Transplanted Gut Bacteria Causes Cardiovascular Changes in Mice

sleep apnea mask
Researchers from the University of Missouri School of Medicine and MU Health Care have found probiotics improved symptoms for recipient, but not donor mice

Researchers from the University of Missouri School of Medicine and MU Health Care have discovered how obstructive sleep apnea- affects the gut microbiome in mice and how transplanting gut bacteria from sleep apnea affected mice can cause cardiovascular changes in the recipient mice.

Obstructive sleep apnea (OSA) is a chronic sleep condition affecting more than 1 billion people worldwide. Evidence suggests OSA can alter the gut microbiome and may promote OSA-associated comorbidities, including diabetes, hypertension, ischemic heart disease, and cognitive problems.

This study examined a group of mice given gut bacteria from mice exposed to conditions that mimic sleep apnea. The researchers compared cardiovascular outcomes in those mice to a separate group that was given bacteria from mice that weren’t exposed to apnea conditions. Over six weeks, the researchers monitored arterial blood pressure, coronary artery and aorta function along with blood analysis measuring a gut-derived metabolite known to promote hardening of the arteries.

“We discovered that the mice with transplanted gut bacteria from donors exposed to sleep apnea conditions experienced a blood pressure increase, higher harmful metabolite levels and impairments in aortic and coronary function,” said study co-author Mohammad Badran, PhD, MSc, B Pharm, assistant professor at MU’s Child Health Research Institute. “In other words, the changes in gut microbiome alone were sufficient to induce some of the changes in cardiovascular function that are characteristically seen in patient with OSA.”

The researchers also gave each group of mice a probiotic to see if beneficial gut bacteria would mitigate the damage caused to the cardiovascular system.

David Gozal, MD
David Gozal, MD

“Our results showed targeted probiotic supplementation exerts protective effects against cardiovascular disease for the mice that received transplanted gut bacteria, but we were surprised to learn that the benefit did not extend to the mice being directly exposed to  apnea conditions,” said senior author David Gozal, MD, the Marie M. and Harry L. Smith Endowed Chair of Pediatrics at the MU School of Medicine. “These findings indicate probiotics alone are insufficient to protect against the many adverse effects induced by chronic sleep apnea, including inflammation, metabolic dysregulation and antioxidant imbalance, and that probiotics may need to be given in conjunction with the standard treatment of OSA which is CPAP to enhance the probiotic benefit.”

Gozal said this data shows that altered gut bacteria is one factor — but not the only one — responsible for modulating sleep apnea-induced cardiovascular disease. However, he said this study reveals that probiotics may be a promising therapy to mitigate the impact of sleep apnea on the cardiovascular system.

In addition to Gozal and Badran, the study authors include fellow MU School of Medicine collaborators Clementine Puech, PhD, postdoctoral fellow; Zachary McAdams, graduate student; and Abdelnaby Khalyfa, PhD, associate professor. Also contributing to the report was Aaron Ericsson, DVM, assistant professor of the MU College of Veterinary Medicine; and Shawn Bender, PhD, associate professor, Department of Biomedical Sciences.

The study, “Gut microbiota mediate vascular dysfunction in a murine model of sleep apnea: effect of probiotics,” was recently published by the European Respiratory Journal. Research reported in this publication was supported by grants from the National Institutes of Health and a grant from the University of Missouri. The contents of this publication do not necessarily represent the official views of the funding agencies.