Anti-Melanogenic Effect of Ethanolic Extract of Sorghum bicolor on IBMX-Induced Melanogenesis in B16/F10 Melanoma Cellsopen access
- Authors
- Han, Hye Ju; Park, Seon Kyeong; Kang, Jin Yong; Kim, Jong Min; Yoo, Seul Ki; Heo, Ho Jin
- Issue Date
- Mar-2020
- Publisher
- Multidisciplinary Digital Publishing Institute (MDPI)
- Keywords
- anti-melanogenesis; B16; F10 melanoma cell; hydroxyoctadecadienoic acid; Sorghum bicolor; 3-isobutyl-1-methylxanthine
- Citation
- Nutrients, v.12, no.3
- Indexed
- SCIE
SCOPUS
- Journal Title
- Nutrients
- Volume
- 12
- Number
- 3
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/6886
- DOI
- 10.3390/nu12030832
- ISSN
- 2072-6643
- Abstract
- To evaluate possibility as a skin whitening agent of Sorghum bicolor (S. bicolor), its antioxidant activity and anti-melanogenic effect on 3-isobutyl-1-methylxanthine (IBMX)-induced melanogenesis in B16/F10 melanoma cells were investigated. The result of total phenolic contents (TPC) indicated that 60% ethanol extract of S. bicolor (ESB) has the highest contents than other ethanol extracts. Antioxidant activity was evaluated using the 2,2'-azino-bis-(3-ethylbenzothiazolin-6-sulfonic acid) diammonium salt (ABTS)/1,1-diphenyl-2-picryl-hydrazyl (DPPH) radical scavenging activities and malondialdehyde (MDA) inhibitory effect. These results showed ESB has significant antioxidant activities. Inhibitory effect against tyrosinase was also assessed using L-tyrosine (IC50 value = 89.25 mu g/mL) and 3,4-dihydroxy-L-phenylalanine (L-DOPA) as substrates. In addition, ESB treatment effectively inhibited melanin production in IBMX-induced B16/F10 melanoma cells. To confirm the mechanism on anti-melanogenic effect of ESB, we examined melanogenesis-related proteins. ESB downregulated melanogenesis by decreasing expression of microphthalmia-associated transcription factor (MITF), tyrosinase and tyrosinase-related protein (TRP)-1. Finally, 9-hydroxyoctadecadienoic acid (9-HODE), 1,3-O-dicaffeoylglycerol and tricin as the main compounds of ESB were analyzed using the ultra-performance liquid chromatography-ion mobility separation-quadrupole time of flight/tandem mass spectrometry (UPLC-IMS-QTOF/MS2). These findings suggest that ESB may have physiological potential to be used skin whitening material.
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