Tacrine and donepezil attenuate the neurotoxic effect of Aβ(25-35) in rat PC12 cells

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Abstract
THE effect of the cholinesterase inhibitors tacrine and donepezil on Aβ(25–35)-induced toxicity was investigated in rat pheochromocytoma PC12 cells by measuring the mitochondrial activity. Tacrine and donepezil was found in clinical relevant concentrations (10−7 − 10−6M) to attenuate Aβ(25–35)-induced toxicity in PC12 cells. The neuroprotective effect of tacrine was blocked in the presence of the nicotinic antagonists mecamylamine (10−5 M) and tubocurarine (10−5 M), suggesting an interaction via nicotinic receptors. This study demonstrates that tacrine and donepezil can exert neuroprotective properties which might be of importance and contribute to the clinical efficacy of cholinesterase inhibitors in the treatment of Alzheimer's disease.