In Vitro Anti-Inflammatory and Skin Protective Effects of Codium fragile Extract on Macrophages and Human Keratinocytes in Atopic Dermatitis

J Microbiol Biotechnol. 2024 Apr 28;34(4):940-948. doi: 10.4014/jmb.2312.12002. Epub 2024 Jan 17.

Abstract

Codium fragile has been traditionally used in oriental medicine to treat enterobiasis, dropsy, and dysuria, and it has been shown to possess many biological properties. Atopic dermatitis (AD) is one of the types of skin inflammation and barrier disruption, which leads to chronic inflammatory skin diseases. In the current investigation, the protective effects of C. fragile extract (CFE) on anti-inflammation and skin barrier improvement were investigated. In LPS-stimulated RAW 264.7 cells, nitric oxide generation and the expression levels of interleukin (IL)-1β, IL-4, IL-6, iNOS, COX-2, and tumor necrosis factor-alpha (TNF)-α were reduced by CFE. CFE also inhibited the phosphorylation of NF-κB-p65, ERK, p-38, and JNK. Additionally, CFE showed inhibitory activity on TSLP and IL-4 expression in HaCaT cells stimulated with TNF-α/interferon-gamma (IFN-γ). Enhanced expression of factors related to skin barrier function, FLG, IVL, and LOR, was confirmed. These findings implied that CFE may be used as a therapeutic agent against AD due to its skin barrier-strengthening and anti-inflammatory activities, which are derived from natural marine products.

Keywords: Codium fragile; atopic dermatitis; barrier function; inflammation.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents* / pharmacology
  • Cell Line
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Cytokines* / metabolism
  • Dermatitis, Atopic* / drug therapy
  • Filaggrin Proteins*
  • HaCaT Cells
  • Humans
  • Keratinocytes* / drug effects
  • Lipopolysaccharides / pharmacology
  • Macrophages* / drug effects
  • Macrophages* / immunology
  • Mice
  • NF-kappa B / metabolism
  • Nitric Oxide* / metabolism
  • Plant Extracts / pharmacology
  • RAW 264.7 Cells
  • Skin / drug effects
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Nitric Oxide
  • Plant Extracts
  • Tumor Necrosis Factor-alpha
  • FLG protein, human
  • Lipopolysaccharides
  • NF-kappa B
  • Cyclooxygenase 2
  • Filaggrin Proteins