Premium
North American opossum Didelphis virginiana as a fetal nephrotoxicity model: Histologic and ultrastructural assessment of uranyl nitrate (UN)‐induced damage
Author(s) -
Liapis Helen,
Vogler George,
Steinhardt George F.
Publication year - 1997
Publication title -
microscopy research and technique
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 118
eISSN - 1097-0029
pISSN - 1059-910X
DOI - 10.1002/(sici)1097-0029(19971101)39:3<285::aid-jemt7>3.0.co;2-j
Subject(s) - uranyl nitrate , nephrotoxicity , necrosis , brush border , fibrosis , kidney , fetus , toxicity , ultrastructure , saline , uranyl acetate , chemistry , pathology , endocrinology , andrology , medicine , biology , pregnancy , biochemistry , vesicle , materials science , uranium , membrane , metallurgy , genetics
We have used our opossum model of fetal nephrotoxicity to investigate uranyl nitrate‐induced morphologic changes in the developing kidney. The present study establishes a renal dose response curve for the uranyl nitrate (UN). We find that pups treated with nonlethal doses of UN do not demonstrate growth retardation compared to saline‐treated controls. The kidneys of UN‐treated pups are heavier than the control animals, an effect less apparent the longer the pups are followed. A low dose of 60 mg/kg of UN administered to small pups causes slight histologic derangement but nevertheless more change than the same dose administered to larger more mature pups. Using a dose of 100 mg/kg of UN that effectively causes nonfatal renal disruption, we examined the kidneys from 4 to 42 days following injection. We find that tubular dilation and epithelial necrosis starts soon after treatment (day 4) and reaches its maximum during the second and third week (11 and 22 days). Architectural restoration appears complete by the end of the third week. By electron microscopy, UN induces sequential structural damage with loss of proximal tubule brush border, epithelial necrosis with intact basement membranes and regeneration at 4, 11, and 22 days. Residual tubular mitochondrial damage is present at 42 days in spite of histologically normal tubules. No apparent lesions are seen in glomeruli. Fibroblastic interstitial proliferation in UN‐treated kidneys at 11 days is not followed by appreciable fibrosis when assessed at 22 and 42 days. As the structural changes caused by 100 mg/ml UN administration in fetal opossum kidneys are reversible, this is a useful model to study the molecular mediators responsible for this form of renal damage and repair. Microsc. Res. Tech. 39:285–296, 1997. © 1997 Wiley‐Liss, Inc.