Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Apr 30;25(2):567-573.
doi: 10.1007/s10068-016-0079-6. eCollection 2016.

Inhibitory effects of mung bean (Vigna radiata L.) seed and sprout extracts on melanogenesis

Affiliations

Inhibitory effects of mung bean (Vigna radiata L.) seed and sprout extracts on melanogenesis

Yoo Min Jeong et al. Food Sci Biotechnol. .

Abstract

Inhibitory effect against melanogenesis and the in vitro tyrosinase inhibitory activity of ethyl acetate (EtOAc) and methylene chloride fractions of 80% methanol extracts of mung bean (Vigna radiata L.) seeds and sprouts were determined. EtOAc extract fractions from mung bean sprouts germinated for 12 h (33.5%), 1 day (56.5%), and 2 days (47.9%) inhibited melanogenesis more effectively than arbutin (16.3%). The in vitro tyrosinase inhibitory activity was higher in an EtOAc extract fraction from mung bean sprouts germinated for 2 days (70.5%). EtOAc extract fractions from mung bean sprouts germinated for 1 day showed excellent whitening effects due to the flavone vitexin. Extracts from mung bean sprouts germinated for 1 day can be used as a novel whitening cosmeceutical ingredient.

Keywords: isovitexin; mung bean; sprout; vitexin; whitening effect.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Kim AR, Park SA, Ha JH, Park SN. Antioxidative and inhibitory activities on melanogenesis of Vitex negundo L. leaf extract. Microbiol. Biotechnol. Lett. 2013;41:135–144.
    1. Ando H, Niki Y, Ito M, Akiyama K, Matsui MS, Yarosh DB, Ichihashi M. Melanosomes are transferred from melanocyte to keratinocytes through the processes of packaging, release, uptake, and dispersion. J. Invest. Dermatol. 2012;132:1222–1229. doi: 10.1038/jid.2011.413. - DOI - PubMed
    1. Seiberg M. Keratinocyte-melanocyte interaction during melanosome transfer. Pigm. Cell Res. 2001;14:236–242. doi: 10.1034/j.1600-0749.2001.140402.x. - DOI - PubMed
    1. Ito S, Wakamatsu K. Quantitative analysis of eumelanin and pheomelanin in humans, mice, and other animals: A comparative review. Pigm. Cell Res. 2003;16:523–531. doi: 10.1034/j.1600-0749.2003.00072.x. - DOI - PubMed
    1. Marmol V, Veermann F. Tyrosinase and related proteins in mammalian pigmentation. FEBS Lett. 1996;381:165–168. doi: 10.1016/0014-5793(96)00109-3. - DOI - PubMed