Inhibition of the pro-inflammatory mediators’ production and anti-inflammatory effect of the iridoid scrovalentinoside

We have studied scrovalentinoside, an iridoid with anti-inflammatory properties isolated from Scrophularia auriculata ssp. pseudoauriculata, as an anti-inflammatory agent in different experimental models of delayed-type hypersensitivity. We found that scrovalentinoside reduced the edema induced by o...

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Bibliographic Details
Published inJournal of ethnopharmacology Vol. 110; no. 3; pp. 419 - 427
Main Authors Bas, Esperanza, Recio, M. Carmen, Abdallah, Mohamed, Máñez, Salvador, Giner, Rosa M., Cerdá-Nicolás, Miguel, Ríos, José-Luis
Format Journal Article
LanguageEnglish
Published Shannon Elsevier Ireland Ltd 04.04.2007
Elsevier
Subjects
NO
LT
PHA
MTT
LPS
IFN
BOC
PBS
IL
NMR
LOX
PG
DTH
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Summary:We have studied scrovalentinoside, an iridoid with anti-inflammatory properties isolated from Scrophularia auriculata ssp. pseudoauriculata, as an anti-inflammatory agent in different experimental models of delayed-type hypersensitivity. We found that scrovalentinoside reduced the edema induced by oxazolone at 0.5 mg/ear and sheep red blood cells at 10 mg/kg. The observed effect occurred during the last phase or inflammatory response; during the earlier phase or induction of the delayed-type hypersensitivity reaction, no significant activity was noted. Thus, scrovalentinoside reduced both the edema and cell infiltration in vivo and reduced lymphocyte proliferation in vitro, affecting the cycle principally during the first 48 h. Whereas cells stimulated with phytohemagglutinin changed from the G 0/G 1 phase to the S and G 2/M phases, when these same cells were treated with scrovalentinoside (100 μM), they remained in the G 0/G 1 phase. Finally, scrovalentinoside inhibited the production of the pro-inflammatory mediators’ TNF-α, IFN-γ, IL-1β, IL-2, IL-4, LTB 4, and NO, but had no effect on the production of the anti-inflammatory cytokine IL-10.
Bibliography:http://dx.doi.org/10.1016/j.jep.2006.09.038
ISSN:0378-8741
1872-7573
DOI:10.1016/j.jep.2006.09.038