Le système nerveux central est la cible la plus probable d'effets biologiques dûs à l'exposition aux radiofréquences (RF) de la téléphonie mobile. Plusieurs études sur l’EEG (électroencéphalogramme) ont montré des variations dans le spectre de la bande alpha pendant et / ou après l'exposition aux radiofréquences, avec les yeux fermés ou pendant le sommeil. Dans ce contexte, l'observation de l'activité électrique spontanée des réseaux neuronaux sous exposition aux radiofréquences représente un outil efficace pour détecter de possibles effets des RF de faible niveau sur le système nerveux. Dans ce travail de thèse, nous avons développé un dispositif expérimental dédié à l'exposition dans la gamme des GHz de réseaux neuronaux et permettant simultanément l’enregistrement de l'activité électrique des neurones. Une cellule électromagnétique transversale (TEM) a été utilisée afin d'exposer les réseaux neuronaux aux signaux GSM-1800 à un niveau de DAS de 3,2 W / kg. L'enregistrement de l'activité électrique neuronale et la détection en termes de spikes et bursts sous exposition ont été réalisées à l'aide de réseaux de micro-électrodes (MEAs). Ce travail démontre la faisabilité de l’étude (culture de réseaux de neurones primaires, enregistrement de l'activité électrique et analyse des signaux obtenus sous exposition aux radiofréquences) et expose des résultats préliminaires. Dans l'expérience principale (16 cultures), il y avait une diminution réversible de 30% du taux moyen de spikes (MFR) et de bursts (BR) pendant les 3 min d’exposition aux RF. Des expériences supplémentaires sont nécessaires pour mieux caractériser cet effet, notamment en termes d'élévation de la température au niveau microscopique. / The central nervous system is the most likely target of mobile telephony radiofrequency field (RF) exposure in terms of biological effects. Several EEG (electroencephalography) studies have reported variations in the alpha-band power spectrum during and/or after RF exposure, in resting EEG and during sleep. In this context, the observation of the spontaneous electrical activity of neuronal networks under RF exposure can be an efficient tool to detect the occurrence of low-level RF effects on the nervous system. In this thesis research work we developed a dedicated experimental setup in the GHz range for the simultaneous exposure of neuronal networks and monitoring of electrical activity. A transverse electromagnetic (TEM) cell was used to expose the neuronal networks to GSM-1800 signals at a SAR level of 3.2 W/kg. Recording of the neuronal electrical activity and detection of the extracellular spikes and bursts under exposure were performed using Micro Electrode Arrays (MEAs). This work provides the proof of feasibility and preliminary results of the integrated investigation regarding exposure setup, culture of the neuronal network, recording of the electrical activity and analysis of the signals obtained under RF exposure. In the main experiment (16 cultures), there was a 30% reversible decrease in mean firing rate (MFR) and bursting rate (BR) during the 3 min exposures to RF. Additional experiments are needed to further characterize this effect, especially in terms of temperature elevation at the microscopic level.

This thesis is concerned with dynamic electrochemistry experiments in which faradaic processes are driven by the application of potential to an electrode immersed in an electrolyte solution. In particular, experimental methods are considered which could be used to study electrochemical systems in a more informative way if the processes occurring at the electrode were better understood. The work develops the theoretical models which describe these experiments, and details the approximations made in each model and the conditions under which they are appropriate. Numerical simulations are reported which demonstrate how the models can be used to infer quantitative details of chemical behaviour from experimentally recorded data. The first system studied in detail is linear sweep voltammetry at a microband electrode array. The diffusional behaviour of an electroactive species is shown to depend on the configuration of the microband array and on the potential scan rate used. Details are given on how experimental conditions can be optimised for the study of electrochemical systems. The next area of work develops the theory of nanoparticle-modified electrodes. Experiments are considered in which an electron transfer reaction is catalysed only at the site of the nanoparticles, whilst the supporting planar electrode remains electrochemically inert. Numerical simulations show how the current measured at these modified electrodes depends on the size and shape of the particles, on the distribution of the particles on the electrode surface, and on the timescale of the experiment. The final theme of work is on electrochemical experiments in poorly conducting solutions. A theoretical model is developed which takes into account the effects of an electric field on the mass transport of electroactive species and on the charge transfer kinetics at the electrode. The model is then used to rationalise the unusual current behaviour that is observed in the anodic stripping of thallium from an amalgam.

