Nordberg Agneta, Darreh-Shori Taher, Peskind Elaine, Soininen Hilkka, Mousavi Malahat, Eagle Gina, Lane Roger
Karolinska Institute, Division of Alzheimer Neurobiology, Karolinska University Hospital Huddinge, Stockholm, Sweden.
Curr Alzheimer Res. 2009 Feb;6(1):4-14. doi: 10.2174/156720509787313961.
The current study aimed to compare the effects of different cholinesterase inhibitors on acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) activities and protein levels, in the cerebrospinal fluid (CSF) of Alzheimer disease (AD) patients.
AD patients aged 50-85 years were randomized to open-label treatment with oral rivastigmine, donepezil or galantamine for 13 weeks. AChE and BuChE activities were assayed by Ellman's colorimetric method. Protein levels were assessed by enzyme-linked immunosorbent assay (ELISA). Primary analyses were based on the Completer population (randomized patients who completed Week 13 assessments). 63 patients were randomized to treatment. Rivastigmine was associated with decreased AChE activity by 42.6% and decreased AChE protein levels by 9.3%, and decreased BuChE activity by 45.6% and decreased BuChE protein levels by 21.8%. Galantamine decreased AChE activity by 2.1% and BuChE activity by 0.5%, but increased AChE protein levels by 51.2% and BuChE protein levels by 10.5%. Donepezil increased AChE and BuChE activities by 11.8% and 2.8%, respectively. Donepezil caused a 215.2% increase in AChE and 0.4% increase in BuChE protein levels. Changes in mean AChE-Readthrough/Synaptic ratios, which might reflect underlying neurodegenerative processes, were 1.4, 0.6, and 0.4 for rivastigmine, donepezil and galantamine, respectively.
The findings suggest pharmacologically-induced differences between rivastigmine, donepezil and galantamine. Rivastigmine provides sustained inhibition of AChE and BuChE, while donepezil and galantamine do not inhibit BuChE and are associated with increases in CSF AChE protein levels. The clinical implications require evaluation.
本研究旨在比较不同胆碱酯酶抑制剂对阿尔茨海默病(AD)患者脑脊液(CSF)中乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BuChE)活性及蛋白水平的影响。
年龄在50 - 85岁的AD患者被随机分为接受口服卡巴拉汀、多奈哌齐或加兰他敏的开放标签治疗,为期13周。采用埃尔曼比色法测定AChE和BuChE活性。通过酶联免疫吸附测定(ELISA)评估蛋白水平。主要分析基于完整人群(完成第13周评估的随机分组患者)。63例患者被随机分组接受治疗。卡巴拉汀使AChE活性降低42.6%,AChE蛋白水平降低9.3%,使BuChE活性降低45.6%,BuChE蛋白水平降低21.8%。加兰他敏使AChE活性降低2.1%,BuChE活性降低0.5%,但使AChE蛋白水平升高51.2%,BuChE蛋白水平升高10.5%。多奈哌齐分别使AChE和BuChE活性升高11.8%和2.8%。多奈哌齐使AChE蛋白水平升高215.2%,BuChE蛋白水平升高0.4%。可能反映潜在神经退行性过程的平均AChE通读/突触比率变化,卡巴拉汀、多奈哌齐和加兰他敏分别为1.4、0.6和0.4。
研究结果表明卡巴拉汀、多奈哌齐和加兰他敏在药理学上存在差异。卡巴拉汀能持续抑制AChE和BuChE,而多奈哌齐和加兰他敏不抑制BuChE,且与脑脊液AChE蛋白水平升高有关。其临床意义有待评估。