Literature DB >> 14648401

Inhibitory effects of a new iridoid, patridoid II and its isomers, on nitric oxide and TNF-alpha production in cultured murine macrophages.

Hye Kyung Ju1, Tae Chul Moon, Eunkyung Lee, Suk-Hwan Baek, Ren-Bo An, KiHwan Bae, Kun Ho Son, Hyun Pyo Kim, Sam Sik Kang, Sung Ho Lee, Jong Keun Son, Hyeun Wook Chang.   

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-alpha (TNF-alpha) 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-alpha production in a dose-dependent manner, with IC (50) values of 14.1 and 17.6 microM, 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.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14648401     DOI: 10.1055/s-2003-45107

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  2 in total

1.  A divergent strategy for the synthesis of secologanin derived natural products.

Authors:  Brandon J English; Robert M Williams
Journal:  J Org Chem       Date:  2010-10-22       Impact factor: 4.354

2.  Synthesis of (+/-)-Oleocanthal via a Tandem Intramolecular Michael Cyclization-HWE Olefination.

Authors:  Brandon J English; Robert M Williams
Journal:  Tetrahedron Lett       Date:  2009-06-10       Impact factor: 2.415

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.