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Generation of TNFα, IFNγ, IL-4, IL-6 and IL-10 in Trichinella spiralis infected mice: effect of the anti-inflammatory compound mimosine.

Authors :
Frydas, S.
Papaioannou, N.
Hatzistilianou, M.
Merlitti, D.
Di Gioacchino, M.
Castellani, M.L.
Conti, P.
Source :
Inflammopharmacology; 2002, Vol. 9 Issue 4, p389-400, 12p, 5 Black and White Photographs, 2 Graphs
Publication Year :
2002

Abstract

The plant amino acid mimosine has been demonstrated to arrest cell cycle progression in the late G1-phase, and inhibits [3H] thymidine incorporation in cultured fibroblasts. In this study, 10 mice were infected with Trichinella spiralis, a nematode parasite, and treated with the antiinflammatory compound L-mimosine to determine if any alteration in the chronic inflammatory state occurred by investigating the host's immunological response. Mimosine was used at 250 μg/bolus for 25 days starting five days before the infection and continuing daily for 35 days then TNFα, IFN-γ, IL-4, IL-6, and IL-10 were determined by ELISA method, after 0, 1, 7, 14, 21, 28, 35 days post-infection, in the serum of treated or untreated animals. When animals with T. spiralis were treated with L-mimosine, inhibition of TNFα was observed within 21 days post-infection, compared with the controls (untreated mice). IFNγ was inhibited only up to the 21[sup st] day, while IL-6 was inhibited up to the 7[sup th] day post-infection and the inhibition of IL-4 was seen mainly at 21[sup st] and 35[sup th] day p.i. Mimosine-treated mice did not statistically affect the secretion of IL-10 (p > 0.05). In healthy animals, the production of cytokines were within the same limits compared with those of non-infected animals treated with L-mimosine. Our studies suggest that mimosine proved to be more effective in inhibiting TNFα and IL-6, which are mainly produced by macrophages and less effective in inhibiting IL-4, which is produced by T-cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09254692
Volume :
9
Issue :
4
Database :
Complementary Index
Journal :
Inflammopharmacology
Publication Type :
Academic Journal
Accession number :
7288151
Full Text :
https://doi.org/10.1163/156856001320290642