Radloff J, Latic N, Pfeiffenberger U, Schüler C, Tangermann S, Kenner L, Erben R G
Department of Biomedical Sciences, University of Veterinary Medicine Vienna, Veterinaerplatz 1, 1210, Vienna, Austria.
Department of Pathobiology, University of Veterinary Medicine Vienna, Vienna, Austria.
Sci Rep. 2021 Jul 21;11(1):14868. doi: 10.1038/s41598-021-94264-8.
C57BL/6 mice are known to be rather resistant to the induction of experimental chronic kidney disease (CKD) by 5/6-nephrectomy (5/6-Nx). Here, we sought to characterize the development of CKD and its cardiac and skeletal sequelae during the first three months after 5/6-Nx in C57BL/6 mice fed a calcium- and phosphate enriched diet (CPD) with a balanced calcium/phosphate ratio. 5/6-NX mice on CPD showed increased renal fibrosis and a more pronounced decrease in glomerular filtration rate when compared to 5/6-Nx mice on normal diet (ND). Interestingly, despite comparable levels of serum calcium, phosphate, and parathyroid hormone (PTH), circulating intact fibroblast growth factor-23 (FGF23) was 5 times higher in 5/6-Nx mice on CPD, relative to 5/6-Nx mice on ND. A time course experiment revealed that 5/6-Nx mice on CPD developed progressive renal functional decline, renal fibrosis, cortical bone loss, impaired bone mineralization as well as hypertension, but not left ventricular hypertrophy. Collectively, our data show that the resistance of C57BL/6 mice to 5/6-Nx can be partially overcome by feeding the CPD, and that the CPD induces a profound, PTH-independent increase in FGF23 in 5/6-Nx mice, making it an interesting tool to assess the pathophysiological significance of FGF23 in CKD.
已知C57BL/6小鼠对通过5/6肾切除术(5/6-Nx)诱导的实验性慢性肾脏病(CKD)具有较强的抵抗力。在此,我们试图描述在给C57BL/6小鼠喂食钙磷比例平衡的富含钙和磷的饮食(CPD)后,5/6-Nx术后前三个月内CKD的发展及其心脏和骨骼后遗症。与喂食正常饮食(ND)的5/6-Nx小鼠相比,喂食CPD的5/6-NX小鼠肾纤维化增加,肾小球滤过率下降更明显。有趣的是,尽管血清钙、磷和甲状旁腺激素(PTH)水平相当,但相对于喂食ND的5/6-Nx小鼠,喂食CPD的5/6-Nx小鼠循环中完整的成纤维细胞生长因子-23(FGF23)高出5倍。一项时间进程实验显示,喂食CPD的5/6-Nx小鼠出现进行性肾功能下降、肾纤维化、皮质骨丢失、骨矿化受损以及高血压,但未出现左心室肥厚。总体而言,我们的数据表明,通过喂食CPD可以部分克服C57BL/6小鼠对5/6-Nx的抵抗力,并且CPD在5/6-Nx小鼠中诱导FGF23显著升高且不依赖于PTH,这使其成为评估FGF23在CKD中病理生理意义的一个有趣工具。