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Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons

The effects of acidic pH on several voltage-dependent ion channels, such as voltage-dependent K(+) and Ca(2+) channels, and hyperpolarization-gated and cyclic nucleotide-activated cation (HCN) channels, were examined using a whole-cell patch clamp technique on mechanically isolated rat mesencephalic...

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Autores principales: Han, Jin-Eon, Cho, Jin-Hwa, Choi, In-Sun, Kim, Do-Yeon, Jang, Il-Sung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343055/
https://www.ncbi.nlm.nih.gov/pubmed/28280415
http://dx.doi.org/10.4196/kjpp.2017.21.2.215
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author Han, Jin-Eon
Cho, Jin-Hwa
Choi, In-Sun
Kim, Do-Yeon
Jang, Il-Sung
author_facet Han, Jin-Eon
Cho, Jin-Hwa
Choi, In-Sun
Kim, Do-Yeon
Jang, Il-Sung
author_sort Han, Jin-Eon
collection PubMed
description The effects of acidic pH on several voltage-dependent ion channels, such as voltage-dependent K(+) and Ca(2+) channels, and hyperpolarization-gated and cyclic nucleotide-activated cation (HCN) channels, were examined using a whole-cell patch clamp technique on mechanically isolated rat mesencephalic trigeminal nucleus neurons. The application of a pH 6.5 solution had no effect on the peak amplitude of voltage-dependent K(+) currents. A pH 6.0 solution slightly, but significantly inhibited the peak amplitude of voltage-dependent K(+) currents. The pH 6.0 also shifted both the current-voltage and conductance-voltage relationships to the depolarization range. The application of a pH 6.5 solution scarcely affected the peak amplitude of membrane currents mediated by HCN channels, which were profoundly inhibited by the general HCN channel blocker Cs(+) (1 mM). However, the pH 6.0 solution slightly, but significantly inhibited the peak amplitude of HCN-mediated currents. Although the pH 6.0 solution showed complex modulation of the current-voltage and conductance-voltage relationships, the midpoint voltages for the activation of HCN channels were not changed by acidic pH. On the other hand, voltage-dependent Ca(2+) channels were significantly inhibited by an acidic pH. The application of an acidic pH solution significantly shifted the current-voltage and conductance-voltage relationships to the depolarization range. The modulation of several voltage-dependent ion channels by an acidic pH might affect the excitability of mesencephalic trigeminal nucleus neurons, and thus physiological functions mediated by the mesencephalic trigeminal nucleus could be affected in acidic pH conditions.
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spelling pubmed-53430552017-03-09 Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons Han, Jin-Eon Cho, Jin-Hwa Choi, In-Sun Kim, Do-Yeon Jang, Il-Sung Korean J Physiol Pharmacol Original Article The effects of acidic pH on several voltage-dependent ion channels, such as voltage-dependent K(+) and Ca(2+) channels, and hyperpolarization-gated and cyclic nucleotide-activated cation (HCN) channels, were examined using a whole-cell patch clamp technique on mechanically isolated rat mesencephalic trigeminal nucleus neurons. The application of a pH 6.5 solution had no effect on the peak amplitude of voltage-dependent K(+) currents. A pH 6.0 solution slightly, but significantly inhibited the peak amplitude of voltage-dependent K(+) currents. The pH 6.0 also shifted both the current-voltage and conductance-voltage relationships to the depolarization range. The application of a pH 6.5 solution scarcely affected the peak amplitude of membrane currents mediated by HCN channels, which were profoundly inhibited by the general HCN channel blocker Cs(+) (1 mM). However, the pH 6.0 solution slightly, but significantly inhibited the peak amplitude of HCN-mediated currents. Although the pH 6.0 solution showed complex modulation of the current-voltage and conductance-voltage relationships, the midpoint voltages for the activation of HCN channels were not changed by acidic pH. On the other hand, voltage-dependent Ca(2+) channels were significantly inhibited by an acidic pH. The application of an acidic pH solution significantly shifted the current-voltage and conductance-voltage relationships to the depolarization range. The modulation of several voltage-dependent ion channels by an acidic pH might affect the excitability of mesencephalic trigeminal nucleus neurons, and thus physiological functions mediated by the mesencephalic trigeminal nucleus could be affected in acidic pH conditions. The Korean Physiological Society and The Korean Society of Pharmacology 2017-03 2017-02-21 /pmc/articles/PMC5343055/ /pubmed/28280415 http://dx.doi.org/10.4196/kjpp.2017.21.2.215 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Han, Jin-Eon
Cho, Jin-Hwa
Choi, In-Sun
Kim, Do-Yeon
Jang, Il-Sung
Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
title Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
title_full Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
title_fullStr Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
title_full_unstemmed Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
title_short Effects of acidic pH on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
title_sort effects of acidic ph on voltage-gated ion channels in rat trigeminal mesencephalic nucleus neurons
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343055/
https://www.ncbi.nlm.nih.gov/pubmed/28280415
http://dx.doi.org/10.4196/kjpp.2017.21.2.215
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