4.7 Article

Protective effects of probiotic Lactobacillus casei Zhang against endotoxin- and D-galactosamine-induced liver injury in rats via anti-oxidative and anti-inflammatory capacities

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 15, Issue 1, Pages 30-37

Publisher

ELSEVIER
DOI: 10.1016/j.intimp.2012.10.026

Keywords

Lactobacillus casei Zhang; Lipopolysaccharide; D-Galactosamine; Liver injury; THF-alpha; TLR4

Funding

  1. National Natural Science Foundation of China [31025019, 30801001, 31270922, 81260622]
  2. China Postdoctoral Science Foundation [20110491553]
  3. Innovation Team Development of the Ministry of Education of China [IRT0967]
  4. China Agriculture Research System [CARS-37]

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Lactobacillus casei Zhang (LcZ) has been recently isolated from the traditional Mongolian beverage koumiss and has a set of favorable probiotic properties, including aciduricity, bile resistance and ability to colonize the gastrointestinal tract. We have previously reported the anti-oxidative properties of LcZ in the hyperlipidemic rats. In this study, the hepatoprotective effects of LcZ against lipopolysaccharide (LPS) and D-galactosamine (D-GalN)-induced liver injury were investigated. We found that pretreatment with LcZ significantly improved survival of rats challenged with LPS/D-GalN. In addition, pretreatment with LcZ significantly decreased alanine transaminase (ALT) and aspartate aminotransferase (AST) levels in LPS/D-GalN-challenged rats, which were accompanied by diminished liver injuries, reduced malondialdehyde (MDA) content and increased superoxide dismutase (SOD) activity in liver homogenates. Pretreatment with LcZ also markedly reduced LPS/D-GalN-induced production of hepatic nitric oxide (NO), activation of inducible nitric oxide synthase (iNOS) and expression of tumor necrosis factor-alpha (TNF-alpha). Furthermore, hepatic toll-like receptor 4 (TLR4) mRNA and protein levels, the phosphorylation of I-kappa B and translocation of nuclear factor kappa B (NF-kappa B) were significantly down-regulated by pretreatment with LcZ. These results suggest that pretreatment with LcZ protects against LPS/D-GalN-induced liver injury in rats via its anti-oxidative and anti-inflammatory capacities. The hepatoprotective effects of LcZ are associated with an inhibition of TLR4 expression and TLR4 signaling. (C) 2012 Elsevier B.V. All rights reserved.

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