Kaurane diterpenes from Isodon japonicus inhibit nitric oxide and prostaglandin E-2 production and NF-kappa B activation in LPS-stimulated macrophageRAW264.7 cells

Citation
By. Hwang et al., Kaurane diterpenes from Isodon japonicus inhibit nitric oxide and prostaglandin E-2 production and NF-kappa B activation in LPS-stimulated macrophageRAW264.7 cells, PLANTA MED, 67(5), 2001, pp. 406-410
Citations number
22
Categorie Soggetti
Pharmacology & Toxicology
Journal title
PLANTA MEDICA
ISSN journal
00320943 → ACNP
Volume
67
Issue
5
Year of publication
2001
Pages
406 - 410
Database
ISI
SICI code
0032-0943(200107)67:5<406:KDFIJI>2.0.ZU;2-O
Abstract
A methanolic extract of the whole plant of Isodon japonicus (Labiatae) show ed potent inhibition on the LPS-induced nitric oxide (NO) and prostaglandin E-2 (PGE(2)) production in RAW264.7 cells. Four known kaurane diterpenes w ere isolated by activity-guided fractionation and their structures were ide ntified as kamebanin (1), kamebacetal A (2), kamebakaurin (3), excisanin A (4), All compounds also inhibited the LPS-induced NF-kappaB activation as a ssessed by NF-kappaB reporter assay and electrophoretic mobility shift assa y (EMSA). Compounds 2-4 showed comparable inhibitory effects on the LPS-ind uced production of NO and PGE(2), and activation of NF-kappaB without affec ting cell viability. These results suggest that kaurane diterpenes could ex ert their inhibitory effects on the production of NO and PGE(2) through the suppression of NF-kappaB activation, and be partially responsible for the anti-inflammatory activities of the genus Isodon.