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Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase

BACKGROUND: Essential oils (EOs), derived from aromatic plants, exhibit properties beneficial to health, such as anti-inflammatory, anti-oxidative, antidiabetic, and antiaging effects. However, the effect of EOs and their interaction in binary combinations against tyrosinase is not yet known. OBJECT...

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Autores principales: You, Zonglin, Li, Yonglian, Chen, Min, Wong, Vincent Kam Wai, Zhang, Kun, Zheng, Xi, Liu, Wenfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Open Academia 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793764/
https://www.ncbi.nlm.nih.gov/pubmed/36590855
http://dx.doi.org/10.29219/fnr.v66.8466
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author You, Zonglin
Li, Yonglian
Chen, Min
Wong, Vincent Kam Wai
Zhang, Kun
Zheng, Xi
Liu, Wenfeng
author_facet You, Zonglin
Li, Yonglian
Chen, Min
Wong, Vincent Kam Wai
Zhang, Kun
Zheng, Xi
Liu, Wenfeng
author_sort You, Zonglin
collection PubMed
description BACKGROUND: Essential oils (EOs), derived from aromatic plants, exhibit properties beneficial to health, such as anti-inflammatory, anti-oxidative, antidiabetic, and antiaging effects. However, the effect of EOs and their interaction in binary combinations against tyrosinase is not yet known. OBJECTIVE: To evaluate the underlying mechanisms of EOs and their interaction in binary combinations against tyrosinas. DESIGN: We explored to investigate the inhibitory effect of 65 EOs and the interaction among cinnamon, bay, and magnolia officinalis in their binary combinations against tyrosinase. In addition, the main constituents of cinnamon, bay, and magnolia officinalis were analyzed by gas chromatography–mass spectrometry (GC–MS). RESULTS: The results showed that the most potent EOs against tyrosinase were cinnamon, bay, and magnolia officinalis with IC(50) values of 25.7, 30.8, and 61.9 μg/mL, respectively. Moreover, the inhibitory mechanism and kinetics studies revealed that cinnamon and bay were reversible and competitive-type inhibitors, and magnolia officinalis was a reversible and mixed-type inhibitor. In addition, these results, assessed in mixtures of three binary combinations, indicated that the combination of cinnamon with bay at different dose and at dose ratio had a strong antagonistic effect against tyrosinase. Magnolia officinalis combined with cinnamon or bay experienced both antagonistic and synergistic effect in anti-tyrosinase activity. CONCLUSION: It is revealed that natural EOs would be promising to be effective anti-tyrosinase agents, and binary combinations of cinnamon, bay, and magnolia officinalis might not have synergistic effects on tyrosinase under certain condition.
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spelling pubmed-97937642022-12-29 Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase You, Zonglin Li, Yonglian Chen, Min Wong, Vincent Kam Wai Zhang, Kun Zheng, Xi Liu, Wenfeng Food Nutr Res Original Article BACKGROUND: Essential oils (EOs), derived from aromatic plants, exhibit properties beneficial to health, such as anti-inflammatory, anti-oxidative, antidiabetic, and antiaging effects. However, the effect of EOs and their interaction in binary combinations against tyrosinase is not yet known. OBJECTIVE: To evaluate the underlying mechanisms of EOs and their interaction in binary combinations against tyrosinas. DESIGN: We explored to investigate the inhibitory effect of 65 EOs and the interaction among cinnamon, bay, and magnolia officinalis in their binary combinations against tyrosinase. In addition, the main constituents of cinnamon, bay, and magnolia officinalis were analyzed by gas chromatography–mass spectrometry (GC–MS). RESULTS: The results showed that the most potent EOs against tyrosinase were cinnamon, bay, and magnolia officinalis with IC(50) values of 25.7, 30.8, and 61.9 μg/mL, respectively. Moreover, the inhibitory mechanism and kinetics studies revealed that cinnamon and bay were reversible and competitive-type inhibitors, and magnolia officinalis was a reversible and mixed-type inhibitor. In addition, these results, assessed in mixtures of three binary combinations, indicated that the combination of cinnamon with bay at different dose and at dose ratio had a strong antagonistic effect against tyrosinase. Magnolia officinalis combined with cinnamon or bay experienced both antagonistic and synergistic effect in anti-tyrosinase activity. CONCLUSION: It is revealed that natural EOs would be promising to be effective anti-tyrosinase agents, and binary combinations of cinnamon, bay, and magnolia officinalis might not have synergistic effects on tyrosinase under certain condition. Open Academia 2022-12-27 /pmc/articles/PMC9793764/ /pubmed/36590855 http://dx.doi.org/10.29219/fnr.v66.8466 Text en © 2022 Zonglin You et al. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 International License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
spellingShingle Original Article
You, Zonglin
Li, Yonglian
Chen, Min
Wong, Vincent Kam Wai
Zhang, Kun
Zheng, Xi
Liu, Wenfeng
Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
title Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
title_full Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
title_fullStr Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
title_full_unstemmed Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
title_short Inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
title_sort inhibition of plant essential oils and their interaction in binary combinations against tyrosinase
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793764/
https://www.ncbi.nlm.nih.gov/pubmed/36590855
http://dx.doi.org/10.29219/fnr.v66.8466
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