THE NEPHROTOXICITY OF INTRAVENOUSLY ADMINISTERED CADMIUM-METALLOTHIONEIN - EFFECT OF DOSE, MODE OF ADMINISTRATION, AND PREEXISTING RENAL CADMIUM BURDEN

Citation
P. Vestergaard et Za. Shaikh, THE NEPHROTOXICITY OF INTRAVENOUSLY ADMINISTERED CADMIUM-METALLOTHIONEIN - EFFECT OF DOSE, MODE OF ADMINISTRATION, AND PREEXISTING RENAL CADMIUM BURDEN, Toxicology and applied pharmacology, 126(2), 1994, pp. 240-247
Citations number
44
Categorie Soggetti
Pharmacology & Pharmacy",Toxicology
ISSN journal
0041008X
Volume
126
Issue
2
Year of publication
1994
Pages
240 - 247
Database
ISI
SICI code
0041-008X(1994)126:2<240:TNOIAC>2.0.ZU;2-N
Abstract
Exogenously administered cadmium-metallothionein (Cd-MT) is highly nep hrotoxic, producing renal damage similar to that seen following chroni c Cd exposure. However, nephrotoxicity following Cd-MT administration occurs at a much lower renal Cd concentration than that following chro nic Cd exposure. In the present study, the sensitivity of female rats to bolus and infused doses of Cd-MT was evaluated. The Cd-MT was admin istered via the jugular vein either as a bolus or infused over a 24-hr period via osmotic minipumps in naive rats and in rats which had been pretreated with 5 mu M CdCl2/kg, sc, five times/week, for 9 weeks. Re nal toxicity was evaluated by urinary lactate dehydrogenase, protein, and MT excretion. In naive rats, a bolus dose of 0.15 mg Cd/kg as Cd-M T was nephrotoxic. In comparison, a two-fold higher infused dose was r equired to cause nephrotoxicity. In Cd-pretreated rats, a bolus dose o f 0.45 mg Cd/kg as Cd-MT was necessary to produce nephrotoxicity, pres umably because Cd pretreatment yielded renal MT levels that were about 15 times higher than the levels in naive animals. Although a bolus do se of 3 mg Cd/kg as CdCl2 resulted in a renal Cd concentration about 1 .5 times that found after administration of 0.15 mg Cd/kg as Cd-MT, it did not produce any nephro-toxicity, The results of this study sugges t that a renal Cd concentration, which is nephrotoxic if the Cd-MT is administered as a bolus dose, is well tolerated if the Cd-MT is delive red at a sustained level over a 24-hr period. Furthermore, the preexis ting renal Cd burden reduces the sensitivity to nephrotoxicity of Cd-M T, presumably due to elevated MT levels available for sequestration of incoming Cd. We conclude that mere accumulation of Cd in the kidney d oes not necessarily result in nephrotoxicity; instead, the circulating Cd-MT level, as well as the intracellular MT concentration, appear to be the more important determinants of nephrotoxicity. (C) 1994 Academ ic Press, Inc.