Secondary Metabolites of Plants as Potential Drugs Research Group, Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05 Hradec Králové, Czech Republic.
School of Pharmacy and Biomedical Sciences, University of Portsmouth, Portsmouth PO1 2DT, UK.
Int J Mol Sci. 2023 Feb 23;24(5):4399. doi: 10.3390/ijms24054399.
Alzheimer's disease (AD) is the most common cause of dementia in elderly people; currently, there is no efficient treatment. Considering the increase in life expectancy worldwide AD rates are predicted to increase enormously, and thus the search for new AD drugs is urgently needed. A great amount of experimental and clinical evidence indicated that AD is a complex disorder characterized by widespread neurodegeneration of the CNS, with major involvement of the cholinergic system, causing progressive cognitive decline and dementia. The current treatment, based on the cholinergic hypothesis, is only symptomatic and mainly involves the restoration of acetylcholine (ACh) levels through the inhibition of acetylcholinesterase (AChE). Since the introduction of the Amaryllidaceae alkaloid galanthamine as an antidementia drug in 2001, alkaloids have been one of the most attractive groups for searching for new AD drugs. The present review aims to comprehensively summarize alkaloids of various origins as multi-target compounds for AD. From this point of view, the most promising compounds seem to be the β-carboline alkaloid harmine and several isoquinoline alkaloids since they can simultaneously inhibit several key enzymes of AD's pathophysiology. However, this topic remains open for further research on detailed mechanisms of action and the synthesis of potentially better semi-synthetic analogues.
阿尔茨海默病(AD)是老年人痴呆症最常见的病因;目前尚无有效的治疗方法。考虑到全球预期寿命的增加,AD 发病率预计会大幅增加,因此急需寻找新的 AD 药物。大量的实验和临床证据表明,AD 是一种复杂的疾病,其特征是中枢神经系统的广泛神经退行性变,主要涉及胆碱能系统,导致进行性认知能力下降和痴呆。目前的治疗方法基于胆碱能假说,仅具有症状缓解作用,主要通过抑制乙酰胆碱酯酶(AChE)来恢复乙酰胆碱(ACh)水平。自 2001 年百合科生物碱加兰他敏被引入作为抗痴呆药物以来,生物碱一直是寻找新的 AD 药物的最具吸引力的药物之一。本综述旨在全面总结各种来源的生物碱作为 AD 的多靶化合物。从这个角度来看,最有前途的化合物似乎是β-咔啉生物碱哈尔明和几种异喹啉生物碱,因为它们可以同时抑制 AD 病理生理学的几种关键酶。然而,这个课题仍有待进一步研究其作用机制的详细情况以及潜在更好的半合成类似物的合成。