Creating high resolution, or high-density, electrode arrays may be the key for improving cochlear implant users' speech perception in noise, comprehension of lexical languages, and music appreciation. Contemporary electrode arrays use multipolar stimulation techniques such as current steering (shifting the spread of neural excitation in between two physical electrodes) and current focusing (narrowing of the neural spread of excitation) to increase resolution and more specifically target the neural population. Another approach to increasing resolution incorporates microelectromechanical systems (MEMS) fabrication to create a thin film microelectrode (TFM) array with a series of high density electrodes. Validating the benefits of high density electrode arrays requires a systems-level approach. This hypothesis will be tested computationally via cochlea and auditory nerve simulations, and in vitro studies will provide structural proof-of-concept. By employing Rattay's activating function and entering it into Litvak's neural probability model, a first order estimation model was obtained of the auditory nerve's response to electrical stimulation. Two different stimulation scenarios were evaluated: current steering vs. a high density electrode and current focusing of contemporary electrodes vs. current focusing of high density electrodes. The results revealed that a high density electrode is more localized than current steering and requires less current. A second order estimation model was also created COMSOL, which provided the resulting potential and current flow when the electrodes were electrically stimulated. The structural tests were conducted to provide a proof of concept for the TFM arrays' ability to contour to the shape of the cochlea. The TFM arrays were integrated with a standard insertion platform (IP). In vitro tests were performed on human cadaver cochleae using the TFM/IP devices. Fluoroscopic images recorded the insertion, and post analysis 3D CT scans and histology were conducted on the specimens. Only three of the ten implanted TFM/IPs suffered severe delamination. This statistic for scala vestibuli excursion is not an outlier when compared to previous data recorded for contemporary cochlear electrode arrays.

The electrochemical behavior of nickel (Ni) in different concentrations of sulfuric acid (H2SO4) was studied via cyclic voltammetry (CV) over a range of potentials (0.0 V– 3.0 V) at room temperature. The presented work displays novel experiments where external forcing by a platinum (Pt) electrode changed the proton concentration at a Ni electrode surface in order to control the frequency and magnitude of periodic oscillations produced. When studying unique phenomena such as the Ni phenomena in this thesis, efficient, durable, and inexpensive technology is always beneficial. A coupled microelectrode array sensor or CMAS which has been used for over four decades to study pitting corrosion, crevice corrosion, intergranular corrosion, galvanic corrosion, and other heterogeneous electrochemical processes were fabricated in a novel, systematic, inexpensive, and time efficient process. The presented work shows how to make the CMAS and proved that they functioned properly.

For almost a century, the electrical properties of the brain and the nervous system have been investigated to gain a better understanding of their mechanisms and to find cures for pathological conditions. Despite the fact that today's advancements in surgical techniques, research, and medical imaging have improved our ability to treat brain disorders, our knowledge of the brain and its functions is still limited. Culturing dissociated cortical neurons on Micro-Electrode Array dishes is a powerful experimental tool for investigating functional and structural characteristics of in-vitro neuronal networks, such as the cellular basis of brain learning, memory and synaptic developmental plasticity. This dissertation focuses on combining MEAs with novel electrophysiology experimental paradigms and statistical data analysis to investigate the mechanisms that regulate brain development at the level of synaptic formation and growth cones. The goal is to use a mathematical approach and specifically designed experiments to investigate whether dissociated neuronal networks can dependably display long and short-term plasticity, which are thought to be the building blocks of memory formation in the brain. Quantifying the functional evolution of dissociated neuronal networks during in- vitro development, using a statistical analysis tool was the first aim of this work. The results of the False Discovery Rate analysis show an evolution in network activity with changes in both the number of statistically significant stimulus/recording pairs as well as the average length of connections and the number of connections per active node. It is therefore proposed that the FDR analysis combined with two metrics, the average connection length and the number of highly connected "supernodes" is a valuable technique for describing neuronal connectivity in MEA dishes. Furthermore, the statistical analysis indicates that cultures dissociated from the same brain tissue display trends in their temporal evolution that are more similar than those obtained with respect to different batches. The second aim of this dissertation was to investigate long and short-term plasticity responsible for memory formation in dissociated neuronal networks. In order to address this issue, a set of experiments was designed and implemented in which the MEA electrode grid was divided into four quadrants, two of which were chronically stimulated, every two days for one hour with a stimulation paradigm that varied over time. Overall network and quadrant responses were then analyzed to quantify what level of plasticity took place in the network and how this was due to the stimulation interruption. The results demonstrate that here were no spatial differences in the stimulus-evoked activity within quadrants. Furthermore, the implemented stimulation protocol induced depression effects in the neuronal networks as demonstrated by the consistently lower network activity following stimulation sessions. Finally, the analysis demonstrated that the inhibitory effects of the stimulation decreased over time, thus suggesting a habituation phenomenon. These findings are sufficient to conclude that electrical stimulation is an important tool to interact with dissociated neuronal cultures, but localized stimuli are not enough to drive spatial synaptic potentiation or depression. On the contrary, the ability to modulate synaptic temporal plasticity was a feasible task to achieve by chronic network stimulation. / Electrical and Computer Engineering

