Lacticaseibacillus casei IB1 Alleviates DSS-Induced Inflammatory Bowel Disease by Regulating the Microbiota and Restoring the Intestinal Epithelial Barrier.
Jianlong LaoShuping YanYanhong YongYin LiZhaohai WenXiaoyong ZhangXiang-Hong JuYouquan LiPublished in: Microorganisms (2024)
Inflammatory bowel disease (IBD) is becoming an increasingly serious health problem in humans and animals. Probiotics can inhibit the development of IBD. Due to the specificity of the strains, the function and mechanism of action of different strains are still unclear. Here, a DSS-induced colitis mouse model was utilized to investigate the ability and mechanism by which Lacticaseibacillus casei IB1 alleviates colitis. Treatment with L. casei IB1 improved DSS-induced colitis in mice, as indicated by increased body weight, colon length, and goblet cell numbers and decreased disease activity index (DAI), proinflammatory factor (TNF-α, IL-1β, and IL-6) levels, and histopathological scores after intake of IB1. IB1 supplementation also improved the expression of tight junction proteins and inhibited the activation of the MAPK and NF-κB signaling pathways to alleviate intestinal inflammation. In addition, IB1 rebalanced the intestinal microbial composition of colitis mice by increasing the abundance of Faecalibaculum and Alistipes and decreasing the abundance of Bacteroides and Escherichia_Shigella . In summary, L. casei IB1 showed great potential for relieving colitis by regulating the microbiota and restoring the epithelial barrier. It can be used as a potential probiotic for the prevention and treatment of UC in the future.
Keyphrases
- signaling pathway
- mouse model
- disease activity
- ulcerative colitis
- rheumatoid arthritis
- body weight
- oxidative stress
- systemic lupus erythematosus
- escherichia coli
- pi k akt
- healthcare
- public health
- ankylosing spondylitis
- stem cells
- blood brain barrier
- human health
- lps induced
- rheumatoid arthritis patients
- diabetic rats
- body mass index
- antibiotic resistance genes
- combination therapy
- cell proliferation
- climate change
- metabolic syndrome
- replacement therapy
- bone marrow
- health information
- nuclear factor
- stress induced