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Lactobacillus fermentum exerts a beneficial effect in an experimental model of rheumatoid arthritis in mice

Published online by Cambridge University Press:  12 May 2008

M. E. Rodríguez-Cabezas
Affiliation:
Department of Pharmacology, University of Granada, Spain
F. Fisac
Affiliation:
Department of Pharmacology, University of Granada, Spain
E. Bailon
Affiliation:
Department of Pharmacology, University of Granada, Spain
M. Comalada
Affiliation:
Department of Pharmacology, University of Granada, Spain
D. Camuesco
Affiliation:
Department of Pharmacology, University of Granada, Spain
J. Xaus
Affiliation:
Puleva Biotech SA, Granada, Spain
A. Concha
Affiliation:
Department of Pathology, Hospital Universitario ‘Virgen de las Nieves’, Granada, Spain
P. Talavera
Affiliation:
Department of Pathology, Hospital Universitario ‘Virgen de las Nieves’, Granada, Spain
A. Nieto
Affiliation:
Health and Progress Foundation, Granada, Spain
A. Zarzuelo
Affiliation:
Department of Pharmacology, University of Granada, Spain
J. Galvez
Affiliation:
Department of Pharmacology, University of Granada, Spain
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Abstract

Type
1st International Immunonutrition Workshop, Valencia, 3–5 October 2007, Valencia, Spain
Copyright
Copyright © The Authors 2008

Previous studies have shown the intestinal anti-inflammatory activity of the probiotic Lactobacillus fermentum CECT 5716 acting as a modulator of the intestinal immune response(Reference Peran, Camuesco and Comalada1). The aim of the present study was to determine the efficacy of this probiotic as a systemic immune modulator in the experimental model of rheumatoid arthritis induced by Mycobacterium butyricum–Freund's adjuvant in mice(Reference Mihara, Nishimoto, Yoshizaki and Suzuki2). Male Balb/C mice (n 10) were given the probiotic in the drinking water (108 colony-forming units (CFU)/ml) for 2 weeks and a control group (n 20) not receiving probiotic was also used for reference. After this period 0.1 ml of a suspension of 10 mg Mycobacterium butyricum in 10 ml Freund's adjuvant was administered subcutaneously in the right paw in treated mice and in half the control group, whereas Freund's adjuvant was administered in the left paw of the mice; normal mice (n 10) only received Freund's adjuvant in both paws. Animals were assessed for clinical arthritis for 4 weeks, and after this period all mice were killed and their arthritic status evaluated by histological analysis of the paws. In addition, the spleens were removed and T-cells were obtained from spleens and activated with concanavalin A and the lymphocyte response evaluated by RT–PCR for the cytokines IL-2 and IL-10.

The results showed that the probiotic treatment ameliorated the severity of the disease since it significantly improved the clinical arthritis score (6.0 (se 0.7) in control mice with arthritis v. 3.3 (se 0.3) in probiotic-treated mice; P<0.05) (Figure 1). Similar findings were obtained by histological analysis. Mycobacterium-induced arthritis also stimulated the expression of IL-2 in the splenocytes, which was also reduced in the probiotic-treated mice. Although IL-10 expression by splenic T-cells was not modified during the course of arthritis in control mice, treatment with the probiotic stimulated the expression of this regulatory cytokine in mice with arthritis. In conclusion, probiotic treatment ameliorated the disease outcome in the Mycobacterium butyricum model of rheumatoid arthritis in mice, showing systemic immunomodulatory properties.

References

1. Peran, L, Camuesco, D, Comalada, M et al. (2006) Int J Colorectal Dis 21, 737746.CrossRefGoogle Scholar
2. Mihara, M, Nishimoto, N, Yoshizaki, K & Suzuki, T (2002) Immunol Lett 4, 223229.CrossRefGoogle Scholar