Planta Med 1989; 55(3): 245-248
DOI: 10.1055/s-2006-961994
Papers

© Georg Thieme Verlag Stuttgart · New York

Antiulcerogenic Compounds Isolated from Chinese Cinnamon

Shigeo Tanaka1 , YoungHwa Yoon1 , Hiroshi Fukui1 , Mamoru Tabata1 , Toshiaki Akira2 , Kanemichi Okano2 , Masakazu Iwai2 , Yoshiro Iga2 , Kazumasa Yokoyama2
  • 1Department of Pharmacognosy, Faculty of Pharmaceutical Sciences, Kyoto University, Sakyo-ku, Kyoto 606, Japan
  • 2Central Research Laboratories, The Green Cross Corporation, Hirakata, Osaka 573, Japan
Weitere Informationen

Publikationsverlauf

1987

Publikationsdatum:
24. Januar 2007 (online)

Abstract

Two active compounds that prevent serotonin-induced ulcerogenesis in rats were isolated from Chinese cinnamon (the stem bark of Cinnamomum cassia) and identified as 3-(2-hydroxyphenyl)-propanoic acid and its O-glucoside, The former compound, administered orally or parenterally to rats at a remarkably low dose (40 µg/kg body weight), also inhibited gastric ulcers induced by the other ulcerogens such as phenylbutazone, ethanol, and water immersion stress, although it failed to prevent in-domethacin-induced ulcers. Pharmacological studies have shown that 3-(2-hydroxyphenyl)-propanoic acid hardly inhibited the secretion of gastric acid, but promoted the gastric blood flow. These results suggest that the antiulcerogenic effect of this compound is probably attributable to the potentiation of defensive factors through the improvement of the circulatory disorder and gastric cytoprotection.

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