Linked Life Data

21549710

Source:http://linkedlifedata.com/resource/pubmed/id/21549710

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-6-27
pubmed:abstractText
We have previously reported that resistin induces hypertrophy and impairs contractility in isolated rat cardiomyocytes. To examine the long-term cardiovascular effects of resistin, we induced in vivo overexpression of resistin using adeno-associated virus serotype 9 injected by tail vein in rats and compared to control animals. Ten weeks after viral injection, overexpression of resistin was associated with increased ratio of left ventricular (LV) weight/body weight, increased end-systolic LV volume and significant decrease in LV contractility, measured by the end-systolic pressure volume relationship slope in LV pressure volume loops, compared to controls. At the molecular level, mRNA expression of ANF and ?-MHC, and protein levels of phospholamban were increased in the resistin group without a change in the level of SERCA2a protein expression. Increased fibrosis by histology, associated with increased mRNA levels of collagen, fibronectin and connective tissue growth factor were observed in the resistin-overexpressing hearts. Resistin overexpression was also associated with increased apoptosis in vivo, along with an apoptotic molecular phenotype in vivo and in vitro. Resistin-overexpressing LV tissue had higher levels of TNF-? receptor 1 and iNOS, and reduced levels of eNOS. Cardiomyocytes overexpressing resistin in vitro produced larger amounts of TNF? in the medium, had increased phosphorylation of I?B? and displayed increased intracellular reactive oxygen species (ROS) content with increased expression and activity of ROS-producing NADPH oxidases compared to controls. Long-term resistin overexpression is associated with a complex phenotype of oxidative stress, inflammation, fibrosis, apoptosis and myocardial remodeling and dysfunction in rats. This phenotype recapitulates key features of diabetic cardiomyopathy. This article is part of Special Issue Item Group entitled "Possible Editorial".
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1095-8584
pubmed:author
pubmed:copyrightInfo
Copyright © 2011 Elsevier Ltd. All rights reserved.
pubmed:issnType
Electronic
pubmed:volume
51
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
144-55
pubmed:meshHeading
pubmed-meshheading:21549710-Animals, pubmed-meshheading:21549710-Apoptosis, pubmed-meshheading:21549710-Biological Markers, pubmed-meshheading:21549710-Blood Glucose, pubmed-meshheading:21549710-Cells, Cultured, pubmed-meshheading:21549710-Fibrosis, pubmed-meshheading:21549710-Gene Expression, pubmed-meshheading:21549710-Gene Expression Regulation, pubmed-meshheading:21549710-Heart, pubmed-meshheading:21549710-Heart Ventricles, pubmed-meshheading:21549710-Hemodynamics, pubmed-meshheading:21549710-Hypertrophy, Left Ventricular, pubmed-meshheading:21549710-Inflammation Mediators, pubmed-meshheading:21549710-Male, pubmed-meshheading:21549710-Myocardium, pubmed-meshheading:21549710-Myocytes, Cardiac, pubmed-meshheading:21549710-Nitric Oxide Synthase, pubmed-meshheading:21549710-Oxidative Stress, pubmed-meshheading:21549710-Rats, pubmed-meshheading:21549710-Rats, Sprague-Dawley, pubmed-meshheading:21549710-Resistin, pubmed-meshheading:21549710-Ventricular Remodeling
pubmed:year
2011
pubmed:articleTitle
Long-term in vivo resistin overexpression induces myocardial dysfunction and remodeling in rats.
pubmed:affiliation
Cardiovascular Research Institute, Mount Sinai School of Medicine, New York, NY, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural