Korean red ginseng polysaccharide as a potential therapeutic agent targeting tau pathology in Alzheimer's disease

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 a...

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Veröffentlicht in:International journal of biological macromolecules 2024-04, Vol.263 (Pt 2), p.130516-130516, Article 130516
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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. •NFP from KRG modulates aggregation and dissociation of tau.•NFP from KRG reduces the tau accumulation and AD-related pathologies in 3xTg mice.•NFP from KRG mitigates hyperphosphorylated tau in okadaic acid-treated HT22 cells.•NFP from KRG alleviates tau-induced neuronal loss in vitro and in vivo.
ISSN:0141-8130
1879-0003
DOI:10.1016/j.ijbiomac.2024.130516