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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,乙酰胆碱酯酶抑制剂,在啮齿动物中受损的学习和记忆的影响

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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:先前的人类研究证明了多胺嘧啶对乙酰胆碱酯酶(ACHE)活性的持续抑制作用;然而,人类和动物中的多奈哌齐的有效浓度尚不清楚。本研究旨在表征在啮齿动物中疼痛抑制和学习中的学习和记忆受损的有效浓度。 Odepezil的药代动力学研究表明,口服处理(3和10mg / kg)分别分别为约1.2 +/- 0.4 h和1.4 +/- 0.5小时的口服治疗后的平均峰血浆浓度;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疼痛活性,并且在无碱基对大碱基治疗后观察到31.5 +/- 5.7%的最大抑制。等离子体疼痛活性与血浆Dentpezil浓度呈负相关。多奈哌齐的药理作用取决于其浓度和疼痛活性;因此,我们在小鼠中评估了多奈哌齐对学习和记忆的影响。 Deypezil治疗(3mg / kg)显着阻止了小鼠中氯化物诱导的记忆损伤的进展。随着大脑中的多胺浓度的增加,自发替换的恢复也有所改善;在大脑中以46.5 +/- 3.5 ng / g观察到最大改善。总之,我们的研究结果表明,Opepezil的浓度可以预测疼痛的抑制活性和药理学作用。此外,46.5 +/- 3.5 ng / g dodepezil是大脑中有效的目标浓度,用于治疗啮齿动物中的学习和记忆障碍。

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