RESUMEN
Electrical activity recordings are critical for evaluating and understanding brain function. We present a novel wireless, implantable, and battery-free device, namely the Wireless Neurosensing System (WiNS), and for the first time, we evaluate multichannel recording capabilities in vivo. For a preliminary evaluation, we performed a benchtop experiment with emulated sinusoidal signals of varying amplitude and frequency, representative of neuronal activity. We later performed and analyzed electrocortical recordings in rats of evoked somatosensory activity in response to three paradigms: hind/fore limb and whisker stimulation. Wired recordings were used for comparison and validation of WiNS. We found that through the channel multiplexing element of WiNS, it is possible to perform multichannel recordings with a maximum sampling rate of â¼10 kHz for a total of eight channels. This sampling rate is appropriate for monitoring the full range of neuronal signals of interest, from low-frequency population recordings of electrocorticography and local field potentials to high-frequency individual neuronal spike recordings. These in vivo experiments demonstrated that the evoked neuronal activity recorded with WiNS is comparable to that recorded with a wired system under identical circumstances. Analysis of critical parameters for interpreting the somatosensory evoked activity showed no statistically significant difference between the parameters obtained by a wired system versus those obtained using WiNS. Therefore, WiNS can match the performance of more invasive recording systems. WiNS is a groundbreaking technology with potential applications throughout neuroscience as it offers a simple alternative to address the pitfalls of battery-powered neuronal implants.
Asunto(s)
Técnicas Biosensibles , Tecnología Inalámbrica , Animales , Electrocorticografía , Diseño de Equipo , Neuronas , RatasRESUMEN
Cortical spreading depression (SD) is a spreading disruption of ionic homeostasis in the brain during which neurons experience complete and prolonged depolarizations. SD is the basis of migraine aura and is increasingly associated with many other brain pathologies. Here, we study the role of glutamate and NMDA receptor dynamics in the context of an ionic electrodiffusion model. We perform simulations in one (1D) and two (2D) spatial dimension. Our 1D simulations reproduce the "inverted saddle" shape of the extracellular voltage signal for the first time. Our simulations suggest that SD propagation depends on two overlapping mechanisms; one dependent on extracellular glutamate diffusion and NMDA receptors and the other dependent on extracellular potassium diffusion and persistent sodium channel conductance. In 2D simulations, we study the dynamics of spiral waves. We study the properties of the spiral waves in relation to the planar 1D wave, and also compute the energy expenditure associated with the recurrent SD spirals.