Nishida Y, Taketani Y, Yamanaka-Okumura H, Imamura F, Taniguchi A, Sato T, Shuto E, Nashiki K, Arai H, Yamamoto H, Takeda E
Department of Clinical Nutrition, Institute of Health Biosciences, University of Tokushima Graduate School, Tokushima, Japan.
Kidney Int. 2006 Dec;70(12):2141-7. doi: 10.1038/sj.ki.5002000. Epub 2006 Oct 25.
Serum fibroblast growth factor 23 (FGF23) is a novel phosphaturic factor and important for the regulation of inorganic phosphate (Pi) homeostasis. In this study, we examined an acute effect of oral Pi loading on serum FGF23 levels to clarify the role in rapid adjustment of serum Pi level. We performed a randomized, double-blind, crossover study in eight healthy male volunteers. The subjects were alternately served one of three test meals containing different Pi amounts (400 mg (P400), 800 mg (P800), and 1200 mg (P1200)) as lunch at noon. The postprandial changes in serum levels of Pi, Ca, 1,25-dihydroxyvitamin D, intact-parathyroid hormone (iPTH), intact-FGF23 (iFGF23), and urinary excretion of Pi and Ca until 8 h after Pi loading were estimated. Serum Pi levels and urinary Pi excretion significantly increased within 1 h after P400 and P800 intake. Serum iPTH levels at 1-2 and 4-6 h after P1200 intake was significantly higher than those of P400 intake. Serum iFGF23 levels slightly decreased up to 8 h after P400 intake and up to 6 h after P800 intake, but not changed in P1200 intake. Significant increase of iFGF23 was observed at 8 h after P1200 intake compared with both P400 and P800 intake. Additionally, negative association was detected between iFGF23 and serum Pi, whereas positive association was observed between iPTH and serum Pi during the short period. We conclude that oral Pi loading cannot rapidly increase serum FGF23 level. FGF23 may be not associated with rapid adaptation of Pi homeostasis.
血清成纤维细胞生长因子23(FGF23)是一种新型的促尿磷排泄因子,对无机磷(Pi)稳态的调节具有重要作用。在本研究中,我们检测了口服Pi负荷对血清FGF23水平的急性影响,以阐明其在血清Pi水平快速调节中的作用。我们对8名健康男性志愿者进行了一项随机、双盲、交叉研究。受试者在中午交替食用三种含不同Pi量(400mg(P400)、800mg(P800)和1200mg(P1200))的试验餐之一作为午餐。评估了Pi负荷后8小时内血清Pi、Ca、1,25-二羟维生素D、完整甲状旁腺激素(iPTH)、完整FGF23(iFGF23)水平的餐后变化以及Pi和Ca的尿排泄情况。摄入P400和P800后1小时内,血清Pi水平和尿Pi排泄显著增加。摄入P1200后1-2小时和4-6小时的血清iPTH水平显著高于摄入P400后的水平。摄入P400后8小时内以及摄入P800后6小时内血清iFGF23水平略有下降,但摄入P1200后未发生变化。与摄入P400和P800相比,摄入P1200后8小时观察到iFGF23显著增加。此外,在短时间内检测到iFGF23与血清Pi之间呈负相关,而iPTH与血清Pi之间呈正相关。我们得出结论,口服Pi负荷不能迅速提高血清FGF23水平。FGF23可能与Pi稳态的快速适应无关。