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Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells

Research on the biological effects of essential oils on human skin cells is scarce. In the current study, we primarily explored the biological activities of 10 essential oils (nine single and one blend) in a pre-inflamed human dermal fibroblast system that simulated chronic inflammation. We measured...

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Autores principales: Han, Xuesheng, Beaumont, Cody, Stevens, Nicole
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805555/
https://www.ncbi.nlm.nih.gov/pubmed/29450150
http://dx.doi.org/10.1016/j.biopen.2017.04.001
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author Han, Xuesheng
Beaumont, Cody
Stevens, Nicole
author_facet Han, Xuesheng
Beaumont, Cody
Stevens, Nicole
author_sort Han, Xuesheng
collection PubMed
description Research on the biological effects of essential oils on human skin cells is scarce. In the current study, we primarily explored the biological activities of 10 essential oils (nine single and one blend) in a pre-inflamed human dermal fibroblast system that simulated chronic inflammation. We measured levels of proteins critical for inflammation, immune responses, and tissue-remodeling processes. The nine single oils were distilled from Citrus bergamia (bergamot), Coriandrum sativum (cilantro), Pelargonium graveolens (geranium), Helichrysum italicum (helichrysum), Pogostemon cablin (patchouli), Citrus aurantium (petitgrain), Santalum album (sandalwood), Nardostachys jatamansi (spikenard), and Cananga odorata (ylang ylang). The essential oil blend (commercial name Immortelle) is composed of oils from frankincense, Hawaiian sandalwood, lavender, myrrh, helichrysum, and rose. All the studied oils were significantly anti-proliferative against these cells. Furthermore, bergamot, cilantro, and spikenard essential oils primarily inhibited protein molecules related to inflammation, immune responses, and tissue-remodeling processes, suggesting they have anti-inflammatory and wound healing properties. Helichrysum and ylang ylang essential oils, as well as Immortelle primarily inhibited tissue remodeling-related proteins, suggesting a wound healing property. The data are consistent with the results of existing studies examining these oils in other models and suggest that the studied oils may be promising therapeutic candidates. Further research into their biological mechanisms of action is recommended. The differential effects of these essential oils suggest that they exert activities by different mechanisms or pathways, warranting further investigation. The chemical composition of these oils was analyzed using gas chromatography–mass spectrometry.
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spelling pubmed-58055552018-02-15 Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells Han, Xuesheng Beaumont, Cody Stevens, Nicole Biochim Open Short communication Research on the biological effects of essential oils on human skin cells is scarce. In the current study, we primarily explored the biological activities of 10 essential oils (nine single and one blend) in a pre-inflamed human dermal fibroblast system that simulated chronic inflammation. We measured levels of proteins critical for inflammation, immune responses, and tissue-remodeling processes. The nine single oils were distilled from Citrus bergamia (bergamot), Coriandrum sativum (cilantro), Pelargonium graveolens (geranium), Helichrysum italicum (helichrysum), Pogostemon cablin (patchouli), Citrus aurantium (petitgrain), Santalum album (sandalwood), Nardostachys jatamansi (spikenard), and Cananga odorata (ylang ylang). The essential oil blend (commercial name Immortelle) is composed of oils from frankincense, Hawaiian sandalwood, lavender, myrrh, helichrysum, and rose. All the studied oils were significantly anti-proliferative against these cells. Furthermore, bergamot, cilantro, and spikenard essential oils primarily inhibited protein molecules related to inflammation, immune responses, and tissue-remodeling processes, suggesting they have anti-inflammatory and wound healing properties. Helichrysum and ylang ylang essential oils, as well as Immortelle primarily inhibited tissue remodeling-related proteins, suggesting a wound healing property. The data are consistent with the results of existing studies examining these oils in other models and suggest that the studied oils may be promising therapeutic candidates. Further research into their biological mechanisms of action is recommended. The differential effects of these essential oils suggest that they exert activities by different mechanisms or pathways, warranting further investigation. The chemical composition of these oils was analyzed using gas chromatography–mass spectrometry. Elsevier 2017-04-26 /pmc/articles/PMC5805555/ /pubmed/29450150 http://dx.doi.org/10.1016/j.biopen.2017.04.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Short communication
Han, Xuesheng
Beaumont, Cody
Stevens, Nicole
Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
title Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
title_full Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
title_fullStr Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
title_full_unstemmed Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
title_short Chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
title_sort chemical composition analysis and in vitro biological activities of ten essential oils in human skin cells
topic Short communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805555/
https://www.ncbi.nlm.nih.gov/pubmed/29450150
http://dx.doi.org/10.1016/j.biopen.2017.04.001
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