人参
高磷酸化
神经退行性变
τ蛋白
疾病
神经保护
Tau病理学
神经炎症
葛兰素史克-3
医学
病理
阿尔茨海默病
神经科学
药理学
化学
生物
激酶
生物化学
替代医学
作者
Sujin Kim,Soo Jung Shin,Yunkwon Nam,Yong Ho Park,Byeong-Hyeon Kim,Hyun Ha Park,Vijay Kumar,Doo-Han Yoo,Yong Yook Lee,Hyang‐Sook Hoe,Minho Moon
标识
DOI:10.1016/j.ijbiomac.2024.130516
摘要
Tau is a microtubule-associated protein that plays a critical role in the stabilization and modulation of neuronal axons. Tau pathology is stronger associated with cognitive decline in patients with Alzheimer's disease (AD) than amyloid beta (Aβ) pathology. Hence, tau targeting is a promising approach for the treatment of AD. Previous studies have demonstrated that the non-saponin fraction with rich polysaccharide (NFP) from Korean red ginseng (KRG) can modulate tau aggregation and exert a therapeutic effect on AD. Therefore, we investigated the efficacy of NFP isolated from KRG on tau pathology in experimental models of AD. Our results showed that NFP from KRG ameliorated deposition and hyperphosphorylation of tau in the brain of 3xTg mice. Moreover, NFP from KRG modulated the aggregation and dissociation of tau K18 in vitro. We demonstrated the alleviatory effects of NFP from KRG on hyperphosphorylated tau and tau kinase in okadaic acid-treated HT22 cells. Furthermore, NFP from KRG mitigated Aβ deposition, neurodegeneration, and neuroinflammation in 3xTg mice. We revealed the neuroprotective effects of NFP from KRG on tau-induced neuronal loss in HT22 cells. Our results indicate that NFP extracted from KRG is a novel therapeutic agent for the treatment of AD associated with tau pathology.
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