方面疗效中等,在阻止疾病进展方面则无效。因此,迫切需要新的药物靶点和给药方法来减缓或逆转AD的进展。在AD潜在治疗作用方面备受关注的一种分子是神经生长因子(NGF)。本综述将展示来自人类和动物的数据,通过以下方式将NGF作为潜在治疗靶点进行推广:(1)概述使用NGF治疗AD背后的假设,(2)回顾NGF在中枢神经系统(CNS)中的正常和AD改变的信号通路及作用,(3)研究从AD动物模型和AD患者获得的NGF治疗结果。