casei CRL 431 during 7 days (Lc), and 7 days selleck chemicals llc post infection for infection control (S), mice given probiotic 7 days before the infection (Lc-S), and mice given continuously probiotic, before and after infection (Lc-S-Lc). Results for healthy mice obtained

the same day of the infected animals were not added Selleckchem LXH254 because there were not significant differences compared to the basal data. Results are expressed as the means ± SD of the total number of positive cells per 2 × 104 counted cells at 1 000X magnification. Means for each value without a common letter differ significantly (P < 0.01). Measurement of cytokines released by immune cells isolated from Peyer's patches of mice untreated or treated with the probiotic strain previous and post infection Cells isolated from Peyer's patches of healthy mice fed 7 days with L. casei CRL 431 (Lc group) increased significantly (p < 0.01) the release of IFNγ and IL-10 compared to the untreated Selleckchem Trichostatin A control (C group). Seven days after infection, the cells from the infection control group (S) increased significantly (p < 0.01) the release of IFNγ and TNFα, compared to the untreated

control (C). However, at this time point, the IFNγ levels in the culture supernatant of cells isolated from the two groups fed with the probiotic strain (Lc-S and Lc-S-Lc groups) decreased significantly (p < 0.01) compared to the infection control (S). The concentration of this cytokine from Lc-S-Lc group was similar to those obtained from healthy mice fed with L. casei (Lc group). The production of TNFα did not show significant differences (p < 0.01) in all the groups after Salmonella infection. Seven days after infection, the cells isolated from S and Lc-S groups showed similar releases of IL-10, without significant differences compared to healthy mice (C and

Inositol oxygenase Lc groups). Continuous probiotic administration before and after infection decreased significantly (p < 0.01) the IL-10 release by the Peyer’s patches mononuclear cells compared to the other infected groups, and the values were similar to those obtained from cells of the untreated control (C) (Table 2). Table 2 Effect of L. casei CRL 431 administration on the cytokines released in cultures of immune cells isolated from Peyer’s patches of mice untreated, treated and infected with S. Typhimurium Experimental groups Cytokine concentration (pg/ml)   TNFα IFNγ IL-10 C 203 ± 32a 139 ± 83a 65 ± 13ac Lc 257 ± 55ac 1175 ± 563bc 187 ± 91b S 336 ± 90bcd 1384 ± 74c 102 ± 42ab Lc-S 328 ± 4b 148 ± 86a 102 ± 24ab Lc-S-Lc 432 ± 20d 592 ± 40b 34 ± 18c The concentration of different cytokines were evaluated in supernatant of cultures of cells isolated from Peyer’s patches of mice at 2 time points: the day of the infection (basal data) for the untreated control (C) and for mice given L.