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Inhibition of Monamine Oxidase by a Flavone and Its Glycoside from Ixeris dentata Nakai

  • Chung, Ha-Sook (Department of Food and Nutrition, Duksung Women's University)
  • Published : 2003.06.01

Abstract

Ixeris dentata Nakai (Compositae) is a perennial herb which has been used as a folk medicine for treating diabetes and gastroenteric troubles in Korea. Active compounds were isolated from the aerial parts of Ixeris dentata through the bioassay-guided fractionation and isolation method evaluated for inhibition of monoamine oxidase (MAO) in vitro. The compounds were identified as 5,7,3',4'-tetrahydroxyflavone (1) and 5,7,3',4'- tetrahydroxyflavone 7-glucoside (2), based on physical and spectroscopic characteristics. Compounds 1 and 2 showed a selective inhibition of type B MAO (MAO-B) activity, with IC/sub 50/ values of 15.3 μM and 36.4 μM, respectively, but did not inhibit type A MAO (MAO-A) activity.

Keywords

References

  1. Volz HP, Gleiter CH. 1998. Monoamine oxidase inhibitors.A perspective on their use in the elderly. Drugs Aging 13: 341-355 https://doi.org/10.2165/00002512-199813050-00002
  2. Steven MC, Russell JM. 2000. Bioactive natural products: Detection, isolation and structure determination. CRC press, New York. p 1-8
  3. Elliott M, Chithan K. 1994. The impact of plant flavonoids on mammalian biology: implications for immunity, inflammation and cancer. In The Flavonoids: Advances in research. Harborne JB, ed. Chapman and Hall, London. p 619-652
  4. Lee MH, Lin RD, Shen LY, Yang LL, Yen KY, Hou WC. 2001. Monoamine oxidase B and free radical scavenging activities of natural flavonoids in Melastoma candidum D.Don. J Agric Food Chem 49: 5551-5555 https://doi.org/10.1021/jf010622j
  5. Chung HS, Woo WS, Lim SJ. 1994. Dentalactone, a sesquiterpene from Ixeris dentata. Phytochem 35: 1583-1584 https://doi.org/10.1016/S0031-9422(00)86898-3
  6. Chung HS, Woo WS, Lim SJ. 1994. Dentatins: Sesquiterpene glucosides from Ixeris dentata. Arch Pharm Res 17: 323-326 https://doi.org/10.1007/BF02974170
  7. Choi JS, Young HS, Kim BW. 1990. Hypoglycemic and hypolipemic effects of Ixeris dentata in diabetic rats. Arch Pharm Res 13: 269-272 https://doi.org/10.1007/BF02856534
  8. Das M, Ram A, Ghosh B. 2003. Luteolin alleviates bronchoconstriction and airway hyperreactivity in ovalbumin sensitized mice. Inflamm Res 52: 101-106 https://doi.org/10.1007/s000110300021
  9. Su CC, Chen GW, Yeh CC, Yang MD, Hung CF, Chung JG. 2003. Luteolin induces N-acetylation and DNA adduct of 2-aminofluorene accompanying N-acetyltransferase activity and gene expression in human bladder cancer T24 cell line. Anticancer Res 23: 355-362
  10. Yee SB, Lee JH, Chung HY, Im KS, Bae SJ, Choi JS, Kim ND. 2003. Inhibitory effects of luteolin isolated from Ixeris sonchifolia Hance on the proliferation of HepG2 human hepatocellular carcinoma cells. Arch Pharm Res 26: 151-156 https://doi.org/10.1007/BF02976662
  11. Chung HS, Hwang KH, Byun SH, Lim SH. 2001. Monoamine oxidase inhibitory activity of green tea produced in China, its processing and province differences. Proceeding of International conferences on O-Cha (tea) culture and science. Shizuoka, Japan
  12. McEwen CM Jr, Sasaki G, Jones DC. 1969. Human liver mitochondrial monoamine oxidase. II. Determination substrate and inhibitor specifies. Biochemistry 8: 3952-3962 https://doi.org/10.1021/bi00838a011
  13. Markham KR. 1975. Isolation techniques for flavonoids. In The flavonoids. Harborne JB, Mabry TJ, Mabry H, eds.Chapman and Hall, London. p 45-126
  14. Mabry TJ, Markham KR, Thomas ME. 1970. Reagents and procedures for the ultraviolet spectral analysis of flavonoids. In The systematic identification of flavonoids. Springer-Verlag, New York. p 35-250
  15. Markham KR, Mabry TJ. 1975. Ultraviolet-visible and proton magnetic resornance spectroscopy of flavonoids. In The flavonoids. Harborne JB, Mabry TJ, Mabry H, eds. Chapman and Hall, London. p 45-126
  16. Markham KR, Ternai B, Stanley R, Geiger H, Mabry TJ.1978. Carbon-13 NMR studies of flavonoids III. Naturally occurring flavonoid glycosides and their acylated derivatives. Tetrahedron 34: 1389-1397 https://doi.org/10.1016/0040-4020(78)88336-7

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