Drug Discovery Biology, Monash Institute of Pharmaceutical Sciences, Monash University, Parkville, VIC, 3052, Australia.
Department of Pharmacology, Monash University, Parkville, VIC, 3052, Australia.
Purinergic Signal. 2022 Sep;18(3):359-381. doi: 10.1007/s11302-022-09883-1. Epub 2022 Jul 23.
Alzheimer's disease (AD) is the most common dementia in the elderly and its increasing prevalence presents treatment challenges. Despite a better understanding of the disease, the current mainstay of treatment cannot modify pathogenesis or effectively address the associated cognitive and memory deficits. Emerging evidence suggests adenosine G protein-coupled receptors (GPCRs) are promising therapeutic targets for Alzheimer's disease. The adenosine A and A receptors are expressed in the human brain and have a proposed involvement in the pathogenesis of dementia. Targeting these receptors preclinically can mitigate pathogenic β-amyloid and tau neurotoxicity whilst improving cognition and memory. In this review, we provide an accessible summary of the literature on Alzheimer's disease and the therapeutic potential of A and A receptors. Although there are no available medicines targeting these receptors approved for treating dementia, we provide insights into some novel strategies, including allosterism and the targeting of oligomers, which may increase drug discovery success and enhance the therapeutic response.
阿尔茨海默病(AD)是老年人中最常见的痴呆症,其发病率的增加带来了治疗挑战。尽管对这种疾病有了更好的了解,但目前的主要治疗方法不能改变发病机制,也不能有效解决相关的认知和记忆缺陷。新出现的证据表明,腺苷 G 蛋白偶联受体(GPCR)是治疗阿尔茨海默病的有前途的治疗靶点。人脑中表达有腺苷 A 和 A 受体,它们在痴呆症的发病机制中具有潜在作用。在临床前靶向这些受体可以减轻致病性β-淀粉样蛋白和 tau 神经毒性,同时改善认知和记忆。在这篇综述中,我们对阿尔茨海默病的文献和 A 和 A 受体的治疗潜力进行了通俗易懂的总结。尽管目前还没有针对这些受体的药物被批准用于治疗痴呆症,但我们提供了一些新策略的见解,包括变构和寡聚物的靶向,这可能会提高药物发现的成功率,并增强治疗反应。