Administration of Lactobacillus salivarius LI01 or Pediococcus pentosaceus LI05 prevents CCl4-induced liver cirrhosis by protecting the intestinal barrier in rats
Alterations in the gut microbiome have been reported in liver cirrhosis, and probiotic interventions are considered a potential treatment strategy. This study aimed to evaluate the effects and mechanisms of Lactobacillus salivarius LI01, Pediococcus pentosaceus LI05, Lactobacillus rhamnosus GG, Clos...
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Veröffentlicht in: | Scientific reports 2017-07, Vol.7 (1), p.1-13, Article 6927 |
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Sprache: | eng |
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Zusammenfassung: | Alterations in the gut microbiome have been reported in liver cirrhosis, and probiotic interventions are considered a potential treatment strategy. This study aimed to evaluate the effects and mechanisms of
Lactobacillus salivarius
LI01,
Pediococcus pentosaceus
LI05,
Lactobacillus rhamnosus
GG,
Clostridium butyricum
MIYAIRI and
Bacillus licheniformis
Zhengchangsheng on CCl
4
-induced cirrhotic rats. Only administration of LI01 or LI05 prevented liver fibrosis and down-regulated the hepatic expression of profibrogenic genes. Serum endotoxins, bacterial translocations (BTs), and destruction of intestinal mucosal ultrastructure were reduced in rats treated with LI01 or LI05, indicating maintenance of the gut barrier as a mechanism; this was further confirmed by the reduction of not only hepatic inflammatory cytokines, such as TNF-α, IL-6, and IL-17A, but also hepatic TLR2, TLR4, TLR5 and TLR9. Metagenomic sequencing of 16S rRNA gene showed an increase in potential beneficial bacteria, such as
Elusimicrobium
and
Prevotella
, and a decrease in pathogenic bacteria, such as
Escherichia
. These alterations in gut microbiome were correlated with profibrogenic genes, gut barrier markers and inflammatory cytokines. In conclusion,
L
.
salivarius
LI01 and
P
.
pentosaceus
LI05 attenuated liver fibrosis by protecting the intestinal barrier and promoting microbiome health. These results suggest novel strategies for the prevention of liver cirrhosis. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-017-07091-1 |