Abstract Title:

Neuroprotective effect of-derived polysaccharides in neuronal HT22 cell damage induced by hydrogen peroxide.

Abstract Source:

Biosci Biotechnol Biochem. 2020 Jan 21:1-12. Epub 2020 Jan 21. PMID: 31960754

Abstract Author(s):

Woo Sik Kim, Yi-Eun Kim, Eun-Ji Cho, Eui-Baek Byun, Woo Yong Park, Ha-Yeon Song, Kwangwook Kim, Sang-Hyun Park, Eui-Hong Byun

Article Affiliation:

Woo Sik Kim


Crude extracts and phytochemical compounds derived fromleaves have been demonstrated to exert neuroprotective effects. However, the neuroprotective effects ofleaves-derived polysaccharide extracts (ALPs) have not been investigated. ALP treatment was shown to induce concentration-dependent antioxidant activity in HT22 cells, and to increase cell viability in HO-treated HT22 cells. These effects were correlated with a decrease in major components of oxidation, including: Ca, ROS, and malondialdehyde (MDA). Mediators of the intracellular response to oxidation, including Bax, cytochrome, and cleaved caspases-3, -8, -9, MAPKs, and NF-κB, were positively influenced by ALP treatment under conditions of HO-mediated oxidative stress. In addition, ALP restored the expression of superoxide dismutase (SOD) and associated signaling pathways (PARP, PI3K/AKT and Nrf2-mediated HO-1/NQO-1) following HOtreatment. These results provide new pharmacological evidence that ALP facilitates neuroprotection via prevention of neuronal oxidative stress and promotion of cell survival signaling pathways.ABTS: 2,2'-azino-bis-(3-ethylbenzothiazoline-6-sulfonicacid); AD: Alzheimer's disease; ALP: polysaccharide extracts isolated fromleaves; ARE: antioxidant response element; DPPH: 1,1-diphenyl-picrylhydrazyl; DCFH-DA: 2',7'-dichlorofluorescin diacetate; ECL: electrochemiluminescence; ERK: extracellular regulated kinase; FBS: Fetal bovine serum; FITC: fluorescein isothiocyanate; FRAP: ferric reducing antioxidant power; HO-1: Heme oxygenase-1; JNK: c-jun N-terminal kinase; MAPKs: mitogen-activated protein kinases; MDA: malondialdehyde; MMP: mitochondrial membrane potential; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide; NQO1: NAD(P)H:quinine oxidoreductase 1, Nrf2: nuclear factor-E2-related factor 2; PD: parkinson's disease; PI3K: phosphatidylinositol-3kinase; PVDF: polyvinylidene difluoride; ROS: reactive oxygen species; SOD: Superoxidedismutase; TPTZ: tripydyltriazine.

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