TY - JOUR
T1 - Cardiometabolic effects of sacubitril/valsartan in a rat model of heart failure with preserved ejection fraction
AU - Moraña-Fernández, Sandra
AU - Vázquez-Abuín, Xocas
AU - Aragón-Herrera, Alana
AU - Anido-Varela, Laura
AU - García-Seara, Javier
AU - Otero-García, Óscar
AU - Rodríguez-Penas, Diego
AU - Campos-Toimil, Manuel
AU - Otero-Santiago, Manuel
AU - Rodrigues, Alexandre
AU - Gonçalves, Alexandre
AU - Pereira Morais, Juliana
AU - Alves, Inês N.
AU - Sousa-Mendes, Cláudia
AU - Falcão-Pires, Inês
AU - Ramón González-Juanatey, José
AU - Feijóo-Bandín, Sandra
AU - Lago, Francisca
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2024/12
Y1 - 2024/12
N2 - 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.
AB - 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.
KW - Diastolic dysfunction
KW - Heart failure with preserved ejection fraction
KW - Metabolome
KW - Sacubitril/valsartan
KW - ZSF1
UR - http://www.scopus.com/inward/record.url?scp=85206618083&partnerID=8YFLogxK
U2 - 10.1016/j.bcp.2024.116571
DO - 10.1016/j.bcp.2024.116571
M3 - Article
AN - SCOPUS:85206618083
SN - 0006-2952
VL - 230
JO - Biochemical pharmacology
JF - Biochemical pharmacology
M1 - 116571
ER -