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Donepezil markedly potentiates memantine neurotoxicity in the adult rat brain

机译:多奈哌齐显着增强成年大鼠大脑中的美金刚胺神经毒性

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摘要

The NMDA antagonist, memantine (Namenda), and the cholinesterase inhibitor, donepezil (Aricept), are currently being used widely, either individually or in combination, for treatment of Alzheimer’s disease (AD). NMDA antagonists have both neuroprotective and neurotoxic properties; the latter is augmented by drugs, such as pilocarpine, that increase cholinergic activity. Whether donepezil, by increasing cholinergic activity, might augment memantine’s neurotoxic potential has not been investigated. In the present study, we determined that a dose of memantine (20 mg/kg ip), considered to be in the therapeutic (neuroprotective) range for rats, causes a mild neurotoxic reaction in the adult rat brain. Co-administration of memantine (20 or 30 mg/kg) with donepezil (2.5 to 10mg/kg) markedly potentiated this neurotoxic reaction, causing neuronal injury at lower doses of memantine, and causing the toxic reaction to become disseminated and lethal to neurons throughout many brain regions. These findings raise questions about using this drug combination in AD, especially in the absence of evidence that the combination is beneficial, or that either drug arrests or reverses the disease process.
机译:NMDA拮抗剂美金刚(Namenda)和胆碱酯酶抑制剂多奈哌齐(Aricept)目前已被广泛使用,无论是单独使用还是组合使用,都可以治疗阿尔茨海默氏病(AD)。 NMDA拮抗剂具有神经保护和神经毒性特性。后者通过诸如毛果芸香碱等药物增强胆碱能活性。尚未通过增加胆碱能活性的多奈哌齐是否可能增强美金刚的神经毒性潜能。在本研究中,我们确定美金刚的剂量(20 mg / kg腹膜内)被认为对大鼠具有治疗(神经保护)作用,其在成年大鼠大脑中引起轻度神经毒性反应。美金刚(20或30 mg / kg)与多奈哌齐(2.5至10mg / kg)的共同给药显着增强了这种神经毒性反应,在较低剂量的美金刚中引起神经元损伤,并导致毒性反应在整个神经元中扩散并致死。许多大脑区域。这些发现引起了关于在AD中使用这种药物组合的疑问,尤其是在没有证据表明该组合是有益的,或者药物阻止或逆转疾病过程的证据的情况下。

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