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Effects of Josamycin on Scratching Behavior in NC/Nga Mice with Atopic Dermatitis-Like Skin Lesions
Katsuhiko Matsui1, Midori Nakamura1, Noriko Obana1
1Department of Clinical Immunology, Meiji Pharmaceutical University.
Abstract:
Our previous study showed that chronic skin colonization by Staphylococcus aureus exacerbated atopic dermatitis (AD) and that control of such skin colonization using antibiotic ointment might relieve AD-related skin inflammation. However, the role of S. aureus colonization in the pruritus accompanying AD was not elucidated. The aim of the present study was to evaluate the effect of topically applied josamycin, a macrolide antibiotic, on the scratching behavior of NC/Nga mice with AD-like skin lesions. Josamycin (0.1%) was topically administered to NC/Nga mice with AD-like skin lesions induced by a mite antigen, Dermatophagoides farinae extract, and the therapeutic effects of josamycin were assessed by measurement of the skin severity score, S. aureus colonization, scratching count, and interleukin (IL)-31 mRNA expression in the skin lesions. Topical treatment with josamycin ointment significantly suppressed the increase of the skin severity score in NC/Nga mice. This suppressive effect was associated with decreases in the S. aureus count on the lesioned skin, scratching behavior of mice and IL-31 mRNA expression in the lesions. The present results show that the severity of AD-like skin inflammation in NC/Nga mice is correlated with the level of S. aureus colonization and subsequent IL-31 production in the skin. Therefore, topical application of josamycin to AD lesions colonized by S. aureus would be beneficial for control of AD by eliminating superficially located S. aureus and by suppressing the IL-31-induced scratching behavior.
Insights
Topical antibiotic josamycin reduced Staphylococcus aureus (S. aureus) colonization and scratching behavior in mice with atopic dermatitis (AD)-like skin lesions. This treatment also decreased skin inflammation and IL-31, suggesting a link between S. aureus and AD itch.
Area of Science:
- Dermatology
- Microbiology
- Immunology
Background:
- Chronic Staphylococcus aureus (S. aureus) colonization worsens atopic dermatitis (AD) and inflammation.
- The role of S. aureus in AD-associated pruritus (itch) remains unclear.
Purpose of the Study:
- To investigate the effect of topical josamycin on scratching behavior in AD-like mouse models.
- To assess josamycin's impact on S. aureus colonization, skin severity, and IL-31 expression.
Main Methods:
- NC/Nga mice with Dermatophagoides farinae-induced AD-like lesions were treated with 0.1% josamycin ointment.
- Evaluations included skin severity scores, S. aureus counts, scratching behavior, and IL-31 mRNA levels.
Main Results:
- Josamycin significantly reduced skin severity scores in treated mice.
- A decrease in S. aureus colonization, scratching behavior, and IL-31 mRNA expression was observed.
- Results indicate a correlation between S. aureus levels, IL-31 production, and AD severity.
Conclusions:
- Topical josamycin is effective in managing AD-like skin inflammation and pruritus.
- Eliminating S. aureus with josamycin suppresses IL-31 production, alleviating itch in AD.
- This suggests josamycin is a potential therapeutic for S. aureus-colonized AD lesions.

