Related Experiment Video
Updated: Jul 29, 2025

Improved Renal Denervation Mitigated Hypertension Induced by Angiotensin II Infusion
Published on: May 26, 2022
Sacubitril/valsartan: research progress of multi-channel therapy for cardiorenal syndrome
Shuangcui Wang1, Yuli Wang2, Yun Deng2
1Oncology Department, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Insights
Cardiorenal syndrome (CRS) involves heart and kidney dysfunction. Sacubitril/valsartan, targeting both renin-angiotensin-aldosterone system (RAAS) and natriuretic peptide (NP) systems, shows promise for treating CRS, though further research is needed.
Area of Science:
- Cardiology
- Nephrology
- Pharmacology
Background:
- Cardiorenal syndrome (CRS) is a complex condition with increasing incidence and mortality.
- Current treatments for CRS are limited, with drugs targeting only the renin-angiotensin-aldosterone system (RAAS) or natriuretic peptide (NP) systems proving ineffective.
- Sacubitril/valsartan simultaneously modulates both RAAS and NP systems.
Purpose of the Study:
- To summarize the pathophysiological mechanisms of CRS.
- To review the preliminary clinical application effects of sacubitril/valsartan in CRS prevention and treatment.
- To provide a pharmacological basis for using sacubitril/valsartan in CRS management.
Main Methods:
- Literature review focusing on RAAS and NP systems in CRS.
- Analysis of existing research on sacubitril/valsartan's effects on cardiovascular and renal function.
- Examination of recent studies, including animal models combining levosimendan and sacubitril/valsartan.
Main Results:
- Sacubitril/valsartan simultaneously regulates RAAS and NP systems, key pathways in CRS.
- Recent research indicates potential cardioprotective and renoprotective effects of combined levosimendan and sacubitril/valsartan in rats.
- Clinical data on sacubitril/valsartan specifically for CRS treatment remains inconclusive.
Conclusions:
- Sacubitril/valsartan presents a potential therapeutic strategy for CRS due to its dual-action mechanism.
- Further clinical studies are warranted to confirm the efficacy and safety of sacubitril/valsartan in treating cardiorenal syndrome.
- Understanding RAAS and NP biomarkers is crucial for advancing CRS pharmacotherapy.
Abstract:
Cardiorenal syndrome (CRS) results from complex interaction between heart and kidneys, inducing simultaneous acute or chronic dysfunction of these organs. Although its incidence rate is increasing with higher mortality in patients, effective clinical treatment drugs are currently not available. The literature suggests that renin-angiotensin-aldosterone system (RAAS) and diuretic natriuretic peptide (NP) system run through CRS. Drugs only targeting the RAAS and NPs systems are not effective. Sacubitril/valsartan contains two agents (sacubitril and valsartan) that can regulate RAAS and NPs simultaneously. In the 2017 American College of Cardiology/American Heart Association/American Heart Failure (HF) ssociation (ACC/AHA/HFSA) guideline, sacubitril/valsartan was recommended as standard therapy for HF patients. The latest research shows that Combined levosimendan and Sacubitril/Valsartan markets are protected the heart and kidney against cardiovascular syndrome in rat. However, fewer studies have reported its therapeutic efficacy in CRS treatment, and their results are inconclusive. Therefore, based on RAAS and NPs as CRS biomarkers, this paper summarizes possible pathophysiological mechanisms and preliminary clinical application effects of sacubitril/valsartan in the prevention and treatment of CRS. This will provide a pharmacological justification for expanding sacubitril/valsartan use to the treatment of CRS.
Related Concept Videos
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System
Heart Failure V: Medical Management
Heart Failure VI: Adjunct Therapies
Cardiomyopathy V: Interprofessional Care
Continuous Renal Replacement Therapy
Antihypertensive Drugs: Direct Renin Inhibitors

