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- W2577668070 endingPage "614" @default.
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- W2577668070 abstract "A novel generation of drugs is introduced in the treatment of heart failure (HF). These drugs, including phosphodiesterase-5 inhibitors, guanylate cyclase stimulators and activators, share the feature that their action is either endothelial-mediated or substitutes for endothelial pathways, in particular the nitric oxide–cyclic guanosine monophosphate pathway, thereby influencing homeostatic balances in virtually each organ system in a pleiotropic fashion. Unfortunately, recent clinical trials with some of these drugs have shown disappointing results, at least in the setting of HF with a preserved ejection fraction. This suggests that their clinical use may require approaches that diverge from traditional pharmacological approaches, the latter often titrated on the effects of drugs on haemodynamic parameters or single biomarkers. In this paper we preconize that HF drugs with an endothelial profile should be applied conform to principles of endothelial physiology and systems pharmacology. This type of drug therapy should be viewed as a systems physio-pharmacological intervention and its clinical use accustomed to systems pharmacological principles, comparable to the systemic endothelial-mediated benefits induced by exercise training in HF. We will review the actions of these drugs and define criteria to which trials with these drugs should comply in order to increase chances of success." @default.
- W2577668070 created "2017-01-26" @default.
- W2577668070 creator A5024401015 @default.
- W2577668070 creator A5036821495 @default.
- W2577668070 creator A5054708047 @default.
- W2577668070 creator A5070351037 @default.
- W2577668070 date "2017-01-19" @default.
- W2577668070 modified "2023-09-24" @default.
- W2577668070 title "The future of pleiotropic therapy in heart failure. Lessons from the benefits of exercise training on endothelial function" @default.
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