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Natural products modulating the hERG channel: heartaches and hope
Covering: 1996–December 2016 The human Ether-à-go-go Related Gene (hERG) channel is a voltage-gated potassium channel playing an essential role in the normal electrical activity in the heart. It is involved in the repolarization and termination of action potentials in excitable cardiac cells. Mutati...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708533/ https://www.ncbi.nlm.nih.gov/pubmed/28497823 http://dx.doi.org/10.1039/c7np00014f |
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author | Kratz, Jadel M. Grienke, Ulrike Scheel, Olaf Mann, Stefan A. Rollinger, Judith M. |
author_facet | Kratz, Jadel M. Grienke, Ulrike Scheel, Olaf Mann, Stefan A. Rollinger, Judith M. |
author_sort | Kratz, Jadel M. |
collection | PubMed |
description | Covering: 1996–December 2016 The human Ether-à-go-go Related Gene (hERG) channel is a voltage-gated potassium channel playing an essential role in the normal electrical activity in the heart. It is involved in the repolarization and termination of action potentials in excitable cardiac cells. Mutations in the hERG gene and hERG channel blockage by small molecules are associated with increased risk of fatal arrhythmias. Several drugs have been withdrawn from the market due to hERG channel-related cardiotoxicity. Moreover, as a result of its notorious ligand promiscuity, this ion channel has emerged as an important antitarget in early drug discovery and development. Surprisingly, the hERG channel blocking profile of natural compounds present in frequently consumed botanicals (i.e. dietary supplements, spices, and herbal medicinal products) is not routinely assessed. This comprehensive review will address these issues and provide a critical compilation of hERG channel data for isolated natural products and extracts over the past two decades (1996–2016). In addition, the review will provide (i) a solid basis for the molecular understanding of the physiological functions of the hERG channel, (ii) the translational potential of in vitro/in vivo results to cardiotoxicity in humans, (iii) approaches for the identification of hERG channel blockers from natural sources, (iv) future perspectives for cardiac safety guidelines and their applications within phytopharmaceuticals and dietary supplements, and (v) novel applications of hERG channel modulation (e.g. as a drug target). |
format | Online Article Text |
id | pubmed-5708533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-57085332018-01-05 Natural products modulating the hERG channel: heartaches and hope Kratz, Jadel M. Grienke, Ulrike Scheel, Olaf Mann, Stefan A. Rollinger, Judith M. Nat Prod Rep Chemistry Covering: 1996–December 2016 The human Ether-à-go-go Related Gene (hERG) channel is a voltage-gated potassium channel playing an essential role in the normal electrical activity in the heart. It is involved in the repolarization and termination of action potentials in excitable cardiac cells. Mutations in the hERG gene and hERG channel blockage by small molecules are associated with increased risk of fatal arrhythmias. Several drugs have been withdrawn from the market due to hERG channel-related cardiotoxicity. Moreover, as a result of its notorious ligand promiscuity, this ion channel has emerged as an important antitarget in early drug discovery and development. Surprisingly, the hERG channel blocking profile of natural compounds present in frequently consumed botanicals (i.e. dietary supplements, spices, and herbal medicinal products) is not routinely assessed. This comprehensive review will address these issues and provide a critical compilation of hERG channel data for isolated natural products and extracts over the past two decades (1996–2016). In addition, the review will provide (i) a solid basis for the molecular understanding of the physiological functions of the hERG channel, (ii) the translational potential of in vitro/in vivo results to cardiotoxicity in humans, (iii) approaches for the identification of hERG channel blockers from natural sources, (iv) future perspectives for cardiac safety guidelines and their applications within phytopharmaceuticals and dietary supplements, and (v) novel applications of hERG channel modulation (e.g. as a drug target). Royal Society of Chemistry 2017-08-01 2017-05-12 /pmc/articles/PMC5708533/ /pubmed/28497823 http://dx.doi.org/10.1039/c7np00014f Text en This journal is © The Royal Society of Chemistry 2017 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Kratz, Jadel M. Grienke, Ulrike Scheel, Olaf Mann, Stefan A. Rollinger, Judith M. Natural products modulating the hERG channel: heartaches and hope |
title | Natural products modulating the hERG channel: heartaches and hope
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title_full | Natural products modulating the hERG channel: heartaches and hope
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title_fullStr | Natural products modulating the hERG channel: heartaches and hope
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title_full_unstemmed | Natural products modulating the hERG channel: heartaches and hope
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title_short | Natural products modulating the hERG channel: heartaches and hope
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title_sort | natural products modulating the herg channel: heartaches and hope |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708533/ https://www.ncbi.nlm.nih.gov/pubmed/28497823 http://dx.doi.org/10.1039/c7np00014f |
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