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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 |