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ISSN : 1738-0294(Print)
ISSN : 2288-8853(Online)
Journal of Mushrooms Vol.11 No.4 pp.254-260
DOI :

갈색 느티만가닥버섯 메탄올 추출물의 항산화 및 tyrosinase 저해 효과

김수철1, 류한민1, 정성미1, 이용현1, 김혜수1, 김종옥2, 조용운1, 조수정1*
경남과학기술대학교 제약공학과1, 남경농산2

Antioxidant and tyrosinase inhibitory activity of Hypsizygus marmoreus (brown cultivar) methanol extracts

Soo Jeong Cho1*, Su Cheol Kim1, Han Min Ryu1, Sung Mi Jung1, Young Hyun Lee1, Hye Soo Kim1, Jong Ok Kim2, Young Un Cho1
1Department of Pharmaceutical Engineering, Gyeongnam National University of Science and Technology, 33 Dongjin-ro, Jinju 660-758, Korea
2Namkyung Co., Ltd, Cheongdo-gun, Gyeongbuk 714-841, Korea
(Received December 11, 2013 / Revised December 23, 2013 / Accepted December 27, 2013)

Abstract

The objective of this study was to evaluate antioxidant effect and tyrosinase inhibitory activity of methanolextracts from Hypsizygus marmoreus. The Hypsizygus marmoreus was divided into two parts (pileus and stipe) andextracted with methanol. Total polyphenolics and flavonoids in the methanol extracts were measured by spectrophotometricmethods and 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging activities have been determined for antioxidantactivities. The total polyphenolics and flavonoids contents of methanol extract of the pileus were higher than methanolextract of the stipes. The total polyphenolics contents in methanol extracts of the pileus and stipes were 8.7 ug/mg and5.6 ug/mg, respectively. The total flavonoids contents in methanol extracts of the pileus and stipes were 2.8 ug/mg and1.4 ug/mg, respectively. The tyrosinase inhibitory activity was proportional to concentration of methanol extract. The tyrosinaseinhibitory activity of the methanol extract (200 mg/ml) of pileus (66.9%) and stipe (57.97%) was lower than thoseof positive control 2% arbutin. The DPPH radical scavenging activity of the methanol extract (20 mg/ml) of pileus andstipes was 52.55% and 30.35%, respectively. Moreover, the effects of methanol extarcts on cell proliferation of B16BL6mouse melanoma cells were investigated using WST-1 assay (4-[3-(4-iodophenyl)-2-(4-nitrophenyl)-2H-5-tetrazolio]-1,3-benzene disulphonate) and B16BL6 mouse melanoma cells treated with methanol extract of 200-2,000 ug/ml were higherproliferation rate than those of 0.04% adenosine.

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