Distinct roles of neuronal phenotypes during neurofeedback adaptation
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Learning adaptation allows the brain to refine motor patterns in response to changing environments rapidly. While population-level neural dynamics and single-neuron activity in motor learning have been widely studied, the contributions of individual neuron types remain poorly understood. Here, we employed a brain-machine interface (BMI) task with perturbations of varying difficulty to investigate single-neuron dynamics underlying neurofeedback adaptation in two rhesus macaques. Cortical neurons were classified based on waveform shape into narrow waveform (NW) and broad waveform (BW) categories, representing putative inhibitory interneurons and excitatory pyramidal neurons, respectively. Compared to BW neurons, NW neurons were more active and more strongly involved in the learning process. Moreover, task difficulty modulated neural responsiveness and coordination within both neuron groups, highlighting differential neuron engagement during motor learning. Our findings provide novel insights into single-neuron mechanisms underlying neurofeedback adaptation and emphasize the distinct functional roles of neuronal phenotypes in rapid learning processes.
Author Summary
Understanding how the brain adapts to changes is crucial for improving treatments for neurological disorders and enhancing brain-machine interface (BMI) technology, which allows control of external devices using neural signals. In our study, we investigated how different types of brain cells contribute to the adaptation process when individuals encounter unexpected challenges during neurofeedback tasks. We discovered that one type of neuron was notably more active and played a more engaged role in rapidly adjusting neural activity compared to another type. These neurons demonstrated stronger coordination in their activity and showed greater responsiveness as the task difficulty increased. Our findings highlight the distinct roles of specific neurons in quickly adapting to neurofeedback tasks, offering insights that could enhance therapies for movement disorders and improve the precision and reliability of brain-controlled prosthetics.