Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by KREPPEL, H.
Right arrow Articles by KLAASSEN, C. D.
Right arrow Search for Related Content
PubMed
Right arrow Articles by KREPPEL, H.
Right arrow Articles by KLAASSEN, C. D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1994 Oxford University Press

research-article

Zinc-Induced Arsenite Tolerance in Mice1

HELMUT KREPPEL2, JIE LIU, YAPING LIU, FRANZ XAVER REICHL2 and CURTIS D. KLAASSEN3

Department of Pharmacology. Toxicology, and Therapeutics, Environmental Health and Occupational Medicine Center, University of Kansas Medical Center Kansas City, Kansas 66160

Received August 16, 1993; accepted February 14, 1994

The mechanism of tolerance to arsenic toxicity is not known. Recently it has been shown that arsenic induces metallothionein (MT), which is a sulthydryl-rich, metal-binding protein that de creases the toxicity of a number of metals. The present studies were designed to examine the role of MT in arsenic toxicity. Zinc (Zn) pretreatment (1000 µmol/kg, Sc) markedly increased hepatic MT (150-fold over controls), and also protected against the lethal effects of arsenite (130 µmol/kg, sc). However, no correlation was found between the ability of various known MT inducers (Zn, Cd, arsenite, monomethylarsenite, {alpha}-hederin, or oleanolic acid) to increase hepatic MT and to protect against arsenic lethality in mice. To examine the mechanism of Zn protection against arsenic toxicity, the subcellular distribution of arsenite in liver, kidney, and small intestine was determined 2 hr after arsenite injection. Zn pretreatment did not markedly alter the amount of arsenic-73 in the cytosol or the various cellular organdIes (nuclei, mitochondria, microsomes) in liver, kidney, or small intestine. There was also very little arsenic-73 bound to MT in the cytosol of the Zn-pretreated mice, as determined by G-75 gel-filtration chromatography. In mice pretreated with Zn (1000 µmol/kg, sc) and subsequently injected with arsenite-73 (115 µmol/kg, sc), the arsenic-73 content in blood, heart, lung, kidneys, spleen, muscle, and skin was lower than in controls, indicating increased arsenic elimination in Zn-pretreated mice. In conclusion, Zn pretreatment protects mice against arsenite toxicity, but the mechanism of tolerance does not appear to be induction of MT.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.