Literature DB >> 8179484

The ambiguous effect of ascorbic acid on chromate induced proteinuria in rats.

D Appenroth1, K Winnefeld, H Schröter, M Rost.   

Abstract

The influence of ascorbic acid (AA, 5 g/kg body weight) on chromate (Cr, 10 mg/kg) induced proteinuria, which is a sensitive parameter of its nephrotoxicity, was investigated in adult female Wistar rats. The concentrations of Cr and ascorbic acid (AA) were determined in renal tissue. Cr nephrotoxicity is related to its intracellular reduction from Cr(VI) to Cr(III). Proteinuria was completely prevented by enhancement of extracellular reduction of Cr(VI) to Cr(III) followed by rapid renal excretion when Cr and AA were given concomitantly. With an interval up to 1 h between Cr and AA, proteinuria was decreased probably by the radical scavenging function of AA. At an interval of 3 h AA enhanced Cr toxicity by increased intracellular Cr reduction. If the interval was increased to 5 h or if Cr was given 24 h after AA, no influence of AA could be detected. Our results confirm that AA is a very effective reductant of Cr which can influence Cr nephrotoxicity in very high concentrations. It depends on the interval between Cr and AA administration whether or not there is a beneficial effect of AA in Cr nephrotoxicity.

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Year:  1994        PMID: 8179484     DOI: 10.1007/s002040050047

Source DB:  PubMed          Journal:  Arch Toxicol        ISSN: 0340-5761            Impact factor:   5.153


  23 in total

Review 1.  Role of physiological antioxidants in chromium(VI)-induced cellular injury.

Authors:  M Sugiyama
Journal:  Free Radic Biol Med       Date:  1992       Impact factor: 7.376

2.  Influence of metyrapone and phenobarbital on sodium dichromate nephrotoxicity in developing rats.

Authors:  D Appenroth; S Gambaryan; K H Friese; H Bräunlich
Journal:  J Appl Toxicol       Date:  1990-06       Impact factor: 3.446

3.  Effect of ascorbic acid on DNA damage, cytotoxicity, glutathione reductase, and formation of paramagnetic chromium in Chinese hamster V-79 cells treated with sodium chromate(VI).

Authors:  M Sugiyama; K Tsuzuki; R Ogura
Journal:  J Biol Chem       Date:  1991-02-25       Impact factor: 5.157

4.  Production of activated species of oxygen during the chromate(VI)-ascorbate reaction: implication in carcinogenesis.

Authors:  Y Lefebvre; H Pézerat
Journal:  Chem Res Toxicol       Date:  1992 Jul-Aug       Impact factor: 3.739

5.  Effect of vitamins C and E on toxicity and mutagenicity of hexavalent chromium in rat and guinea pig.

Authors:  D Chorvatovicová; E Ginter; A Kosinová; Z Zloch
Journal:  Mutat Res       Date:  1991-01       Impact factor: 2.433

6.  Uptake of 51Cr-chromate by human erythrocytes-a role of glutathione.

Authors:  J Aaseth; J Alexander; T Norseth
Journal:  Acta Pharmacol Toxicol (Copenh)       Date:  1982-04

7.  Age dependent differences in sodium dichromate nephrotoxicity in rats.

Authors:  D Appenroth; H Bräunlich
Journal:  Exp Pathol       Date:  1988

8.  Chromate nephrotoxicity in developing rats. Significance of Cr(VI) reduction in rat kidney tissue.

Authors:  D Appenroth; M Friedrich; K H Friese; H Bräunlich
Journal:  J Trace Elem Electrolytes Health Dis       Date:  1991-03

Review 9.  Antioxidant functions of vitamins. Vitamins E and C, beta-carotene, and other carotenoids.

Authors:  H Sies; W Stahl; A R Sundquist
Journal:  Ann N Y Acad Sci       Date:  1992-09-30       Impact factor: 5.691

10.  Chromate metabolism in liver microsomes.

Authors:  K W Jennette
Journal:  Biol Trace Elem Res       Date:  1979-03       Impact factor: 3.738

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