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Drugs acting at TRPM7 channels inhibit seizure‐like activity

Transient receptor potential cation subfamily M7 (TRPM7) channels are ion channels permeable to divalent cations. They are abundantly expressed with particularly high expression in the brain. Previous studies have highlighted the importance of TRPM7 channels in brain diseases such as stroke and trau...

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Detalles Bibliográficos
Autores principales: Khalil, Aytakin, Shekh‐Ahmad, Tawfeeq, Kovac, Stjepana, Wykes, Robert C., Horgen, F. David, Fleig, Andrea, Walker, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472385/
https://www.ncbi.nlm.nih.gov/pubmed/37328275
http://dx.doi.org/10.1002/epi4.12773
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author Khalil, Aytakin
Shekh‐Ahmad, Tawfeeq
Kovac, Stjepana
Wykes, Robert C.
Horgen, F. David
Fleig, Andrea
Walker, Matthew C.
author_facet Khalil, Aytakin
Shekh‐Ahmad, Tawfeeq
Kovac, Stjepana
Wykes, Robert C.
Horgen, F. David
Fleig, Andrea
Walker, Matthew C.
author_sort Khalil, Aytakin
collection PubMed
description Transient receptor potential cation subfamily M7 (TRPM7) channels are ion channels permeable to divalent cations. They are abundantly expressed with particularly high expression in the brain. Previous studies have highlighted the importance of TRPM7 channels in brain diseases such as stroke and traumatic brain injury, yet evidence for a role in seizures and epilepsy is lacking. Here, we show that carvacrol, a food additive that inhibits TRPM7 channels, and waixenicin A, a novel selective and potent TRPM7 inhibitor, completely suppressed seizure‐like activity in rodent hippocampal‐entorhinal brain slices exposed to pentylenetetrazole or low magnesium. These findings support inhibition of TRPM7 channels as a novel target for antiseizure medications.
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spelling pubmed-104723852023-09-02 Drugs acting at TRPM7 channels inhibit seizure‐like activity Khalil, Aytakin Shekh‐Ahmad, Tawfeeq Kovac, Stjepana Wykes, Robert C. Horgen, F. David Fleig, Andrea Walker, Matthew C. Epilepsia Open Short Research Articles Transient receptor potential cation subfamily M7 (TRPM7) channels are ion channels permeable to divalent cations. They are abundantly expressed with particularly high expression in the brain. Previous studies have highlighted the importance of TRPM7 channels in brain diseases such as stroke and traumatic brain injury, yet evidence for a role in seizures and epilepsy is lacking. Here, we show that carvacrol, a food additive that inhibits TRPM7 channels, and waixenicin A, a novel selective and potent TRPM7 inhibitor, completely suppressed seizure‐like activity in rodent hippocampal‐entorhinal brain slices exposed to pentylenetetrazole or low magnesium. These findings support inhibition of TRPM7 channels as a novel target for antiseizure medications. John Wiley and Sons Inc. 2023-06-20 /pmc/articles/PMC10472385/ /pubmed/37328275 http://dx.doi.org/10.1002/epi4.12773 Text en © 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Research Articles
Khalil, Aytakin
Shekh‐Ahmad, Tawfeeq
Kovac, Stjepana
Wykes, Robert C.
Horgen, F. David
Fleig, Andrea
Walker, Matthew C.
Drugs acting at TRPM7 channels inhibit seizure‐like activity
title Drugs acting at TRPM7 channels inhibit seizure‐like activity
title_full Drugs acting at TRPM7 channels inhibit seizure‐like activity
title_fullStr Drugs acting at TRPM7 channels inhibit seizure‐like activity
title_full_unstemmed Drugs acting at TRPM7 channels inhibit seizure‐like activity
title_short Drugs acting at TRPM7 channels inhibit seizure‐like activity
title_sort drugs acting at trpm7 channels inhibit seizure‐like activity
topic Short Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472385/
https://www.ncbi.nlm.nih.gov/pubmed/37328275
http://dx.doi.org/10.1002/epi4.12773
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