<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Aragon-Herrera A</submitter><funding>Predoctoral research grant from the PFIS Program of the Spanish Ministry of Science and Instituto de Salud Carlos III (Spain)</funding><funding>Axencia Galega de Innovación (GAIN): Axudas do programa de consolidación e estruturación de unidades de investigación competitivas</funding><funding>Xunta de Galicia</funding><funding>PFIS Program of the Spanish Ministry of Science and Instituto de Salud Carlos III</funding><funding>National Institute of Health “Fondo de Investigaciones Sanitarias del Instituto de Salud Carlos III” Madrid, Spain</funding><funding>Axencia Galega de Innovación</funding><funding>European Regional Development Fund (FEDER) and European Union framework MSCA-RISE-H2020 Programme</funding><funding>Predoctoral research grant from Xunta de Galicia</funding><funding>National Institute of Health "Fondo de Investigaciones Sanitarias del Instituto de Salud Carlos III" Madrid, Spain</funding><pagination>1021</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9317583</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(7)</volume><pubmed_abstract>The pleiotropic hormone relaxin-2 plays a pivotal role in the physiology and pathology of the cardiovascular system. Relaxin-2 exerts relevant regulatory functions in cardiovascular tissues through the specific receptor relaxin family peptide receptor 1 (RXFP1) in the regulation of cardiac metabolism; the induction of vasodilatation; the reversion of fibrosis and hypertrophy; the reduction of inflammation, oxidative stress, and apoptosis; and the stimulation of angiogenesis, with inotropic and chronotropic effects as well. Recent preclinical and clinical outcomes have encouraged the potential use of relaxin-2 (or its recombinant form, known as serelaxin) as a therapeutic strategy during cardiac injury and/or in patients suffering from different cardiovascular disarrangements, especially he</pubmed_abstract><journal>Journal of personalized medicine</journal><pubmed_title>Relaxin-2 as a Potential Biomarker in Cardiovascular Diseases.</pubmed_title><pmcid>PMC9317583</pmcid><funding_grant_id>PI21/01145, RETICS Programme RD16/0012/0014 and CIBER de Enfermedades Cardiovascula-res (CIBERCV)</funding_grant_id><funding_grant_id>734899</funding_grant_id><funding_grant_id>Project number 734899</funding_grant_id><funding_grant_id>Not applicable</funding_grant_id><funding_grant_id>PI21/01145</funding_grant_id><funding_grant_id>RD16/0012/0014</funding_grant_id><funding_grant_id>GPC IN607B 2021 108</funding_grant_id><pubmed_authors>Lago F</pubmed_authors><pubmed_authors>Rosello-Lleti E</pubmed_authors><pubmed_authors>Morana-Fernandez S</pubmed_authors><pubmed_authors>Gualillo O</pubmed_authors><pubmed_authors>Gonzalez-Juanatey JR</pubmed_authors><pubmed_authors>Portoles M</pubmed_authors><pubmed_authors>Aragon-Herrera A</pubmed_authors><pubmed_authors>Feijoo-Bandin S</pubmed_authors><pubmed_authors>Tarazon E</pubmed_authors><pubmed_authors>Anido-Varela L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Relaxin-2 as a Potential Biomarker in Cardiovascular Diseases.</name><description>The pleiotropic hormone relaxin-2 plays a pivotal role in the physiology and pathology of the cardiovascular system. Relaxin-2 exerts relevant regulatory functions in cardiovascular tissues through the specific receptor relaxin family peptide receptor 1 (RXFP1) in the regulation of cardiac metabolism; the induction of vasodilatation; the reversion of fibrosis and hypertrophy; the reduction of inflammation, oxidative stress, and apoptosis; and the stimulation of angiogenesis, with inotropic and chronotropic effects as well. Recent preclinical and clinical outcomes have encouraged the potential use of relaxin-2 (or its recombinant form, known as serelaxin) as a therapeutic strategy during cardiac injury and/or in patients suffering from different cardiovascular disarrangements, especially he</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-04-25T16:52:41.693Z</modification><creation>2022-08-06T22:42:03.644Z</creation></dates><accession>S-EPMC9317583</accession><cross_references><pubmed>35887517</pubmed><doi>10.3390/jpm12071021</doi></cross_references></HashMap>