Inhibitory effect of Psidium guajava water extract in the development of 2,4-dinitrochlorobenzene-induced atopic dermatitis in NC/Nga mice

Food Chem Toxicol. 2012 Aug;50(8):2923-9. doi: 10.1016/j.fct.2012.04.044. Epub 2012 May 17.

Abstract

Atopic dermatitis (AD) is a chronic, relapsing, and inflammatory skin disease associated with eczematous symptoms and IgE hyperproduction. Psidium guajava is an important food crop and medicinal plant with anti-oxidant, anti-inflammatory, and anti-allergic activities, supporting its traditional uses. Our previous studies have shown that P. guajava extract inhibits Th2 chemokine expression by suppressing the activation of NF-κB and STAT1 co-stimulated with TNF-α and INF-γ. In this study, we investigated the inhibitory effect of P. guajava water extract (PGW) on 2,4-dinitrochlorobenzene (DNCB)-induced AD-like skin lesions in NC/Nga mice. Treatment of cream containing PGW onto DNCB-induced AD-like skin lesions in NC/Nga mice ameliorated lesion intensity scores, levels of IgE, thymus and activation-regulated chemokine (TARC), TNF-α, and IL-4 in serum and ears. In contrast, PGW increased level of the immunosuppressive cytokine IL-10. Histological analyses demonstrated decreased thickening of the epidermis/dermis as well as dermal infiltration by inflammatory cells. These results suggest that cream containing PGW may be a potential therapeutic modality for AD and adjunctive agent to control pruritus in AD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Cytokines / metabolism
  • DNA Primers
  • Dermatitis, Atopic / chemically induced*
  • Dermatitis, Atopic / metabolism
  • Dermatitis, Atopic / pathology
  • Dinitrochlorobenzene / toxicity*
  • Immunoglobulin E / metabolism
  • Male
  • Mice
  • Plant Extracts / pharmacology*
  • Psidium / chemistry*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Water / chemistry

Substances

  • Cytokines
  • DNA Primers
  • Dinitrochlorobenzene
  • Plant Extracts
  • Water
  • Immunoglobulin E