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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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 |
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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 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.</description><identifier>ISSN: 0006-2952</identifier><identifier>ISSN: 1873-2968</identifier><identifier>EISSN: 1873-2968</identifier><identifier>DOI: 10.1016/j.bcp.2024.116571</identifier><identifier>PMID: 39424202</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>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</subject><ispartof>Biochemical pharmacology, 2024-12, Vol.230 (Pt 1), p.116571, Article 116571</ispartof><rights>2024 Elsevier Inc.</rights><rights>Copyright © 2024 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c235t-85c2bd42bef57f9c6433d2f4e523e3d9d4127ea77e9dcaaf94a066b43b7ac7b13</cites><orcidid>0000-0003-3089-0684</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006295224005719$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39424202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moraña-Fernández, Sandra</creatorcontrib><creatorcontrib>Vázquez-Abuín, Xocas</creatorcontrib><creatorcontrib>Aragón-Herrera, Alana</creatorcontrib><creatorcontrib>Anido-Varela, Laura</creatorcontrib><creatorcontrib>García-Seara, Javier</creatorcontrib><creatorcontrib>Otero-García, Óscar</creatorcontrib><creatorcontrib>Rodríguez-Penas, Diego</creatorcontrib><creatorcontrib>Campos-Toimil, Manuel</creatorcontrib><creatorcontrib>Otero-Santiago, Manuel</creatorcontrib><creatorcontrib>Rodrigues, Alexandre</creatorcontrib><creatorcontrib>Gonçalves, Alexandre</creatorcontrib><creatorcontrib>Pereira Morais, Juliana</creatorcontrib><creatorcontrib>Alves, Inês N.</creatorcontrib><creatorcontrib>Sousa-Mendes, Cláudia</creatorcontrib><creatorcontrib>Falcão-Pires, Inês</creatorcontrib><creatorcontrib>González-Juanatey, José Ramón</creatorcontrib><creatorcontrib>Feijóo-Bandín, Sandra</creatorcontrib><creatorcontrib>Lago, Francisca</creatorcontrib><title>Cardiometabolic effects of sacubitril/valsartan in a rat model of heart failure with preserved ejection fraction</title><title>Biochemical pharmacology</title><addtitle>Biochem Pharmacol</addtitle><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.</description><subject>Aminobutyrates - pharmacology</subject><subject>Aminobutyrates - therapeutic use</subject><subject>Angiotensin Receptor Antagonists - pharmacology</subject><subject>Angiotensin Receptor Antagonists - therapeutic use</subject><subject>Animals</subject><subject>Biphenyl Compounds - pharmacology</subject><subject>Diastolic dysfunction</subject><subject>Disease Models, Animal</subject><subject>Drug Combinations</subject><subject>Heart Failure - drug therapy</subject><subject>Heart Failure - metabolism</subject><subject>Heart Failure - physiopathology</subject><subject>Heart failure with preserved ejection fraction</subject><subject>Male</subject><subject>Metabolome</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Zucker</subject><subject>Sacubitril/valsartan</subject><subject>Stroke Volume - drug effects</subject><subject>Stroke Volume - physiology</subject><subject>Tetrazoles - pharmacology</subject><subject>Tetrazoles - therapeutic use</subject><subject>Valsartan</subject><subject>ZSF1</subject><issn>0006-2952</issn><issn>1873-2968</issn><issn>1873-2968</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rGzEQhkVpaNwkP6CXomMvdvS1X-RUTJMGArk0ZzGSRlhmd7WRdh3y7yvXbo89zQx63wf0EPKFsw1nvL7db4ydNoIJteG8rhr-gax428i16Or2I1kxxuqyV-KSfM55fzzbmn8il7JTQpXeikxbSC7EAWcwsQ-Wovdo50yjpxnsYsKcQn97gD5DmmGkYaRAE8x0iA77Y2yH5YV6CP2SkL6FeUenhBnTAR3FfaGFOFKf4M9yTS58geHNeV6Rl_sfv7Y_10_PD4_b709rK2Q1r9vKCuOUMOirxne2VlI64RVWQqJ0nVNcNAhNg52zAL5TwOraKGkasI3h8op8O3GnFF8XzLMeQrbY9zBiXLKWnLeSKdmqEuWnqE0x54ReTykMkN41Z_ooWu91Ea2PovVJdOl8PeMXM6D71_hrtgTuTgEsnzwETDrbgKNFF1JRol0M_8H_BtpTkB0</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Moraña-Fernández, Sandra</creator><creator>Vázquez-Abuín, Xocas</creator><creator>Aragón-Herrera, Alana</creator><creator>Anido-Varela, Laura</creator><creator>García-Seara, Javier</creator><creator>Otero-García, Óscar</creator><creator>Rodríguez-Penas, Diego</creator><creator>Campos-Toimil, Manuel</creator><creator>Otero-Santiago, Manuel</creator><creator>Rodrigues, Alexandre</creator><creator>Gonçalves, Alexandre</creator><creator>Pereira Morais, Juliana</creator><creator>Alves, Inês N.