Dietary Regulation of Keap1/Nrf2/ARE Pathway: Focus on Plant-Derived Compounds and Trace Minerals

被引:179
作者
Stefanson, Amanda L. [1 ]
Bakovic, Marica [1 ]
机构
[1] Univ Guelph, Dept Human Hlth & Nutr Sci, Guelph, ON N1G 2W1, Canada
关键词
Nrf2; NF kappa B; Keap1; oxidative stress; glutathione; antioxidant enzymes; phase; 2; enzymes; nutrient: gene interactions; phytochemicals; trace minerals; zinc; selenium; NF-KAPPA-B; GLUTAMATE-CYSTEINE LIGASE; DRUG-METABOLIZING-ENZYMES; CUL3-BASED E3 LIGASE; OXIDATIVE STRESS; HEME OXYGENASE-1; GENE-EXPRESSION; INDUCED HEPATOTOXICITY; GLUTATHIONE SYNTHESIS; TRANSCRIPTION FACTOR;
D O I
10.3390/nu6093777
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
It has become increasingly evident that chronic inflammation underpins the development of many chronic diseases including cancer, cardiovascular disease and type 2 diabetes. Oxidative stress is inherently a biochemical dysregulation of the redox status of the intracellular environment, which under homeostatic conditions is a reducing environment, whereas inflammation is the biological response to oxidative stress in that the cell initiates the production of proteins, enzymes, and other compounds to restore homeostasis. At the center of the day-to-day biological response to oxidative stress is the Keap1/Nrf2/ARE pathway, which regulates the transcription of many antioxidant genes that preserve cellular homeostasis and detoxification genes that process and eliminate carcinogens and toxins before they can cause damage. The Keap1/Nrf2/ARE pathway plays a major role in health resilience and can be made more robust and responsive by certain dietary factors. Transient activation of Nrf2 by dietary electrophilic phytochemicals can upregulate antioxidant and chemopreventive enzymes in the absence of actual oxidative stress inducers. Priming the Keap1/Nrf2/ARE pathway by upregulating these enzymes prior to oxidative stress or xenobiotic encounter increases cellular fitness to respond more robustly to oxidative assaults without activating more intense inflammatory NFB-mediated responses.
引用
收藏
页码:3777 / 3801
页数:25
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