Curcumin alleviates arsenic trioxide-induced neural damage in the murine striatal region

Arsenic-induced neurotoxicity, with dose-dependent effects, is well-documented in rodents. Curcumin (CUR), a cost-effective plant polyphenol, shows neuroprotective effects by modulating oxidative stress, apoptosis, and neurochemistry. This study evaluates curcumin's neuroprotective potential against arsenic trioxide (As₂O₃) in the mouse striatal region.

Healthy adult male mice were chronically administered with varying concentrations of As₂O₃ (2, 4 and 8 mg/kg bw) alone and along with CUR (100 mg/kg bw) orally for 45 days. Towards the end of the experimental period, the animals were subjected to behavioural paradigms including open field task, novel object recognition, rota-rod, and Morris water maze. Striatal tissues were freshly collected from the animals on day 46 for biochemical analyses (MDA, GPx, and GSH). Additionally, perfusion-fixed brains were processed for morphological observations.

Behavioural study showed an apparent decrease in certain cognitive functions (learning and memory) and locomotor activity in mice exposed to As₂O₃ compared to controls. Simultaneous treatment of As₂O₃ (2, 4 and 8 mg/kg bw) and curcumin (100 mg/kg bw) alleviated the As-induced locomotor and cognitive deficits. As₂O₃ alone exposure also exhibited a significant increase in oxidative stress marker (MDA) and a decrease in antioxidant enzyme levels (GPx, GSH). Morphological alterations were noted in mice subjected to elevated doses of As₂O₃ (4 and 8 mg/kg bw). However, these changes were reversed in mice who received As₂O₃ + CUR co-treatment.

Collectively, our findings indicate that curcumin offers neuroprotection to the striatal region against As₂O₃-induced behavioral deficits, as well as biochemical and morphological alterations.

Graphical abstract illuminating the adverse effects of Arsenic trioxide (As₂O₃) exposure on the basal ganglia of mice along with the potential neuroprotective benefits of curcumin supplementation.