Planta Med 2003; 69(10): 950-953
DOI: 10.1055/s-2003-45107
Letter
© Georg Thieme Verlag Stuttgart · New York

Inhibitory Effects of a New Iridoid, Patridoid II and its Isomers, on Nitric Oxide and TNF-α Production in Cultured Murine Macrophages

Hye Kyung Ju1 , Tae Chul Moon1 , Eunkyung Lee1 , Suk-Hwan Baek2 , Ren-Bo An3 , KiHwan Bae3 , Kun Ho Son4 , Hyun Pyo Kim5 , Sam Sik Kang6 , Sung Ho Lee1 , Jong Keun Son1 , Hyeun Wook Chang1
  • 1College of Pharmacy, Yeungnam University, Gyongsan, Korea
  • 2Department of Biochemistry and Molecular Biology, College of Medicine, Yeungnam University, Daegu, Korea
  • 3College of Pharmacy, Chungnam National University, Taejin, Korea
  • 4Department of Food and Nutrition, Andong National University, Andong, Korea
  • 5College of Pharmacy, Kangwon National University, Chunchen, Korea
  • 6Natural Products Research Institute, Seoul National University, Seoul, Korea
This research was supported by a grant (PF0320302-00) from Plant Diversity Research Center of 21st Century Frontier Research Program funded by the Ministry of Science and Technology of Korea Government
Further Information

Publication History

Received: March 21, 2003

Accepted: July 26, 2003

Publication Date:
02 December 2003 (online)

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Abstract

Patridoids I, II and IIA, are new iridoids isolated from the whole plants of Patrinia saniculaefolia. These compounds were examined by assessing their effects on the production of tumor necrosis factor-α (TNF-α) as well as by investigating the expression of two enzymes, inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2), in the lipopolysaccharide (LPS)-stimulated murine macrophage-like cell line, Raw 264.7. Among them, patridoid II consistently inhibited nitric oxide (NO) and TNF-α production in a dose-dependent manner, with IC50 values of 14.1 and 17.6 μM, respectively. Western Blotting probed with specific anti-iNOS antibodies showed that the decrease in the quantity of the NO product was accompanied by a decrease in the iNOS protein level. However, all three patridoids did not affect the COX-2 protein expression level in the LPS-stimulated macrophages. In addition, the C-5 isomer of patridoid II, patridoid I, only slightly affected the production of NO. Moreover, the C-3 isomer of patridoid II, patridoid IIA, did not inhibit proinflammatory cytokines and NO production. These results suggest that the orientations of the C-3 and C-5 methoxy groups in the patridoids have a significant role in the expression of their biological activity.

References

Hyeun Wook Chang

College of Pharmacy

Yeungnam University

712-749 Gyongsan

Korea

Phone: +82-53-810-2811

Fax: 82-53-811-3871

Email: hwchang@yu.ac.kr