Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition

Abstract Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by immune dysregulation and excessive cytokine production. This study aimed to explore the potential of Camellia sinensis L. water extract (CSE) as a treatment for AD by the impact of CSE on inflammatory responses i...

Full description

Saved in:
Bibliographic Details
Main Authors: Min Jung Kim, Ye Jin Yang, Ga-Yul Min, Ji Woong Heo, Jae Dong Son, Young Zoo You, Hun Hwan Kim, Gon Sup Kim, Hu-Jang Lee, Ju-Hye Yang, Kwang Il Park
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-025-86678-5
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832594810126467072
author Min Jung Kim
Ye Jin Yang
Ga-Yul Min
Ji Woong Heo
Jae Dong Son
Young Zoo You
Hun Hwan Kim
Gon Sup Kim
Hu-Jang Lee
Ju-Hye Yang
Kwang Il Park
author_facet Min Jung Kim
Ye Jin Yang
Ga-Yul Min
Ji Woong Heo
Jae Dong Son
Young Zoo You
Hun Hwan Kim
Gon Sup Kim
Hu-Jang Lee
Ju-Hye Yang
Kwang Il Park
author_sort Min Jung Kim
collection DOAJ
description Abstract Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by immune dysregulation and excessive cytokine production. This study aimed to explore the potential of Camellia sinensis L. water extract (CSE) as a treatment for AD by the impact of CSE on inflammatory responses in keratinocytes, particularly concerning the production of inflammatory cytokines and the modulation of signaling pathways relevant to AD pathogenesis. CSE was obtained via hot water extraction from Camellia sinensis L. Ultra-high-performance liquid chromatography (UPLC) analyzed catechin and caffeine content. Cell viability was assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), polyphenol and flavonoid content were determined. 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay measured antioxidant activity. Enzyme-Linked Immunosorbent Assay (ELISA), western blotting, and Immunofluorescence (IF) assays examined cytokines, pathways, and protein localization, respectively. Molecular docking assessed compound binding with inflammation-related proteins. UPLC identified six CSE components including epigallocatechin (EGC) epicatechin (EC), caffeine (CF), catechin (C), epigallocatechin gallate (EGCG), and epicatechin gallate (ECG). CSE demonstrated a significant reduction in the production of inflammatory cytokines interleukin (IL)-2 and IL-6 in TNF-α/IFN-γ activated keratinocytes. Treatment with CSE inhibited the mitogen-activated protein kinase (MAPK) pathway, which resulted in decreased phosphorylation of p38, Jun N-terminal kinase (JNK), and extracellular signal-regulated kinase (ERK). Exposure of TNF-α/IFN-γ- stimulated human keratinocytes (HaCaT) cells to CSE resulted in a 200 µg/mL dependent inhibition of p65 and signal transducer and activator of transcription 1 (STAT-1) translocation from the cytosol to the nucleus, as confirmed through immunofluorescence (IF) staining. Molecular docking simulations provided insights into the underlying mechanisms of CSE action, which supported its potential as a therapeutic agent for AD. CSE might be a potential candidate for its therapeutic efficacy for inflammatory skin conditions like AD. Thus, based on this evidence, the authors suggest that CSE should be studied further for its anti-inflammatory activities and topical application in the treatment of AD.
format Article
id doaj-art-11bb27c01aee4332b0ad403740033944
institution Kabale University
issn 2045-2322
language English
publishDate 2025-01-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj-art-11bb27c01aee4332b0ad4037400339442025-01-19T12:18:46ZengNature PortfolioScientific Reports2045-23222025-01-0115111410.1038/s41598-025-86678-5Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibitionMin Jung Kim0Ye Jin Yang1Ga-Yul Min2Ji Woong Heo3Jae Dong Son4Young Zoo You5Hun Hwan Kim6Gon Sup Kim7Hu-Jang Lee8Ju-Hye Yang9Kwang Il Park10Department of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityKorean Medicine (KM) Application Center, Korea Institute of Oriental MedicineDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityKorean Medicine (KM) Application Center, Korea Institute of Oriental MedicineDepartment of Veterinary Physiology, College of Veterinary Medicine, Gyeongsang National UniversityAbstract Atopic dermatitis (AD) is a chronic inflammatory skin disease characterized by immune dysregulation and excessive cytokine production. This study aimed to explore the potential of Camellia sinensis L. water extract (CSE) as a treatment for AD by the impact of CSE on inflammatory responses in keratinocytes, particularly concerning the production of inflammatory cytokines and the modulation of signaling pathways relevant to AD pathogenesis. CSE was obtained via hot water extraction from Camellia sinensis L. Ultra-high-performance liquid chromatography (UPLC) analyzed catechin and caffeine content. Cell viability was assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), polyphenol and flavonoid content were determined. 