Neuropeptides concentrations in the skin of a murine (NC/Nga mice) model of atopic dermatitis

J Dermatol Sci. 2003 Oct;33(1):55-65. doi: 10.1016/s0923-1811(03)00155-5.

Abstract

Background: It has been reported that the expression of neuropeptides (NPs), and the density and structure of peripheral nerves in atopic dermatitis (AD) are different from those in normal skin.

Objective: We investigated the role of NPs, in the development of AD with quantitative study of substance P (SP) and calcitonin gene-related peptide (CGRP) in the skin of AD-model mice.

Methods: We measured the NPs in the skin of mice (NC/Nga as AD-model mice, BALB/c and C57BL/6 as control) by enzyme-linked immunosorbentassay (ELISA). Peripheral nerve fibers and SP in the skin were stained by immunohistochemical staining, using anti-PGP9.5 antibody and anti-SP antibody.

Results: Under conventional condition, SP concentration in AD-like skin lesions of NC/Nga mice was higher than that in non-affected skin of the same mice. Under specific pathogen-free condition, SP concentration in the skin of NC/Nga mice was higher than that in the skin of BALB/c and C57BL/6 mice. In contrast, CGRP concentration in the skin lesions was lower than that in non-affected skin of NC/Nga mice. SP was detected not only in the nerve fibers in the dermis but also in mast cells in the inflammatory areas.

Conclusions: The skin of NC/Nga mice contains more SP congenitally, and environmental factors may aggravate this abnormal condition. We hypothesize that increase of SP accompanied with a decrease of CGRP in the skin may play important roles in the pathogenesis and development of AD.

MeSH terms

  • Animals
  • Back
  • Calcitonin Gene-Related Peptide / metabolism*
  • Dermatitis, Atopic / metabolism*
  • Dermatitis, Atopic / pathology
  • Disease Models, Animal
  • Enzyme-Linked Immunosorbent Assay
  • Immunoglobulin E / analysis
  • Immunohistochemistry / methods
  • Mice
  • Mice, Inbred Strains
  • Osmolar Concentration
  • Skin / metabolism*
  • Skin / pathology
  • Species Specificity
  • Staining and Labeling
  • Substance P / metabolism*

Substances

  • Substance P
  • Immunoglobulin E
  • Calcitonin Gene-Related Peptide