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Substance P alterations in skin and brain of chronically stressed atopic-like mice

Background  Stress is known to worsen the symptoms of atopic eczema (AE). Substance P is likely to play an important role in the development and pathogenesis of AE. Objective  To examine a possible connection between chronic mild stress and changes in the expression of substance P and its receptor (...

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Bibliographic Details
Published in:Journal of the European Academy of Dermatology and Venereology 2013-02, Vol.27 (2), p.199-205
Main Authors: Grip, L., Lonne-Rahm, S.-B., Holst, M., Johansson, B., Nordlind, K., Theodorsson, E., El-Nour, H.
Format: Article
Language:English
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Summary:Background  Stress is known to worsen the symptoms of atopic eczema (AE). Substance P is likely to play an important role in the development and pathogenesis of AE. Objective  To examine a possible connection between chronic mild stress and changes in the expression of substance P and its receptor (R) neurokinin (NK) 1 in the skin and stress‐related brain regions in NC/Nga atopic‐like mice. Methods  The mice were divided into three groups (eight animals per group): SE (stressed eczematous), NSE (non‐stressed eczematous) and SC (stressed control). Ears and brains of the mice were investigated using immunohistochemistry and RT‐PCR. Results  In the skin, there was a decrease in the number of substance P immunoreactive nerve fibres in SE compared with SC group. RT‐PCR showed a strong tendency to an increase in mRNA for NK1R in the skin of SE compared with NSE mice. There was an increase in the number of mast cells and the degree of their degranulation in the SE compared with both other groups. A decrease in substance P immunoreactivity in medial hippocampus was found in SE compared with NSE animals. In prefrontal cortex and central amygdala, there were no significant differences in substance P immunoreactivity between the three groups. Conclusion  Exposure to chronic mild stress in NC/Nga atopic‐like mice may result in altered expression patterns of substance P in the skin and hippocampus.
ISSN:0926-9959
1468-3083
1468-3083
DOI:10.1111/j.1468-3083.2011.04443.x