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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Journal of Applied T...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Journal of Applied Toxicology
Article . 2008 . Peer-reviewed
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Toxicological evaluation of subchronic exposure to diphenyl diselenide in rats

Authors: Flavia Carla, Meotti; Vanessa Corralo, Borges; Juliano, Perottoni; Cristina Wayne, Nogueira;

Toxicological evaluation of subchronic exposure to diphenyl diselenide in rats

Abstract

AbstractThe aim of this study was to investigate the effects caused by subchronic exposure to diphenyl diselenide in rats. Adult Wistar rats were exposed to diphenyl diselenide (5–300 µmol kg−1, subcutaneously) once a day for 14 days. The subchronic administration of diphenyl diselenide at a dose of 300 µmol kg−1 significantly increased aspartate aminotransferase (AST) and alanine aminotransferase (ALT) activities in plasma. Conversely, this exposure did not alter lactate dehydrogenase (LDH) activity, urea and creatinine levels in plasma. The activity of δ‐aminolevulinate dehydratase (δ‐ALA‐D) from liver and kidney was inhibited by high dosages of diphenyl diselenide. Diphenyl diselenide did not alter renal Na+/K+ATPase. A decline in body weight gain was associated with a decrease in food consumption in rats treated with 100 or 300 µmol kg−1 diphenyl diselenide. At these dosages (100 and 300 µmol kg−1), diphenyl diselenide did not cause histological alterations in the liver of rats. Taken together, these results demonstrated that subchronic exposure to diphenyl diselenide at high doses induced minor toxicological effects. Copyright © 2007 John Wiley & Sons, Ltd.

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Keywords

Male, L-Lactate Dehydrogenase, Body Weight, Alanine Transaminase, Porphobilinogen Synthase, Rats, Eating, Liver, Creatinine, Organoselenium Compounds, Benzene Derivatives, Animals, Urea, Aspartate Aminotransferases, Chemical and Drug Induced Liver Injury, Rats, Wistar, Sodium-Potassium-Exchanging ATPase

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Powered by OpenAIRE graph
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
14
Average
Average
Top 10%
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