2,2-diphenyl-1-picrylhydrazyl (DPPH) assay measured antioxidant activity. Enzyme-Linked Immunosorbent Assay (ELISA), western blotting, and Immunofluorescence (IF) assays examined cytokines, pathways, and protein localization, respectively. Molecular docking assessed compound binding with inflammation-related proteins. UPLC identified six CSE components including epigallocatechin (EGC) epicatechin (EC), caffeine (CF), catechin (C), epigallocatechin gallate (EGCG), and epicatechin gallate (ECG). CSE demonstrated a significant reduction in the production of inflammatory cytokines interleukin (IL)-2 and IL-6 in TNF-α/IFN-γ activated keratinocytes. Treatment with CSE inhibited the mitogen-activated protein kinase (MAPK) pathway, which resulted in decreased phosphorylation of p38, Jun N-terminal kinase (JNK), and extracellular signal-regulated kinase (ERK). Exposure of TNF-α/IFN-γ- stimulated human keratinocytes (HaCaT) cells to CSE resulted in a 200 µg/mL dependent inhibition of p65 and signal transducer and activator of transcription 1 (STAT-1) translocation from the cytosol to the nucleus, as confirmed through immunofluorescence (IF) staining. Molecular docking simulations provided insights into the underlying mechanisms of CSE action, which supported its potential as a therapeutic agent for AD. CSE might be a potential candidate for its therapeutic efficacy for inflammatory skin conditions like AD. Thus, based on this evidence, the authors suggest that CSE should be studied further for its anti-inflammatory activities and topical application in the treatment of AD.https://doi.org/10.1038/s41598-025-86678-5Anti-inflammationAntioxidantAtopic dermatitisCamellia sinensis L.Ultra performance liquid chromatography
spellingShingle Min Jung Kim
Ye Jin Yang
Ga-Yul Min
Ji Woong Heo
Jae Dong Son
Young Zoo You
Hun Hwan Kim
Gon Sup Kim
Hu-Jang Lee
Ju-Hye Yang
Kwang Il Park
Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition
Scientific Reports
Anti-inflammation
Antioxidant
Atopic dermatitis
Camellia sinensis L.
Ultra performance liquid chromatography
title Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition
title_full Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition
title_fullStr Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition
title_full_unstemmed Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition
title_short Anti-inflammatory and antioxidant properties of Camellia sinensis L. extract as a potential therapeutic for atopic dermatitis through NF-κB pathway inhibition
title_sort anti inflammatory and antioxidant properties of camellia sinensis l extract as a potential therapeutic for atopic dermatitis through nf κb pathway inhibition
topic Anti-inflammation
Antioxidant
Atopic dermatitis
Camellia sinensis L.
Ultra performance liquid chromatography
url https://doi.org/10.1038/s41598-025-86678-5
work_keys_str_mv AT minjungkim antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT yejinyang antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT gayulmin antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT jiwoongheo antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT jaedongson antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT youngzooyou antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT hunhwankim antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT gonsupkim antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT hujanglee antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT juhyeyang antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition
AT kwangilpark antiinflammatoryandantioxidantpropertiesofcamelliasinensislextractasapotentialtherapeuticforatopicdermatitisthroughnfkbpathwayinhibition