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@ARTICLE{Maybeck:825324,
author = {Maybeck, Vanessa and Schnitker, Jan and Li, Wenfang and
Heuschkel, M. and Offenhäusser, Andreas},
title = {{A}n evaluation of extracellular {MEA} versus optogenetic
stimulation of cortical neurons},
journal = {Biomedical physics $\&$ engineering express},
volume = {2},
number = {5},
issn = {2057-1976},
address = {Bristol},
publisher = {IOP Publ.},
reportid = {FZJ-2016-07787},
pages = {055017},
year = {2016},
abstract = {Objective. The importance of extracellular neural
stimulation has driven the development of multiple
technologies. Of growing importance is accurately
stimulating single neurons in dense networks. It is unlikely
that one approach is best for all applications, however
comparisons between methods are lacking. We aim to show the
strengths and suitable applications for two tools;
micro-electrode array (MEA) stimulation and optogenetics.
Approach. We compare MEA-based electrical stimulation to
Channelrhodopsin 2 based optogenetic stimulation of
dissociated cortical neurons in vitro. Effectivity is
compared based on stimulation success rate, spatial and
temporal accuracy, and reproducibility. We discuss how
necessities of each method may limit performance in each
category. Main Results. MEA stimulation outperformed
optogenetic stimulation in the speed with which an action
potential could be generated. The relation between the size
of the stimulating point (electrode or illumination spot)
and the area of stimulated tissue was similar in both
methods. However, technical difficulties in maintaining low
impedance from very small electrodes allows higher spatial
specificity in optogenetic stimulation. If simultaneous
recording and stimulation are desired, MEA stimulation
artifacts were far more impairing than light induce
artifacts on MEA recordings. Significance. The like versus
like comparison of stimulation technologies provides an
incomplete evaluation tool for researchers desiring to apply
these technologies. This comparison highlights advantages
for specific applications and should promote more
cross-topic evaluations.},
cin = {ICS-8},
ddc = {610},
cid = {I:(DE-Juel1)ICS-8-20110106},
pnm = {552 - Engineering Cell Function (POF3-552)},
pid = {G:(DE-HGF)POF3-552},
typ = {PUB:(DE-HGF)16},
doi = {10.1088/2057-1976/2/5/05517},
url = {https://juser.fz-juelich.de/record/825324},
}