The Role of Gut Microbiota in Male Erectile Dysfunction of RatsOriginal paper
What was studied?
This study investigated whether high-fat-diet (HFD) induced disruption of the gut microbiota contributes to erectile dysfunction (ED) in rats. Researchers compared erectile function and stool-based 16S rRNA sequencing profiles between rats fed a normal diet (ND) and rats fed an HFD for 24 weeks. To test whether the microbiota itself was responsible for this effect, they performed fecal microbiota transplantation (FMT), transplanting stool from ND-group and HFD-group rats into new groups of rats and again assessing erectile function, microbiota composition, and serum metabolomics after another 24 weeks.
Who was studied?
The subjects were male Sprague-Dawley rats, aged 8 weeks at the start of the experiment. They were randomly divided into a normal diet group and a high-fat diet group for the initial phase, then two additional groups of rats received fecal microbiota transplants from those donor groups. No human subjects were studied; the findings come entirely from this rat model.
What were the most important findings?
Erectile function and intestinal microbiota species diversity were both significantly lower in the HFD group compared to the ND group, and overall microbiota community structure differed markedly between the two groups. Critically, rats that received fecal microbiota transplants from HFD-diet donors (HFD-FMT group) also developed significantly lower erectile function than rats transplanted with normal-diet microbiota (ND-FMT group). The microbiota community characteristics in the FMT recipient groups mirrored those of their respective donor groups, and serum metabolomic differences were also detected between groups.
What are the greatest implications of this study?
These findings suggest that HFD-induced gut microbiota dysbiosis is not merely associated with erectile dysfunction but can causally transmit impaired erectile function, since transplanting dysbiotic microbiota alone reproduced the deficit in previously unexposed rats. This supports a gut-microbiota-to-erectile-function axis, potentially mediated through microbial metabolites detectable in serum. The results point to the gut microbiome as a possible target for future diagnostic or therapeutic strategies in diet-related erectile dysfunction, though this remains to be tested in humans.