Anti-psoriatic properties of paeoniflorin: suppression of the NF-kappaB pathway and Keratin 17

Eur J Dermatol. 2020 Jun 1;30(3):243-250. doi: 10.1684/ejd.2020.3770.

Abstract

Background: Psoriasis is a common inflammatory skin disease characterized by hyperproliferation of epidermal keratinocytes, however, there is still no curative therapy for psoriasis. Paeoniflorin (PF), a Chinese herbal medicine, has shown anti-inflammatory effects.

Objectives: We aimed to illustrate the effect and associated mechanism of PF on keratinocyte proliferation using the IMQ-induced psoriasis mouse model.

Materials and methods: The anti-psoriatic effect of PF in vivo and in vitro was assessed by western blot, RT-PCR, immunofluorescence, cell counting kit-8 and haematoxylin/eosin staining.

Results: In vivo, epidermal thickness, dermal infiltrated lymphocytes and the level of several antimicrobial peptides, pro-inflammatory cytokines, and K17 were significantly reduced in mice with topical application of PF. In vitro, PF inhibited the proliferation of HaCaT cells in a dose-dependent manner, down-regulated K17 expression, and suppressed NF-kappaB activation.

Conclusion: Our findings indicate that PF may inhibit the proliferation of keratinocytes by targeting K17, suggesting that PF might be a potential target in the treatment of psoriasis.

Keywords: K17; paeoniflorin; proliferation; psoriasis.

MeSH terms

  • Administration, Cutaneous
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Cell Proliferation / drug effects*
  • Cytokines / metabolism
  • Down-Regulation / drug effects
  • Female
  • Glucosides / pharmacology*
  • Glucosides / therapeutic use
  • HaCaT Cells
  • Humans
  • Imiquimod
  • Keratin-17 / metabolism*
  • Keratinocytes / physiology
  • Keratins / metabolism
  • Mice
  • Monoterpenes / pharmacology*
  • Monoterpenes / therapeutic use
  • NF-kappa B / metabolism*
  • Psoriasis / chemically induced
  • Psoriasis / drug therapy*
  • Psoriasis / metabolism
  • Psoriasis / pathology
  • Signal Transduction / drug effects

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Glucosides
  • Keratin-17
  • Krt17 protein, mouse
  • Monoterpenes
  • NF-kappa B
  • peoniflorin
  • Keratins
  • Imiquimod