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Barnett, C. R.

Publications and source records attributed to Barnett, C. R..

2 recordsLinked to original sources

Long-term neuron tracking reveals balance of stability and plasticity in functional properties

Neural stability is essential for executing learned motor behaviors while plasticity provides the flexibility needed to adapt to new tasks and environments. Although low-dimensional neural population dynamics exhibit long-term stability, the extent to which individual neurons retain their functional properties over time and balance the need for both stability and plasticity remains an open question. Tracking individual neurons across multiple recording sessions is crucial to addressing this question, yet conventional methods face challenges such as electrode drift, waveform variability, and large inter-electrode distances that limit the number of channels a neuron is observed on. Here, we introduce a waveform-based neuron tracking method optimized for standard microelectrode arrays, enabling the identification of the same neurons across sessions without relying on spatial overlap, a strategy commonly leveraged with high-density electrode arrays. We apply this method to assess the longitudinal stability of multiple neural properties, including firing rates, inter-spike intervals, tuning properties, and spike-field interactions. Our findings reveal that while spike waveform properties remain stable, certain functional properties such as ISI and tuning can exhibit gradual shifts, suggesting a balance between neural stability and plasticity. Understanding the persistence of individual neural signals provides insight into learning and adaptation while advancing the study of neural stability and plasticity over extended timescales. Beyond basic neuroscience, this framework has potential to enhance the long-term reliability of brain-machine interfaces and closed-loop deep brain stimulation systems that rely on chronic neural sensing.

neuroscience↗

Volitional Regulation and Transferable Patterns of Midbrain Oscillations

Dopaminergic brain areas are crucial for cognition and their dysregulation is linked to neuropsychiatric disorders typically treated with pharmacological interventions. These treatments often have side effects and variable effectiveness, underscoring the need for alternatives. We introduce the first demonstration of neurofeedback using local field potentials (LFP) from the ventral tegmental area (VTA). This approach leverages the real-time temporal resolution of LFP and ability to target deep brain. In our study, non-human primates learned to regulate VTA beta power using a customized normalized metric to stably quantify VTA LFP signal modulation. The subjects demonstrated flexible and specific control with different strategies for specific frequency bands, revealing new insights into the plasticity of VTA neurons contributing to oscillatory activity that is functionally relevant to many aspects of cognition. Excitingly, the subjects showed transferable patterns, a key criterion for clinical applications beyond training settings. This work provides a foundation for neurofeedback-based treatments, which may be a promising alternative to conventional approaches and open new avenues for understanding and managing neuropsychiatric disorders. Significance statementThis study demonstrates, for the first time, that neurofeedback using local field potentials (LFP) from the ventral tegmental area (VTA) is feasible in non-human primates. By leveraging the temporal resolution and ability to target deep brain regions, this approach provides a novel way to modulate brain activity linked to dopamine-related functions. The findings reveal that subjects can flexibly control VTA LFP signals and transfer learned strategies to new settings, offering potential for developing neurofeedback-based treatments. This research opens new avenues for managing neuropsychiatric disorders, presenting an alternative to traditional pharmacological interventions that often have side effects and limited effectiveness. The study highlights the plasticity of VTA neurons and their relevance to cognition and mood regulation.

neuroscience↗