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Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices

U0126 (1,4-diamino-2,3-dicyano-1,4-bis (2-aminophenylthio) butadiene), a widely used mitogen-activated protein kinase kinase (MEK) inhibitor, was found to accelerate voltage-gated K(+) channel (K(V)) inactivation in heterologous cells expressing several types of K(V). The goal of this study was to e...

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Autores principales: Wang, Jin-Zhao, Long, Cheng, Li, Kai-Yuan, Xu, Hua-Tai, Yuan, Li-Lian, Wu, Gang-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995919/
https://www.ncbi.nlm.nih.gov/pubmed/29892075
http://dx.doi.org/10.1038/s41598-018-27235-1
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author Wang, Jin-Zhao
Long, Cheng
Li, Kai-Yuan
Xu, Hua-Tai
Yuan, Li-Lian
Wu, Gang-Yi
author_facet Wang, Jin-Zhao
Long, Cheng
Li, Kai-Yuan
Xu, Hua-Tai
Yuan, Li-Lian
Wu, Gang-Yi
author_sort Wang, Jin-Zhao
collection PubMed
description U0126 (1,4-diamino-2,3-dicyano-1,4-bis (2-aminophenylthio) butadiene), a widely used mitogen-activated protein kinase kinase (MEK) inhibitor, was found to accelerate voltage-gated K(+) channel (K(V)) inactivation in heterologous cells expressing several types of K(V). The goal of this study was to examine whether U0126 at a concentration thought to specifically inhibit MEK signaling also inhibits K(V) in native neurons of primary cultures or brain slices. U0126 caused a dose-dependent inhibition of both the transient (I(A)) and sustained (I(DR)) components of K(+) currents in hippocampal neurons. U0126 also exhibited much higher potency on the I(A) and I(DR) than the classical K(V) blockers 4-aminopyridine (4-AP) and tetraethylammonium (TEA). Consistent with its inhibitory effect on K(V), U0126 broadened action potential duration, profoundly affected the repolarizing phase, and dramatically reduced firing frequency in response to current pulse injections. Despite the potent and reversible action of U0126 on K(v) channels, PD98059, a structurally-unrelated MEK inhibitor, did not induce such an effect, suggesting U0126 may act independently of MEK inhibition. Together, these results raise cautions for using U0126 as a specific inhibitor for studying MEK signaling in neurons; on the other hand, further studies on the blocking mechanisms of U0126 as a potent inhibitor of K(V) may provide useful insights into the structure-function relationship of K(V) in general.
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spelling pubmed-59959192018-06-21 Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices Wang, Jin-Zhao Long, Cheng Li, Kai-Yuan Xu, Hua-Tai Yuan, Li-Lian Wu, Gang-Yi Sci Rep Article U0126 (1,4-diamino-2,3-dicyano-1,4-bis (2-aminophenylthio) butadiene), a widely used mitogen-activated protein kinase kinase (MEK) inhibitor, was found to accelerate voltage-gated K(+) channel (K(V)) inactivation in heterologous cells expressing several types of K(V). The goal of this study was to examine whether U0126 at a concentration thought to specifically inhibit MEK signaling also inhibits K(V) in native neurons of primary cultures or brain slices. U0126 caused a dose-dependent inhibition of both the transient (I(A)) and sustained (I(DR)) components of K(+) currents in hippocampal neurons. U0126 also exhibited much higher potency on the I(A) and I(DR) than the classical K(V) blockers 4-aminopyridine (4-AP) and tetraethylammonium (TEA). Consistent with its inhibitory effect on K(V), U0126 broadened action potential duration, profoundly affected the repolarizing phase, and dramatically reduced firing frequency in response to current pulse injections. Despite the potent and reversible action of U0126 on K(v) channels, PD98059, a structurally-unrelated MEK inhibitor, did not induce such an effect, suggesting U0126 may act independently of MEK inhibition. Together, these results raise cautions for using U0126 as a specific inhibitor for studying MEK signaling in neurons; on the other hand, further studies on the blocking mechanisms of U0126 as a potent inhibitor of K(V) may provide useful insights into the structure-function relationship of K(V) in general. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995919/ /pubmed/29892075 http://dx.doi.org/10.1038/s41598-018-27235-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wang, Jin-Zhao
Long, Cheng
Li, Kai-Yuan
Xu, Hua-Tai
Yuan, Li-Lian
Wu, Gang-Yi
Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices
title Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices
title_full Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices
title_fullStr Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices
title_full_unstemmed Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices
title_short Potent block of potassium channels by MEK inhibitor U0126 in primary cultures and brain slices
title_sort potent block of potassium channels by mek inhibitor u0126 in primary cultures and brain slices
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995919/
https://www.ncbi.nlm.nih.gov/pubmed/29892075
http://dx.doi.org/10.1038/s41598-018-27235-1
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