Simultaneous multisite detection of quantal release from PC12 cells using micro graphitic-diamond multi electrode arrays
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Updated: Jan 21, 2026

How to Culture, Record and Stimulate Neuronal Networks on Micro-electrode Arrays MEAs
Published on: May 30, 2010
Giulia Tomagra1, Claudio Franchino1, Alberto Pasquarelli2
1Department of Drug and Science Technology, NIS Inter-departmental Centre, University of Torino, Corso Raffaello 30, 10125 Torino, Italy.
Abstract:
Micro graphitic - diamond - multi electrode arrays (μG-D-MEAs) are suitable for measuring multisite quantal dopamine (DA) release from PC12 cells. Following cell stimulation with high extracellular KCl and electrode polarization at +650 mV, amperometric spikes are detected with a mean frequency of 0.60 ± 0.16 Hz. In each recording, simultaneous detection of secretory events is occurred in approximately 50% of the electrodes. Kinetic spike parameters and background noise are preserved among the different electrodes. Comparing the amperometric spikes recorder under control conditions with those recorders from PC12 cells previously incubated for 30 min with the dopamine precursor Levodopa (L-DOPA, 20 μM) it appears that the quantal size of amperometric spikes is increased by 250% and the half-time width (t1/2) by over 120%. On the contrary, L-DOPA has no effect on the frequency of secretory events. Overall, these data demonstrate that the μG-D-MEAs represent a reliable bio-sensor to simultaneously monitor quantal exocytotic events from different cells and in perspective can be exploited as a drug-screening tool.
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