</creator><creator>Sousa-Mendes, Cláudia</creator><creator>Falcão-Pires, Inês</creator><creator>González-Juanatey, José Ramón</creator><creator>Feijóo-Bandín, Sandra</creator><creator>Lago, Francisca</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3089-0684</orcidid></search><sort><creationdate>202412</creationdate><title>Cardiometabolic effects of sacubitril/valsartan in a rat model of heart failure with preserved ejection fraction</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c235t-85c2bd42bef57f9c6433d2f4e523e3d9d4127ea77e9dcaaf94a066b43b7ac7b13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aminobutyrates - pharmacology</topic><topic>Aminobutyrates - therapeutic use</topic><topic>Angiotensin Receptor Antagonists - pharmacology</topic><topic>Angiotensin Receptor Antagonists - therapeutic use</topic><topic>Animals</topic><topic>Biphenyl Compounds - pharmacology</topic><topic>Diastolic dysfunction</topic><topic>Disease Models, Animal</topic><topic>Drug Combinations</topic><topic>Heart Failure - drug therapy</topic><topic>Heart Failure - metabolism</topic><topic>Heart Failure - physiopathology</topic><topic>Heart failure with preserved ejection fraction</topic><topic>Male</topic><topic>Metabolome</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Zucker</topic><topic>Sacubitril/valsartan</topic><topic>Stroke Volume - drug effects</topic><topic>Stroke Volume - physiology</topic><topic>Tetrazoles - pharmacology</topic><topic>Tetrazoles - therapeutic use</topic><topic>Valsartan</topic><topic>ZSF1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moraña-Fernández, Sandra</creatorcontrib><creatorcontrib>Vázquez-Abuín, Xocas</creatorcontrib><creatorcontrib>Aragón-Herrera, Alana</creatorcontrib><creatorcontrib>Anido-Varela, Laura</creatorcontrib><creatorcontrib>García-Seara, Javier</creatorcontrib><creatorcontrib>Otero-García, Óscar</creatorcontrib><creatorcontrib>Rodríguez-Penas, Diego</creatorcontrib><creatorcontrib>Campos-Toimil, Manuel</creatorcontrib><creatorcontrib>Otero-Santiago, Manuel</creatorcontrib><creatorcontrib>Rodrigues, Alexandre</creatorcontrib><creatorcontrib>Gonçalves, Alexandre</creatorcontrib><creatorcontrib>Pereira Morais, Juliana</creatorcontrib><creatorcontrib>Alves, Inês N.</creatorcontrib><creatorcontrib>Sousa-Mendes, Cláudia</creatorcontrib><creatorcontrib>Falcão-Pires, Inês</creatorcontrib><creatorcontrib>González-Juanatey, José Ramón</creatorcontrib><creatorcontrib>Feijóo-Bandín, Sandra</creatorcontrib><creatorcontrib>Lago, Francisca</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moraña-Fernández, Sandra</au><au>Vázquez-Abuín, Xocas</au><au>Aragón-Herrera, Alana</au><au>Anido-Varela, Laura</au><au>García-Seara, Javier</au><au>Otero-García, Óscar</au><au>Rodríguez-Penas, Diego</au><au>Campos-Toimil, Manuel</au><au>Otero-Santiago, Manuel</au><au>Rodrigues, Alexandre</au><au>Gonçalves, Alexandre</au><au>Pereira Morais, Juliana</au><au>Alves, Inês N.</au><au>Sousa-Mendes, Cláudia</au><au>Falcão-Pires, Inês</au><au>González-Juanatey, José Ramón</au><au>Feijóo-Bandín, Sandra</au><au>Lago, Francisca</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cardiometabolic effects of sacubitril/valsartan in a rat model of heart failure with preserved ejection fraction</atitle><jtitle>Biochemical pharmacology</jtitle><addtitle>Biochem Pharmacol</addtitle><date>2024-12</date><risdate>2024</risdate><volume>230</volume><issue>Pt 1</issue><spage>116571</spage><pages>116571-</pages><artnum>116571</artnum><issn>0006-2952</issn><issn>1873-2968</issn><eissn>1873-2968</eissn><abstract>[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.</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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