Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/123545
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dc.contributor.authorLeo, C.H.-
dc.contributor.authorJelinic, M.-
dc.contributor.authorNg, H.H.-
dc.contributor.authorTare, M.-
dc.contributor.authorParry, L.J.-
dc.date.issued2016-
dc.identifier.citationTrends in Pharmacological Sciences, 2016; 37(6):498-507-
dc.identifier.issn0165-6147-
dc.identifier.issn1873-3735-
dc.identifier.urihttp://hdl.handle.net/2440/123545-
dc.description.abstractVascular dysfunction is an important hallmark of cardiovascular disease. It is characterized by increased sensitivity to vasoconstrictors, decreases in the endothelium-derived vasodilators nitric oxide (NO) and prostacyclin (PGI2), and endothelium-derived hyperpolarization (EDH). Serelaxin (recombinant human relaxin) has gained considerable attention as a new vasoactive drug, largely through its beneficial therapeutic effects in acute heart failure. In this review we first describe the contribution of endogenous relaxin to vascular homeostasis. We then provide a comprehensive overview of the novel mechanisms of serelaxin action in blood vessels that differentiate it from other vasodilator drugs and explain how this peptide could be used more widely as a therapeutic to alleviate vascular dysfunction in several cardiovascular diseases.-
dc.description.statementofresponsibilityChen Huei Leo, Maria Jelinic, Hooi Hooi Ng, MarianneTare, Laura J.Parry-
dc.language.isoen-
dc.publisherElsevier-
dc.rights© 2016 Published by Elsevier Ltd.-
dc.source.urihttp://dx.doi.org/10.1016/j.tips.2016.04.001-
dc.subjectSerelaxin; vascular dysfunction; endothelium; prostanoids; nitric oxide-
dc.titleSerelaxin: a novel therapeutic for vascular diseases-
dc.typeJournal article-
dc.identifier.doi10.1016/j.tips.2016.04.001-
dc.relation.grantNHMRC-
pubs.publication-statusPublished-
dc.identifier.orcidParry, L.J. [0000-0002-6883-3418]-
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