» Articles » PMID: 34204204

Water Extract of Prevents Inflammatory Skin Diseases In Vitro Models

Overview
Journal Plants (Basel)
Date 2021 Jul 2
PMID 34204204
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

Atopic dermatitis (AD) is a chronic inflammatory skin disease caused by immune hypersensitivity reaction. The cause of AD is unclear, but its symptoms have a negative effect on quality of life; various treatment methods to alleviate these symptoms are underway. In the present study, we aimed to evaluate in vitro antioxidant and anti-inflammatory effects of water extract (RCW) on AD. Total phenolic compounds and flavonoid content of RCW were 4242.40 ± 54.84 mg GAE/g RCE and 1010.99 ± 14.75 mg CE/g RCW, respectively. RCW reduced intracellular reactive oxygen species level and increased the action of antioxidant enzymes, such as catalase, superoxide dismutase, and glutathione peroxidase in tumor necrosis factor-α (TNF-α)/interferon-γ (IFN-γ)-stimulated HaCaT cells. Moreover, mRNA expression of the pro-inflammatory cytokines, including TNF-α, interleukin-1β, and interleukin-6, was downregulated by RCW in the TNF-α/IFN-γ-stimulated cells. The levels of inflammatory chemokines (thymus- and activation-regulated chemokine; eotaxin; macrophage-derived chemokine; regulated on activation, normal T-cell expressed and secreted; and granulocyte-macrophage colony-stimulating factor) and intercellular adhesion molecule-1 were decreased in the TNF-α/IFN-γ-stimulated HaCaT cells after RCW treatment. Additionally, the mRNA expression levels of filaggrin and involucrin, proteins that form the skin, were increased by RCW. Furthermore, RCW inhibited the nuclear factor kappa-light-chain-enhancer of the activated B cells pathway in the TNF-α/IFN-γ-stimulated HaCaT cells. Collectively, the present investigation indicates that RCW is a potent substance that inhibits AD.

Citing Articles

Inhibitory effect of Sanguisorba hakusanensis Makino ethanol extract on atopic dermatitis-like responses in NC/Nga mice and human keratinocytes.

Song H, Park S, Kim H, Jang S, Choo B, Kim H Sci Rep. 2023; 13(1):14594.

PMID: 37670127 PMC: 10480230. DOI: 10.1038/s41598-023-41676-3.


Design and Evaluation of Paeonol-Loaded Liposomes in Thermoreversible Gels for Atopic Dermatitis.

Wang Y, Yue Y, Jia R, Liu X, Cheng Z, Cheng Y Gels. 2023; 9(3).

PMID: 36975647 PMC: 10047988. DOI: 10.3390/gels9030198.

References
1.
Ji H, Li X . Oxidative Stress in Atopic Dermatitis. Oxid Med Cell Longev. 2016; 2016:2721469. PMC: 4781995. DOI: 10.1155/2016/2721469. View

2.
Vestergaard C, Kirstejn N, Gesser B, Mortensen J, Matsushima K, Larsen C . IL-10 augments the IFN-gamma and TNF-alpha induced TARC production in HaCaT cells: a possible mechanism in the inflammatory reaction of atopic dermatitis. J Dermatol Sci. 2001; 26(1):46-54. DOI: 10.1016/s0923-1811(00)00160-2. View

3.
Seo K, Lee J, Park J, Jang G, Kim H, Lee Y . Differences in anti-inflammatory effect of immature and mature of Rubus coreanus fruits on LPS-induced RAW 264.7 macrophages via NF-κB signal pathways. BMC Complement Altern Med. 2019; 19(1):89. PMC: 6485102. DOI: 10.1186/s12906-019-2496-6. View

4.
Thyssen J, Kezic S . Causes of epidermal filaggrin reduction and their role in the pathogenesis of atopic dermatitis. J Allergy Clin Immunol. 2014; 134(4):792-9. DOI: 10.1016/j.jaci.2014.06.014. View

5.
Kiyohara C, Tanaka K, Miyake Y . Genetic susceptibility to atopic dermatitis. Allergol Int. 2008; 57(1):39-56. DOI: 10.2332/allergolint.R-07-150. View