Planta Med 2006; 72(3): 199-203
DOI: 10.1055/s-2005-916175
Original Paper
Pharmacology
© Georg Thieme Verlag KG Stuttgart · New York

New Lanostanes and Naphthoquinones Isolated from Antrodia salmonea and their Antioxidative Burst Activity in Human Leukocytes

Chien-Chang Shen1 , 2 , Yuh-Chiang Shen1 , 3 , Yea-Hwey Wang4 , Lie-Chwen Lin1 , Ming-Jaw Don1 , Kuo-Tong Liou5 , Wen-Yen Wang6 , Yu-Chang Hou6 , Tun-Tschu Chang7
  • 1National Research Institute of Chinese Medicine, Taipei, Taiwan
  • 2Department of Biochemistry, National Yang-Ming University, Taipei, Taiwan
  • 3Institute of Biomedical Sciences, National Chung-Hshing University, Taichung, Taiwan
  • 4Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan
  • 5Department of Chinese Martial Arts, Chinese Culture University, Taipei, Taiwan
  • 6Departments of Surgery and Chinese Medicine, Tao-Yuan General Hospital, Department of Health, Taiwan
  • 7Division of Forest Protection, Taiwan Forestry Research Institute, Taipei, Taiwan
Further Information

Publication History

Received: March 17, 2005

Accepted: July 27, 2005

Publication Date:
05 December 2005 (online)

Abstract

Four new compounds were isolated from the basidiomata of the fungus Antrodia salmonea, a newly identified species of Antrodia (Aphyllophorales) in Taiwan. These new compounds are named as lanosta-8,24-diene-3β,15α,21-triol (1), 24-methylenelanost-8-ene-3β,15α,21-triol (2), 2,3-dimethoxy-5-(2′,5′-dimethoxy-3′,4′-methylenedioxyphenyl)-7-methyl-[1] [4]-naphthoquinone (3), and 2,3-dimethoxy-6-(2′,5′-dimethoxy-3′,4′-methylenedioxyphenyl)-7-methyl-[1] [4]-naphthoquinone (4), respectively. Their structures were elucidated by spectroscopic methods. An in vitro cellular functional assay was performed to evaluate their anti-oxidative burst activity in human leukocytes. They showed inhibitory effects against phorbol 12-myristate-13-acetate (PMA), a direct protein kinase C activator, induced oxidative burst in neutrophils (PMN) and mononuclear cells (MNC) with 50 % inhibitory concentration (IC50) ranging from 3.5 to 25.8 μM. The potency order of these compounds in PMA-activated leukocytes was as 1 > 3 > 4 > 2. They were relatively less effective in formyl-Met-Leu-Phe (fMLP), a G-protein coupled receptor agonist, induced oxidative burst, except for compounds 3 and 4 in fMLP-activated PMN. These results indicated that three (1, 3, and 4) of these four newly identified compounds displayed anti-oxidative effect in human leukocytes with different potency and might confer anti-inflammatory activity to these drugs.

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Tun-Tschu Chang

Division of Forest Protection

Taiwan Forestry Research Institute

No. 53, Nai-Hai Road

Taipei 100

Taiwan

Republic of China

Phone: +886-2-23078901

Fax: +886-2-23078755

Email: ttchang@serv.tfri.gov.tw

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