4.7 Article

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

Journal

FOOD AND CHEMICAL TOXICOLOGY
Volume 50, Issue 8, Pages 2923-2929

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2012.04.044

Keywords

Psidium guajava; Atopic dermatitis; IgE; TARC

Funding

  1. Technology Development Program for Ministry for Food, Agriculture, Forestry, and Fisheries, Republic of Korea [20090237]
  2. Priority Research Centers Program through the National Research Foundation of Korea (NRF)
  3. Ministry of Education, Science and Technology, Republic of Korea
  4. Korea Institute of Marine Science & Technology Promotion (KIMST) [20090237] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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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-kappa B and STAT1 co-stimulated with TNF-alpha and INF-gamma. 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-alpha, 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. (C) 2012 Elsevier Ltd. All rights reserved.

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