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体内乙酰胆碱释放常规分析的改进方法:在有和没有酯酶抑制剂的情况下进行定量分析。

Improved method for the routine analysis of acetylcholine release in vivo: quantitation in the presence and absence of esterase inhibitor.

作者信息

Greaney M D, Marshall D L, Bailey B A, Acworth I N

机构信息

ESA, Inc., Bedford, MA 01730.

出版信息

J Chromatogr. 1993 Dec 22;622(2):125-35. doi: 10.1016/0378-4347(93)80258-6.

DOI:10.1016/0378-4347(93)80258-6
PMID:8150861
Abstract

An improved high-performance liquid chromatographic (HPLC) method using electrochemical detection (ED) is described capable of routinely measuring the low levels of acetylcholine (ACh) typically found in rat brain microdialysis samples. Microdialysis was performed in the striatum of the urethane anesthetized rat using a 4-mm membrane length, high recovery (40% at 1.0 microliters/min; ambient conditions), loop-design probe perfused with an artificial cerebrospinal fluid (aCSF) solution containing physiologically normal calcium levels (1.2 mM). The HPLC method utilizes a polymeric stationary phase to resolve choline (Ch) from ACh. These analytes are then converted to hydrogen peroxide (H2O2) by a solid-phase reactor (containing immobilized choline oxidase and acetylcholinesterase enzymes). The H2O2 is detected amperometrically and quantitated on a platinum (Pt) working electrode (+300 mV; with a unique analytical cell featuring a solid-state palladium reference electrode). Two designs of the Pt working electrode were examined, differing only in the support material used (Kel-F or PEEK). The Kel-F/Pt electrode had a limit of detection (LOD) for both analytes of < 30 fmol per 10 microliters with a signal-to-noise ratio of 3:1. Striatal microdialysis perfusates were monitored for ACh and Ch over a 0-1000 nM range of neostigmine (NEO) in the CSF perfusion medium. Using the 4-mm probe, basal ACh and Ch levels were detected with a NEO level as low as 10 nM and were found to be 37 +/- 3 fmol and 22 +/- 1 pmol per 10 microliters (mean +/- S.E.M., n = 6 replicates) respectively. In similar experiments using 3-mm concentric probes comparable (lower) levels of ACh were found with the 50 and 1000 nM NEO doses (n = 4-21 animals). ACh could not be reliably quantitated when animals were perfused with the 10 nM dose of NEO (n = 4). The PEEK/Pt electrode had an improved LOD of < 20 fmol per 10 microliters due to a two- to three-fold decrease in the background noise component. Basal striatal levels of ACh in the absence of NEO approached the LOD and were found to be 15 +/- 2 fmol per 10 microliters; Ch was 5 +/- 1 pmol per 10 microliters (n = 2, mean of five basal samples). The analytical system requires very little maintenance; a simple electrochemical electrode cleaning step eliminates the need for routine polishing of the Pt electrode and the mobile phase is stable for up to one week.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

描述了一种改进的高效液相色谱(HPLC)方法,该方法使用电化学检测(ED),能够常规测量大鼠脑微透析样品中通常存在的低水平乙酰胆碱(ACh)。在乌拉坦麻醉的大鼠纹状体中进行微透析,使用4毫米膜长、高回收率(1.0微升/分钟时为40%;环境条件下)、环设计的探针,用含有生理正常钙水平(1.2毫摩尔)的人工脑脊液(aCSF)溶液灌注。HPLC方法利用聚合物固定相将胆碱(Ch)与ACh分离。然后这些分析物通过固相反应器(含有固定化胆碱氧化酶和乙酰胆碱酯酶)转化为过氧化氢(H2O2)。H2O2通过安培法检测,并在铂(Pt)工作电极(+300毫伏;具有独特的分析池,配备固态钯参比电极)上进行定量。研究了两种Pt工作电极设计,仅在使用的支撑材料(Kel-F或PEEK)上有所不同。Kel-F/Pt电极对两种分析物的检测限(LOD)均<30飞摩尔/10微升,信噪比为3:1。在脑脊液灌注介质中,对新斯的明(NEO)0 - 1000纳摩尔范围内的纹状体微透析灌注液进行ACh和Ch监测。使用4毫米探针,在NEO水平低至10纳摩尔时检测到基础ACh和Ch水平,发现分别为37±3飞摩尔/10微升和22±1皮摩尔/10微升(平均值±标准误,n = 6次重复)。在使用3毫米同心探针的类似实验中,50和1000纳摩尔NEO剂量下发现了相当(较低)水平的ACh(n = 4 - 21只动物)。当动物用10纳摩尔剂量的NEO灌注时,ACh无法可靠定量(n = 4)。由于背景噪声成分降低了两到三倍,PEEK/Pt电极的LOD有所改善,<20飞摩尔/10微升。在无NEO时,纹状体基础ACh水平接近检测限,发现为15±2飞摩尔/10微升;Ch为5±1皮摩尔/10微升(n = 2,五个基础样品的平均值)。该分析系统几乎不需要维护;简单的电化学电极清洁步骤无需对Pt电极进行常规抛光,流动相可稳定长达一周。(摘要截断于400字)

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