Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro.

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Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro. / Chan, C. Y.; Hounsgaard, J.; Nicholson, C.

In: The Journal of Physiology, Vol. 402, No. 1, 01.08.1988, p. 751-771.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Chan, CY, Hounsgaard, J & Nicholson, C 1988, 'Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro.', The Journal of Physiology, vol. 402, no. 1, pp. 751-771. https://doi.org/10.1113/jphysiol.1988.sp017232

APA

Chan, C. Y., Hounsgaard, J., & Nicholson, C. (1988). Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro. The Journal of Physiology, 402(1), 751-771. https://doi.org/10.1113/jphysiol.1988.sp017232

Vancouver

Chan CY, Hounsgaard J, Nicholson C. Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro. The Journal of Physiology. 1988 Aug 1;402(1):751-771. https://doi.org/10.1113/jphysiol.1988.sp017232

Author

Chan, C. Y. ; Hounsgaard, J. ; Nicholson, C. / Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro. In: The Journal of Physiology. 1988 ; Vol. 402, No. 1. pp. 751-771.

Bibtex

@article{86f292acd15141f591015017e9613b3c,
title = "Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro.",
abstract = "1. Transmembrane potential (TMP) responses of Purkinje cells (PCs) in isolated turtle cerebellum to externally applied quasi‐steady‐state electric fields aligned with the dendritic axis were continuously measured using simultaneous intracellular and extracellular recording. TMP was obtained by subtraction of extracellular voltage fields from intracellular potential recorded at the same depth in the cerebellum. 2. The applied field changed the TMP with the polarity and amplitude dependent on the location on the PC membrane. This response at a given location increased linearly with external field up to a threshold level, beyond which active responses appeared. 3. The basic effect on TMP consisted of depolarization in the half of the dendrite towards which the fields were directed, and hyperpolarization in the other half. A pooled TMP depth‐profile shows a steady increase in polarization from the middle of the molecular layer towards each end. This profile correlates with that predicted from previously proposed cable models, giving them empirical support for the first time. 4. Active responses were triggered by the field‐induced depolarization. Tetrodotoxin (TTX)‐sensitive action potentials arose with the primary depolarization in the somatic region. Notched, Ca2+‐dependent action potentials arose with primary depolarization in the distal and mid‐dendritic regions. 5. A TTX‐sensitive voltage plateau was triggered by TMP‐depolarization in the proximal region. It in turn activated Na+‐spike trains. The frequency of spiking was proportional to the external field. At around 160 spikes/s, the Na+ spikes inactivated, and the TMP level rose to a more depolarized plateau. This latter plateau was also TTX‐sensitive. 6. During depolarization of the distal dendritic region, sometimes a Ca2+‐dependent plateau was observed. It appears to be associated with a small conductance increase. 7. Field‐induced hyperpolarization suppressed local spiking and voltage plateaux, but remote Ca2+ spikes with reduced amplitude appeared in recordings from the proximal region. Similarly, in the distal region, low‐amplitude, remote Na+ spikes and a Na+ plateau were observed superimposed on the hyperpolarizing baseline. The Na+ plateau apparently did not contribute to shunting of membrane currents in the distal dendrite. 8. The phase characteristics of the action potentials correlate with the modulation pattern noted in our extracellular study (Chan & Nicholson, 1986). Thus, the extracellular units ({"}giant spikes{"}) were probably Na+ spikes activated in the soma and spread distally. Occasionally Ca2+ spikes, with a higher threshold, might also be activated to give dual‐phase response.(ABSTRACT TRUNCATED AT 400 WORDS)",
author = "Chan, {C. Y.} and J. Hounsgaard and C. Nicholson",
year = "1988",
month = aug,
day = "1",
doi = "10.1113/jphysiol.1988.sp017232",
language = "English",
volume = "402",
pages = "751--771",
journal = "The Journal of Physiology",
issn = "0022-3751",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Effects of electric fields on transmembrane potential and excitability of turtle cerebellar Purkinje cells in vitro.

AU - Chan, C. Y.

AU - Hounsgaard, J.

AU - Nicholson, C.

