Department of Medical Biology, Faculty of Medicine, Atatürk University, Erzurum 25240, Turkey.
Department of Pharmacy, University G. d'Annunzio Chieti-Pescara, Via deiVestini 31, Chieti 66100, Italy.
Curr Drug Deliv. 2022;19(8):860-873. doi: 10.2174/1567201819666211228153801.
Alzheimer's Disease (AD) is one of the most important neurodegenerative diseases, accounting for 60% of all dementia cases. AD is a progressive neurodegenerative disease that occurs due to the production of β-amyloid (Aβ) protein and accumulation of hyper-phosphorylated tau protein; it causes breakage in the synaptic bonds and neuronal deaths to a large extent. Millions of people worldwide suffer from AD because there is no definitive drug for disease prevention, treatment, or slowing down its progression. Over the last decade, multiple target applications have been developed for AD treatments. These targets include Aβ accumulations, hyper-phosphorylated tau proteins, mitochondrial dysfunction, and oxidative stress, resulting in toxicity. Various natural or semisynthetic antioxidant formulations have been shown to protect brain cells from Aβ-induced toxicity and provide promising potentials for AD treatment. Ferulic acid (FA), a high-capacity antioxidant molecule, is naturally synthesized from certain plants. FA has been shown to have different substantial biological properties, such as anticancer, antidiabetic, antimicrobial, anti-inflammatory, hepatoprotective, and cardioprotective actions, etc. Furthermore, FA exerts neuroprotection via preventing Aβ-fibril formation, acting as an anti-inflammatory agent, and inhibiting free radical generation and acetylcholinesterase (AChE) enzyme activity. In this review, we present key biological roles of FA and several FA derivatives in preventing Aβ-induced neurotoxicity, protecting against free radical attacks, and exhibiting enzyme inhibitions and evaluate them as possible therapeutic agents for the treatment of AD.
阿尔茨海默病(AD)是最重要的神经退行性疾病之一,占所有痴呆病例的 60%。AD 是一种进行性神经退行性疾病,由于β-淀粉样蛋白(Aβ)蛋白的产生和过度磷酸化 tau 蛋白的积累而发生;它在很大程度上导致突触连接的断裂和神经元死亡。全球数百万人患有 AD,因为目前没有针对疾病预防、治疗或减缓其进展的明确药物。在过去的十年中,已经开发出多种针对 AD 治疗的靶向应用。这些靶点包括 Aβ 积累、过度磷酸化 tau 蛋白、线粒体功能障碍和氧化应激导致的毒性。各种天然或半合成抗氧化配方已被证明可保护脑细胞免受 Aβ诱导的毒性,并为 AD 治疗提供有希望的潜力。阿魏酸(FA)是一种高容量抗氧化分子,天然存在于某些植物中。FA 已被证明具有不同的实质性生物学特性,如抗癌、抗糖尿病、抗菌、抗炎、保肝和心脏保护等作用。此外,FA 通过防止 Aβ-纤维形成、作为抗炎剂以及抑制自由基生成和乙酰胆碱酯酶(AChE)酶活性来发挥神经保护作用。在这篇综述中,我们介绍了 FA 及其几种 FA 衍生物在预防 Aβ 诱导的神经毒性、防止自由基攻击以及表现出酶抑制作用方面的关键生物学作用,并将其评估为治疗 AD 的潜在治疗剂。