This work characterized an in vitro 3-D neural co-culture model electrophysiologically via multi electrode arrays (MEAs), and morphologically via immunocytochemistry. Since MEA surface insulation SU-8 2000 can be used in neural micro- and multi- electrode arrays, this investigation first developed techniques to make SU-8 2000 cytocompatible. The in vitro 3-D neural co-culture model was then used to study viability and electrophysiological responses to physical injury as well as drugs known to affect network signaling. 1) SU-8 2000 cytotoxicity to neuronal cultures was linked to both poor adhesive properties and toxic components, such as solvents and photo acid generator elements. Surface treatments of oxygen plasma or parylene coating following optimal combinations of heat and isopropanol sonication showed improvement in SU-8 2000 cytocompatibility. 2) The 3-D neural networks within the 3-D co-cultures maintained considerable process outgrowth and complex 3-D structure. The cultures were viable up to three weeks in vitro with functional synaptic connections and spontaneous electrophysiological activity that was responsive to chemical modulation. This electrophysiological activity was modulated by synaptic inhibition. 3) Injury experiments demonstrated that both shear and compression loading significantly increased acute membrane permeability of cells in a strain rate dependent manner. Cell death correlated with higher membrane permeability, and shear resulted in more death than compression in these 3-D cultures. While techniques were developed for making a major micro-fabrication material cytocompatible, engineering the 3-D neural co-culture resulted in a more physiologically-representative neural tissue platform, allowing an increased understanding of structure-function relationships. Overall, this research established and characterized a neural culture system for the mechanistic study of cell growth, cell-cell and cell-matrix interactions, as well as the responses to chemical or mechanical perturbations. This is the first investigation of the network-level electrophysiological activity of 3-D dissociated cultures. This system can be used to model various pathological states in vitro, testing various reparative drugs; cell-, and tissue-engineering based strategies; as well as for pre-animal and pre-clinical testing of neural implants.

The central nervous system is the most likely target of mobile telephony radiofrequency field (RF) exposure in terms of biological effects. Several EEG (electroencephalography) studies have reported variations in the alpha-band power spectrum during and/or after RF exposure, in resting EEG and during sleep. In this context, the observation of the spontaneous electrical activity of neuronal networks under RF exposure can be an efficient tool to detect the occurrence of low-level RF effects on the nervous system. In this thesis research work we developed a dedicated experimental setup in the GHz range for the simultaneous exposure of neuronal networks and monitoring of electrical activity. A transverse electromagnetic (TEM) cell was used to expose the neuronal networks to GSM-1800 signals at a SAR level of 3.2 W/kg. Recording of the neuronal electrical activity and detection of the extracellular spikes and bursts under exposure were performed using Micro Electrode Arrays (MEAs). This work provides the proof of feasibility and preliminary results of the integrated investigation regarding exposure setup, culture of the neuronal network, recording of the electrical activity and analysis of the signals obtained under RF exposure. In the main experiment (16 cultures), there was a 30% reversible decrease in mean firing rate (MFR) and bursting rate (BR) during the 3 min exposures to RF. Additional experiments are needed to further characterize this effect, especially in terms of temperature elevation at the microscopic level.

