Neuroprotective effect of Citrus unshiu immature peel and nobiletin inhibiting hydrogen peroxide-induced oxidative stress in HT22 murine hippocampal neuronal cells

被引:45
作者
Cho, Hyun Woo [1 ]
Jung, Su Young [2 ]
Lee, Gyeong Hwan [1 ]
Cho, Jung Hee [1 ]
Choi, In Young [1 ]
机构
[1] Jeonnam Dev Inst Korean Tradit Med, Res & Dev Team, Jangheung Gun 529851, Jeonnam, South Korea
[2] Chonbuk Natl Univ Hosp, Clin Trial Ctr Funct Foods, Geonjiro 561712, Jeonju, South Korea
关键词
Citrus unshiu immature peel; neuroprotective effect; nobiletin; oxidative stress; NF-KAPPA-B; PC12; CELLS; ALZHEIMERS-DISEASE; ACTIVATION; APOPTOSIS; DAMAGE; P38; PHOSPHORYLATION; ANTIOXIDANTS; EXTRACTS;
D O I
10.4103/0973-1296.166047
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Background: Oxidative stress-induced cell damage is common in the etiology of several neurobiological disorders, including Alzheimer's disease and Parkinson's disease. In a case study, nobiletin-rich Citrus reticulata peels could prevent the progression of cognitive impairment in donepezil-preadministered Alzheimer's disease patients. Objective: In this study, we investigated the effects and underlying mechanism of nobiletin and Citrus unshiu immature peel (CUIP) water extract, which contains nobiletin as a major compound, on hydrogen peroxide-induced oxidative stress in HT22 cells, a murine hippocampal neuronal model. Materials and Methods: HT22 cells were treated with hydrogen peroxide in the presence or absence of various concentrations of CUIP and nobiletin. Cytotoxicity and apoptotic protein levels were measured by 3-(4,5-dimethythiazol-2-yl)-2,5-diphenyl tetrazolium bromide assay and Western blotting. Results: Pretreatment with CUIP and nobiletin inhibited cell death due to hydrogen peroxide. Hydrogen peroxide-induced the expression of phospho-Jun N-terminal kinases (p-JNK) and p-p38 proteins in HT22 cells; however CUIP and nobiletin suppressed p-JNK and p-p38 without changing JNK or p38. Regarding apoptosis, caspase 3, B-cell lymphoma 2 (Bcl-2), and Bax protein expression was determined. CUIP and nobiletin suppressed caspase 3 and Bax expression, but they induced Bcl-2 expression in HT22 cells. Conclusion: These results show that CUIP and nobiletin can protect against hydrogen peroxide-induced cell death in HT22 neurons via mitogen-activated protein kinases and apoptotic pathways.
引用
收藏
页码:S284 / S289
页数:6
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