The Effects of Essential Oils on Skin Homeostasis and Inflammation Using Human Keratinocyte HaCaT cells

Authors

    Chisato Tanaka, Ayaki Okada, Miyako Nedachi, Shinzo Noda, Naoko Takahashi-Ando Department of Applied Chemistry, Graduate School of Science and Engineering, Toyo University, Tokyo, Japan Department of Applied Chemistry, Graduate School of Science and Engineering, Toyo University, Tokyo, Japan Research Institute of Industrial Technology, Toyo University, Tokyo, Japan Aroma-Health-Tech Laboratory, Japan Department of Applied Chemistry, Graduate School of Science and Engineering, Toyo University, Tokyo, Japan; Research Institute of Industrial Technology, Toyo University, Tokyo, Japan

Keywords:

Atopic dermatitis, HaCaT, TARC, Chemokine, Patchouli

Abstract

Some essential oils used in aromatherapy are known to have antibacterial, anti-inflammatory, and/or antioxidant effects although it has not been scientifically validated. In this study, we screened essential oils with antiinflammatory effects using an in-vitro inflammation model. Inflammatory cytokines were added to the human epidermal keratinocytes HaCaT to induce the expression of inflammatory and thymus and activationregulated chemokine (CCL17/TARC). As a result, 7 of the 46 kinds of essential oils, including German chamomile and patchouli, were found to suppress IFN-γ- and TNF-α-induced TARC. Moreover, both essential oils were shown to suppress TARC induction, disregarding the countries of origin and product manufacturers. We also performed RTPCR to examine the inflammation- and skin homeostasis-related gene expression fluctuation. The expressions of inflammatory chemokines and the genes responsible for the skin barrier function, such as filaggrin, fluctuated when inflammatory cytokines were applied to HaCaT cells. Then, we examined the effect of patchouli on the expression of several genes in HaCaT cells. As a result, patchouli was found to suppress the inflammatory chemokine expression induction to some extent and modulate MLN64 and MMP2 expressions. From the above, it was strongly suggested that some essential oils may have effects to suppress skin inflammation.

References

Japanese Dermatological Association, Japanese Society of Allergology, Atopic Dermatitis Treatment Guidelines Development Committee, et al., 2018, Atopic Dermatitis Treatment Guidelines 2018. Journal of the Japanese Dermatological Association, 128(12): 2431–2502. https://doi.org/10.14924/Dermatol.128.2431

Avena-Woods C, 2017, Overview of Atopic Dermatitis. Am J Manag Care, 23 (8 Suppl): S115–S123.

Rathi SK, Kumrah L, 2011, Topical Corticosteroid-Induced Rosacea-Like Dermatitis: A Clinical Study of 110 cases.Indian J Dermatol Venereol Leprol, 77(1): 42–46. https://doi.org/10.4103/0378-6323.74974

Rapaport MJ, Lebwohl M, 2003, Corticosteroid Addiction and Withdrawal in the Atopic: The Red Burning Skin Syndrome. Clin Dermatol, 21(3): 201–214. https://doi.org/10.1016/s0738-081x(02)00365-6

Takahashi-Ando N, Jones MA, Fujisawa S, et al., 2015, Patient-Reported Outcomes after Discontinuation of Long-Term Topical Corticosteroid Treatment for Atopic Dermatitis: A Targeted Cross-Sectional Survey. Drug Healthc Patient Saf, 7: 57–62. https://doi.org/10.2147/DHPS.S78016

Brunner PM, Guttman-Yassky E, Leung DYM, 2017, The Immunology of Atopic Dermatitis and Its Reversibility with Broad-Spectrum and Targeted Therapies. J Allergy Clin Immunol, 139(4S): S65–S76. https://doi.org/10.1016/j.jaci.2017.01.011

Kataoka Y, 2014, Thymus and Activation-Regulated Chemokine as a Clinical Biomarker in Atopic Dermatitis. J Dermatol, 41(3): 221–229. https://doi.org/10.1111/1346-8138.12440

Saeki H, 2013, Biomarker of Atopic Dermatitis: Focusing on Serum TARC/CCL17 Level as Severity Marker. Japanese Journal of Allergology, 62(2): 131–137. https://doi.org/10.15036/arerugi.62.131

Yu B, Koga T, Urabe K, et al., 2002, Differential regulation of thymus- and activation-regulated chemokine induced by IL-4, IL-13, TNF-alpha and IFN-gamma in human keratinocyte and fibroblast. J Dermatol Sci, 30(1): 29–36. https://doi.org/10.1016/s0923-1811(02)00046-4