PY - 1988/8/1

Y1 - 1988/8/1

N2 - 1. Transmembrane potential (TMP) responses of Purkinje cells (PCs) in isolated turtle cerebellum to externally applied quasi‐steady‐state electric fields aligned with the dendritic axis were continuously measured using simultaneous intracellular and extracellular recording. TMP was obtained by subtraction of extracellular voltage fields from intracellular potential recorded at the same depth in the cerebellum. 2. The applied field changed the TMP with the polarity and amplitude dependent on the location on the PC membrane. This response at a given location increased linearly with external field up to a threshold level, beyond which active responses appeared. 3. The basic effect on TMP consisted of depolarization in the half of the dendrite towards which the fields were directed, and hyperpolarization in the other half. A pooled TMP depth‐profile shows a steady increase in polarization from the middle of the molecular layer towards each end. This profile correlates with that predicted from previously proposed cable models, giving them empirical support for the first time. 4. Active responses were triggered by the field‐induced depolarization. Tetrodotoxin (TTX)‐sensitive action potentials arose with the primary depolarization in the somatic region. Notched, Ca2+‐dependent action potentials arose with primary depolarization in the distal and mid‐dendritic regions. 5. A TTX‐sensitive voltage plateau was triggered by TMP‐depolarization in the proximal region. It in turn activated Na+‐spike trains. The frequency of spiking was proportional to the external field. At around 160 spikes/s, the Na+ spikes inactivated, and the TMP level rose to a more depolarized plateau. This latter plateau was also TTX‐sensitive. 6. During depolarization of the distal dendritic region, sometimes a Ca2+‐dependent plateau was observed. It appears to be associated with a small conductance increase. 7. Field‐induced hyperpolarization suppressed local spiking and voltage plateaux, but remote Ca2+ spikes with reduced amplitude appeared in recordings from the proximal region. Similarly, in the distal region, low‐amplitude, remote Na+ spikes and a Na+ plateau were observed superimposed on the hyperpolarizing baseline. The Na+ plateau apparently did not contribute to shunting of membrane currents in the distal dendrite. 8. The phase characteristics of the action potentials correlate with the modulation pattern noted in our extracellular study (Chan & Nicholson, 1986). Thus, the extracellular units ("giant spikes") were probably Na+ spikes activated in the soma and spread distally. Occasionally Ca2+ spikes, with a higher threshold, might also be activated to give dual‐phase response.(ABSTRACT TRUNCATED AT 400 WORDS)

AB - 1. Transmembrane potential (TMP) responses of Purkinje cells (PCs) in isolated turtle cerebellum to externally applied quasi‐steady‐state electric fields aligned with the dendritic axis were continuously measured using simultaneous intracellular and extracellular recording. TMP was obtained by subtraction of extracellular voltage fields from intracellular potential recorded at the same depth in the cerebellum. 2. The applied field changed the TMP with the polarity and amplitude dependent on the location on the PC membrane. This response at a given location increased linearly with external field up to a threshold level, beyond which active responses appeared. 3. The basic effect on TMP consisted of depolarization in the half of the dendrite towards which the fields were directed, and hyperpolarization in the other half. A pooled TMP depth‐profile shows a steady increase in polarization from the middle of the molecular layer towards each end. This profile correlates with that predicted from previously proposed cable models, giving them empirical support for the first time. 4. Active responses were triggered by the field‐induced depolarization. Tetrodotoxin (TTX)‐sensitive action potentials arose with the primary depolarization in the somatic region. Notched, Ca2+‐dependent action potentials arose with primary depolarization in the distal and mid‐dendritic regions. 5. A TTX‐sensitive voltage plateau was triggered by TMP‐depolarization in the proximal region. It in turn activated Na+‐spike trains. The frequency of spiking was proportional to the external field. At around 160 spikes/s, the Na+ spikes inactivated, and the TMP level rose to a more depolarized plateau. This latter plateau was also TTX‐sensitive. 6. During depolarization of the distal dendritic region, sometimes a Ca2+‐dependent plateau was observed. It appears to be associated with a small conductance increase. 7. Field‐induced hyperpolarization suppressed local spiking and voltage plateaux, but remote Ca2+ spikes with reduced amplitude appeared in recordings from the proximal region. Similarly, in the distal region, low‐amplitude, remote Na+ spikes and a Na+ plateau were observed superimposed on the hyperpolarizing baseline. The Na+ plateau apparently did not contribute to shunting of membrane currents in the distal dendrite. 8. The phase characteristics of the action potentials correlate with the modulation pattern noted in our extracellular study (Chan & Nicholson, 1986). Thus, the extracellular units ("giant spikes") were probably Na+ spikes activated in the soma and spread distally. Occasionally Ca2+ spikes, with a higher threshold, might also be activated to give dual‐phase response.(ABSTRACT TRUNCATED AT 400 WORDS)

UR - http://www.scopus.com/inward/record.url?scp=0023772536&partnerID=8YFLogxK

U2 - 10.1113/jphysiol.1988.sp017232

DO - 10.1113/jphysiol.1988.sp017232

M3 - Journal article

C2 - 3236254

AN - SCOPUS:0023772536

VL - 402

SP - 751

EP - 771

JO - The Journal of Physiology

JF - The Journal of Physiology

SN - 0022-3751

IS - 1

ER -

ID: 237699919