Glossogyne tenuifolia Essential Oil Prevents Forskolin-Induced Melanin Biosynthesis via Altering MITF Signaling Cascade

Author:

Lin Wan-Teng1ORCID,Chen Yi-Ju23ORCID,Kuo Hsin-Ning1ORCID,Yu Cheng-Yeh4,Abomughaid Mosleh Mohammad5ORCID,Senthil Kumar K. J.46ORCID

Affiliation:

1. Department of Hospitality Management, College of Agriculture and Health, Tunghai University, Taichung 407224, Taiwan

2. Department of Surgery, Taichung Veterans General Hospital, Taichung 40705, Taiwan

3. Department of Animal Science and Biotechnology, College of Agriculture and Health, Tunghai University, Taichung 407224, Taiwan

4. Bachelor Program of Biotechnology, National Chung Hsing University, Taichung 402, Taiwan

5. Department of Medical Laboratory Sciences, College of Applied Medical Sciences, University of Bisha, Bisha 67714, Saudi Arabia

6. Center for General Education, National Chung Hsing University, Taichung 402, Taiwan

Abstract

Glossogyne tenuifolia (Labill.) Cass. ex Cass (Compositae) is a herbaceous plant that is endemic to Taiwan. Traditional Chinese Medicine has utilized it as a treatment for fever, inflammation, and liver preservation. Recent research has unveiled its bioactivities, including anti-inflammation, anti-cancer, antiviral, antioxidant, anti-fatigue, hepatoprotection, and immune modulation elements. Nevertheless, its effect on skin health remains to be investigated. Thus, we investigated the impact of G. tenuifolia essential oil (GTEO) on forskolin (FRK)-induced melanin biosynthesis and its mechanisms in B16-F10 murine melanoma in vitro. Treatment of GTEO resulted in a substantial decrease in FRK-induced melanin production, accompanied by a significant decrease in tyrosinase mRNA and protein expression levels. Additionally, our data demonstrated that the decrease in tyrosinase expression resulted from the suppression of MITF, as indicated by the reduced movement of MITF into the cell nucleus. Moreover, GTEO prompted a prolonged ERK1/2 activation, leading to the decline of MITF through proteasomal degradation, and it was verified that GTEO had no inhibitory impact on MITF activity in ERK1/2 inhibitor-treated cells. Additional studies demonstrated that α-pinene and D-limonene, which are the primary components in GTEO, showed strong melanin and tyrosinase inhibitory effects, indicating that α-pinene and D-limonene may contribute to its anti-melanogenic effects. Collectively, these data presented compelling proof that GTEO, along with its primary components α-pinene and D-limonene, show great potential as natural sources for developing innovative skin-whitening agents in the field of cosmetics.

Funder

National Science and Technology Council, Taiwan

Tunghai University

Publisher

MDPI AG

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