It would be of great value to have a precise and non-damaging neuromodulation technique in the field of basic neuroscience research and for clinical treatment of neurological diseases. Infrared neural modulation (INM) is a new modulation modality developed in the last decade, which uses pulsed or continues infrared (IR) light with a wavelength of 1200 to 2200 nm to directly alter neural signals. INM includes both infrared neural stimulation (INS) and infrared neural inhibition (INI). INM is widely investigated for use on peripheral nerves, cochlear nerve fibers, cardiac cells, and the central nervous system. This technique holds the advantages of contact-free and high spatiotemporal precision compared to the traditional electrical stimulation. It does not depend on genetic modification and exogenous absorbers as other optical techniques, such as the optogenetic technique and the enhanced near-infrared neural stimulation (e-NIR). These advantages make INM a viable technique for research and clinical applications. The primary mechanism of the INM is believed to be a photothermal effect, where the IR laser energy absorbed by water leads to a rapid local temperature change. However, so far the details of the mechanism of action potential (AP) generation and inhibition remain elusive. Another issueis that the cells may be endangeredbythe heat exposure, consequently triggering a physiologicalmalfunction or even permanent damage.These concernshave hindered the transfer of the INM technique to the clinical therapy.Therefore, the general aim of this study was to improve the understanding of the details of how INM affects the cells. Laser parameters for safe and efficient stimulation were investigated on the basis of being useful for clinical applications. A tailored heating model and in vitro INM experiments on cortex neurons were used to reach this goal.The first paper was a feasibility study. A 1550nm laser with a beam spot diameter of around 6 mm was used to irradiate the rat cortex neurons, which were seeded on multi-electrode arrays (MEA) and formed well-connected networks. A heating model based on an estimated laser beam (standard Gaussian distribution) was used to simulate temperaturechanges. The damage signal ratio (DSR),based on the temperature,was calculated to predict the heat damage. The average spike rate of all the working electrodes from two MEAs was used to evaluate the degree of theinhibition of the neural networks. Results IVshowed that it is possible to use the 1550 nm laser to safely inhibit the neural network activity and that the degree of the INI is dependent on the power of the laser.The second paper wasan application and mechanism study. The aim of this study was to investigate the safety, efficiency, and cellular mechanism of INI. The same laser as in paper Iwas used in this study. A 20 X objective was used to decrease the beam spot diameteraround 240 μm. The measured laser profile (high order Gaussian beam) was used in the heating model to predict the temperature. The model was verified by local temperature measurements viamicropipette. The action potential rates, measured by the MEA electrodes, were quantified for different temperatures. Bicuculline was added to the cortex neuron cultures to induce hyperexcitation of the neural network. The results showed that the INI is temperature dependent and that the temperature needs to be less than 46 °C at 30 s laser irradiation for safe inhibition. The IR laser couldalso be used to inhibit the hyperexcitedactivity. The degree of inhibition, for the assessed subpopulation of neurons, was better correlated with the action potential amplitude than the width of it and INIcan be accomplished without inhibitory synapses / <p>QC 20180920</p><p></p>

The process of respiration is a pattern of spontaneity and automatic motor control that originate in the brainstem. The mechanism by which the brainstem detects CO2 is termed central CO2 chemoreception (CCR). Since the early 1960’s there have been tremendous efforts placed on identification of central CO2 chemoreceptors (molecules that detect CO2). Even with these efforts, what a central CO2 chemoreceptor looks like remain unknown. To test the hypothesis that inward rectifier K+ (Kir) channels are CO2 sensing molecules in CCR, a series of experiments were carried out. 1) The first question asked was whether the Kir4.1-Kir5.1 channel is expressed in brainstem chemosensitive nuclei. Immunocytochemistry was performed on transverse medullary and pontine sections using antibodies raised against Kir4.1 and Kir5.1. Positive immunoassays for both Kir4.1 and Kir5.1 subunits were found in CO2 chemosensitive neurons. In the LC the Kir4.1 and Kir5.1 were co-expressed with the neurokinin-1 receptor that is the natural receptor for substance P. 2) The second question asked was whether the Kir4.1-Kir5.1 channel is subject to modulation by neurotransmitters critical for respiratory control. My studies demonstrated that indeed the Kir4.1-Kir5.1 channel is subject to modulation by substance P, serotonin and thyrotropin releasing hormone. 3) I performed studies to demonstrate the intracellular signaling system underlying the Kir4.1-Kir5.1 channel modulation by these neurotransmitters. The modulation by all three neurotransmitters was dependent upon the activation of protein kinase C (PKC). The Kir4.1-Kir5.1 but not the Kir4.1 channel was modulated by PKC. Both the Kir4.1 and Kir5.1 subunits can be phosphorylated by PKC in vitro. However, systematic mutational analysis failed to reveal the phosphorylation site. 4) The fourth question asked was whether Kir channels share a common pH gating mechanism that can be identified. Experiments were performed to understand the gating of the Kir6.2+SUR1 channel as specific sites for ligand binding and gating have been demonstrated. I identified a functional gate that was shared by multiple ligands that is Phe168 in the Kir6.2. Other Kir channels appear to share a similar gating mechanism. Taken together, these studies demonstrate the modulation of Kir channels in central CO2 chemoreception.