Instituto de Neurociencias de Alicante, Universidad Miguel Hernández-CSIC, San Juan de Alicante, Spain.
PLoS One. 2010 Jan 14;5(1):e8701. doi: 10.1371/journal.pone.0008701.
Many studies have been conducted in an extensive effort to identify alterations in blood cholinesterase levels as a consequence of disease, including the analysis of acetylcholinesterase (AChE) in plasma. Conventional assays using selective cholinesterase inhibitors have not been particularly successful as excess amounts of butyrylcholinesterase (BuChE) pose a major problem.
Here we have estimated the levels of AChE activity in human plasma by first immunoprecipitating BuChE and measuring AChE activity in the immunodepleted plasma. Human plasma AChE activity levels were approximately 20 nmol/min/mL, about 160 times lower than BuChE. The majority of AChE species are the light G(1)+G(2) forms and not G(4) tetramers. The levels and pattern of the molecular forms are similar to that observed in individuals with silent BuChE. We have also compared plasma AChE with the enzyme pattern obtained from human liver, red blood cells, cerebrospinal fluid (CSF) and brain, by sedimentation analysis, Western blotting and lectin-binding analysis. Finally, a selective increase of AChE activity was detected in plasma from Alzheimer's disease (AD) patients compared to age and gender-matched controls. This increase correlates with an increase in the G(1)+G(2) forms, the subset of AChE species which are increased in Alzheimer's brain. Western blot analysis demonstrated that a 78 kDa immunoreactive AChE protein band was also increased in Alzheimer's plasma, attributed in part to AChE-T subunits common in brain and CSF.
Plasma AChE might have potential as an indicator of disease progress and prognosis in AD and warrants further investigation.
为了确定疾病导致的血液胆碱酯酶水平的变化,人们进行了许多研究,包括对血浆中乙酰胆碱酯酶(AChE)的分析。使用选择性胆碱酯酶抑制剂的常规检测方法并不特别成功,因为过量的丁酰胆碱酯酶(BuChE)是一个主要问题。
在这里,我们首先通过免疫沉淀 BuChE 来估计人血浆中的 AChE 活性,然后测量免疫沉淀后的血浆中的 AChE 活性。人血浆 AChE 活性水平约为 20nmol/min/mL,大约是 BuChE 的 160 倍。大多数 AChE 是轻 G(1)+G(2)形式,而不是 G(4)四聚体。分子形式的水平和模式与沉默 BuChE 个体中观察到的相似。我们还通过沉降分析、Western blot 和凝集素结合分析,将血浆 AChE 与从人肝、红细胞、脑脊液(CSF)和脑获得的酶模式进行了比较。最后,与年龄和性别匹配的对照组相比,阿尔茨海默病(AD)患者的血浆中 AChE 活性选择性增加。这种增加与 G(1)+G(2)形式的增加相关,而 G(1)+G(2)是阿尔茨海默氏脑增加的 AChE 物种亚组。Western blot 分析表明,AD 患者的血浆中也增加了 78kDa 免疫反应性 AChE 蛋白带,部分归因于脑和 CSF 中常见的 AChE-T 亚基。
血浆 AChE 可能作为 AD 疾病进展和预后的指标具有潜力,值得进一步研究。