Department of Neurological Sciences, 'Dino Ferrari' Center, University of Milan, Fondazione Cà Granda, IRCCS Ospedale Maggiore Policlinico, Via F. Sforza 35, 20122, Milan, Italy.
Ther Adv Neurol Disord. 2011 Jul;4(4):203-16. doi: 10.1177/1756285611404470.
The first drugs developed for Alzheimer's disease (AD), acetylcholinesterase inhibitors (AChEI), increase acetylcholine levels, previously demonstrated to be reduced in AD. To date, four AChEI are approved for the treatment of mild-to-moderate AD. A further therapeutic option available for moderate-to-severe AD is memantine. These treatments are symptomatic, whereas drugs under development are intended to modify the pathological steps leading to AD, thus acting on the evolution of the disease. For this reason they are have been termed 'disease-modifying' drugs. To block the progression of the disease they have to interfere with the pathogenic steps responsible for the clinical symptoms, including the deposition of extracellular amyloid beta (Aβ) plaques and of intracellular neurofibrillary tangles, inflammation, oxidative damage, iron deregulation and cholesterol metabolism. In this review, new perspectives will be discussed. In particular, several approaches will be described, including interference with Aβ deposition by anti-Aβ aggregation agents, vaccination, γ-secretase inhibitors or selective Aβ-lowering agents; interference with tau deposition by methylthioninium chloride; and reduction of inflammation and oxidative damage.
用于治疗阿尔茨海默病(AD)的首批药物,乙酰胆碱酯酶抑制剂(AChEI),可增加乙酰胆碱水平,此前研究表明 AD 患者的乙酰胆碱水平降低。迄今为止,已有四种 AChEI 获批用于治疗轻中度 AD。对于中重度 AD,另一种可用的治疗选择是美金刚。这些治疗方法是对症的,而正在开发的药物旨在改变导致 AD 的病理步骤,从而作用于疾病的发展。因此,它们被称为“疾病修饰”药物。为了阻止疾病的进展,它们必须干预导致临床症状的致病步骤,包括细胞外淀粉样β(Aβ)斑块和细胞内神经原纤维缠结、炎症、氧化损伤、铁失调和胆固醇代谢的沉积。在这篇综述中,将讨论新的观点。特别是,将描述几种方法,包括通过抗 Aβ聚集剂、疫苗、γ-分泌酶抑制剂或选择性 Aβ降低剂来干扰 Aβ沉积;通过氯化甲噻嗪来干扰 tau 沉积;以及减轻炎症和氧化损伤。