Role
of hepatic and pancreatic oxidative stress in arsenic
induced
diabetic condition in Wistar rats
Hitesh
Vashrambhai Patel and Kiran Kalia*?
Laboratory
of Biochemistry, BRD School of Biosciences, Sardar Patel University, Vallabh
Vidya Nagar ? 388 120, India
*Corresponding
Author email : kirankalia_in@yahoo.com
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Publication
Data
Paper received:
30 August 2011
Revised received:
17 January 2012
Accepted:
19 March 2012
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Abstract
Arsenic,
a potent environmental toxicant has been reported to induce diabetes
mellitus, but its potential biological mechanism(s) has not been much
investigated. The present study was designed to correlate pancreatic and
hepatic oxidative stress with arsenic induced diabetes mellitus in
experimental animals. Male albino Wistar rats were administered with low (1.5
mg kg-1?b.wt.)
and high (5.0 mg kg-1?b.wt.)
sodium arsenite orally for 4 week. Hyperglycemic condition was observed in
arsenic exposed groups as indicated by increased (P<0.001) fasting plasma
glucose, glycosylated hemoglobin (HbA1c) and impaired glucose tolerance
(IGT), which were accompanied by an increase in the level of lipid
peroxidation (P<0.001), protein oxidation (P<0.05 at low dose and
P<0.001 at high dose) and nitric oxide (NO) (P<0.001) in hepatic and
pancreatic tissue compared to control. Furthermore, superoxide dismutase
(SOD) (P<0.001), catalase (CAT) (P<0.001) and glutathione-S-transferase
(GST) (P<0.05 at low dose and P<0.001 at high dose) activities were
elevated, while glutathione peroxidase (GPx) (P<0.05 at low dose and
P<0.001 at high dose) and GSH level showed significant (P<0.001)
depletion in both studied tissue of arsenic exposed rats compared to control.
Arsenic induced hepatotoxicity was manifested by an increase (P<0.001) in
serum ALT, AST and ALP. Arsenic exposure leads to accumulation of arsenic
(P<0.05) and significant (P<0.05) depletion of copper and zinc level in
hepatic and pancreatic tissue as compared to control. Our data suggests that
sub-chronic arsenic exposure induces diabetic condition which may be mediated
due to increased oxidative stress in hepatic and pancreatic tissue.
Key words
Arsenic,
Oxidative stress, Diabetes mellitus, Rat
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