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卡巴拉汀对人体脑脊液乙酰胆碱酯酶的优先抑制作用。

Preferential cerebrospinal fluid acetylcholinesterase inhibition by rivastigmine in humans.

作者信息

Kennedy J S, Polinsky R J, Johnson B, Loosen P, Enz A, Laplanche R, Schmidt D, Mancione L C, Parris W C, Ebert M H

机构信息

Department of Psychiatry, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.

出版信息

J Clin Psychopharmacol. 1999 Dec;19(6):513-21. doi: 10.1097/00004714-199912000-00005.

Abstract

This study sought to examine the feasibility of prolonged assessment of acetylcholinesterase (AChE) activity in the cerebrospinal fluid (CSF) of volunteers and to test the hypothesis that rivastigmine (ENA-713; Exelon, Novartis Pharma AG, Basel, Switzerland) selectively inhibits AChE in CSF in humans at a dose producing minimal inhibition of the peripheral enzyme. Lumbar CSF samples were collected continuously (0.1 mL x min(-1)) for 49 hours from eight healthy volunteers who took either placebo or a single oral dose of rivastigmine (3 mg). CSF specimens and samples of blood cells and blood plasma were analyzed at intervals for rivastigmine and its metabolite NAP 226-90 ([-] [3-([1-dimethylaminolethyl)-phenol]), erythrocyte AChE activity, CSF AChE activity, and plasma and CSF butyrylcholinesterase (BuChE) activity. Safety evaluations were performed 23 hours after drug dosing and at the end of the study. Evaluable data were obtained from six subjects. The mean time to maximal rivastigmine plasma concentration (tmax) was 0.83 +/- 0.26 hours, the mean maximal plasma concentration (Cmax) was 4.88 +/- 3.82 ng x mL(-1), the mean plasma area under the concentration versus time curve (AUC0-infinity) was 7.43 +/- 4.74 ng x hr x mL(-1), and the mean plasma t1/2 was 0.85 +/- 0.115 hours. The concentration of rivastigmine in CSF was lower than the quantification limit for assay (0.65 ng x mL(-1)), but NAP 226-90 reached a mean Cmax of 3.14 +/- 0.57 ng x mL(-1). Only minimal inhibition of erythrocyte AChE activity (approximately 3%) was observed. Inhibition of AChE in the CSF after rivastigmine administration was significantly greater than after placebo for up to 8.4 hours after the dose and was maximal (40%) at 2.4 hours. Plasma BuChE activity was significantly lower after rivastigmine than after placebo, but this was not clinically relevant. BuChE activity in CSF was significantly lower after rivastigmine than after placebo for up to 3.6 hours after dosing, but this difference was not sustained. This study confirms the feasibility of using continuous measurement of AChE activity in CSF over prolonged periods, that rivastigmine markedly inhibits CSF AChE after a single oral dose of 3 mg, and that the inhibition of central AChE is substantially greater than that of peripheral AChE or BuChE.

摘要

本研究旨在探讨对志愿者脑脊液(CSF)中乙酰胆碱酯酶(AChE)活性进行长时间评估的可行性,并检验以下假设:卡巴拉汀(ENA - 713;艾斯能,诺华制药有限公司,瑞士巴塞尔)在产生对外周酶最小抑制作用的剂量下,能选择性抑制人体脑脊液中的AChE。从8名服用安慰剂或单次口服3 mg卡巴拉汀的健康志愿者中连续49小时(0.1 mL×min⁻¹)采集腰椎脑脊液样本。每隔一段时间分析脑脊液标本、血细胞和血浆样本中的卡巴拉汀及其代谢产物NAP 226 - 90([-][3 - ([1 - 二甲基氨基乙基]) - 苯酚])、红细胞AChE活性、脑脊液AChE活性以及血浆和脑脊液丁酰胆碱酯酶(BuChE)活性。在给药23小时后和研究结束时进行安全性评估。从6名受试者获得了可评估数据。卡巴拉汀血浆浓度达峰值的平均时间(tmax)为0.83±0.26小时,平均最大血浆浓度(Cmax)为4.88±3.82 ng×mL⁻¹,浓度 - 时间曲线下的平均血浆面积(AUC0 - ∞)为7.43±4.74 ng×hr×mL⁻¹,平均血浆半衰期(t1/2)为0.85±0.115小时。脑脊液中卡巴拉汀的浓度低于测定的定量限(0.65 ng×mL⁻¹),但NAP 226 - 90的平均Cmax达到3.14±0.57 ng×mL⁻¹。仅观察到红细胞AChE活性有最小程度的抑制(约3%)。给药后卡巴拉汀对脑脊液中AChE的抑制作用在给药后长达8.4小时内显著大于安慰剂组,在2.4小时时达到最大抑制(40%)。卡巴拉汀给药后血浆BuChE活性显著低于安慰剂组,但这在临床上无相关性。给药后卡巴拉汀组脑脊液中BuChE活性在长达3.6小时内显著低于安慰剂组,但这种差异未持续存在。本研究证实了长时间连续测量脑脊液中AChE活性的可行性,单次口服3 mg卡巴拉汀后能显著抑制脑脊液中的AChE,且对中枢AChE的抑制作用明显大于对外周AChE或BuChE的抑制作用。

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