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The NO-cGMP-PKG Axis in HFpEF: From Pathological Mechanisms to Potential Therapies

Zhulan Cai, Cencen Wu, Yuan Xu, Jiageng Cai, Menglin Zhao, Lingyun Zu

2022Aging and Disease52 citationsDOIOpen Access PDF

Abstract

Heart failure with preserved ejection fraction (HFpEF) accounts for almost half of all heart failure (HF) cases worldwide. Unfortunately, its incidence is expected to continue to rise, and effective therapy to improve clinical outcomes is lacking. Numerous efforts currently directed towards the pathophysiology of human HFpEF are uncovering signal transduction pathways and novel therapeutic targets. The nitric oxide-cyclic guanosine phosphate-protein kinase G (NO-cGMP-PKG) axis has been described as an important regulator of cardiac function. Suppression of the NO-cGMP-PKG signalling pathway is involved in the progression of HFpEF. Therefore, the NO-cGMP-PKG signalling pathway is a potential therapeutic target for HFpEF. In this review, we aim to explore the mechanism of NO-cGMP-PKG in the progression of HFpEF and to summarize potential therapeutic drugs that target this signalling pathway.

Topics & Concepts

MedicineCyclic guanosine monophosphateHeart failure with preserved ejection fractioncGMP-dependent protein kinaseHeart failureNitric oxideSignal transductionPathologicalInternal medicineTherapeutic approachCardiologyPharmacologyEjection fractionCell biologyBiologyDiseaseCyclin-dependent kinase 2CancerCell cycleNitric Oxide and Endothelin EffectsHeart Failure Treatment and ManagementReceptor Mechanisms and Signaling
The NO-cGMP-PKG Axis in HFpEF: From Pathological Mechanisms to Potential Therapies | Litcius