Department of Chemical and Biological Engineering, Chalmers University of Technology, Kemivägen 10, SE-41296 Göteborg, Sweden.
J Neurosci Methods. 2013 Oct 15;219(2):292-6. doi: 10.1016/j.jneumeth.2013.08.012. Epub 2013 Aug 19.
We have developed a superfusion method utilizing an open-volume microfluidic device for administration of pharmacologically active substances to selected areas in brain slices with high spatio-temporal resolution. The method consists of a hydrodynamically confined flow of the active chemical compound, which locally stimulates neurons in brain slices, applied in conjunction with electrophysiological recording techniques to analyze the response. The microfluidic device, which is a novel free-standing multifunctional pipette, allows diverse superfusion experiments, such as testing the effects of different concentrations of drugs or drug candidates on neurons in different cell layers with high positional accuracy, affecting only a small number of cells. We demonstrate herein the use of the method with electrophysiological recordings of pyramidal cells in hippocampal and prefrontal cortex brain slices from rats, determine the dependence of electric responses on the distance of the superfusion device from the recording site, document a multifold gain in solution exchange time as compared to whole slice perfusion, and show that the device is able to store and deliver up to four solutions in a series. Localized solution delivery by means of open-volume microfluidic technology also reduces reagent consumption and tissue culture expenses significantly, while allowing more data to be collected from a single tissue slice, thus reducing the number of laboratory animals to be sacrificed for a study.
我们开发了一种利用开放式体积微流控装置的灌流方法,可实现对脑片选定区域的药物以高时空分辨率给药。该方法包括局部刺激脑片中神经元的活性化合物的水力限制流动,与电生理记录技术结合使用,以分析响应。微流控装置是一种新颖的独立多功能移液器,允许进行各种灌流实验,例如在不同细胞层中以高定位精度测试不同浓度的药物或药物候选物对神经元的影响,仅影响少数细胞。我们在此展示了使用该方法进行电生理记录的情况,包括来自大鼠海马和前额叶皮层脑片的锥体细胞,确定了电响应与灌流装置与记录部位的距离之间的关系,记录了与全切片灌流相比溶液交换时间的倍数增加,并表明该装置能够连续存储和输送多达四种溶液。通过开放式体积微流控技术进行局部溶液输送还可以显著减少试剂消耗和组织培养费用,同时允许从单个组织切片中收集更多数据,从而减少用于研究的实验动物数量。