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Original Research Article | OPEN ACCESS

Methanol Partition Fraction of Ethanol Extract of Discorea nipponica Makino Inhibits Melanogenesis

Hsiou-Yu Ding1, Pei-Wen Lin2, Hui-Wen Wang1, Te-Sheng Chang2

1Institute of Cosmetics Science, Chia Nan University of Pharmacy and Science, 60, Sec. 1 Erh-Jen Rd, Jen-Te District; 2Department of Biological Science and Technology, National University of Tainan, 33 Sec. 2 Su-Lin St, Tainan, Taiwan.

For correspondence:-  Te-Sheng Chang   Email: mozyme2001@gmail.com   Tel:+88662602137

Received: 28 January 2014        Accepted: 18 April 2014        Published: 23 May 2014

Citation: Ding H, Lin P, Wang H, Chang T. Methanol Partition Fraction of Ethanol Extract of Discorea nipponica Makino Inhibits Melanogenesis. Trop J Pharm Res 2014; 13(5):719-726 doi: 10.4314/tjpr.v13i5.10

© 2014 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the inhibitory effect of the methanol fraction of Dioscorea nipponica Makino ethanol extract (DNM) on melanogenesis both in vitro and in vivo.
Methods: Cultured mouse B16 melanoma cell and zebra fish were used to evaluate the melanogenesis inhibitory activity of DNM in vitro and in vivo, respectively. In B16 cells, inhibitory effects on intracellular melanogenesis, tyrosinase activity and reactive oxygen species (ROS) were determined after DNM treatment. In zebra fish, both toxic and anti-melanogenic activities of DNM on developed larvae were evaluated.
Results: In B16 cells, the results show that DNM dose-dependently inhibited melanogenesis at non-toxic concentrations. Surprisingly, however, DNM had no effect on intracellular tyrosinase activity or the amount of the enzyme in B16 cells. On the other hand, DNM showed strong antioxidant activities against cell-free 2,2-diphenyl-1-picryl-hydrazl (DPPH) and 2,2’-azino-bis (3-etnylbenzthiazoline-6-sulphaonic acid) (ABTS+) free radical and intracellular ROS in B16 cells. In zebra fish, DNM significantly and dose-dependently inhibited skin melanogenesis of zebra fish larvae at non-toxic concentrations.
Conclusion: The findings demonstrate that DNM inhibits melanogenesis in vitro in B16 melanoma cells and in vivo in zebrafish. Furthermore, DNM exhibits potent inhibition of melanogenesis probably as a result of its antioxidant activity in the cells.

Keywords: Dioscorea nipponica, Makino, Melanogenesis, Tyrosinase, Antioxidant, Melanoma, Zebra fish

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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