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

[Display omitted] 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 f...

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Veröffentlicht in:Biochemical pharmacology 2024-12, Vol.230 (Pt 1), p.116571, Article 116571
Hauptverfasser: Moraña-Fernández, Sandra, Vázquez-Abuín, Xocas, Aragón-Herrera, Alana, Anido-Varela, Laura, García-Seara, Javier, Otero-García, Óscar, Rodríguez-Penas, Diego, Campos-Toimil, Manuel, Otero-Santiago, Manuel, Rodrigues, Alexandre, Gonçalves, Alexandre, Pereira Morais, Juliana, Alves, Inês N., Sousa-Mendes, Cláudia, Falcão-Pires, Inês, González-Juanatey, José Ramón, Feijóo-Bandín, Sandra, Lago, Francisca
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container_issue Pt 1
container_start_page 116571
container_title Biochemical pharmacology
container_volume 230
creator Moraña-Fernández, Sandra
Vázquez-Abuín, Xocas
Aragón-Herrera, Alana
Anido-Varela, Laura
García-Seara, Javier
Otero-García, Óscar
Rodríguez-Penas, Diego
Campos-Toimil, Manuel
Otero-Santiago, Manuel
Rodrigues, Alexandre
Gonçalves, Alexandre
Pereira Morais, Juliana
Alves, Inês N.
Sousa-Mendes, Cláudia
Falcão-Pires, Inês
González-Juanatey, José Ramón
Feijóo-Bandín, Sandra
Lago, Francisca
description [Display omitted] 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.
doi_str_mv 10.1016/j.bcp.2024.116571
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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. 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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.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>39424202</pmid><doi>10.1016/j.bcp.2024.116571</doi><orcidid>https://orcid.org/0000-0003-3089-0684</orcidid></addata></record>
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subjects Aminobutyrates - pharmacology
Aminobutyrates - therapeutic use
Angiotensin Receptor Antagonists - pharmacology
Angiotensin Receptor Antagonists - therapeutic use
Animals
Biphenyl Compounds - pharmacology
Diastolic dysfunction
Disease Models, Animal
Drug Combinations
Heart Failure - drug therapy
Heart Failure - metabolism
Heart Failure - physiopathology
Heart failure with preserved ejection fraction
Male
Metabolome
Rats
Rats, Inbred SHR
Rats, Zucker
Sacubitril/valsartan
Stroke Volume - drug effects
Stroke Volume - physiology
Tetrazoles - pharmacology
Tetrazoles - therapeutic use
Valsartan
ZSF1
title Cardiometabolic effects of sacubitril/valsartan in a rat model of heart failure with preserved ejection fraction
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