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Combined administration of selenium and meso-2, 3-dimercaptosuccinic acid on arsenic mobilization and tissue oxidative stress in chronic arsenic-exposed male rats
Objective : The present study describes the effect of selenium either alone or in combination with meso-2, 3-dimercaptosuccinic acid (DMSA) against chronic arsenic poisoning in rats. Materials and Methods : Male Wistar rats were exposed to 100 ppm sodium arsenite in drinking water for eight months a...
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Published in: | Indian journal of pharmacology 2007-03, Vol.39 (2), p.107 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Objective : The present study describes the effect of selenium either
alone or in combination with meso-2, 3-dimercaptosuccinic acid (DMSA)
against chronic arsenic poisoning in rats. Materials and Methods : Male
Wistar rats were exposed to 100 ppm sodium arsenite in drinking water
for eight months and treated thereafter with DMSA (0.3 mmol/kg orally)
either individually or in combination with selenium (Se, 6.3 or 12.6
µmol/kg, intraperitoneally) once daily for five days. The effects
of these treatments in influencing the arsenic (As)-induced changes in
heme synthesis, hepatic, renal or brain oxidative stress were evaluated
along with the As concentration in blood and soft tissues. Results :
Exposure to As significantly altered biochemical parameters related to
the heme synthesis pathway, blood and organ (liver, kidney and brain)
oxidative stress while increasing body As burden in animals. Treatment
with DMSA alone significantly reduced the adverse effects related to
most of these biochemical parameters as well as the As concentration in
blood and tissues. On the other hand, co-administration of Se with DMSA
had only limited additional beneficial effects (particularly tissue
oxidative stress) over the individual effect of DMSA. Conclusion : The
above results suggest that Se administration during chelation affected
by other agents had some beneficial effects on oxidative stress with no
major additional beneficial effect on arsenic depletion. |
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ISSN: | 0253-7613 1998-3751 |
DOI: | 10.4103/0253-7613.32530 |