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东莨菪碱诱导的认知障碍大鼠中多奈哌齐的全身暴露和脑摄取减少。

Reduced systemic exposure and brain uptake of donepezil in rats with scopolamine-induced cognitive impairment.

作者信息

Zhao Jiajia, Ren Tianjing, Yang Mengbi, Zhang Yufeng, Wang Qianwen, Zuo Zhong

机构信息

School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong SAR.

出版信息

Xenobiotica. 2020 Apr;50(4):389-400. doi: 10.1080/00498254.2019.1643514. Epub 2019 Aug 1.

Abstract
  1. Donepezil (DPZ) is an acetylcholinesterase (AchE) inhibitor used in the mild to moderately severe Alzheimer's disease. Among its major metabolites, 6--desmethyl DPZ (6-DDPZ), 5--desmethyl DPZ (5-DDPZ) and DPZ -oxide, the anti-AchE activities of 5-DDPZ and DPZ -oxide have never been clearly identified before. Besides, there is no report on simultaneous determination of DPZ and its three metabolites in the brain, thus their uptake in hippocampus and cortex are unknown. Therefore, the current studies are proposed aiming to: (1) investigate the anti-AchE activities and brain uptake of DPZ and its three metabolites and (2) compare their pharmacokinetics and brain uptake between normal and scopolamine-induced rats.2. DPZ and its three metabolites demonstrated anti-AchE activities with the IC in the order of DPZ (7.20 × 10μM), 6-DDPZ (1.14 × 10μM), 5-DDPZ (4.03 × 10μM) and DPZ -oxide (1.61 μM). They were also evenly distributed in the brain and retained much longer in the brain than that in plasma in normal rats.3. Compared to normal rats, C, AUC and AUC of DPZ were reduced by 52.0%, 31.2% and 30.1%, respectively; T of DPZ and its three metabolites were prolonged and their brain uptake were decreased in scopolamine-induced rats, suggesting the potential reduced absorption of DPZ.
摘要
  1. 多奈哌齐(DPZ)是一种用于轻度至中度严重阿尔茨海默病的乙酰胆碱酯酶(AchE)抑制剂。在其主要代谢产物中,6-去甲基DPZ(6-DDPZ)、5-去甲基DPZ(5-DDPZ)和DPZ-氧化物,5-DDPZ和DPZ-氧化物的抗AchE活性以前从未被明确鉴定过。此外,尚无关于同时测定脑中DPZ及其三种代谢产物的报道,因此它们在海马体和皮质中的摄取情况未知。因此,提出了当前的研究旨在:(1)研究DPZ及其三种代谢产物的抗AchE活性和脑摄取情况,以及(2)比较正常大鼠和东莨菪碱诱导的大鼠之间它们的药代动力学和脑摄取情况。2. DPZ及其三种代谢产物表现出抗AchE活性,其IC50顺序为DPZ(7.20×10⁻⁶μM)、6-DDPZ(1.14×10⁻⁵μM)、5-DDPZ(4.03×10⁻⁵μM)和DPZ-氧化物(1.61μM)。它们在脑中也均匀分布,并且在正常大鼠脑中保留的时间比在血浆中长得多。3. 与正常大鼠相比,DPZ的Cmax、AUC和AUC分别降低了52.0%、31.2%和30.1%;在东莨菪碱诱导的大鼠中,DPZ及其三种代谢产物的Tmax延长,它们的脑摄取减少,这表明DPZ的吸收可能降低。

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