Ophiopogonin D ameliorates DNCB-induced atopic dermatitis-like lesions in BALB/c mice and TNF-α- inflamed HaCaT cell

Biochem Biophys Res Commun. 2020 Jan 29;522(1):40-46. doi: 10.1016/j.bbrc.2019.10.190. Epub 2019 Nov 15.

Abstract

Atopic dermatitis (AD) can occur in both children and adults, and the symptoms include itching and eczema, which in turn cause patients to suffer. Ophiopogonin D (OP-D) is a steroidal glycoside from Radix Ophiopogon japonicus, which is well known as an effective anti-inflammatory herbal medicine in many Asian countries. In this study, we aimed to investigate the anti-inflammatory effects of OP-D, using an AD mouse model and inflamed HaCaT cells. Through a histopathological analysis, we were able to confirm the suppressive effects of OP-D on skin thickening and the mast cell activation in AD-like mouse back skin tissues stimulated by DNCB. In addition, we detected significant decreases in cytokine expression levels through multiplex assessment assays of the OP-D-treated mice blood. We observed the anti-inflammatory effect of OP-D in the spleen, causing weight loss in the spleen and in the mRNA expression levels related to diverse cytokines. In human keratinocytes inflamed by TNF-α, OP-D inhibited p38 and ERK protein activation and showed a reduction of NF-κB nuclear translocation. Furthermore, OP-D attenuated pro-inflammatory cytokine mRNA expressions in TNF-α-inflamed HaCaT cells. Accordingly, we came to the conclusion that OP-D is a potential natural drug which can be used in order to treat inflammatory skin diseases, such as AD.

Keywords: Allergic contact dermatitis; Atopic dermatitis; Epidermal thickness; HaCaT cells; Inflammatory skin disease; Ophiopogonin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Cell Line
  • Cytokines / metabolism
  • Dermatitis, Atopic / chemically induced
  • Dermatitis, Atopic / drug therapy*
  • Dinitrochlorobenzene / pharmacology
  • Female
  • Humans
  • Inflammation
  • Keratinocytes / drug effects*
  • Mice
  • Mice, Inbred BALB C
  • Saponins / pharmacology*
  • Skin / drug effects
  • Spirostans / pharmacology*
  • Spleen / drug effects
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Cytokines
  • Dinitrochlorobenzene
  • Saponins
  • Spirostans
  • Tumor Necrosis Factor-alpha
  • ophiopogonin D