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Kawasaki, Masashi
Pluta, Scott R.
Kawasaki, Masashi
author Pluta, Scott R.
Kawasaki, Masashi
spellingShingle Pluta, Scott R.
Kawasaki, Masashi
Journal of Neurophysiology
Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
Physiology
General Neuroscience
author_sort pluta, scott r.
spelling Pluta, Scott R. Kawasaki, Masashi 0022-3077 1522-1598 American Physiological Society Physiology General Neuroscience http://dx.doi.org/10.1152/jn.00731.2009 <jats:p> Mormyrid weakly electric fish actively sense their surroundings by continuously emitting discrete pulses of electricity separated by varying intervals of silence. The temporal pattern of this pulsing behavior is related to context. While resting in the absence of an overt stimulus, baseline interpulse intervals (IPIs) mostly range 200–450 ms, and sequential variation is relatively high. Spontaneously, or following the presentation of a novel stimulus, IPIs transiently shorten during the performance of an electromotor “burst” display. We made intracellular whole cell recordings in vivo from neurons in the lateral nucleus of the torus semicircularis while the fish's dynamic pulsing behavior modified the temporal pattern of stimulation. Stimulation was designed to simulate the spatial patterns of AM that occur during the electrolocation of a resistive object. We discovered that toral neurons selectively respond to stimulation during a particular mode of electromotor activity. Two types of temporally selective neurons were discovered: baseline-selective neurons that displayed significantly higher postsynaptic potential (PSP) amplitude and spike count per electric organ discharge (EOD) during baseline electromotor activity and burst-selective neurons that displayed significantly higher PSP amplitude and spike count per EOD during electromotor burst displays. Interval-dependent changes in the strength of excitation and inhibition contributed to their selectivity. </jats:p> Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing Journal of Neurophysiology
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title Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_unstemmed Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_full Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_fullStr Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_full_unstemmed Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_short Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_sort temporal selectivity in midbrain electrosensory neurons identified by modal variation in active sensing
topic Physiology
General Neuroscience
url http://dx.doi.org/10.1152/jn.00731.2009
publishDate 2010
physical 498-507
description <jats:p> Mormyrid weakly electric fish actively sense their surroundings by continuously emitting discrete pulses of electricity separated by varying intervals of silence. The temporal pattern of this pulsing behavior is related to context. While resting in the absence of an overt stimulus, baseline interpulse intervals (IPIs) mostly range 200–450 ms, and sequential variation is relatively high. Spontaneously, or following the presentation of a novel stimulus, IPIs transiently shorten during the performance of an electromotor “burst” display. We made intracellular whole cell recordings in vivo from neurons in the lateral nucleus of the torus semicircularis while the fish's dynamic pulsing behavior modified the temporal pattern of stimulation. Stimulation was designed to simulate the spatial patterns of AM that occur during the electrolocation of a resistive object. We discovered that toral neurons selectively respond to stimulation during a particular mode of electromotor activity. Two types of temporally selective neurons were discovered: baseline-selective neurons that displayed significantly higher postsynaptic potential (PSP) amplitude and spike count per electric organ discharge (EOD) during baseline electromotor activity and burst-selective neurons that displayed significantly higher PSP amplitude and spike count per EOD during electromotor burst displays. Interval-dependent changes in the strength of excitation and inhibition contributed to their selectivity. </jats:p>
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author Pluta, Scott R., Kawasaki, Masashi
author_facet Pluta, Scott R., Kawasaki, Masashi, Pluta, Scott R., Kawasaki, Masashi
author_sort pluta, scott r.
container_issue 1
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container_title Journal of Neurophysiology
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description <jats:p> Mormyrid weakly electric fish actively sense their surroundings by continuously emitting discrete pulses of electricity separated by varying intervals of silence. The temporal pattern of this pulsing behavior is related to context. While resting in the absence of an overt stimulus, baseline interpulse intervals (IPIs) mostly range 200–450 ms, and sequential variation is relatively high. Spontaneously, or following the presentation of a novel stimulus, IPIs transiently shorten during the performance of an electromotor “burst” display. We made intracellular whole cell recordings in vivo from neurons in the lateral nucleus of the torus semicircularis while the fish's dynamic pulsing behavior modified the temporal pattern of stimulation. Stimulation was designed to simulate the spatial patterns of AM that occur during the electrolocation of a resistive object. We discovered that toral neurons selectively respond to stimulation during a particular mode of electromotor activity. Two types of temporally selective neurons were discovered: baseline-selective neurons that displayed significantly higher postsynaptic potential (PSP) amplitude and spike count per electric organ discharge (EOD) during baseline electromotor activity and burst-selective neurons that displayed significantly higher PSP amplitude and spike count per EOD during electromotor burst displays. Interval-dependent changes in the strength of excitation and inhibition contributed to their selectivity. </jats:p>
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spelling Pluta, Scott R. Kawasaki, Masashi 0022-3077 1522-1598 American Physiological Society Physiology General Neuroscience http://dx.doi.org/10.1152/jn.00731.2009 <jats:p> Mormyrid weakly electric fish actively sense their surroundings by continuously emitting discrete pulses of electricity separated by varying intervals of silence. The temporal pattern of this pulsing behavior is related to context. While resting in the absence of an overt stimulus, baseline interpulse intervals (IPIs) mostly range 200–450 ms, and sequential variation is relatively high. Spontaneously, or following the presentation of a novel stimulus, IPIs transiently shorten during the performance of an electromotor “burst” display. We made intracellular whole cell recordings in vivo from neurons in the lateral nucleus of the torus semicircularis while the fish's dynamic pulsing behavior modified the temporal pattern of stimulation. Stimulation was designed to simulate the spatial patterns of AM that occur during the electrolocation of a resistive object. We discovered that toral neurons selectively respond to stimulation during a particular mode of electromotor activity. Two types of temporally selective neurons were discovered: baseline-selective neurons that displayed significantly higher postsynaptic potential (PSP) amplitude and spike count per electric organ discharge (EOD) during baseline electromotor activity and burst-selective neurons that displayed significantly higher PSP amplitude and spike count per EOD during electromotor burst displays. Interval-dependent changes in the strength of excitation and inhibition contributed to their selectivity. </jats:p> Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing Journal of Neurophysiology
spellingShingle Pluta, Scott R., Kawasaki, Masashi, Journal of Neurophysiology, Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing, Physiology, General Neuroscience
title Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_full Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_fullStr Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_full_unstemmed Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_short Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
title_sort temporal selectivity in midbrain electrosensory neurons identified by modal variation in active sensing
title_unstemmed Temporal Selectivity in Midbrain Electrosensory Neurons Identified by Modal Variation in Active Sensing
topic Physiology, General Neuroscience
url http://dx.doi.org/10.1152/jn.00731.2009