Neurological Disorder Research Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University (HBKU), Qatar Foundation, Doha P.O. Box 5825, Qatar.
Center of Basic Research, Biomedical Research Foundation of the Academy of Athens, 11527 Athens, Greece.
Int J Mol Sci. 2023 Jul 11;24(14):11326. doi: 10.3390/ijms241411326.
AD is the most common neurodegenerative disorder characterized by progressive memory impairment and cognitive deficits. The pathology of AD is still unclear; however, several studies have shown that the aggregation of the Aβ peptide in the CNS is an exclusively pathological process involved in AD. Currently, there is no proven medication to cure or prevent the disease progression. Nevertheless, various therapeutic approaches for AD show only relief of symptoms and mostly work on cognitive recovery. However, one of the promising approaches for therapeutic intervention is to use inhibitors for blocking the Aβ peptide aggregation process. Recently, herbal phenolic compounds have been shown to have a therapeutic property for treatment of AD due to their multifaceted action. In this study, we investigated the effectiveness of SA, Gn Rb1, and DMyr on inhibiting the aggregation and toxicity of Aβ40 and Aβ42 using different biochemical and cell-based assays. Our results showed that SA and DMyr inhibit Aβ40 and Aβ42 fibrillation, seeded aggregation, and toxicity. Gn Rb1 did not have any effect on the aggregation or toxicity induced by Aβ40 and Aβ42. Moreover, SA and DMyr were able to disaggregate the preformed fibrils. Overall, these compounds may be used alone or synergistically and could be considered as a lead for designing new compounds that could be used as effective treatment of AD and related disorders.
AD 是最常见的神经退行性疾病,其特征是进行性记忆障碍和认知缺陷。AD 的病理学仍不清楚;然而,几项研究表明,Aβ肽在中枢神经系统中的聚集是一种专门的病理过程,与 AD 有关。目前,尚无治愈或预防疾病进展的有效药物。然而,针对 AD 的各种治疗方法仅能缓解症状,主要作用于认知恢复。然而,一种有前途的治疗干预方法是使用抑制剂来阻断 Aβ肽聚集过程。最近,由于其多方面的作用,草药酚类化合物已被证明具有治疗 AD 的治疗特性。在这项研究中,我们使用不同的生化和基于细胞的测定法,研究了 SA、Gn Rb1 和 DMyr 对抑制 Aβ40 和 Aβ42 聚集和毒性的有效性。我们的结果表明,SA 和 DMyr 抑制 Aβ40 和 Aβ42 的纤维形成、种子聚集和毒性。Gn Rb1 对 Aβ40 和 Aβ42 诱导的聚集和毒性没有任何影响。此外,SA 和 DMyr 能够解聚原纤维。总的来说,这些化合物可以单独使用或协同使用,并可被视为设计新化合物的先导,这些新化合物可有效治疗 AD 和相关疾病。