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Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels
Recent clinical data support the clinical use of oral lavender oil in patients suffering from subsyndromal anxiety. We identified the molecular mechanism of action that will alter the perception of lavender oil as a nonspecific ingredient of aromatherapy to a potent anxiolytic inhibiting voltage dep...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639265/ https://www.ncbi.nlm.nih.gov/pubmed/23637742 http://dx.doi.org/10.1371/journal.pone.0059998 |
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author | Schuwald, Anita M. Nöldner, Michael Wilmes, Thomas Klugbauer, Norbert Leuner, Kristina Müller, Walter E. |
author_facet | Schuwald, Anita M. Nöldner, Michael Wilmes, Thomas Klugbauer, Norbert Leuner, Kristina Müller, Walter E. |
author_sort | Schuwald, Anita M. |
collection | PubMed |
description | Recent clinical data support the clinical use of oral lavender oil in patients suffering from subsyndromal anxiety. We identified the molecular mechanism of action that will alter the perception of lavender oil as a nonspecific ingredient of aromatherapy to a potent anxiolytic inhibiting voltage dependent calcium channels (VOCCs) as highly selective drug target. In contrast to previous publications where exorbitant high concentrations were used, the effects of lavender oil in behavioral, biochemical, and electrophysiological experiments were investigated in physiological concentrations in the nanomolar range, which correlate to a single dosage of 80 mg/d in humans that was used in clinical trials. We show for the first time that lavender oil bears some similarities with the established anxiolytic pregabalin. Lavender oil inhibits VOCCs in synaptosomes, primary hippocampal neurons and stably overexpressing cell lines in the same range such as pregabalin. Interestingly, Silexan does not primarily bind to P/Q type calcium channels such as pregabalin and does not interact with the binding site of pregabalin, the α2δ subunit of VOCCs. Lavender oil reduces non-selectively the calcium influx through several different types of VOCCs such as the N-type, P/Q-type and T-type VOCCs. In the hippocampus, one brain region important for anxiety disorders, we show that inhibition by lavender oil is mainly mediated via N-type and P/Q-type VOCCs. Taken together, we provide a pharmacological and molecular rationale for the clinical use of the oral application of lavender oil in patients suffering from anxiety. |
format | Online Article Text |
id | pubmed-3639265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36392652013-05-01 Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels Schuwald, Anita M. Nöldner, Michael Wilmes, Thomas Klugbauer, Norbert Leuner, Kristina Müller, Walter E. PLoS One Research Article Recent clinical data support the clinical use of oral lavender oil in patients suffering from subsyndromal anxiety. We identified the molecular mechanism of action that will alter the perception of lavender oil as a nonspecific ingredient of aromatherapy to a potent anxiolytic inhibiting voltage dependent calcium channels (VOCCs) as highly selective drug target. In contrast to previous publications where exorbitant high concentrations were used, the effects of lavender oil in behavioral, biochemical, and electrophysiological experiments were investigated in physiological concentrations in the nanomolar range, which correlate to a single dosage of 80 mg/d in humans that was used in clinical trials. We show for the first time that lavender oil bears some similarities with the established anxiolytic pregabalin. Lavender oil inhibits VOCCs in synaptosomes, primary hippocampal neurons and stably overexpressing cell lines in the same range such as pregabalin. Interestingly, Silexan does not primarily bind to P/Q type calcium channels such as pregabalin and does not interact with the binding site of pregabalin, the α2δ subunit of VOCCs. Lavender oil reduces non-selectively the calcium influx through several different types of VOCCs such as the N-type, P/Q-type and T-type VOCCs. In the hippocampus, one brain region important for anxiety disorders, we show that inhibition by lavender oil is mainly mediated via N-type and P/Q-type VOCCs. Taken together, we provide a pharmacological and molecular rationale for the clinical use of the oral application of lavender oil in patients suffering from anxiety. Public Library of Science 2013-04-29 /pmc/articles/PMC3639265/ /pubmed/23637742 http://dx.doi.org/10.1371/journal.pone.0059998 Text en © 2013 Schuwald et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schuwald, Anita M. Nöldner, Michael Wilmes, Thomas Klugbauer, Norbert Leuner, Kristina Müller, Walter E. Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels |
title | Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels |
title_full | Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels |
title_fullStr | Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels |
title_full_unstemmed | Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels |
title_short | Lavender Oil-Potent Anxiolytic Properties via Modulating Voltage Dependent Calcium Channels |
title_sort | lavender oil-potent anxiolytic properties via modulating voltage dependent calcium channels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639265/ https://www.ncbi.nlm.nih.gov/pubmed/23637742 http://dx.doi.org/10.1371/journal.pone.0059998 |
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