TY - JOUR
T1 - A system for MEA-based multisite stimulation
AU - Jimbo, Yasuhiko
AU - Kasai, Nahoko
AU - Torimitsu, Keiichi
AU - Tateno, Takashi
AU - Robinson, Hugh P.C.
N1 - Funding Information:
Manuscript received September 4, 2001; revised July 31, 2002. This work was supported by Core Research for Evolutional Science Technology of Japan Science and Technology Corporation, and by the Toyota Physical and Chemical Research Institute. Asterisk indicates corresponding author. Y. Jimbo is with NTT Basic Research Laboratories, NTT Corporation, Kanagawa 243-0198, Japan (e-mail: jimbo@will.brl.ntt.co.jp). N. Kasai and K. Torimitsu are with NTT Basic Research Laboratories, NTT Corporation, Kanagawa 243-0198, Japan. T. Tateno is with Osaka University, Osaka 560-8531, Japan. H. P. C. Robinson is with the University of Cambridge, Cambridge CB2 3EG, U.K. Digital Object Identifier 10.1109/TBME.2002.805470
PY - 2003/2/1
Y1 - 2003/2/1
N2 - The capability for multisite stimulation is one of the biggest potential advantages of microelectrode arrays (MEAs). There remain, however, several technical problems which have hindered the development of a practical stimulation system. An important design goal is to allow programmable multisite stimulation, which produces minimal interference with simultaneous extracellular and patch or whole cell clamp recording. Here, we describe a multisite stimulation and recording system with novel interface circuit modules, in which preamplifiers and transistor transistor logic-driven solid-state switching devices are integrated. This integration permits PC-controlled remote switching of each substrate electrode. This allows not only flexible selection of stimulation sites, but also rapid switching of the selected sites between stimulation and recording, within 1.2 ms. This allowed almost continuous monitoring of extracellular signals at all the substrate-embedded electrodes, including those used for stimulation. In addition, the vibration-free solid-state switching made it possible to record whole-cell synaptic currents in one neuron, evoked from multiple sites in the network. We have used this system to visualize spatial propagation patterns of evoked responses in cultured networks of cortical neurons. This MEA-based stimulation system is a useful tool for studying neuronal signal processing in biological neuronal networks, as well as the process of synaptic integration within single neurons.
AB - The capability for multisite stimulation is one of the biggest potential advantages of microelectrode arrays (MEAs). There remain, however, several technical problems which have hindered the development of a practical stimulation system. An important design goal is to allow programmable multisite stimulation, which produces minimal interference with simultaneous extracellular and patch or whole cell clamp recording. Here, we describe a multisite stimulation and recording system with novel interface circuit modules, in which preamplifiers and transistor transistor logic-driven solid-state switching devices are integrated. This integration permits PC-controlled remote switching of each substrate electrode. This allows not only flexible selection of stimulation sites, but also rapid switching of the selected sites between stimulation and recording, within 1.2 ms. This allowed almost continuous monitoring of extracellular signals at all the substrate-embedded electrodes, including those used for stimulation. In addition, the vibration-free solid-state switching made it possible to record whole-cell synaptic currents in one neuron, evoked from multiple sites in the network. We have used this system to visualize spatial propagation patterns of evoked responses in cultured networks of cortical neurons. This MEA-based stimulation system is a useful tool for studying neuronal signal processing in biological neuronal networks, as well as the process of synaptic integration within single neurons.
KW - Electrical stimulation
KW - MEA
KW - Neuron
KW - Spike
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U2 - 10.1109/TBME.2002.805470
DO - 10.1109/TBME.2002.805470
M3 - Article
C2 - 12665038
AN - SCOPUS:0037297071
SN - 0018-9294
VL - 50
SP - 241
EP - 248
JO - IEEE Transactions on Biomedical Engineering
JF - IEEE Transactions on Biomedical Engineering
IS - 2
ER -