Han Na, Wen Yuanyuan, Liu Zhihui, Zhai Jianxiu, Li Sikai, Yin Jun
Development and Utilization Key Laboratory of Northeast Plant Materials, School of Traditional Chinese Materia, Shenyang Pharmaceutical University, Shenyang, China.
Front Pharmacol. 2022 Oct 12;13:960112. doi: 10.3389/fphar.2022.960112. eCollection 2022.
Alzheimer's disease (AD) is a serious neurodegenerative disease associated with the memory and cognitive impairment. The occurrence of AD is due to the accumulation of amyloid -protein (Aβ) plaques and neurofibrillary tangles (NFTs) in the brain tissue as well as the hyperphosphorylation of Tau protein in neurons, doing harm to the human health and even leading people to death. The development of neuroprotective drugs with small side effects and good efficacy is focused by scientists all over the world. Natural drugs extracted from herbs or plants have become the preferred resources for new candidate drugs. Lignans were reported to effectively protect nerve cells and alleviate memory impairment, suggesting that they might be a prosperous class of compounds in treating AD. To explore the roles and mechanisms of lignans in the treatment of neurological diseases, providing proofs for the development of lignans as novel anti-AD drugs. Relevant literature was extracted and retrieved from the databases including China National Knowledge Infrastructure (CNKI), Elsevier, Science Direct, PubMed, SpringerLink, and Web of Science, taking lignan, anti-inflammatory, antioxidant, apoptosis, nerve regeneration, nerve protection as keywords. The functions and mechanisms of lignans against AD were summerized. Lignans were found to have the effects of regulating vascular disorders, anti-infection, anti-inflammation, anti-oxidation, anti-apoptosis, antagonizing NMDA receptor, suppressing AChE activity, improving gut microbiota, so as to strengthening nerve protection. Among them, dibenzocyclooctene lignans were most widely reported and might be the most prosperous category in the develpment of anti-AD drugs. Lignans displayed versatile roles and mechanisms in preventing the progression of AD in and models, supplying potential candidates for the treatment of nerrodegenerative diseases.
阿尔茨海默病(AD)是一种与记忆和认知障碍相关的严重神经退行性疾病。AD的发生是由于脑组织中淀粉样蛋白(Aβ)斑块和神经原纤维缠结(NFTs)的积累以及神经元中Tau蛋白的过度磷酸化,损害人体健康甚至导致死亡。开发副作用小、疗效好的神经保护药物受到全世界科学家的关注。从草药或植物中提取的天然药物已成为新候选药物的首选资源。据报道,木脂素可有效保护神经细胞并减轻记忆障碍,这表明它们可能是治疗AD的一类有前景的化合物。为了探索木脂素在治疗神经疾病中的作用和机制,为开发新型抗AD药物提供依据。以木脂素、抗炎、抗氧化、细胞凋亡、神经再生、神经保护为关键词,从中国知网(CNKI)、爱思唯尔、科学Direct、PubMed、SpringerLink和Web of Science等数据库中提取和检索相关文献。总结了木脂素抗AD的作用和机制。发现木脂素具有调节血管紊乱、抗感染、抗炎、抗氧化、抗细胞凋亡、拮抗NMDA受体、抑制乙酰胆碱酯酶活性、改善肠道微生物群等作用,从而增强神经保护作用。其中,二苯并环辛烯木脂素的报道最为广泛,可能是抗AD药物开发中最有前景的类别。木脂素在预防AD进展的体内和体外模型中发挥了多种作用和机制,为神经退行性疾病的治疗提供了潜在的候选药物。