Lactobacillus rhamnosus GG ameliorates noise-induced cognitive deficits and systemic inflammation in rats by modulating the gut-brain axis

Front Cell Infect Microbiol. 2023 Apr 26:13:1067367. doi: 10.3389/fcimb.2023.1067367. eCollection 2023.

Abstract

Background: Environmental noise exposure is linked to neuroinflammation and imbalance of the gut microbiota. Promoting gut microbiota homeostasis may be a key factor in relieving the deleterious non-auditory effects of noise. This study aimed to investigate the effect of Lactobacillus rhamnosus GG (LGG) intervention on noise-induced cognitive deficits and systemic inflammation in rats.

Methods: Learning and memory were assessed using the Morris water maze, while 16S rRNA sequencing and gas chromatography-mass spectrometry were used to analyze the gut microbiota and short-chain fatty acid (SCFA) content. Endothelial tight junction proteins and serum inflammatory mediators were assessed to explore the underlying pathological mechanisms.

Results: The results indicated that Lactobacillus rhamnosus GG intervention ameliorated noise-induced memory deterioration, promoted the proliferation of beneficial bacteria, inhibited the growth of harmful bacteria, improved dysregulation of SCFA-producing bacteria, and regulated SCFA levels. Mechanistically, noise exposure led to a decrease in tight junction proteins in the gut and hippocampus and an increase in serum inflammatory mediators, which were significantly alleviated by Lactobacillus rhamnosus GG intervention.

Conclusion: Taken together, Lactobacillus rhamnosus GG intervention reduced gut bacterial translocation, restored gut and blood-brain barrier functions, and improved gut bacterial balance in rats exposed to chronic noise, thereby protecting against cognitive deficits and systemic inflammation by modulating the gut-brain axis.

Keywords: Lactobacillus rhamnosus GG; cognition; gut microbiota; gut-brain axis; inflammation; noise.

MeSH terms

  • Animals
  • Brain-Gut Axis
  • Cognition
  • Inflammation / metabolism
  • Inflammation Mediators
  • Lacticaseibacillus rhamnosus*
  • Probiotics* / therapeutic use
  • RNA, Ribosomal, 16S
  • Rats
  • Tight Junction Proteins

Substances

  • RNA, Ribosomal, 16S
  • Tight Junction Proteins
  • Inflammation Mediators

Grants and funding

This work was supported by National Natural Science Foundation of China (No. 81673136) and Scientific Research Projects (No. JK20202A020453, 20WQ042) awarded to BC.