摘要
阿尔茨海默病是一种常见的和最慢性的神经系统疾病(NDs),与认知功能障碍相关。病理上,阿尔茨海默病(AD)的特征是存在β-淀粉样蛋白(Aβ)斑块、高磷酸化Tau蛋白和神经纤维缠结,然而,持续性氧化-硝化应激、内质网应激、线粒体功能障碍、炎症细胞因子、凋亡前蛋白和神经递质水平的改变是其发病的共同病因。利斯的明、美金刚胺、加兰他明和多奈哌齐是FDA批准的用于AD症状管理的药物,而他克林因肝毒性而被停用。这些已批准的药物仅发挥症状缓解和表现出较差的患者依从性。在目前的情况下,已发表的大量证据表明,自然发生的生物活性分子通过其抗氧化、抗炎、抗凋亡和神经递质调节特性具有神经保护潜力。尽管它们具有强大的治疗意义,但它们的疗效和可能的临床结果引起了关注。因此,为了克服这些缺陷,人们合成了许多受自然资源启发的杂环和环烃化合物,并显示出改善的治疗活性。计算研究(分子对接)已用于预测这些天然生物活性以及天然来源的合成化合物对活化B细胞(NF-kB)乙酰胆碱酯酶,α/β分泌酶核因子kappa-轻链增强子的结合亲和力,核因子红系2相关因子2(Nrf2)等神经靶点。因此,本文就阿尔茨海默病的分子病因进行了综述,重点讨论了天然产物的药物治疗、化学和药理方面以及从天然来源合成和半合成分子的多靶点设计配体(MTDL)以及一些重要的临床试验。
关键词: 神经退行性变,自然产物,Tau蛋白,分子对接,痴呆,计算研究;临床试验
图形摘要
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