Anti-Melanogenic Effects of Cnidium monnieri Extract via p38 Signaling-Mediated Proteasomal Degradation of Tyrosinase

Author:

Choi Soon Ho1ORCID,Kim Hyunggun2ORCID,Hwang-Bo Jeon3,Kim Kyoung Mi4ORCID,Kwon Jeong Eun3ORCID,Lee Sung Ryul5ORCID,Hwang Sun Ha3ORCID,Kang Se Chan3ORCID,Lee Yeong-Geun3ORCID

Affiliation:

1. Research Institute, APRG Inc., Yongin 16950, Republic of Korea

2. Department of Biomechatronic Engineering, Sungkyunkwan University, Suwon 16419, Republic of Korea

3. Department of Biopharmaceutical Biotechnology and Graduate School of Biotechnology, Kyung Hee University, Yongin 17104, Republic of Korea

4. Research Center, CureBio Therapeutics Co., Ltd., Suwon 16229, Republic of Korea

5. Department of Convergence Biomedical Science, Cardiovascular and Metabolic Disease Center, College of Medicine, Inje University, Busan 47392, Republic of Korea

Abstract

Cnidium monnieri fructus is widely used in traditional Oriental medicine for treating female genital disorders, male impotence, frigidity, and skin-related conditions in East Asia. However, the role of C. monnieri fructus extract (CMFE) in melanin synthesis is not well elucidated. This study aimed to investigate the anti-melanogenesis effect and mechanism of action of CMFE in α-MSH-stimulated B16F10 cells. Intracellular melanin content and tyrosinase activity were measured in α-MSH-stimulated B16F10 cells treated with various concentrations of CMFE (0.5–5 μg/mL). mRNA and protein levels of tyrosinase and MITF were evaluated using qRT-PCR and ting. CMFE’s effect on the proteasomal degradation of tyrosinase was confirmed using a proteasomal degradation inhibitor, MG132. CMFE treatment activated p38, a protein associated with proteasomal degradation. Treatment with CMFE at up to 5 μg/mL showed no significant cytotoxicity. CMFE significantly reduced α-MSH-stimulated melanin production (43.29 ± 3.55% decrease, p < 0.05) and cellular tyrosinase activity (31.14 ± 3.15% decrease, p < 0.05). Although mRNA levels of MITF and tyrosinase increased, CMFE suppressed tyrosinase protein levels. The suppressive effect of CMFE on tyrosinase protein was blocked by MG132. CMFE inhibited melanogenesis by promoting the proteasome degradation of tyrosinase through p38 activation. These findings suggest that CMFE has the potential to be a natural whitening agent for inhibiting melanogenesis.

Publisher

MDPI AG

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