Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16716
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dc.contributor.authorSingh, Jagdeep SS-
dc.contributor.authorBurrell, Louise M-
dc.contributor.authorCherif, Myriam-
dc.contributor.authorSquire, Iain B-
dc.contributor.authorClark, Andrew L-
dc.contributor.authorLang, Chim C-
dc.date2017-07-08-
dc.date.accessioned2017-07-13T01:31:12Z-
dc.date.available2017-07-13T01:31:12Z-
dc.date.issued2017-10-
dc.identifier.citationHeart 2017;103(2): 1569-1577en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16716-
dc.description.abstractNatriuretic peptides, especially B-type natriuretic peptide (BNP), have primarily been regarded as biomarkers in heart failure (HF). However, they are also possible therapeutic agents due to their potentially beneficial physiological effects. The angiotensin receptor-neprilysin inhibitor, sacubitril/valsartan, simultaneously augments the natriuretic peptide system (NPS) by inhibiting the enzyme neprilysin (NEP) and inhibits the renin-angiotensin-aldosterone system (RAAS) by blocking the angiotensin II receptor. It has been shown to improve mortality and hospitalisation outcomes in patients with HF due to left ventricular systolic dysfunction. The key advantage of sacubitril/valsartan has been perceived to be its ability to augment BNP, while its other effects have largely been overlooked. This review highlights the important effects of sacubitril/valsartan, beyond just the augmentation of BNP. First we discuss how NPS physiology differs between healthy individuals and those with HF by looking at mechanisms like the overwhelming effects of RAAS on the NPS, natriuretic peptide receptor desensitisation and absolute natriuretic deficiency. Second, this review explores other hormones that are augmented by sacubitril/valsartan such as bradykinin, substance P and adrenomedullin that may contribute to the efficacy of sacubitril/valsartan in HF. We also discuss concerns that sacubitril/valsartan may interfere with amyloid-β homeostasis with potential implications on Alzheimer's disease and macular degeneration. Finally, we explore the concept of 'autoinhibition' which is a recently described observation that humans have innate NEP inhibitory capability when natriuretic peptide levels rise above a threshold. There is speculation that autoinhibition may provide a surge of natriuretic and other vasoactive peptides to rapidly reverse decompensation. We contend that by pre-emptively inhibiting NEP, sacubitril/valsartan is inducing this surge earlier during decompensation, resulting in the better outcomes observed.en_US
dc.subjectAlzheimer’s diseaseen_US
dc.subjectB-type natriuretic peptideen_US
dc.subjectSacubitril/valsartanen_US
dc.subjectAngiotensin receptor-neprilysin inhibitoren_US
dc.subjectBradykininen_US
dc.subjectMechanism of actionen_US
dc.subjectNatriuretic peptidesen_US
dc.titleSacubitril/valsartan: beyond natriuretic peptidesen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleHearten_US
dc.identifier.affiliationDivision of Molecular and Clinical Medicine, Ninewells Hospital and Medical School, University of Dundee, Dundee, UKen_US
dc.identifier.affiliationMedicine (University of Melbourne)en_US
dc.identifier.affiliationNovartis Pharmaceuticals, Frimley Business Park, Frimley, Surrey, UKen_US
dc.identifier.affiliationDepartment of Cardiovascular Sciences, University of Leicester and Leicester NIHR Cardiovascular Biomedical Research Unit, Glenfield Hospital, Leicester, UKen_US
dc.identifier.affiliationDepartment of Academic Cardiology, University of Hull, Daisy Building, Castle Hill Hospital, Castle Road, Cottingham, UKen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/28689178en_US
dc.identifier.doi10.1136/heartjnl-2017-311295en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0003-1863-7539en_US
dc.type.austinJournal Articleen_US
local.name.researcherBurrell, Louise M
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
crisitem.author.deptCardiology-
crisitem.author.deptGeneral Medicine-
crisitem.author.deptMedicine (University of Melbourne)-
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