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Cited 15 time in webofscience Cited 17 time in scopus
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Inhibition Effects of Mangosenone F from Garcinia mangostana on Melanin Formation in B16F10 Cells

Authors
Ryu, Hyung WonJeong, Seong HunCurtis-Long, Marcus J.Jung, SuninLee, Ji WonWo, Hyun SimCho, Jung KeunPark, 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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