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April 2013 Vol. 1 Issue 2
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Merit Research Journal of Environmental Science
and Toxicology Vol. 1(2) pp. 005-011, April,
2013
Copyright © 2013 Merit Research Journals |
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Full
Length Research Paper
Toxicological Influence of ethanol and
biochemical changes in rats exposed to cadmium |
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1Department of Biology,
King Abdulaziz University, P. O. Box: 80203 Jeddah, 21589, KSA.
2Department of Biology, Taif University, Taif, P. O.
Box 21944, Taif, KSA.
E-mail:
saj_vip.99@hotmail.com
Accepted March 26, 2013 |
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The present study
was performed to assess the function of the liver and kidney in
rats exposed to 50 mg Cd/l (as cadmium chloride) and/or 10%
(w/v) ethanol (EtOH) for 12 weeks. The activities of alanine
aminotransferase (ALAT) and asparate aminotransferase (AspAT) in
serum were measured as indicators of the liver function. As
parameters of the kidney function, creatinine, total protein and
urea concentrations in serum and urine, as well as urinary
alkaline phosphatase (ALP) activity were determined, and
creatinine clearance was calculated. Daily Cd intake ranged from
3.17 to 4.28 mg/kg body weight and from 2.41 to 3.17 mg/kg body
weight in the Cd and Cd + EtOH groups, respectively. The daily
intake of 10% EtOH ranged from 47.5 to 86.9 g/kg body weight in
the EtOH and from 47.3 to 63.4 g/kg body weight in the Cd + EtOH-exposed
rats. Cd and EtOH, independently of separate or combined
application, changed liver and kidney function. Rats treated
with Cd alone and those co-exposed to both substances showed
qualitatively similar. Some functional (increased serum AspAT
and urinary ALP, decreased urinary urea) and functional changes
in the liver and kidney were more evident in the case of
combined exposure, while others were more evident after single
exposure. However, a decrease in creatinine clearance, noted
only in the animals treated with Cd and EtOH, shows that
functional changes indicating renal insufficiency are more
serious in the co-exposed group. Due to lower Cd and EtOH intake
(resulting from a stronger aversion to drinking water containing
both substances) in the co-exposed rats, as compared to the Cd-
and EtOH-treated groups, it is difficult to draw a definite
conclusion from this study. The findings, however, seem to
indicate that EtOH increases Cd nephrotoxicity in rats, and thus
may suggest a higher risk of kidney damage in alcoholics exposed
to Cd. Unfortunately, this study does not provide clear evidence
if, and to what extent, EtOH influences Cd hepatotoxicity.
Keywords: hepatotoxicity- nephrotoxicity- cadmium-
ethanol- rats
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