Literature DB >> 7621806

Interaction of metals during their uptake and accumulation in rabbit renal cortical slices.

R L Keith1, S J McGuinness, A J Gandolfi, T P Lowe, Q Chen, Q Fernando.   

Abstract

The uptake and accumulation of metals occurs in the kidney, which is a key site for interaction between metal nephrotoxicants. The uptake/accumulation and interaction of CdCl2, HgCl2, K2Cr2O7, and NaAsO2 was examined in precision-cut rabbit renal cortical slices. Slices were incubated with 10(-6) to 10(-3) M of a single metal toxicant or combinations of metal toxicants for 12 hr in DME-F12 media. Slices were blotted and sandwiched between two mylar films stretched across XRF sample cups. Quantitation of the metal in the slices was performed by proton-induced X-ray emission analysis (PIXE). The uptake of the metals was rapid, often reaching a maximum between 3 to 6 hr; the accumulation of Hg was highest, followed in order by Cd, Cr, and As. When two metals were present together, substantial alterations were observed in the uptake of the metals in the slices. HgCl2 hindered the uptake of K2Cr2O7, NaAsO2, CdCl2 (in this order), whereas these metals facilitated the uptake of HgCl2. However, a decreased uptake of both metals was often noted after exposure to other combinations of metals. PIXE analysis of metal content in slices is attractive since all elements (atomic number > 20) can be determined simultaneously. This information will be particularly useful in studying potential toxic interactions.

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Year:  1995        PMID: 7621806      PMCID: PMC1519335          DOI: 10.1289/ehp.95103s177

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  10 in total

1.  Arsenic-cadmium interaction in rats: toxic effects in the heart and tissue metal shifts.

Authors:  L Yáñez; L Carrizales; M T Zanatta; J J Mejía; L Batres; F Díaz-Barriga
Journal:  Toxicology       Date:  1991-04-08       Impact factor: 4.221

2.  Preparation of positional renal slices for study of cell-specific toxicity.

Authors:  C E Ruegg; A J Gandolfi; R B Nagle; C L Krumdieck; K Brendel
Journal:  J Pharmacol Methods       Date:  1987-04

3.  The effect of sodium chromate pretreatment on mercuric chloride-induced nephrotoxicity.

Authors:  S Sparrow; L Magos; R Snowden
Journal:  Arch Toxicol       Date:  1988       Impact factor: 5.153

4.  Rat kidney epithelial cell culture for metal toxicity studies.

Authors:  M G Cherian
Journal:  In Vitro Cell Dev Biol       Date:  1985-09

5.  Differential patterns of injury to the proximal tubule of renal cortical slices following in vitro exposure to mercuric chloride, potassium dichromate, or hypoxic conditions.

Authors:  C E Ruegg; A J Gandolfi; R B Nagle; K Brendel
Journal:  Toxicol Appl Pharmacol       Date:  1987-09-15       Impact factor: 4.219

6.  Arsenic-copper interaction in the kidney of the rat.

Authors:  G Schmolke; B Elsenhans; C Ehtechami; W Forth
Journal:  Hum Exp Toxicol       Date:  1992-09       Impact factor: 2.903

7.  Acute (24 hr) toxicity of a combination of four nephrotoxicants in rats compared with the toxicity of the individual compounds.

Authors:  D Jonker; M A Jones; P J van Bladeren; R A Woutersen; H P Til; V J Feron
Journal:  Food Chem Toxicol       Date:  1993-01       Impact factor: 6.023

8.  The effect of potassium dichromate and mercuric chloride on urinary excretion and organ and subcellular distribution of [203Hg]mercuric chloride in rats.

Authors:  J M Baggett; W O Berndt
Journal:  Toxicol Lett       Date:  1985-12       Impact factor: 4.372

9.  Cadmium uptake by primary cultures of rat renal cortical epithelial cells: influence of cell density and other metal ions.

Authors:  T Endo; Z A Shaikh
Journal:  Toxicol Appl Pharmacol       Date:  1993-08       Impact factor: 4.219

10.  Elemental analysis of renal slices by proton-induced X-ray emission.

Authors:  T Lowe; Q Chen; Q Fernando; R Keith; A J Gandolfi
Journal:  Environ Health Perspect       Date:  1993-09       Impact factor: 9.031

  10 in total

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