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Title: p-Chloro-diphenyl diselenide reverses memory impairment-related to stress caused by corticosterone and modulates hippocampal [(3)H]glutamate uptake in mice. Author: Zborowski VA, Sari MH, Heck SO, Stangherlin EC, Neto JS, Nogueira CW, Zeni G. Journal: Physiol Behav; 2016 Oct 01; 164(Pt A):25-33. PubMed ID: 27211333. Abstract: Chronic stress or chronically high levels of glucocorticoids can result in memory impairment. This study aimed to investigate if 4,4'-dichloro-diphenyl diselenide (p-ClPhSe)2 reverses memory impairment-related to stress caused by corticosterone administration in mice and its possible mechanism of action. Swiss mice received corticosterone (20μg/ml) in their drinking water during four weeks. In the last week, the animals were treated with (p-ClPhSe)2 (1 or 5mg/kg) by the intragastric route (i.g.) once a day for 7days. The cognitive performance of mice was assessed through the object recognition test (ORT), the object location test (OLT) and the step-down passive avoidance test (SDPA), some of predictive tests of memory. Biochemical parameters were determined and locomotor activity of mouse was performed to gain insight in (p-ClPhSe)2 toxicity. The findings demonstrated that treatment with (p-ClPhSe)2 in both doses was effective in reversing memory deficits in the ORT, the OLT and the SDPA caused by corticosterone exposure in mice. Treatment with (p-ClPhSe)2 at both doses reversed the increase in the [(3)H] glutamate uptake by hippocampal slices of mice treated with corticosterone. By contrast, [(3)H] glutamate uptake by brain cortical slices was not altered in mice exposed to corticosterone. The Na(+)K(+)ATPase activity was not altered in hippocampus and cerebral cortices of mice treated with corticosterone. There was no sign of toxicity in mice treated with (p-ClPhSe)2. This organoselenium compound reversed memory impairment-related to stress caused by corticosterone and modulated hippocampal [(3)H]glutamate uptake in mice.[Abstract] [Full Text] [Related] [New Search]