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Effects of high‐affinity nerve growth factor receptor inhibitors on symptoms in the NC/Nga mouse atopic dermatitis model
Author(s) -
Takano N.,
Sakurai T.,
Ohashi Y.,
Kurachi M.
Publication year - 2007
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/j.1365-2133.2006.07636.x
Subject(s) - nerve growth factor , tropomyosin receptor kinase a , pathogenesis , atopic dermatitis , receptor , medicine , low affinity nerve growth factor receptor , epidermis (zoology) , endocrinology , immunology , anatomy
Summary Background Nerve growth factor (NGF) is an important substance in the skin, where it modulates nerve maintenance and repair. However, the direct link between NGF and pruritic diseases such as atopic dermatitis is not yet fully understood. Our previous study showed that NGF plays an important role in the pathogenesis of atopic dermatitis‐like skin lesions in NC/Nga mice. NGF mediates its effects by binding to two classes of transmembrane receptors, a high‐affinity receptor (tropomyosin‐related kinase A, TrkA) and a low‐affinity receptor (p75). Objectives To determine the significance of NGF receptors in the pathogenesis of atopic dermatitis, the effects of TrkA inhibitors AG879 and K252a on the symptoms of NC/Nga mice were evaluated. Methods Male NC/Nga mice with severe skin lesions were used. AG879 or K252a was applied to the rostral part of the back of mice five times a week. The dermatitis score for the rostral back was assessed once a week. The scratching behaviour was measured using an apparatus, MicroAct (Neuroscience, Tokyo, Japan). Immunofluorescence examinations were made in the rostral back skin for nerve fibres, NGF and TrkA receptor. Results Repeated applications of AG879 or K252a significantly improved the established dermatitis and scratching behaviour, and decreased nerve fibres in the epidermis. NGF was observed more weakly in keratinocytes, and a lower expression of TrkA was observed in stratum germinativum of the epidermis of mice treated with AG879 or K252a compared with those treated with vehicle. Conclusions We suggest that NGF plays an important role in the pathogenesis of atopic dermatitis‐like skin lesions via the high‐affinity NGF receptor. These findings provide a new potential therapeutic approach for the amelioration of symptoms of atopic dermatitis.