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Updated: Jun 13, 2025

Probiotic Studies in Neonatal Mice Using Gavage
Published on: January 27, 2019
Bifidobacterium regulates premature infant gut metabolites, reducing serum inflammatory factors: a randomised
He Wang1,2, Dongmei Chen1,2, Huamei Li1,2
1The Graduate School of Fujian Medical University, Fuzhou, Fujian, China.
Insights
Bifidobacterium BB-12 supplementation in premature infants increased beneficial gut amino acids and reduced inflammatory markers, leading to improved feeding tolerance. This probiotic intervention shows promise for managing inflammation and feeding issues in preterm neonates.
Area of Science:
- Neonatal nutrition and gut microbiome research
- Immunology and inflammatory pathways in preterm infants
- Probiotic effects on infant health outcomes
Background:
- Premature infants often experience intestinal dysbiosis and inflammation.
- Feeding intolerance is a common complication in preterm neonates.
- The role of specific probiotics like Bifidobacterium BB-12 in modulating infant gut health is under investigation.
Purpose of the Study:
- To investigate the impact of Bifidobacterium BB-12 on intestinal metabolites in premature infants.
- To assess the effect of Bifidobacterium BB-12 on serum inflammatory markers.
- To evaluate the influence of Bifidobacterium BB-12 on the incidence of feeding intolerance.
Main Methods:
- A randomized controlled trial involving 71 premature infants (gestational age ≤32 weeks).
- Infants were assigned to either a probiotic group (Bifidobacterium BB-12) or a control group.
- Faecal and blood samples were collected at 2 and 4 weeks for metabolite and inflammatory marker analysis (TLR4, NF-κB, IL-1β, TNF-α).
Main Results:
- The probiotic group exhibited higher levels of intestinal amino acids, including glutamine, glutamic acid, and kynurenine.
- Significantly lower serum levels of inflammatory markers (TLR4, NF-κB, IL-1β, TNF-α) were observed in the probiotic group.
- The incidence of feeding intolerance was notably lower in infants receiving Bifidobacterium BB-12.
Conclusions:
- Bifidobacterium BB-12 administration increases beneficial amino acids in the preterm infant gut.
- This probiotic reduces key serum inflammatory markers and pro-inflammatory cytokine secretion.
- Bifidobacterium BB-12 supplementation alleviates systemic inflammation, thereby improving feeding tolerance and reducing intolerance incidence.
Background:
Analyse the effects of Bifidobacterium BB-12 on intestinal metabolites and serum inflammatory factors in premature infants.
Methods:
71 premature infants at gestational age of ≤32 weeks were randomly divided into the probiotic (n = 36) and control (n = 35) groups. Faecal and blood samples were collected from the two groups of premature infants at the 2nd and 4th week of life for intestinal metabolite detection and assessment of the level of the serum inflammatory markers TLR4, NF- κ B, IL-1β, and TNF- α.
Results:
Compared to the control group, the probiotic group contained more amino acids, these elements were enriched on multiple amino acid metabolic pathways, and the probiotic group showed significantly lower levels of the serum inflammatory markers TLR4, NF-κB, IL-1β, and TNF-α. Finally, the probiotic group showed a lower incidence of feeding intolerance.
Conclusions:
The administration of Bifidobacterium BB-12 is associated with increasing the levels of glutamine, glutamic acid, and kynurenine in the gut of premature infants, and associated with reducing the levels of TLR4 and NF-κB in the serum, further decreasing the secretion of the pro-inflammatory factors IL-1β and TNF-α, and alleviating systemic inflammatory reactions, thereby reducing the incidence of feeding intolerance.
Impact:
1. The use of Bifidobacterium BB-12 in premature infants can increase the levels of amino acids in the intestine. 2. Increases in Bifidobacterium BB-12 may decrease the serum levels of TLR4, NF-κB, IL-1β, and TNF-α. 3. Kynurenine may improve the prognosis of preterm infants by reducing inflammation. 4. Bifidobacterium BB-12 may improve the feeding tolerance of premature infants, thus reducing the incidence of feeding intolerance.
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