Choi JH, Jin SW, Park BH, et al., 2013, Cultivated Ginseng Inhibits 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis-Like Skin Lesions in NC/Nga Mice and TNF-α/IFN-γ-Induced TARC Activation in HaCaT cells. Food Chem Toxicol, 56: 195–203. https://doi.org/10.1016/j.fct.2013.02.037

Jeong S-J, Lim H-S, Seo C-S, et al., 2015, Traditional Herbal Formula Jakyagamcho-Tang (Paeonia lactiflora and Glycyrrhiza uralensis) Impairs Inflammatory Chemokine Production by Inhibiting Activation of STAT1 and NF-κB in HaCaT Cells. Phytomedicine, 22(2): 326–332. https://doi.org/10.1016/j.phymed.2014.12.002

Ohira T, Miyazawa M, 2016, Advanced Technologies for Terpenoids. CMC Publishing Co., Ltd., Tokyo.

Slominski AT, Zmijewski MA, Skobowiat C, et al., 2012, Sensing the Environment: Regulation of Local and Global Homeostasis by the Skin Neuroendocrine System. Adv Anat Embryol Cell Biol, 212: v–115. https://doi.org/10.1007/978-3-642-19683-6_1

Slominski A, Zbytek B, Nikolakis G, et al., 2013, Steroidogenesis in the Skin: Implications for Local Immune Functions. J Steroid Biochem Mol Biol, 137: 107–123. https://doi.org/10.1016/j.jsbmb.2013.02.006

Kikuchi H, 2009, Unlimited Potential of Liposomes and Their Application to Medical Field. Membrane, 34(6): 328–335. https://doi.org/10.5360/membrane.34.328

Akbarzadeh A, Rezaei-Sadabady R, Davaran S, et al., 2013, Liposome: Classification, Preparation, and Applications. Nanoscale Res Lett, 8(1): 102. https://doi.org/10.1186/1556-276X-8-102

Marongiu L, Donini M, Bovi M, et al., The Inclusion into PLGA Nanoparticles Enable α-Bisabolol to Efficiently Inhibit the Human Dendritic Cell Pro-Inflammatory Activity. J Nanopart Res, 16: 2254. https://doi.org/10.1007/s11051-014-2554-4

Khalesi ZB, Beiranvand SP, Bokaie M, 2019, Efficacy of Chamomile in the Treatment of Premenstrual Syndrome: A Systematic Review. J Pharmacopuncture, 22(4): 204–209. https://doi.org/10.3831/KPI.2019.22.028

Hu G, Peng C, Xie X, et al., 2017, Availability, Pharmaceutics, Security, Pharmacokinetics, and Pharmacological Activities of Patchouli Alcohol. Evid Based Complement Alternat Med, 2017: 4850612. https://doi.org/10.1155/2017/4850612

Zhang Z, Chen X, Chen H, et al., 2016, Anti-Inflammatory Activity of β-Patchoulene Isolated from Patchouli Oil in Mice. Eur J Pharmacol, 781: 229–238. https://doi.org/10.1016/j.ejphar.2016.04.028

Kee J-Y, Jeon Y-D, Kim D-S, et al., 2017, Korean Red Ginseng Improves Atopic Dermatitis-Like Skin Lesions by Suppressing Expression of Proinflammatory Cytokines and Chemokines in vivo and in vitro. J Ginseng Res, 41(2):134–143. https://doi.org/10.1016/j.jgr.2016.02.003

Seo M-D, Kang TJ, Lee CH, et al., 2012, HaCaT Keratinocytes and Primary Epidermal Keratinocytes Have Different Transcriptional Profiles of Cornified Envelope-Associated Genes to T Helper Cell Cytokines. Biomol Ther (Seoul), 20(2): 171–176. https://doi.org/10.4062/biomolther.2012.20.2.171

Cha K-J, Song C-S, Lee J-S, et al., 2019, Chaenomeles sinensis Koehne Extract Suppresses the Development of

Atopic Dermatitis-Like Lesions by Regulating Cytokine and Filaggrin Expression in NC/Nga Mice. Int J Med Sci, 16(12): 1604–1613. https://doi.org/10.7150/ijms.37854

Slominski AT, Manna PR, Tuckey RC, 2015, On the Role of Skin in the Regulation of Local and Systemic Steroidogenic Activities. Steroids, 103: 72–88. https://doi.org/10.1016/j.steroids.2015.04.006

Pham QL, Jang H-J, Kim K-B, 2017, Anti-Wrinkle Effect of Fermented Black Ginseng on Human Fibroblasts. Int J Mol Med, 39(3): 681–686. https://doi.org/10.3892/ijmm.2017.2858

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Published

2023-12-31