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dc.date.accessioned 2019-11-08T13:31:18Z
dc.date.available 2019-11-08T13:31:18Z
dc.date.issued 2014
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/85202
dc.description.abstract Aims Cardiomyocyte swelling occurs in multiple pathological situations and has been associated with contractile dysfunction, cell death, and enhanced propensity to arrhythmias.We investigate whether hypotonic swelling promotes nitric oxide (NO) release in cardiomyocytes, and whether it impacts on swelling-induced contractile dysfunction. Methods and results Superfusing rat cardiomyocytes with a hypotonic solution (HS; 217 mOsm), increased cell volume, reduced myocyte contraction and Ca2+ transient, and increased NO-sensitive 4-amino-5-methylamino-2', 7'-difluorofluorescein diacetate (DAF-FM) fluorescence. When cells were exposed to HS + 2.5 mMof theNOsynthase inhibitor L-NAME, cell swelling occurred in the absence of NOrelease. Swelling-induced NO release was also prevented by the nitric oxide synthase 1 (NOS1) inhibitor, nitroguanidine, and significantly reduced in NOS1 knockout mice. Additionally, colchicine (inhibitor of microtubule polymerization) prevented the increase in DAF-FM fluorescence induced by HS, indicating that microtubule integrity is necessary for swelling-inducedNOrelease. The swelling-induced negative inotropic effectwas exacerbated in the presence of either L-NAME, nitroguandine, the guanylate cyclase inhibitor, ODQ, or the PKG inhibitor, KT5823, suggesting that NOS1-derived NO provides contractile support via a cGMP/PKG-dependent mechanism. Indeed, ODQ reduced Ca2+ wave velocity and both ODQ and KT5823 reduced the HS-induced increment in ryanodine receptor (RyR2, Ser2808) phosphorylation, suggesting that in this context, cGMP/PKG may contribute to preserve contractile function by enhancing sarcoplasmic reticulum Ca2+ release. Conclusions Our findings suggest a novel mechanism for NO release in cardiomyocytes with putative pathophysiological relevance determined, at least in part, by its capability to reduce the extent of contractile dysfunction associated with hypotonic swelling. en
dc.format.extent 456-466 es
dc.language en es
dc.subject Contractile dysfunction es
dc.subject Hypotonic swelling es
dc.subject Ischaemia reperfusion es
dc.subject Nitric oxide es
dc.title Hypotonic swelling promotes nitric oxide release in cardiac ventricular myocytes: Impact on swelling-induced negative inotropic effect en
dc.type Articulo es
sedici.identifier.other doi:10.1093/cvr/cvu230 es
sedici.identifier.other eid:2-s2.0-84927933021 es
sedici.identifier.issn 0008-6363 es
sedici.creator.person Gonano, Luis Alberto es
sedici.creator.person Morell, Malena es
sedici.creator.person Burgos, Juan Ignacio es
sedici.creator.person Dulce, Raúl Ariel es
sedici.creator.person De Giusti, Verónica Celeste es
sedici.creator.person Aiello, Ernesto Alejandro es
sedici.creator.person Hare, J. M. es
sedici.creator.person Vila Petroff, Martín Gerardo es
sedici.subject.materias Ciencias Médicas es
sedici.description.fulltext true es
mods.originInfo.place Centro de Investigaciones Cardiovasculares es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Cardiovascular Research es
sedici.relation.journalVolumeAndIssue vol. 104, no. 3 es
sedici.rights.sherpa * Color: green * Pre-print del autor: si * Post-print del autor: si * Versión de editor/PDF:no * Condiciones: >>Pre-print si only be posted prior to acceptance >>Pre-print must be accompanied by set statement (see link) >>Pre-print must not be replaced with post-print, instead a link to published version with amended set statement should be made >>Pre-print on author's personal website, employer website, free public server or pre-prints in subject area >>Post-print on author's personal website immediately >>Post-print in Institutional repositories or Central repositories after 12 months embargo >>Publisher's version/PDF no be used >>Published source must be acknowledged >>Must link to publisher version >>Set phrase to accompany archived copy (see policy) >>The publisher will deposit in PubMed Central on behalf of NIH authors >>Publisher last contacted on 19/02/2015 * Link a Sherpa: http://sherpa.ac.uk/romeo/issn/0008-6363/es/


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)