Rapid recovery (20 ms) of human 600 Hz electroencephalographic wavelets after double stimulation of sensory nerves

Non-invasive scalp-recordings of human somatosensory evoked potentials (SEP) contain high-frequency (600 Hz) wavelet bursts, presumably generated by synchronized thalamocortical and/or intracortical population spikes. Here, double pulse stimulation (interval 20 ms) in 12 healthy subjects revealed si...

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Published inNeuroscience letters Vol. 286; no. 2; pp. 83 - 86
Main Authors Mackert, Bruno-Marcel, Weisenbach, Simon, Nolte, Guido, Curio, Gabriel
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 02.06.2000
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Abstract Non-invasive scalp-recordings of human somatosensory evoked potentials (SEP) contain high-frequency (600 Hz) wavelet bursts, presumably generated by synchronized thalamocortical and/or intracortical population spikes. Here, double pulse stimulation (interval 20 ms) in 12 healthy subjects revealed significantly different burst recovery for mixed vs. sensory-only nerves. For median nerves the second burst response was decreased (11/11 subjects), possibly due to interfering reafferent (e.g. muscle spindle) input. In contrast, for sensory-only superficial radial nerves (containing less fibers than median nerves), weak bursts were detected in 6/11 subjects and were found fully recovered in 4/6 subjects. This potential for rapid burst recovery at 20 ms intervals renders contributions from neurons emitting bursts based on slowly recovering low-threshold calcium spikes unlikely and favors the generation of macroscopic SEP bursts by specialized cell populations, e.g. inhibitory interneurons and/or chattering cells the latter of which are capable to discharge rapidly repeating (50 Hz) high-frequency (600 Hz) bursts of fast sodium spikes.
AbstractList Non-invasive scalp-recordings of human somatosensory evoked potentials (SEP) contain high-frequency (600 Hz) wavelet bursts, presumably generated by synchronized thalamocortical and/or intracortical population spikes. Here, double pulse stimulation (interval 20 ms) in 12 healthy subjects revealed significantly different burst recovery for mixed vs. sensory-only nerves. For median nerves the second burst response was decreased (11/11 subjects), possibly due to interfering reafferent (e.g. muscle spindle) input. In contrast, for sensory-only superficial radial nerves (containing less fibers than median nerves), weak bursts were detected in 6/11 subjects and were found fully recovered in 4/6 subjects. This potential for rapid burst recovery at 20 ms intervals renders contributions from neurons emitting bursts based on slowly recovering low-threshold calcium spikes unlikely and favors the generation of macroscopic SEP bursts by specialized cell populations, e.g. inhibitory interneurons and/or chattering cells the latter of which are capable to discharge rapidly repeating (50 Hz) high-frequency (600 Hz) bursts of fast sodium spikes.
Non-invasive scalp-recordings of human somatosensory evoked potentials (SEP) contain high-frequency (600 Hz) wavelet bursts, presumably generated by synchronized thalamocortical and/or intracortical population spikes. Here, double pulse stimulation (interval 20 ms) in 12 healthy subjects revealed significantly different burst recovery for mixed vs. sensory-only nerves. For median nerves the second burst response was decreased (11/11 subjects), possibly due to interfering reafferent (e.g. muscle spindle) input. In contrast, for sensory-only superficial radial nerves (containing less fibers than median nerves), weak bursts were detected in 6/11 subjects and were found fully recovered in 4/6 subjects. This potential for rapid burst recovery at 20 ms intervals renders contributions from neurons emitting bursts based on slowly recovering low-threshold calcium spikes unlikely and favors the generation of macroscopic SEP bursts by specialized cell populations, e.g. inhibitory interneurons and/or chattering cells the latter of which are capable to discharge rapidly repeating (50 Hz) high-frequency (600 Hz) bursts of fast sodium spikes.Non-invasive scalp-recordings of human somatosensory evoked potentials (SEP) contain high-frequency (600 Hz) wavelet bursts, presumably generated by synchronized thalamocortical and/or intracortical population spikes. Here, double pulse stimulation (interval 20 ms) in 12 healthy subjects revealed significantly different burst recovery for mixed vs. sensory-only nerves. For median nerves the second burst response was decreased (11/11 subjects), possibly due to interfering reafferent (e.g. muscle spindle) input. In contrast, for sensory-only superficial radial nerves (containing less fibers than median nerves), weak bursts were detected in 6/11 subjects and were found fully recovered in 4/6 subjects. This potential for rapid burst recovery at 20 ms intervals renders contributions from neurons emitting bursts based on slowly recovering low-threshold calcium spikes unlikely and favors the generation of macroscopic SEP bursts by specialized cell populations, e.g. inhibitory interneurons and/or chattering cells the latter of which are capable to discharge rapidly repeating (50 Hz) high-frequency (600 Hz) bursts of fast sodium spikes.
Author Weisenbach, Simon
Mackert, Bruno-Marcel
Nolte, Guido
Curio, Gabriel
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Issue 2
Keywords Somatosensory evoked potentials
Radial nerve
Median nerve
Primary somatosensory cortex
Recovery behavior
Double pulse stimulation
High frequency activity (600 Hz)
Human
Somatosensory cortex
Stimulus
Electrophysiology
Sensory nerve
Electroencephalography
Somatosensory evoked potential
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Snippet Non-invasive scalp-recordings of human somatosensory evoked potentials (SEP) contain high-frequency (600 Hz) wavelet bursts, presumably generated by...
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SubjectTerms Action Potentials - physiology
Biological and medical sciences
Double pulse stimulation
Electric Stimulation
Electroencephalography
Evoked Potentials, Somatosensory - physiology
Fundamental and applied biological sciences. Psychology
High frequency activity (600 Hz)
Humans
Median nerve
Median Nerve - physiology
Neural Conduction - physiology
Neural Pathways - cytology
Neural Pathways - physiology
Neurons, Afferent - cytology
Neurons, Afferent - physiology
Peripheral Nerves - cytology
Peripheral Nerves - physiology
Primary somatosensory cortex
Radial nerve
Radial Nerve - physiology
Recovery behavior
Somatosensory Cortex - cytology
Somatosensory Cortex - physiology
Somatosensory evoked potentials
Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors
Time Factors
Vertebrates: nervous system and sense organs
Title Rapid recovery (20 ms) of human 600 Hz electroencephalographic wavelets after double stimulation of sensory nerves
URI https://dx.doi.org/10.1016/S0304-3940(00)01086-7
https://www.ncbi.nlm.nih.gov/pubmed/10825642
https://www.proquest.com/docview/17693966
https://www.proquest.com/docview/71137979
Volume 286
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