TY - JOUR A1 - Hardt, Stefanie A1 - Valek, Lucie A1 - Zeng-Brouwers, Jinyang A1 - Wilken-Schmitz, Annett A1 - Schäfer, Liliana A1 - Tegeder, Irmgard T1 - Progranulin deficient mice develop nephrogenic diabetes insipidus T2 - Aging and disease N2 - Loss-of-function mutations of progranulin are associated with frontotemporal dementia in humans, and its deficiency in mice is a model for this disease but with normal life expectancy and mild cognitive decline on aging. The present study shows that aging progranulin deficient mice develop progressive polydipsia and polyuria under standard housing conditions starting at middle age (6-9 months). They showed high water licking behavior and doubling of the normal daily drinking volume, associated with increased daily urine output and a decrease of urine osmolality, all maintained during water restriction. Creatinine clearance, urine urea, urine albumin and glucose were normal. Hence, there were no signs of osmotic diuresis or overt renal disease, other than a concentrating defect. In line, the kidney morphology and histology revealed a 50% increase of the kidney weight, kidney enlargement, mild infiltrations of the medulla with pro-inflammatory cells, widening of tubules but no overt signs of a glomerular or tubular pathology. Plasma vasopressin levels were on average about 3-fold higher than normal levels, suggesting that the water loss resulted from unresponsiveness of the collecting tubules towards vasopressin, and indeed aquaporin-2 immunofluorescence in collecting tubules was diminished, whereas renal and hypothalamic vasopressin were increased, the latter in spite of substantial astrogliosis in the hypothalamus. The data suggest that progranulin deficiency causes nephrogenic diabetes insipidus in mice during aging. Possibly, polydipsia in affected patients - eventually interpreted as psychogenic polydipsia - may point to a similar concentrating defect. KW - Progranulin KW - aging KW - polyuria KW - polydipsia KW - knockout mice KW - hypothalamus KW - vasopressin Y1 - 2018 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/48357 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-483577 SN - 2152-5250 N1 - Copyright: © 2017 Hardt S et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. VL - 9 IS - 5 SP - 817 EP - 830 PB - JKL International CY - [s. l.] ER -