Planta Med 2002; 68(8): 685-689
DOI: 10.1055/s-2002-33810
Original Paper
Pharmacology
© Georg Thieme Verlag Stuttgart · New York

Inhibition of Inducible Nitric Oxide Synthesis by Catalposide from Catalpa ovata

Hyuncheol Oh1 , Hyun-Ock Pae2 , Gi-Su Oh2 , Seung Yeob Lee3 , Kyu-Yun Chai2 , Choong Eui Song4 , Tae-Oh Kwon2, 3 , Hun-Taeg Chung2 , Ho-Sub Lee1
  • 1Professional Graduate School of Oriental Medicine, Wonkwang University, Iksan, Chonbuk, Republic of Korea
  • 2Medicinal Resources Research Center, Wonkwang University, Iksan, Chonbuk, Republic of Korea
  • 3College of Life Science and Natural Resources, Wonkwang University, Iksan, Chonbuk, Republic of Korea
  • 4Life Sciences Division, Korea Institute of Science and Technology, Cheongryang, Seoul, Republic of Korea
Further Information

Publication History

Received: November 5, 2001

Accepted: March 17, 2002

Publication Date:
09 September 2002 (online)

Abstract

Catalposide (1) and two related iridoids were isolated from the stem of Catalpa ovata (Bignoniaceae) by bioassay guided fractionation. Catalposide (1) significantly inhibited the production of nitric oxide (NO) in lipopolysaccharide (LPS)-stimulated RAW 264.7 macrophages in a dose-dependent manner. RT-PCR and Western blot analyses demonstrated that catalposide (1) suppressed the expression of inducible nitric oxide synthase (iNOS) gene and iNOS protein. Catalposide (1) also inhibited the activation of LPS-induced NF-κB as analyzed by electrophoretic mobility shift assay (EMSA). In addition to the inhibitory effect on NO production in LPS-stimulated RAW 264.7 cells, catalposide (1) significantly inhibited the NO production in cytokine-stimulated human DLD-1 and rat vascular smooth muscle (VSM) cells in a dose-dependent manner.

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Prof. Ho-Sub Lee

Professional Graduate School of Oriental Medicine

Wonkwang University

Iksan 570-749

Korea

Email: host@wonkwang.ac.kr

Fax: +82-63-850-7324

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