Atopic Dermatitis: a Short Summary
- Rhododendrol (Rhododenol, RD) created a big problem in Japan, when 14000 induced cases of vitiligo-like lesions were reported.
- It is known that Rhodoendol is cytoxic against melanocytes in a Tyrosinase dependent way cytotoxicity
The authors suggest a new mouse model for the study of this effect:
- hk14-scf/HRM Tg Mice become albino (fully depigmented) through suppression of melanin synthesis through tyrosinase activity
- with application of 30%RD 3 times per day on the back:
- depigmentation was visible on day 14
- Melan A decreased on day 7
- After stopping the application of RD:
- Electron Microscopy shows autophagosomes in mouse melanocyte after 4 days.
- Repigmentation is visible 49 days with recovery of basal melanocytes
- with application of 30%RD 3 times per day on the back:
Note:
- when applying RD50%, no mean change in the number of malanocytes (per high power filed under the microscope) was seen compared
- with untreated controls (this could suggest that high concentrations are more toxic than
- control albino mice showed no change at 30% or 50% concentration (this suggests that RD activity is specific to melanocytes, more specific to the synthesis of melanin)
Contributors
Dr Christophe Hsu – dermatologist. Geneva, Switzerland
Source of information: p13-18 Abe Y. et al. A mouse model of leukoderma induced by Rhododendrol (Rhododenol). JSID Annual Meeting (Japanese Society of Investigative Dermatology, 日本研究皮膚科学会) 2014 – Osaka, Japan
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