Interactions between the gut microbiome, associated metabolites and the manifestation and progression of heart failure with preserved ejection fraction in ZSF1 rats

Abstract Background: Heart failure with preserved ejection fraction (HFpEF) is associated with systemic inflammation, obesity, metabolic syndrome, and gut microbiome changes. Increased trimethylamine-N-oxide (TMAO) levels are predictive for mortality in HFpEF. The TMAO precursor trimethylamine (TMA) is synthesized by the intestinal microbiome, crosses the intestinal barrier and is metabolized to TMAO by hepatic flavin-containing mono-oxygenase 3 (FMO3). The intricate interactions of microbiome alterations and TMAO in relation to HFpEF manifestation and progression are analyzed here. Methods: Healthy lean (L-ZSF1, n=12) and obese ZSF1 rats with HFpEF (O-ZSF1, n=12) were studied. HFpEF was confirmed by transthoracic echocardiography and detection of N-terminal pro-brain natriuretic peptide (NT-proBNP). TMAO, amino acids and carnitine were measured using mass-spectroscopy. The intestinal epithelial barrier was analyzed by immunohistochemistry and in-vitro impedance measurements. Hepatic FMO3 quantity was determined by Western blot. The fecal microbiome after 8, 13 and 20 weeks was assessed using 16s rRNA amplicon sequencing. Results: Increased levels of TMAO, carnitine (+46%) and the cardiac stress marker NT-proBNP (+25%) as well as a pronounced amino acid imbalance were observed in obese rats with HFpEF. Anatomy and zonula occludens protein density in the intestinal epithelium remained unchanged, but endothelial barrier function was impaired in O-ZSF1. FMO3 was decreased by 20% in the histologically normal livers of O-ZSF1. Alpha diversity, as indicated by the Shannon diversity index, was comparable at eight weeks of age, but decreased when HFpEF manifested in O-ZSF1 at 13 weeks of age. Bray-Curtis dissimilarity (Beta-Diversity) was shown to be effective in differentiating L-ZSF1 from O-ZSF1 at 20 weeks of age. Members of the microbial families Lactobacillaceae, Ruminococcaceae, Erysipelotrichaceae and Lachnospiraceaewere significantly differentially abundant in O-ZSF1 and L-ZSF1 rats. Conclusions: In the ZSF1 HFpEF rat model, increased dietary intake is associated with alterations in gut microbiome composition and bacterial metabolites, an impaired intestinal barrier, and changes in pro-inflammatory and health-predictive metabolic profiles. HFpEF as well as its most common comorbidities obesity and metabolic syndrome and the alterations described here evolve in parallel and are likely to be interrelated and mutually reinforcing. Dietary adaption may have a positive impact on all entities.