Trace element status is known to be;altered ill the diabetic state. Current
evidence suggests that reactive oxygen intermediates (ROI's) do participat
e in the destruction of pancreatic beta cells in STZ-induced Type 1 diabete
s. The copper and zinc status of diabetic patients and their descendants wa
s also found to have changed. The aim of this study was to evaluate the pot
ential usefulness of copper sulfate in the treatment of STZ-induced type T
diabetes. We used C57BL6 female mice, in whom copper sulfate treatment was
started at 6 weeks of age followed by an IP injection of 40 mg/kg body weig
ht of STZ for five consecutive days. Its effects were evaluated at 10 weeks
of age. The treatment with copper sulfate significantly decreased blood gl
ucose levels, levels of lipid peroxidation and mRNA expression of the enzym
e iNOS and the cytokines IFN-gamma and IL-4. Histological analysis of the p
ancreas revealed that, three out of five animals in the copper sulfate trea
ted groups showed absence of mononuclear cell infiltration and no change in
the shape and size of islets as compared to pancreas of the STZ-induced di
abetic group of animals. In conclusion, our observations indicate that copp
er sulfate treatment call exert beneficial effects in diabetes with preserv
ation of beta -cell function in vivo. Copper sulfate could be exerting thes
e beneficial effects either by acting directly by reducing free radicals or
through reduction in glucose levels. (C) 2001 Elsevier Science Ireland Ltd
. All rights reserved.