Planta Med 2007; 73(14): 1478-1481
DOI: 10.1055/s-2007-990245
Pharmacology
Letter
© Georg Thieme Verlag KG Stuttgart · New York

Decursin and Decursinol Angelate Selectively Inhibit NADH-Fumarate Reductase of Ascaris suum

Kazuro Shiomi1 , 2 , Hiroko Hatano2 , Hiromi Morimoto3 , Hideaki Ui1 , Kimitoshi Sakamoto4 , Kiyoshi Kita4 , Hiroshi Tomoda3 , Eun Woo Lee5 , Tae Ryeon Heo6 , Hirokazu Kawagishi7 , Satoshi  Omura1 , 2
  • 1Kitasato Institute for Life Sciences, Kitasato University, Tokyo, Japan
  • 2The Kitasato Institute, Tokyo, Japan
  • 3School of Pharmacy, Kitasato University, Tokyo Japan
  • 4Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
  • 5PNE Co. Ltd., 907-12 Daechidong, Kangnam-Gu, Seoul, Korea
  • 6Faculty of Biological Engineering, Inha University, Incheon, Korea
  • 7Graduate School of Science and Technology, Shizuoka University, Shizuoka, Japan
Further Information

Publication History

Received: August 24, 2006 Revised: May 8, 2007

Accepted: July 6, 2007

Publication Date:
18 October 2007 (online)

Abstract

NADH-fumarate reductase (NFRD) is a key enzyme in many anaerobic helminths. Decursin and decursinol angelate have been isolated from the roots of Angelica gigas Nakai (Apiaceae) as NFRD inhibitors. They inhibited Ascaris suum NFRD with IC50 values of 1.1 and 2.7 μM, respectively. Their target is the electron transport enzyme complex I. Since the inhibitory activities of decursin against bovine heart complexes are weak, it is a selective inhibitor of the nematode complex I. In contrast, decursinol angelate moderately inhibits bovine heart complexes II and III. Decursinol inhibits A. suum NFRD to a similar extent, but its target is complex II. It also inhibits bovine heart complexes II and III.

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Prof. Kazuro Shiomi

Kitasato Institute for Life Sciences

Kitasato University

5-9-1 Shirokane

Minato-ku

Tokyo 108-8641

Japan

Phone: +81-3-5791-6439

Fax: +81-3-5791-6131

Email: shiomi@lisci.kitasato-u.ac.jp