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dc.date.accessioned | 2020-10-13T12:55:35Z | |
dc.date.available | 2020-10-13T12:55:35Z | |
dc.date.issued | 2012 | |
dc.identifier.uri | http://sedici.unlp.edu.ar/handle/10915/106764 | |
dc.description.abstract | The objective of this study was to establish whether 1) hyperactivity of renin-angiotensin-aldosterone system (RAAS) produces apoptosis in early stages of cardiac disease; and 2) Ca2+-calmodulin-dependent protein kinase II (CaMKII) is involved in these apoptotic events. Two models of hypertrophy were used at an early stage of cardiac disease: spontaneously hypertensive rats (SHR) and isoproterenol-treated rats (Iso-rats). At 4 mo, SHR showed blood pressure, aldosterone serum levels, used as RAAS activity index, and left ventricular mass index, used as hypertrophy index, above control values by 84.2 6 2.6 mmHg, 211.2 6 25.8%, and 8.6 6 1.1 mg/mm, respectively. There was also an increase in apoptotis (Bax-to-Bcl-2 ratio and terminal deoxynucleotidyl transferase dUTP-mediated nick-end labeling positive cells) associated with an enhancement of CaMKII activity with respect to age-matched controls (phosphorylated-CaMKII, 98.7 6 14.1 above control). Similar results were observed in 4-mo-old Isorats. Cardiac function studied by echocardiography remained unaltered in all groups. Enalapril treatment significantly prevented hypertrophy, apoptosis, and CaMKII activity. Moreover, intracellular Ca2+ handling in isolated myocytes was similar between SHR, Iso-rats, and their aged-matched controls. However, SHR and Iso-rats showed a significant increase in superoxide anion generation (lucigenin) and lipid peroxidation (thiobarbituric acid reactive substance). In transgenic mice with targeted cardiomyocyte expression of a CaMKII inhibitory peptide (AC3-I) or a scrambled control peptide (AC3-C), Iso treatment increased thiobarbituric acid reactive substance in both strains, whereas it increased CaMKII activity and apoptosis only in AC3-C mice. Endogenous increases in RAAS activity induce ROS and CaMKII-dependent apoptosis in vivo. CaMKII activation could not be associated with intracellular Ca2+ increments and was directly related to the increase in oxidative stress. | en |
dc.format.extent | 2110-2120 | es |
dc.language | en | es |
dc.subject | angiotensin II | es |
dc.subject | Ca2+-calmodulin-dependent protein kinase II | es |
dc.subject | reactive oxygen species | es |
dc.subject | hypertrophy | es |
dc.subject | apoptosis | es |
dc.title | Early apoptosis in different models of cardiac hypertrophy induced by high renin-angiotensin system activity involves CaMKII | en |
dc.type | Articulo | es |
sedici.identifier.uri | http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC3774203&blobtype=pdf | es |
sedici.identifier.other | pmid:22492934 | es |
sedici.identifier.other | pmcid:PMC3774203 | es |
sedici.identifier.other | doi:10.1152/japplphysiol.01383.2011 | es |
sedici.identifier.issn | 8750-7587 | es |
sedici.creator.person | Vélez Rueda, Jorge Omar | es |
sedici.creator.person | Palomeque, Julieta | es |
sedici.creator.person | Mattiazzi, Alicia Ramona | 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 | Journal of Applied Physiology | es |
sedici.relation.journalVolumeAndIssue | vol. 112, no. 12 | es |