Inhibition Effects of Mangosenone F from Garcinia mangostana on Melanin Formation in B16F10 Cells
- Authors
- Ryu, Hyung Won; Jeong, Seong Hun; Curtis-Long, Marcus J.; Jung, Sunin; Lee, Ji Won; Wo, Hyun Sim; Cho, Jung Keun; Park, Ki Hun
- Issue Date
- 29-Aug-2012
- Publisher
- AMER CHEMICAL SOC
- Keywords
- mangostenone F; alpha-glucosidase; endo H; cytotoxicity; melanogenesis
- Citation
- JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, v.60, no.34, pp 8372 - 8378
- Pages
- 7
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
- Volume
- 60
- Number
- 34
- Start Page
- 8372
- End Page
- 8378
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/22070
- DOI
- 10.1021/jf3015987
- ISSN
- 0021-8561
- Abstract
- Melanogenesis can be controlled by tyrosinase inhibition or by blocking the maturation processes of tyrosinase and its related proteins. Mangostenone F was isolated from the seedcases of Garcinia mangostana. Mangostenone F Was shown to be inactive against tyrosinase (IC50 > 200 mu M) but was a potent alpha-glucosidase inhibitor in vitro (IC50 = 21.0 mu M). Mangastenone F was found to inhibit production of melanin in the mouse melanoma cell line B16F10. Importantly, unlike. most glycosidase, inhibitors, mangostenone F displayed very low cytotoxicity (EC50 > 200 mu M). The Western blot for expression levels of proteins involved in melanogenesis showed that mangostenone F down-regulated :tyrosinase and TRP-2 expression. Treating B16F10 cells with mangostenone F significantly increased the susceptibility of tyrosinase to endoglycosidase H digestion, indicating that tyrosinase was unable to mature fully and pass to the trans-golgi apparatus. Consistent with these data, in lysate assays, mangosterione F was shown to be a better inhibitor of alpha-glucosidases than deoxynojirimycin, a representative glycosidase inhibitor.
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