4.4 Article

Lactobacillus acidophilus modulates inflammatory activity by regulating the TLR4 and NF-B expression in porcine peripheral blood mononuclear cells after lipopolysaccharide challenge

Journal

BRITISH JOURNAL OF NUTRITION
Volume 115, Issue 4, Pages 567-575

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0007114515004857

Keywords

Inflammatory cytokines; Lactobacillus acidophilus; Lipopolysaccharide; Peripheral blood mononuclear cells; Toll-like receptor 4

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A total of forty weaned pigs ((LandracexYorkshire)xDuroc) were used to evaluate the effects of Lactobacillus acidophilus on inflammatory activity after lipopolysaccharide (LPS) challenge. Experimental treatments were as follows: (T1) control diet+saline challenge; (T2) control diet with 01 % L. acidophilus+saline challenge; (T3) control diet+LPS challenge; and (T4) control diet with 01 % L. acidophilus+LPS challenge. On d-14, piglets were challenged with saline (T1 and T2) or LPS (T3 and T4). Blood samples were obtained at 0, 2, 4, 6 and 12 h after being challenged and analysed for immune cell cytokine production and gene expression pattern. The L. acidophilus treatment increased the average daily weight gain (ADWG) and average daily feed intake (ADFI) compared with the control diet. With the control diet, the LPS challenge (T3) increased the number of immune cells and expression of TNF- and IL-6 compared with the saline challenge (T1). Whereas with the saline challenge L. acidophilus treatment (T2) increased the number of leucocytes and CD4 compared with the control diet (T1), with the LPS challenge L. acidophilus treatment (T4) decreased the number of leucocytes, lymphocytes, CD4+ and CD8+ and expression of TNF- and IL-6 compared with the control diet (T3). L. acidophilus treatment decreased the expression of TRL4 and NF-B in peripheral blood mononuclear cells (PBMC) after LPS challenge, which leads to inhibition of TNF-, IFN-, IL-6, IL-8 and IL1B1 and to induction of IL-4 and IL-10. We suggested that L. acidophilus improved ADWG and ADFI and protected against LPS-induced inflammatory responses by regulating TLR4 and NF-B expression in porcine PBMC.

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