scholarly journals Novel neural signal features permit robust machine-learning of natural tactile- and proprioception-dominated dorsal column nuclei signals

2019 ◽  
Author(s):  
Alastair J Loutit ◽  
Jason R Potas

Neural prostheses enable users to effect movement through a variety of actuators by translating brain signals into movement control signals. However, to achieve more natural limb movements from these devices, restoration of somatosensory feedback and advances in neural decoding of motor control-related brain signals are required. We used a machine-learning approach to assess signal features for their capacity to enhance decoding performance of neural signals evoked by natural tactile and proprioceptive somatosensory stimuli, recorded from the surface of the dorsal column nuclei in urethane-anaesthetised rats. We determined signal features that are highly informative for decoding somatosensory stimuli, yet these appear underutilised in neuroprosthetic applications. We found that proprioception-dominated stimuli generalise across animals better than tactile-dominated stimuli, and we demonstrate how information that signal features contribute to neural decoding changes over a time-course of dynamic somatosensory events. These findings may improve neural decoding for various applications including novel neuroprosthetic design.

2019 ◽  
Author(s):  
Alexandria M. H. Lesicko ◽  
Daniel A. Llano

ABSTRACTThe lateral cortex of the inferior colliculus (LCIC) is parcellated into two neurochemical compartments: one that comprises periodic neurochemical modules rich in GABAergic and cholinergic terminals and an extramodular matrix rich in calretinin neurons. We recently found that projections from auditory structures (auditory cortex and central nucleus of the IC) target the extramodular matrix, while somatosensory structures (somatosensory cortex and dorsal column nuclei) target the modules. What is peculiar about this finding of segregated inputs is that previous work has found that many LCIC neurons respond to both auditory and somatosensory stimuli. To investigate how these pathways interact, here we use laser photostimulation of caged glutamate to interrogate local LCIC circuits in brain slices from mouse. We found that most cell types in the LCIC receive inputs only from their home domain, but that GABAergic neurons in the modules serve as a bridge between modules and extramodular space. Further, we found that residence in- or out-of a module strongly predicted the output connectivity of that cell. These data suggest that distinct processing streams are seen in the LCIC and that GABAergic cells in modules serve to link these streams.


1978 ◽  
Vol 133 (3) ◽  
pp. 231-238 ◽  
Author(s):  
W. E. Haefely

SummaryAfter a brief review of the characteristic somatic and psychotropic effects of benzodiazepines evidence is presented which supports a specific facilitatory action of these drugs on GABA ergic synapses within the mammalian central nervous system. Benzodiazepines enhance presynaptic inhibition in the spinal cord and dorsal column nuclei as well as postsynaptic inhibition in dorsal column nuclei, hippocampus, hypothalamus, cerebral cortex, cerebellar cortex, which are all examples of recurrent and collateral inhibition mediated by GABA ergic intrinsic neurones. In addition, the compounds also enhance the inhibitory effect of GABA ergic long projection neurones in the substantia nigra and the lateral vestibular nucleus of Deiters. Several problems remain to be solved, such as the exact site at which benzodiazepines initiate their action (pre-synaptically at GABA ergic nerve endings or postsynaptically at the target cells) and the possible existence of endogenous ligands for the benzodiazepine receptor. Some suspected implications which studies on benzodiazepine binding sites could have for a deeper understanding of the mode of action of these drugs are discussed.


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