Volume 10, Issue 7 pp. 581-584
Research Article

Inhibitory Effect of Poria cocos on 12-O-Tetradecanoylphorbol-13-Acetate-Induced Ear Oedema and Tumour Promotion in Mouse Skin

Tomohiro Kaminaga

Tomohiro Kaminaga

College of Pharmacy, Nihon University, 7-1, Narashinodai 7-chome, Funabashi-shi, Chiba 274, Japan

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Ken Yasukawa

Corresponding Author

Ken Yasukawa

College of Pharmacy, Nihon University, 7-1, Narashinodai 7-chome, Funabashi-shi, Chiba 274, Japan

College of Pharmacy, Nihon University, 7-1, Narashinodai 7-chome, Funabashi-shi, Chiba 274, JapanSearch for more papers by this author
Michio Takido

Michio Takido

College of Pharmacy, Nihon University, 7-1, Narashinodai 7-chome, Funabashi-shi, Chiba 274, Japan

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Takaaki Tai

Takaaki Tai

Central Research Laboratory, Kotaro Pharmaceutical Co. Ltd, Suga-cho 47-3, Takatsuki-shi, Osaka 569, Japan

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Yoshiki Nunoura

Yoshiki Nunoura

Central Research Laboratory, Kotaro Pharmaceutical Co. Ltd, Suga-cho 47-3, Takatsuki-shi, Osaka 569, Japan

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Abstract

The methanol extract from the sclerotium of Poria cocos was found to inhibit 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced tumour promotion in two-stage carcinogenesis in mouse skin. From the active fraction of the extract, eight lanostane-type triterpene acids and four 3,4-secolanostane-type triterpene acids were isolated. The isolated compounds showed inhibitory activity against TPA-induced ear inflammatory oedema. The 50% inhibitory dose of pachymic acid, 3-O-acetyl-16α-hydroxytrametenolic acid, dehydropachymic acid, dehydroeburiconic acid, 3β-hydroxylanosta-7,9(11),24-trien-21-oic acid, poricoic acid A and poricoic acid B for TPA-induced inflammation was 17–44 μg/ear, at a grade corresponding to that of hydrocortisone.

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