author_facet Dougherty, Patrick M.
Chen, Jinghong
Dougherty, Patrick M.
Chen, Jinghong
author Dougherty, Patrick M.
Chen, Jinghong
spellingShingle Dougherty, Patrick M.
Chen, Jinghong
Journal of Neurophysiology
Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
Physiology
General Neuroscience
author_sort dougherty, patrick m.
spelling Dougherty, Patrick M. Chen, Jinghong 0022-3077 1522-1598 American Physiological Society Physiology General Neuroscience http://dx.doi.org/10.1152/jn.00187.2016 <jats:p> The input-output and discharge properties of neurons are shaped by both passive and active electrophysiological membrane properties. Whole cell patch-clamp recordings in lamina I–III neurons in an isolated preparation of the whole spinal cord of juvenile rats with attached dorsal roots and dorsal root ganglia were used to further define which of these properties provides the most impactful classification strategy. A total of 95 neurons were recorded in segment L5 and were classified based on the responses to L4 dorsal root stimulation. The results showed that high-threshold and silent neurons had higher membrane resistance and more negative resting membrane potential than low-threshold or wide-dynamic-range neurons. Rheobase in low-threshold and wide-dynamic-range neurons was significantly lower than that of high-threshold or silent neurons. Four types of firing patterns were identified in response to depolarizing current injections. Low-threshold cells most frequently showed a phasic firing pattern characterized by a short initial burst of action potentials, single spiking or irregular firing bursts at the onset of a depolarizing pulse. High-threshold and wide-dynamic-range neurons were characterized by tonic firing with trains of spikes occurring at regular intervals throughout the current pulse. The majority of silent neurons displayed a delayed onset of firing in response to current injection. These results indicate that the passive membrane properties of spinal neurons are tuned to optimize the responses to particular subsets of afferent stimuli. </jats:p> Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro Journal of Neurophysiology
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title Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_unstemmed Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_full Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_fullStr Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_full_unstemmed Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_short Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_sort relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
topic Physiology
General Neuroscience
url http://dx.doi.org/10.1152/jn.00187.2016
publishDate 2016
physical 1137-1151
description <jats:p> The input-output and discharge properties of neurons are shaped by both passive and active electrophysiological membrane properties. Whole cell patch-clamp recordings in lamina I–III neurons in an isolated preparation of the whole spinal cord of juvenile rats with attached dorsal roots and dorsal root ganglia were used to further define which of these properties provides the most impactful classification strategy. A total of 95 neurons were recorded in segment L5 and were classified based on the responses to L4 dorsal root stimulation. The results showed that high-threshold and silent neurons had higher membrane resistance and more negative resting membrane potential than low-threshold or wide-dynamic-range neurons. Rheobase in low-threshold and wide-dynamic-range neurons was significantly lower than that of high-threshold or silent neurons. Four types of firing patterns were identified in response to depolarizing current injections. Low-threshold cells most frequently showed a phasic firing pattern characterized by a short initial burst of action potentials, single spiking or irregular firing bursts at the onset of a depolarizing pulse. High-threshold and wide-dynamic-range neurons were characterized by tonic firing with trains of spikes occurring at regular intervals throughout the current pulse. The majority of silent neurons displayed a delayed onset of firing in response to current injection. These results indicate that the passive membrane properties of spinal neurons are tuned to optimize the responses to particular subsets of afferent stimuli. </jats:p>
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author Dougherty, Patrick M., Chen, Jinghong
author_facet Dougherty, Patrick M., Chen, Jinghong, Dougherty, Patrick M., Chen, Jinghong
author_sort dougherty, patrick m.
container_issue 3
container_start_page 1137
container_title Journal of Neurophysiology
container_volume 116
description <jats:p> The input-output and discharge properties of neurons are shaped by both passive and active electrophysiological membrane properties. Whole cell patch-clamp recordings in lamina I–III neurons in an isolated preparation of the whole spinal cord of juvenile rats with attached dorsal roots and dorsal root ganglia were used to further define which of these properties provides the most impactful classification strategy. A total of 95 neurons were recorded in segment L5 and were classified based on the responses to L4 dorsal root stimulation. The results showed that high-threshold and silent neurons had higher membrane resistance and more negative resting membrane potential than low-threshold or wide-dynamic-range neurons. Rheobase in low-threshold and wide-dynamic-range neurons was significantly lower than that of high-threshold or silent neurons. Four types of firing patterns were identified in response to depolarizing current injections. Low-threshold cells most frequently showed a phasic firing pattern characterized by a short initial burst of action potentials, single spiking or irregular firing bursts at the onset of a depolarizing pulse. High-threshold and wide-dynamic-range neurons were characterized by tonic firing with trains of spikes occurring at regular intervals throughout the current pulse. The majority of silent neurons displayed a delayed onset of firing in response to current injection. These results indicate that the passive membrane properties of spinal neurons are tuned to optimize the responses to particular subsets of afferent stimuli. </jats:p>
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spelling Dougherty, Patrick M. Chen, Jinghong 0022-3077 1522-1598 American Physiological Society Physiology General Neuroscience http://dx.doi.org/10.1152/jn.00187.2016 <jats:p> The input-output and discharge properties of neurons are shaped by both passive and active electrophysiological membrane properties. Whole cell patch-clamp recordings in lamina I–III neurons in an isolated preparation of the whole spinal cord of juvenile rats with attached dorsal roots and dorsal root ganglia were used to further define which of these properties provides the most impactful classification strategy. A total of 95 neurons were recorded in segment L5 and were classified based on the responses to L4 dorsal root stimulation. The results showed that high-threshold and silent neurons had higher membrane resistance and more negative resting membrane potential than low-threshold or wide-dynamic-range neurons. Rheobase in low-threshold and wide-dynamic-range neurons was significantly lower than that of high-threshold or silent neurons. Four types of firing patterns were identified in response to depolarizing current injections. Low-threshold cells most frequently showed a phasic firing pattern characterized by a short initial burst of action potentials, single spiking or irregular firing bursts at the onset of a depolarizing pulse. High-threshold and wide-dynamic-range neurons were characterized by tonic firing with trains of spikes occurring at regular intervals throughout the current pulse. The majority of silent neurons displayed a delayed onset of firing in response to current injection. These results indicate that the passive membrane properties of spinal neurons are tuned to optimize the responses to particular subsets of afferent stimuli. </jats:p> Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro Journal of Neurophysiology
spellingShingle Dougherty, Patrick M., Chen, Jinghong, Journal of Neurophysiology, Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro, Physiology, General Neuroscience
title Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_full Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_fullStr Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_full_unstemmed Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_short Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_sort relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
title_unstemmed Relationship of membrane properties, spike burst responses, laminar location, and functional class of dorsal horn neurons recorded in vitro
topic Physiology, General Neuroscience
url http://dx.doi.org/10.1152/jn.00187.2016