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Studies of the Anti-amnesic Effects and Mechanisms of Single and Combined Use of Donepezil and Ginkgo Ketoester Tablet on Scopolamine-Induced Memory Impairment in Mice

机译:多奈哌齐和银杏酮酸酯片联合使用对东pol碱引起的小鼠记忆障碍的抗遗忘作用及其机制的研究

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摘要

Ginkgo ketoester tablets (GT) and donepezil were a clinically used combination for the treatment of Alzheimer's disease (AD). The aim of the study was undertaken to investigate the antiamnesic effects of the two drugs alone and in combination through in vivo models of the Morris water maze along with in vitro antioxidants, acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE). The potential mechanisms were speculated by the activities of acetylcholine (ACh), AChE, superoxide dismutase (SOD), and malondialdehyde (MDA) and the protein expression of brain-derived neurotrophic factor (BDNF) and tyrosine protein kinase B (TrkB). The combination group showed a concentration-dependent inhibition of cholinesterase and antioxidation. As far as its mechanism was concerned, the combination of two drugs exerted excellent effects on oxidative stress, cholinergic pathway damage, and inactivation of the BDNF-TrkB signaling pathway. Additionally, to elucidate the binding mechanism of GT active ingredients into the structure of AChE, the results of molecular docking studies indicated that hydrogen and/or hydrophobic bonds might play an important role in their binding process. Thus, the combination of drugs could treat AD perfectly and further verify the scientific rationality of clinical medication.
机译:银杏酮酸酯片(GT)和多奈哌齐是临床上用于治疗阿尔茨海默氏病(AD)的组合。进行研究的目的是通过在莫里斯水迷宫的体内模型以及体外抗氧化剂,乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BuChE)的体内模型研究两种药物的抗记忆效应。潜在的机制由乙酰胆碱(ACh),AChE,超氧化物歧化酶(SOD)和丙二醛(MDA)的活性以及脑源性神经营养因子(BDNF)和酪氨酸蛋白激酶B(TrkB)的蛋白表达来推测。联合治疗组表现出胆碱酯酶的浓度依赖性抑制作用和抗氧化作用。就其机理而言,两种药物的组合对氧化应激,胆碱能途径损害和BDNF-TrkB信号传导途径的失活均具有出色的作用。此外,为阐明GT活性成分与AChE结构的结合机理,分子对接研究的结果表明,氢和/或疏水键可能在其结合过程中起重要作用。因此,药物组合可以完美治疗AD,并进一步验证临床药物的科学合理性。

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