| Literature DB >> 31449775 |
Elise Bouderlique1, Ellie Tang1, Joëlle Perez1, Amélie Coudert2, Dominique Bazin3, Marie-Christine Verpont1, Christophe Duranton4, Isabelle Rubera4, Jean-Philippe Haymann5, Georges Leftheriotis6, Ludovic Martin7, Michel Daudon5, Emmanuel Letavernier8.
Abstract
Most kidney stones are made of calcium oxalate crystals. Randall's plaque, an apatite deposit at the tip of the renal papilla, is considered to at the origin of these stones. Hypercalciuria may promote Randall's plaque formation and growth. We analyzed whether long-term exposure of Abcc6-/- mice (a murine model of Randall's plaque) to vitamin D supplementation, with or without a calcium-rich diet, would accelerate the formation of Randall's plaque. Eight groups of mice (including Abcc6-/- and wild type) received vitamin D alone (100,000 UI/kg every 2 weeks), a calcium-enriched diet alone (calcium gluconate 2 g/L in drinking water), both vitamin D supplementation and a calcium-rich diet, or a standard diet (controls) for 6 months. Kidney calcifications were assessed by 3-dimensional microcomputed tomography, μ-Fourier transform infrared spectroscopy, field emission-scanning electron microscopy, transmission electron microscopy, and Yasue staining. At 6 months, Abcc6-/- mice exposed to vitamin D and calcium supplementation developed massive Randall's plaque when compared with control Abcc6-/- mice (P < 0.01). Wild-type animals did not develop significant calcifications when exposed to vitamin D. Combined administration of vitamin D and calcium significantly accelerates Randall's plaque formation in a murine model. This original model raises concerns about the cumulative risk of vitamin D supplementation and calcium intakes in Randall's plaque formation.Entities:
Year: 2019 PMID: 31449775 DOI: 10.1016/j.ajpath.2019.07.013
Source DB: PubMed Journal: Am J Pathol ISSN: 0002-9440 Impact factor: 4.307