{"title":"Molecular Nutritional Study of Phosphate and Vitamin D Metabolism","authors":"I. Kaneko","doi":"10.4327/jsnfs.73.3","DOIUrl":null,"url":null,"abstract":"Summary : The biological phosphate regulatory system plays an important role in longevity and aging. Recent work focusing on the aging suppressor gene Klotho suggests that “ phosphate accelerates aging ” , thereby di-recting the focus toward various diseases caused by an abnormal phosphate balance mediated by the fibroblast growth factor 23 ( FGF 23) /Klotho/Vitamin D axis. In the present study, using knock-out mice and cultured cells, we revealed that the FGF 23 /Klotho/Vitamin D axis mediates mineral homeostasis from early develop-ment to late adulthood. Our findings suggest that the biological vitamin D status in chronic diseases can control aging. Analysis of methods to suppress aging by modifying phosphate and vitamin D metabolism in association with the prevention or improvement of progressive chronic kidney disease or cerebral dysfunction could help to promote a healthy life and slow the aging process through a nutritional approach.","PeriodicalId":19296,"journal":{"name":"Nippon Eiyo Shokuryo Gakkaishi","volume":"22 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-01-01","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.73.3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Summary : The biological phosphate regulatory system plays an important role in longevity and aging. Recent work focusing on the aging suppressor gene Klotho suggests that “ phosphate accelerates aging ” , thereby di-recting the focus toward various diseases caused by an abnormal phosphate balance mediated by the fibroblast growth factor 23 ( FGF 23) /Klotho/Vitamin D axis. In the present study, using knock-out mice and cultured cells, we revealed that the FGF 23 /Klotho/Vitamin D axis mediates mineral homeostasis from early develop-ment to late adulthood. Our findings suggest that the biological vitamin D status in chronic diseases can control aging. Analysis of methods to suppress aging by modifying phosphate and vitamin D metabolism in association with the prevention or improvement of progressive chronic kidney disease or cerebral dysfunction could help to promote a healthy life and slow the aging process through a nutritional approach.