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Recovery of pigmentation following selective photothermolysis in adult zebrafish skin: clinical implications for laser toning treatment of melasma

Authors
Kim, Jae HwanKim, Do HyunKim, Ji HaeLee, Sang GeunKim, Hyeon SooPark, Hae ChulKim, Il-Hwan
Issue Date
12월-2012
Publisher
TAYLOR & FRANCIS INC
Keywords
laser; melanosome; photothermolysis; tyrosinase; zebrafish
Citation
JOURNAL OF COSMETIC AND LASER THERAPY, v.14, no.6, pp.277 - 285
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF COSMETIC AND LASER THERAPY
Volume
14
Number
6
Start Page
277
End Page
285
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/106760
DOI
10.3109/14764172.2012.738908
ISSN
1476-4172
Abstract
In recent years, laser toning has gained popularity for the treatment of melasma, and tyrosinase inhibitors are conventionally used to prevent its recurrence after this treatment. The effectiveness of this treatment modality, however, is still questionable, and additional in vivo studies are needed to validate the method. In this study, we used adult zebrafish skin as an adult melanocyte regenerative system and examined the simulated human skin response to laser toning. Melanosomes regenerated after selective photothermolysis, and these organelles showed a bi-directional translocation pattern in accordance with the changes of intact melanosome patterns. Furthermore, a tyrosinase inhibitor, 1-phenyl-2-thiourea (PTU), completely blocked melanosome regeneration after laser irradiation, but this inhibitor failed to prevent melanosome regeneration after the medication was discontinued. Finally, arbutin and kojic acid, the commercially available tyrosinase inhibitors, slowed down but did not completely block melanosome regeneration. Based on these findings, we describe the limitations of laser toning treatment of melasma and the combined use of tyrosinase inhibitors. We suggest that melanosomes in adult zebrafish skin can be utilized for studying melanosome regeneration response to laser irradiation and for developing a system to assess the comparative efficacy of melanogenic regulatory compounds.
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