Inhibition of MCP-1 and MIP-2 Chemokines in Murine Trichinellosis: Effect of the Anti-Inflammatory Compound L-Mimosine

Author:

Frydas S.1,Papaioannou N.1,Papazahariadou M.,Hatzistilianou M.2,Karagouni E.3,Trakatelli M.4,Brellou G.1,Petrarca C.5,Castellani M. L.5,Conti P.5,Riccioni G.6,Patruno A.7,Grilli A.7

Affiliation:

1. Department of Pathology, Veterinary Faculty

2. II° Department of Pediatrics; Aristotle University of Thessaloniki

3. Laboratory of Parasite Immunology, Hellenic Pasteur Institute, Athens

4. Department of Biochemistry, Aristotle University of Thessaloniki, Greece

5. Immunology Division, University of Chieti School of Medicine

6. Department of Internal Medicine, University of Chieti School of Medicine, Chieti, Italy

7. Biology Division, University of Chieti School of Medicine, Chieti, Italy

Abstract

Mimosine, is a plant amino-acid which has been reported to block DNA replication in mammalian cells and to arrest cells reversibly towards the end of the G1 phase or at the beginning of the S phase. In this study, 42 mice were infected with T. spiralis, a nematode parasite, and treated with the anti-inflammatory compound L-mimosine, to determine if any alteration in the chronic inflammatory state occurred, by investigating the host's immunological response. MCP-1, a C-C chemokine and MIP-2, a C-X-C chemokine were tested and measured in the sera of infected animals, after 1, 10, 20, 30, 40, 50 and 60 days postinfection, by ELISA method. The diaphragm/muscle and the masseters of the infected mice, were tested for inflammatory response. We found that MCP-1 was partially inhibited by L-mimosine, while MIP-2 was totally inhibited. Moreover, in sections of the diaphragm and masseters, the infiltration of inflammatory cells such as macrophages, lymphocytes and eosinophils were more intense in untreated animals compared to those treated with L-mimosine. These findings show, that L-mimosine may have an inhibitory effect on MCP-1 and MIP-2 serum levels in Trichinellosis and may influence the recruitment of inflammatory cells and the intensity of the inflammatory reaction in this parasitic disease.

Publisher

SAGE Publications

Subject

Pharmacology,Immunology,Immunology and Allergy

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