Cardiometabolic effects of sacubitril/valsartan in a rat model of heart failure with preserved ejection fraction

Biochem Pharmacol. 2024 Dec;230(Pt 1):116571. doi: 10.1016/j.bcp.2024.116571. Epub 2024 Oct 16.

Abstract

The promising results obtained in the PARADIGM-HF trial prompted the approval of sacubitril/valsartan (SAC/VAL) as a first-in-class treatment for heart failure with reduced ejection fraction (HFrEF) patients. The effect of SAC/VAL treatment was also studied in patients with heart failure with preserved ejection fraction (HFpEF) and, although improvements in New York Heart Association (NYHA) class, HF hospitalizations, and cardiovascular deaths were observed, these results were not so promising. However, the demand for HFpEF therapies led to the approval of SAC/VAL as an alternative treatment, although further studies are needed. We aimed to elucidate the effects of a 9-week SAC/VAL treatment in cardiac function and metabolism using a preclinical model of HFpEF, the Zucker Fatty and Spontaneously Hypertensive (ZSF1) rats. We found that SAC/VAL significantly improved diastolic function parameters and modulated respiratory quotient during exercise. Ex-vivo studies showed that SAC/VAL treatment significantly decreased heart, liver, spleen, and visceral fat weights; cardiac hypertrophy and percentage of fibrosis; lipid infiltration in liver and circulating levels of cholesterol and sodium. Moreover, SAC/VAL reduced glycerophospholipids, cholesterol, and cholesteryl esters while increasing triglyceride levels in cardiac tissue. In conclusion, SAC/VAL treatment improved diastolic and hepatic function, respiratory metabolism, reduced hypercholesterolemia and cardiac fibrosis and hypertrophy, and was able to modulate cardiac metabolic profile. Our findings might provide further insight into the therapeutic benefits of SAC/VAL treatment in obese patients with HFpEF.

Keywords: Diastolic dysfunction; Heart failure with preserved ejection fraction; Metabolome; Sacubitril/valsartan; ZSF1.

MeSH terms

  • Aminobutyrates* / pharmacology
  • Aminobutyrates* / therapeutic use
  • Angiotensin Receptor Antagonists / pharmacology
  • Angiotensin Receptor Antagonists / therapeutic use
  • Animals
  • Biphenyl Compounds* / pharmacology
  • Disease Models, Animal
  • Drug Combinations*
  • Heart Failure* / drug therapy
  • Heart Failure* / metabolism
  • Heart Failure* / physiopathology
  • Male
  • Rats
  • Rats, Inbred SHR*
  • Rats, Zucker*
  • Stroke Volume* / drug effects
  • Stroke Volume* / physiology
  • Tetrazoles / pharmacology
  • Tetrazoles / therapeutic use
  • Valsartan*

Substances

  • Valsartan
  • Biphenyl Compounds
  • Aminobutyrates
  • sacubitril and valsartan sodium hydrate drug combination
  • Drug Combinations
  • Tetrazoles
  • Angiotensin Receptor Antagonists