Department of Life Sciences, School of Sciences, European University Cyprus, Nicosia 1516, Cyprus.
Int J Mol Sci. 2024 Aug 7;25(16):8630. doi: 10.3390/ijms25168630.
Alzheimer's disease (AD), a progressive neurodegenerative disorder, manifests through dysregulation of brain function and subsequent loss of bodily control, attributed to β-amyloid plaque deposition and TAU protein hyperphosphorylation and aggregation, leading to neuronal death. Concurrently, similar cannabinoids to the ones derived from are present in the endocannabinoid system, acting through receptors CBR and CBR and other related receptors such as Trpv-1 and GPR-55, and are being extensively investigated for AD therapy. Given the limited efficacy and adverse effects of current available treatments, alternative approaches are crucial. Therefore, this review aims to identify effective natural and synthetic cannabinoids and elucidate their beneficial actions for AD treatment. PubMed and Scopus databases were queried (2014-2024) using keywords such as "Alzheimer's disease" and "cannabinoids". The majority of natural (Δ-THC, CBD, AEA, etc.) and synthetic (JWH-133, WIN55,212-2, CP55-940, etc.) cannabinoids included showed promise in improving memory, cognition, and behavioral symptoms, potentially via pathways involving antioxidant effects of selective CBR agonists (such as the BDNF/TrkB/Akt pathway) and immunomodulatory effects of selective CBR agonists (TLR4/NF-κB p65 pathway). Combining anticholinesterase properties with a cannabinoid moiety may enhance therapeutic responses, addressing cholinergic deficits of AD brains. Thus, the positive outcomes of the vast majority of studies discussed support further advancing cannabinoids in clinical trials for AD treatment.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,表现为大脑功能失调和随后的身体控制丧失,归因于β-淀粉样斑块沉积和 TAU 蛋白过度磷酸化和聚集,导致神经元死亡。同时,内源性大麻素系统中存在与来源于 的大麻素类似的物质,通过 CBR 和 CBR 受体以及其他相关受体(如 Trpv-1 和 GPR-55)发挥作用,并正在广泛研究用于 AD 治疗。鉴于目前可用治疗方法的疗效有限和不良反应,需要寻找替代方法。因此,本综述旨在确定有效的天然和合成大麻素,并阐明它们对 AD 治疗的有益作用。使用“阿尔茨海默病”和“大麻素”等关键词在 PubMed 和 Scopus 数据库中进行了检索(2014-2024 年)。包括的大多数天然(Δ-THC、CBD、AEA 等)和合成(JWH-133、WIN55,212-2、CP55-940 等)大麻素都显示出改善记忆、认知和行为症状的潜力,可能通过涉及选择性 CBR 激动剂的抗氧化作用(如 BDNF/TrkB/Akt 途径)和选择性 CBR 激动剂的免疫调节作用(TLR4/NF-κB p65 途径)。将抗胆碱酯酶特性与大麻素部分结合可能会增强治疗反应,解决 AD 大脑的胆碱能缺陷。因此,讨论的绝大多数研究的积极结果支持进一步推进大麻素在 AD 治疗的临床试验中应用。