ABSTRACT
Neural activation by infrared nerve stimulation (INS) gains growing interest as a potential alternative to conventional electric nerve stimulation, since unambiguous advantages like contact-free operation, enhanced spatial selectivity and lack of (electrical) stimulation artifacts are promising for both future electrophysiological research and clinical application. For the systematic investigation of laser nerve activation, we recently introduced a novel experimental approach. Comprising a defined focused beam profile, it enables remote controlled, contact-free pulsed laser stimulation of the rat sciatic nerve, simultaneous to high-speed temperature measurement in vivo. Up to now, successful neural activation with single laser pulses (2 - 6 mJ) was observed in all performed experiments, however, it strongly depended on the particular nerve location. Hence, we depict the investigation of spatial dependency of the nerve response and identify `regions of excitability' on the nerve surface, that are highly susceptible to INS. By means of thermal imaging, we simultaneously monitored the nerve surface temperature, where we observed progressing temperature build-up during single pulse stimulation with repetition rates above 4 Hz. In this work, we present current results of our ongoing research.
Subject(s)
Infrared Rays , Lasers , Sciatic Nerve/radiation effects , Animals , Electric Stimulation , RatsABSTRACT
Glioma patients often suffer from epileptic seizures because of the tumor's impact on the brain physiology. Using the rat glioma cell line C6 as a model system, we performed long-term live recordings of the electrical activity of glioma populations in an ultrasensitive detection method. The transducer exploits large-area electrodes that maximize double-layer capacitance, thus increasing the sensitivity. This strategy allowed us to record glioma electrical activity. We show that although glioma cells are nonelectrogenic, they display a remarkable electrical burst activity in time. The low-frequency current noise after cell adhesion is dominated by the flow of Na+ ions through voltage-gated ion channels. However, after an incubation period of many hours, the current noise markedly increased. This electric bursting phenomenon was not associated with apoptosis because the cells were viable and proliferative during the period of increased electric activity. We detected a rapid cell culture medium acidification accompanying this event. By using specific inhibitors, we showed that the electrical bursting activity was prompted by extracellular pH changes, which enhanced Na+ ion flux through the psalmotoxin 1-sensitive acid-sensing ion channels. Our model of pH-triggered bursting was unambiguously supported by deliberate, external acidification of the cell culture medium. This unexpected, acidosis-driven electrical activity is likely to directly perturb, in vivo, the functionality of the healthy neuronal network in the vicinity of the tumor bulk and may contribute to seizures in glioma patients.
Subject(s)
Electrophysiological Phenomena , Glioma/physiopathology , Hydrogen-Ion Concentration , Neurons/cytology , Animals , Cell Line, Tumor , Humans , Nerve Net , Rats , Sodium Channels/physiologyABSTRACT
Microelectrode arrays (MEA) record extracellular local field potentials of cells adhered to the electrodes. A disadvantage is the limited signal-to-noise ratio. The state-of-the-art background noise level is about 10 µVpp. Furthermore, in MEAs low frequency events are filtered out. Here, we quantitatively analyze Au electrode/electrolyte interfaces with impedance spectroscopy and noise measurements. The equivalent circuit is the charge transfer resistance in parallel with a constant phase element that describes the double layer capacitance, in series with a spreading resistance. This equivalent circuit leads to a Maxwell-Wagner relaxation frequency, the value of which is determined as a function of electrode area and molarity of an aqueous KCl electrolyte solution. The electrochemical voltage and current noise is measured as a function of electrode area and frequency and follow unambiguously from the measured impedance. By using large area electrodes the noise floor can be as low as 0.3 µVpp. The resulting high sensitivity is demonstrated by the extracellular detection of C6 glioma cell populations. Their minute electrical activity can be clearly detected at a frequency below about 10 Hz, which shows that the methodology can be used to monitor slow cooperative biological signals in cell populations.