{"title":"食物因子调控药物代谢系统的生物防御功能研究","authors":"T. Kitakaze","doi":"10.4327/jsnfs.75.291","DOIUrl":null,"url":null,"abstract":"( PAHs ) are mediated mainly by the aryl hydrocarbon receptor ( AhR ) . Therefore, reduction of AhR activity is a promising strategy for prevention of xe-nobiotic-induced toxicity. Activation of nuclear factor-erythroid 2 -related factor 2 ( Nrf 2) results in enhanced antioxidant capacity and protection against environmental stressors by inducing phase II drug-metabolizing enzymes. The author revealed that luteolin and kaempferol coordinately prevent AhR-induced phase I drug-metabolizing enzyme, and a physiological concentration of luteolin, achievable from dietary consumption, activated Nrf 2 . Moreover, B[a]P-induced AhR activation caused lipid accumulation in the liver through circadian disruption; however, luteolin and kaempferol inhibited the circadian disruption caused by AhR activation. These results indicate that luteolin and kaempferol enhance biological defense function against xenobiotic-in-duced toxicity through the regulation of the drug metabolism system.","PeriodicalId":19296,"journal":{"name":"Nippon Eiyo Shokuryo Gakkaishi","volume":"85 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Study on Biological Defense Function though Regulation of Drug Metabolism System by Food Factors\",\"authors\":\"T. Kitakaze\",\"doi\":\"10.4327/jsnfs.75.291\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"( PAHs ) are mediated mainly by the aryl hydrocarbon receptor ( AhR ) . Therefore, reduction of AhR activity is a promising strategy for prevention of xe-nobiotic-induced toxicity. Activation of nuclear factor-erythroid 2 -related factor 2 ( Nrf 2) results in enhanced antioxidant capacity and protection against environmental stressors by inducing phase II drug-metabolizing enzymes. The author revealed that luteolin and kaempferol coordinately prevent AhR-induced phase I drug-metabolizing enzyme, and a physiological concentration of luteolin, achievable from dietary consumption, activated Nrf 2 . Moreover, B[a]P-induced AhR activation caused lipid accumulation in the liver through circadian disruption; however, luteolin and kaempferol inhibited the circadian disruption caused by AhR activation. These results indicate that luteolin and kaempferol enhance biological defense function against xenobiotic-in-duced toxicity through the regulation of the drug metabolism system.\",\"PeriodicalId\":19296,\"journal\":{\"name\":\"Nippon Eiyo Shokuryo Gakkaishi\",\"volume\":\"85 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Nippon Eiyo Shokuryo Gakkaishi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4327/jsnfs.75.291\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nippon Eiyo Shokuryo Gakkaishi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4327/jsnfs.75.291","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Study on Biological Defense Function though Regulation of Drug Metabolism System by Food Factors
( PAHs ) are mediated mainly by the aryl hydrocarbon receptor ( AhR ) . Therefore, reduction of AhR activity is a promising strategy for prevention of xe-nobiotic-induced toxicity. Activation of nuclear factor-erythroid 2 -related factor 2 ( Nrf 2) results in enhanced antioxidant capacity and protection against environmental stressors by inducing phase II drug-metabolizing enzymes. The author revealed that luteolin and kaempferol coordinately prevent AhR-induced phase I drug-metabolizing enzyme, and a physiological concentration of luteolin, achievable from dietary consumption, activated Nrf 2 . Moreover, B[a]P-induced AhR activation caused lipid accumulation in the liver through circadian disruption; however, luteolin and kaempferol inhibited the circadian disruption caused by AhR activation. These results indicate that luteolin and kaempferol enhance biological defense function against xenobiotic-in-duced toxicity through the regulation of the drug metabolism system.