Department of Clinical Nutrition and Food Management, Institute of Biomedical Sciences, University of Tokushima Graduate School, 3-18-15 Kuramoto-cho, Tokushima, 770-8503, Japan.
Department of Health and Nutrition, Faculty of Nursing and Nutrition, The University of Shimane, 151 Nishihayashigi, Izumo, Shimane, 693-8550, Japan.
Calcif Tissue Int. 2019 Jun;104(6):667-678. doi: 10.1007/s00223-019-00525-0. Epub 2019 Jan 23.
Inorganic phosphate (Pi) is an essential nutrient for maintaining various biological functions, particularly during growth periods. Excess intake of dietary Pi increases the secretion of fibroblast growth factor 23 (FGF23) and parathyroid hormone to maintain plasma Pi levels. FGF23 is a potent phosphaturic factor that binds to the α-klotho/FGFR complex in the kidney to promote excretion of Pi into the urine. In addition, excess intake of dietary Pi decreases renal α-klotho expression. Down-regulation or lack of α-klotho induces a premature aging-like phenotype, resulting from hyperphosphatemia, and leading to conditions such as ectopic calcification and osteoporosis. However, it remains unclear what effects dietary Pi has on α-klotho expression at different life stages, especially during growth periods. To investigate this, we used C57BL/6J mice in two life stages during growing period. Weaned (3 weeks old) and periadolescent (7 weeks old) were randomly divided into seven experimental groups and fed with 0.02, 0.3, 0.6, 0.9, 1.2, 1.5, or 1.8% Pi diets for 7 days. As a result, elevated plasma Pi and FGF23 levels and decreased renal α-klotho expression were observed in weaned mice fed with a high Pi diet. In addition, a high Pi diet clearly induced renal calcification in the weaned mice. However, in the periadolescent group, renal calcification was not observed, even in the 1.8% Pi diet group. The present study indicates that a high Pi diet in weaned mice has much greater adverse effects on renal α-klotho expression and pathogenesis of renal calcification compared with periadolescent mice.
无机磷酸盐 (Pi) 是维持各种生物功能的必需营养素,特别是在生长期间。饮食中 Pi 的过量摄入会增加成纤维细胞生长因子 23 (FGF23) 和甲状旁腺激素的分泌,以维持血浆 Pi 水平。FGF23 是一种有效的磷排泄因子,它与肾脏中的 α-klotho/FGFR 复合物结合,促进 Pi 排泄到尿液中。此外,饮食 Pi 的过量摄入会降低肾脏 α-klotho 的表达。α-klotho 的下调或缺失会导致类似早衰的表型,这是由于高磷血症引起的,并导致异位钙化和骨质疏松等疾病。然而,目前尚不清楚饮食 Pi 在不同生命阶段,特别是在生长期间,对 α-klotho 表达有何影响。为了研究这一点,我们在生长期间使用了 C57BL/6J 小鼠的两个生命阶段。断奶 (3 周龄) 和青春期 (7 周龄) 被随机分为七个实验组,并喂食 0.02、0.3、0.6、0.9、1.2、1.5 或 1.8% Pi 饮食 7 天。结果表明,高 Pi 饮食喂养的断奶小鼠血浆 Pi 和 FGF23 水平升高,肾脏 α-klotho 表达降低。此外,高 Pi 饮食明显诱导断奶小鼠肾脏钙化。然而,在青春期组中,即使在 1.8% Pi 饮食组中,也未观察到肾脏钙化。本研究表明,与青春期小鼠相比,断奶小鼠高 Pi 饮食对肾脏 α-klotho 表达和肾脏钙化发病机制的不良影响更大。