Bifidobacterium longum is frequently
utilized and has broad prospects for preventing liver injury. The
current research assessed the antioxidant capacity of B. longum BL-10 and probed its mechanism for ameliorating
lipopolysaccharide (LPS)-induced acute liver injury (ALI). B. longum BL-10-encoded 15 antioxidant genes showed
strong reducing power activity and scavenging activity of DPPH, hydroxyl
radicals, and superoxide anions. The intragastric administration of B. longum BL-10 resulting in a marked reduction in
liver function indicators (alanine aminotransferase, aspartate aminotransferase,
total bilirubin, and total bile acid) and proinflammatory cytokines
(TNF-α, IFN-γ, and IL-6) was indicative of ALI recovery.
Following 16s RNA analysis, B. longum BL-10 significantly altered the richness of genera, as for the Escherichia–Shigella, Lachnospiraceae_NK4A136_group, and Clostridia_UCG-014, dramatically contributing to
the formation of acetic acid and butyric acid. Meanwhile, their metabolites
regulated the TLR4/NF-κB signaling pathways to alleviate hepatic
injury symptoms. Overall, all the results demonstrated that B. longum BL-10 had excellent efficiency in preventing
LPS-induced ALI.
Intestine is the largest digestive and immune organ in the human body with an intact intestinal mucosal barrier. Lactobacillus plantarum is an important strain of probiotics in the intestine for...
Ulcerative colitis (UC) is challenging to treat and severely impacts patients and families. A previous study reported immunomodulatory and reduction of pro-inflammatory properties for the Lactiplantibacillus plantarum L15. This study aimed to analyze the preventive properties and mechanistic actions in an in vivo colitis model. The histopathological alteration, inflammation cytokines, and intestinal barrier function were analyzed. Subsequently, the cecal gut microbiota contents and products from different groups were detected. Finally, gene expressions related to the NF-κB signaling process were evaluated. L. plantarum L15 significantly decreased disease activity index (DAI), myeloperoxidase activity (MPO), pro-inflammatory cytokine (TNF-α, IL-1β, and IL-6) level, and increased weight change, colon length, and production of inflammation-suppressing cytokines. Furthermore, this strain supplementation substantially increased ZO-1, Occludin, and Claudin-1, and MUC2 mRNA expression levels with a corresponding decrease in serum lipopolysaccharide and D-lactic acid contents. In addition, L. plantarum L15 improved gut microbiota composition and increased short-chain fatty acid (SCFAs) in the colon content, which significantly reduced the transfer of NF-κB p65 to the nucleus. Our findings provide a theoretical basis for L. plantarum L15 as a preventive candidate for UC.
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