Abstract. Powdered Cesfrurn diurnum leaves, mixed with two diets differing in calcium and phosphorus contents, produced nephrocalcinosis in young chicks regardless of serum calcium elevation. The calcific deposits, found in both proximal and distal portions of cortical tubules, began either in the cytoplasm or in lysosomal bodies as a unilaminar spheroid structure containing apatite crystals. The ultrastructural characteristics of intraluminal concretions suggested that they were formed intracellularly but later were extruded into the lumen. The extent of calcific deposits increased with duration and with hypercalcemia. Although Cestrum contains an analog of 1,25-dihydroxycholecalciferol, neither mitochondria nor basal lamina contained calcific deposits described in nephroca1cinos:s secondary to hypervitaminosis D.The appearance of nephrocalcinosis following large doses of vitamin D was first reported in 1928 [14]. In recent years, great advances have been made in the understanding of vitamin D metabolism, and its biologically active metabolite has been isolated. We now know that vitamin D is converted in the liver into 25-hydroxycholecalciferol, which is the main circulating form of the vitamin in blood [3]. This metabolite is hydroxylated further in the kidney to 1,25-dihydroxycholeca1-ciferol, but this conversion is regulated closely according to the need of the organism.Thus, when excess vitamin D is given to normal animals, it is converted to 25-hydroxycholecalciferol without subsequent production of 1,25-dihydroxycholecalciferol. Consequently, the serum of animals with experimental hypervitaminosis D shows a high concentration of 25-hydroxycholecalciferol, while the concentration of 1,25-dihydroxycholecalciferol remains relatively low [4].It has been established that 1,25-dihydroxycholecalciferol is the most active metabolite of vitamin D [3, 41, but induction of nephrocalcinosis by pure 1,25-dihydroxycholecalciferol has not been reported. Renal calcification, however, is seen frequently among animals feeding on plants such as Solunum mulucoxylon [2] and Trisetumflavescens [6], which contain an analog of 1,25-dihydroxycholecalciferol. On the other hand, neither cattle nor horses feeding on Cesrrzim diurnum, another plant 62