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The Effects of Donepezil an Acetylcholinesterase Inhibitor on Impaired Learning and Memory in Rodents

机译:乙酰胆碱酯酶抑制剂多奈哌齐对啮齿动物学习和记忆障碍的影响

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摘要

A previous study in humans demonstrated the sustained inhibitory effects of donepezil on acetylcholinesterase (AChE) activity; however, the effective concentration of donepezil in humans and animals is unclear. This study aimed to characterize the effective concentration of donepezil on AChE inhibition and impaired learning and memory in rodents. A pharmacokinetic study of donepezil showed a mean peak plasma concentration of donepezil after oral treatment (3 and 10 mg/kg) of approximately 1.2 ± 0.4 h and 1.4 ± 0.5 h, respectively; absolute bioavailability was calculated as 3.6%. Further, AChE activity was inhibited by increasing plasma concentrations of donepezil, and a maximum inhibition of 31.5 ± 5.7% was observed after donepezil treatment in hairless rats. Plasma AChE activity was negatively correlated with plasma donepezil concentration. The pharmacological effects of donepezil are dependent upon its concentration and AChE activity; therefore, we assessed the effects of donepezil on learning and memory using a Y-maze in mice. Donepezil treatment (3 mg/kg) significantly prevented the progression of scopolamine-induced memory impairment in mice. As the concentration of donepezil in the brain increased, the recovery of spontaneous alternations also improved; maximal improvement was observed at 46.5 ± 3.5 ng/g in the brain. In conclusion, our findings suggest that the AChE inhibitory activity and pharmacological effects of donepezil can be predicted by the concentration of donepezil. Further, 46.5 ± 3.5 ng/g donepezil is an efficacious target concentration in the brain for treating learning and memory impairment in rodents.
机译:先前在人体中的研究表明多奈哌齐对乙酰胆碱酯酶(AChE)活性具有持续抑制作用。但是,多奈哌齐在人和动物中的有效浓度尚不清楚。这项研究旨在表征多奈哌齐对AChE抑制和啮齿类动物学习与记忆受损的有效浓度。多奈哌齐的药代动力学研究表明,口服治疗后多奈哌齐的平均血浆峰值浓度(3和10 mg / kg)分别约为1.2±0.4 h和1.4±0.5 h。绝对生物利用度计算为3.6%。此外,通过增加多奈哌齐的血浆浓度抑制了AChE活性,多奈哌齐治疗无毛大鼠后最大抑制率为31.5±5.7%。血浆AChE活性与血浆多奈哌齐浓度呈负相关。多奈哌齐的药理作用取决于其浓度和AChE活性。因此,我们使用Y迷宫评估了多奈哌齐对学习和记忆的影响。多奈哌齐治疗(3 mg / kg)显着阻止了东pol碱引起的小鼠记忆力损害的进展。随着脑中多奈哌齐浓度的增加,自发交替的恢复也得到改善。在大脑中观察到最大改善,为46.5±3.5 ng / g。总之,我们的发现表明多奈哌齐的浓度可以预测多奈哌齐的AChE抑制活性和药理作用。此外,46.5±3.5 ng / g多奈哌齐是大脑中治疗啮齿类动物学习和记忆障碍的有效目标浓度。

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