Korean red ginseng polysaccharide as a potential therapeutic agent targeting tau pathology in Alzheimer's disease
- Authors
- Kim, Sujin; Shin, Soo Jung; Nam, Yunkwon; Park, Yong Ho; Kim, Byeong-Hyeon; Park, Hyun Ha; Kumar, Vijay; Yoo, Doo-Han; Lee, Yong Yook; Hoe, Hyang-Sook; Moon, Minho
- Issue Date
- Apr-2024
- Publisher
- ELSEVIER
- Keywords
- Alzheimer's disease; Tau pathology; Red ginseng polysaccharide
- Citation
- INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, v.263
- Journal Title
- INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
- Volume
- 263
- URI
- http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/1166
- DOI
- 10.1016/j.ijbiomac.2024.130516
- ISSN
- 0141-8130
1879-0003
- Abstract
- 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 (A beta) 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 A beta 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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Collections - 연구본부 > 퇴행성 뇌질환 연구그룹 > 1. Journal Articles
- 연구본부 > 치매 연구그룹 > 1. Journal Articles
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