Combined treatment with capsaicin and resveratrol enhances neuroprotection against glutamate-induced toxicity in mouse cerebral cortical neurons

被引:62
作者
Lee, Jong-Geol [1 ]
Yon, Jung-Min [1 ]
Lin, Chunmei [1 ]
Jung, Young [1 ]
Jung, Ki Youn [1 ]
Nam, Sang-Yoon [1 ]
机构
[1] Chungbuk Natl Univ, Lab Vet Anat, Coll Vet Med, Res Inst Vet Med, Cheongju 361763, South Korea
基金
新加坡国家研究基金会;
关键词
Glutamate; Capsaicin; Resveratrol; Neuroprotection; Cortical neuron; CENTRAL-NERVOUS-SYSTEM; HIPPOCAMPAL-NEURONS; INDUCED APOPTOSIS; INFLAMMATORY CYTOKINES; INDUCED NEUROTOXICITY; OXIDATIVE STRESS; BCL-X; INVOLVEMENT; RAT; RECEPTOR;
D O I
10.1016/j.fct.2012.08.040
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Capsaicin and resveratrol as natural products have a variety of beneficial effects. However, capsaicin is also a neurotoxic agent, rendering its effect on the nervous system confusing. The aim of this study was to investigate whether capsaicin and/or resveratrol have a protective effect against glutamate (Glu)-induced neurotoxicity. After exposure to glutamate for 15 min, cerebral cortical neurons of ICR mouse fetuses on embryonic days 15-16 were post-treated with capsaicin and/or resveratrol for 24 h. Glu induced a significant reduction in cell viability, but the cell viability increased significantly with capsaicin or resveratrol treatment and further was highest in the neurons co-treated with both phytochemicals. Glu-induced reactive oxygen species generation and apoptotic neuronal death also significantly decreased by a combined treatment with both phytochemicals. Due to Glu insults, the reduced mRNA levels of cytoplasmic glutathione peroxidase, copper/zinc and manganese superoxide dismutases, and Bcl-x(L) and the overexpressed mRNA levels of interleukin-1 beta and tumor necrosis factor-alpha were significantly restored by post-treatment of capsaicin and/or resveratrol. These findings indicate that capsaicin and resveratrol are neuroprotective against Glu-induced toxicity and that the combined treatment of both phytochemicals can enhance the neuroprotection, suggesting a useful therapeutic application in the treatment of neurodegenerative disorders. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3877 / 3885
页数:9
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