Planta Med 1981; 42(5): 17-21
DOI: 10.1055/s-2007-971540
Research Articles

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Inhibition of Type A and Type B Monoamine Oxidases by Naturally Occurring Xanthones

O. Suzuki1 , Y. Katsumata2 , M. Oya2 , V. M. Chari3 , B. Vermes5 , H. Wagner3 , K. Hostettmann4
  • 1Department of Legal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan
  • 2Department of Legal Medicine, Nagoya University School of Medicine, Nagoya, Japan
  • 3Institut für Pharmazeutische Biologie der Universität München, München, Federal Republic of Germany
  • 4Pharmazeutisches Institut, Eidgenössische Technische Hochschule, Zürich, Switzerland
  • 5Institute for Organic Chemistry, Technical University, Budapest, Hungary
Further Information

Publication History

Publication Date:
30 March 2007 (online)

Abstract

Eleven naturally occurring xanthones were tested for in vitro inhibition of type A and type B monoamine oxidases (MAO's), prepared by treating rat brain mitochondria with selective inhibitors. All compounds showed various potencies of inhibition for both types of MAO. 1-Hydroxy-3,8-dimethoxy-xanthone and 1,3-dihydroxy-7,8-dimethoxy-xanthone were most potent for type A MAO, while they were rather weak for type B MAO, showing that these compounds can be regarded as type A inhibitors. The xanthones bearing 1,3-dihydroxy-groups generally exhibited potent inhibition for both types. The 3-O-glucosides of xanthones were much weaker than their corresponding genuine aglycones for both types.

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