Karolinska Institutet, Division of Alzheimer Neurobiology, Karolinska University Hospital Huddinge, Stockholm,
Curr Alzheimer Res. 2010 Feb;7(1):67-73. doi: 10.2174/156720510790274455.
Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by cognitive decline associated with a deficit in cholinergic function. Inhibitors of acetylcholinesterase (AChE) and/or butyrylcholinesterase (BuChE), such as donepezil, galantamine or rivastigmine, are widely prescribed as symptomatic treatments for AD. These agents exhibit a wide variation in their pharmacological properties. Here we review clinical data from 1998 to 2009 investigating the effect of different cholinesterase inhibitor treatments on the levels and activities of cholinesterases in the cerebrospinal fluid (CSF) of AD patients. These studies suggest that treatment with rapidly-reversible cholinesterase inhibitors (e.g. donepezil, galantamine, tacrine) are associated with marked and significant upregulation of AChE activities and protein levels in the CSF of AD patients. In contrast, pseudo-irreversible cholinesterase inhibition (e.g. rivastigmine) is associated with a significant decrease in both CSF AChE and BuChE activities, with no upregulation of CSF protein levels. Additionally, donepezil is associated with a decrease in the level of the AChE-R isoform relative to the synaptic AChE-S isoform, whereas rivastigmine seems to increase this ratio. These findings suggest that these agents exert different effects on CSF cholinesterases. The clinical effects of these pharmacological differences are yet to be fully established.
阿尔茨海默病(AD)是一种进行性神经退行性疾病,其特征是认知能力下降,与胆碱能功能缺陷有关。乙酰胆碱酯酶(AChE)和/或丁酰胆碱酯酶(BuChE)抑制剂,如多奈哌齐、加兰他敏或利伐斯的明,被广泛用作 AD 的对症治疗药物。这些药物在药理学特性上存在很大差异。在这里,我们回顾了 1998 年至 2009 年的临床数据,这些数据研究了不同的胆碱酯酶抑制剂治疗对 AD 患者脑脊液(CSF)中胆碱酯酶水平和活性的影响。这些研究表明,快速可逆性胆碱酯酶抑制剂(如多奈哌齐、加兰他敏、他克林)的治疗与 AD 患者 CSF 中 AChE 活性和蛋白水平的显著上调有关。相比之下,假性不可逆性胆碱酯酶抑制(如利伐斯的明)与 CSF 中 AChE 和 BuChE 活性的显著降低以及 CSF 蛋白水平的无上调有关。此外,多奈哌齐与 AChE-R 同工型相对于突触 AChE-S 同工型的水平降低有关,而利伐斯的明似乎增加了这种比值。这些发现表明这些药物对 CSF 胆碱酯酶有不同的作用。这些药理学差异的临床效果尚未完全确定。