Melanogenesis-Inhibitory Activity and Cancer Chemopreventive Effect of Glucosylcucurbic Acid from Shea (Vitellaria paradoxa) Kernels

被引:20
作者
Zhang, Jie [1 ]
Kurita, Masahiro [1 ]
Ebina, Kodai [1 ]
Ukiya, Motohiko [1 ]
Tokuda, Harukuni [2 ]
Yasukawa, Ken [3 ]
Masters, Eliot T. [4 ]
Shimizu, Naoto [5 ]
Akihisa, Momoko [6 ]
Feng, Feng [7 ]
Akihisa, Toshihiro [1 ,8 ]
机构
[1] Nihon Univ, Coll Sci & Technol, Chiyoda Ku, Tokyo 1018308, Japan
[2] Kanazawa Univ, Grad Sch Med Sci, Kanazawa, Ishikawa 9208640, Japan
[3] Nihon Univ, Sch Pharm, Funabashi, Chiba 2748555, Japan
[4] NMIT, World Agroforestry Ctr ICRAF, Nelson 7010, New Zealand
[5] Agilent Technol Japan Ltd, Applicat Ctr, Hachioji, Tokyo 1920033, Japan
[6] Tokyo Med & Dent Univ, Dept Endocrinol & Metab, Hosp Med, Bunkyo Ku, Tokyo 1138519, Japan
[7] China Pharmaceut Univ, Dept Nat Med Chem, Nanjing 210009, Peoples R China
[8] Akihisa Med Clin, Sanda, Hyogo 6691311, Japan
关键词
Vitellaria paradoxa; Shea kernel; Glucosylcucurbic acid; Melanogenesis inhibition; EpsteinBarr virus early antigen (EBV-EA); Anti-inflammatory activity; Mouse skin carcinogenesis; PLANT-GROWTH REGULATORS; CUCURBITA-PEPO L; PHENOLIC-COMPOUNDS; METHYL CUCURBATE; ANGELICA-KEISKEI; TRITERPENE; BIOSYNTHESIS; CONSTITUENTS; GLYCOSIDES; SEEDLINGS;
D O I
10.1002/cbdv.201400424
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two jasmonate derivatives, glucosylcucurbic acid (1) and methyl glucosylcucurbate (2), were isolated from the MeOH extract of defatted shea (Vitellaria paradoxa; Sapotaceae) kernels. These and their deglucosylated derivatives, cucurbic acid (3) and methyl cucurbate (4), were evaluated for their melanogenesis-inhibitory and cancer chemopreventive potencies. Compounds 1, 3, and 4 exhibited potent melanogenesis-inhibitory activities in -melanocyte-stimulating hormone (-MSH)-stimulated B16 melanoma cells. Western-blot analysis revealed that compounds 1 and 3 reduced the protein levels of MITF (=microphthalmia-associated transcription factor), tyrosinase, TRP-1 (=tyrosine-related protein 1), and TRP-2 mostly in a concentration-dependent manner. In addition, compound 1 exhibited inhibitory effects against EpsteinBarr virus early antigen (EBV-EA) activation induced with 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells, against TPA-induced inflammation in mice, and against skin tumor promotion in an in vivo two-stage mouse skin carcinogenesis test based on 7,12-dimethylbenz[a]anthracene (DMBA) as initiator, and with TPA as promoter.
引用
收藏
页码:547 / 558
页数:12
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