Department of Pharmacology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Curr Drug Targets. 2018;19(8):927-937. doi: 10.2174/1389450118666170328122527.
Neurodegenerative disease is an incurable disease which involves the degeneration or death of the nerve cells. Alzheimer's Disease (AD) is a neurodegenerative disease discovered in 1906 by Alois Alzheimer, a German clinical psychiatrist and neuroanatomist. The main pathological hallmarks of this disease are the formation of extracellular amyloid β (Aβ) plaques and intracellular neurofibrillary tangle (NFT). The accumulation of the amyloid protein aggregates in the brain of AD patients leads to oxidative stress and inflammation. Other postulated reasons for the development of this disease are cholinergic depletion and excessive glutamatergic neurotransmission. The current drugs approved and marketed for the treatment of AD are cholinesterase inhibitors (ChEIs) and N-methyl-Daspartate (NMDA) receptor antagonists. The function of ChEIs is to avoid cholinergic depletion; whereas the function of NMDA receptor antagonist is to block excessive glutamatergic neurotransmission. Unfortunately, the current drugs prescribed for AD show only modest improvement in terms of symptomatic relief and delay the progression of the disease. This review will discuss about several polyphenolic compounds as potential natural treatment options for AD. Three compounds are highlighted in this review - Curcumin (Cur), Resveratrol (Rsv) and Epigallocatechin-3- gallate (EGCG). These compounds have huge potential for AD treatment, especially due to their low frequency of adverse events. However, the current conventional pharmaceutical drugs remain as the mainstay of treatment for AD.
神经退行性疾病是一种不可治愈的疾病,涉及神经细胞的退化或死亡。阿尔茨海默病(AD)是一种神经退行性疾病,于 1906 年由德国临床精神病学家和神经解剖学家 Alois Alzheimer 发现。这种疾病的主要病理特征是细胞外淀粉样β(Aβ)斑块和细胞内神经原纤维缠结(NFT)的形成。AD 患者大脑中淀粉样蛋白聚集物的积累导致氧化应激和炎症。这种疾病发展的其他假定原因是胆碱能耗竭和谷氨酸能神经传递过度。目前批准和上市用于治疗 AD 的药物是胆碱酯酶抑制剂(ChEIs)和 N-甲基-D-天冬氨酸(NMDA)受体拮抗剂。ChEIs 的作用是避免胆碱能耗竭;而 NMDA 受体拮抗剂的作用是阻断过度的谷氨酸能神经传递。不幸的是,目前为 AD 开具的药物仅在症状缓解和延缓疾病进展方面有适度的改善。本综述将讨论几种多酚化合物作为 AD 的潜在天然治疗选择。在本综述中强调了三种化合物 - 姜黄素(Cur)、白藜芦醇(Rsv)和表没食子儿茶素-3-没食子酸酯(EGCG)。这些化合物在 AD 治疗方面具有巨大的潜力,尤其是由于它们不良反应的发生率低。然而,目前的传统药物仍然是 AD 治疗的主要方法。