کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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4328424 | 1614174 | 2009 | 5 صفحه PDF | دانلود رایگان |
A 7-day treatment with memantine (25 mg/kg, i.p.), a drug that is currently prescribed for the treatment of Alzheimer's disease, increased the levels of brain-derived neurotrophic factor (BDNF) and reduced the expression of the neuron-specific K+/Cl− co-transporter, KCC2, in the hippocampus and cerebral cortex of mice. Knowing that KCC2 maintains low intracellular Cl− concentrations, which drive Cl− influx in response to GABAA receptor activation, we monitored the behavioural response to the GABAA receptor enhancer, diazepam, in mice pre-treated for 7 days with saline or 25 mg/kg of memantine. Memantine treatment substantially attenuated motor impairment induced by an acute challenge with diazepam (6 mg/kg, i.p.), as assessed by the rotarod test and the horizontal wire test. We suggest that a prolonged treatment with memantine induces changes in the activity of GABAA receptors that might contribute to the therapeutic and/or toxic effects of the drug.
Journal: Brain Research - Volume 1265, 10 April 2009, Pages 75–79