Cho Jung-Eun, Kim Jin Ryoun
Othmer-Jacobs Department of Chemical and Biological Engineering, Polytechnic Institute of New York University, 6 MetroTech Center, Brooklyn, NY 11201, USA.
Recent Pat CNS Drug Discov. 2011 Sep 1;6(3):222-33. doi: 10.2174/157488911796958002.
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by neuropathological features comprising amyloid deposits and neuronal losses in brain. In AD, aggregation of a β amyloid peptide (Aβ), produced from proteolytic cleavage of amyloid precursor protein, is believed to be implicated in the pathophysiological cascade leading to neuronal death. Most AD drugs currently available can only alleviate symptoms rather than modify the underlying molecular cause of AD. In this review, we describe and discuss the recent patents issued within the past two years focusing on therapeutic interventions targeting at various Aβ-associated pathological mechanisms of AD. The described therapeutic strategies include 1) reduction of synthesis of Aβ, 2) inhibition of Aβ aggregation, 3) immunotherapeutic/enzymatic clearance of Aβ, 4) targeting other amyloidogenic proteins interacting with Aβ and 5) amelioration of Aβ downstream toxic effects. Important issues to be considered for further improvement of therapeutic efficacy of these approaches are also discussed.
阿尔茨海默病(AD)是一种神经退行性疾病,其神经病理学特征包括大脑中的淀粉样蛋白沉积和神经元丧失。在AD中,淀粉样前体蛋白经蛋白水解裂解产生的β淀粉样肽(Aβ)聚集,被认为与导致神经元死亡的病理生理级联反应有关。目前可用的大多数AD药物只能缓解症状,而不能改变AD潜在的分子病因。在本综述中,我们描述并讨论了过去两年内发布的近期专利,这些专利聚焦于针对AD各种与Aβ相关病理机制的治疗干预措施。所描述的治疗策略包括:1)减少Aβ的合成;2)抑制Aβ聚集;3)免疫治疗/酶促清除Aβ;4)靶向与Aβ相互作用的其他淀粉样蛋白生成蛋白;5)改善Aβ下游毒性作用。还讨论了为进一步提高这些方法的治疗效果而需考虑的重要问题。