Dysbiotic microbiota contributes to the extent of acute myocardial infarction in rats

Sci Rep. 2022 Oct 3;12(1):16517. doi: 10.1038/s41598-022-20826-z.

Abstract

Increasing evidence suggests that the intestinal microbiota composition could play a role in specific pathologies such as hypertension, obesity and diabetes. This study aims to demonstrate that the intestinal microbiota modulated by a diet creating dysbiosis increased the size of the myocardial infarction and that probiotics could attenuate this effect. To do this, microbiota transplants from rats fed a dysbiotic or non-dysbiotic diet in the presence or absence of probiotics were performed for 10 days on rats whose microbiota had been previously suppressed by antibiotic therapy. Then, the anterior coronary artery of the transplanted rats was occluded for 30 min. Infarct size was measured after 24 h of reperfusion, while signaling pathways were evaluated after 15 min of reperfusion. Intestinal resistance, plasma concentration of LPS (lipopolysaccharides), activation of NF-κB and Akt and composition of the microbiota were also measured. Our results demonstrate a larger infarct size in animals transplanted with the dysbiotic microbiota without probiotics compared to the other groups, including those that received the dysbiotic microbiota with probiotics. This increase in infarct size correlates with a higher firmicutes/bacteroidetes ratio, NF-kB phosphorylation and plasma LPS concentration, and a decrease in intestinal barrier resistance and Akt. These results indicate that dysbiotic microbiota promotes an increase in infarct size, an effect that probiotics can attenuate.

MeSH terms

  • Animals
  • Anti-Bacterial Agents
  • Dysbiosis
  • Lipopolysaccharides
  • Microbiota*
  • Myocardial Infarction* / pathology
  • Myocardial Infarction* / therapy
  • NF-kappa B / metabolism
  • Probiotics*
  • Proto-Oncogene Proteins c-akt
  • Rats

Substances

  • Anti-Bacterial Agents
  • Lipopolysaccharides
  • NF-kappa B
  • Proto-Oncogene Proteins c-akt