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dc.contributor.authorNakagawa-Toyama, Yumiko
dc.contributor.authorZhang, Songwen
dc.contributor.authorKrieger, Monty
dc.date.accessioned2013-01-23T14:58:34Z
dc.date.available2013-01-23T14:58:34Z
dc.date.issued2012-10
dc.date.submitted2012-04
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/76336
dc.description.abstractBackground: Mice with a deficiency in the HDL receptor SR-BI and low expression of a modified apolipoprotein E gene (SR-BI KO/ApoeR61h/h) called ‘HypoE’ when fed an atherogenic, ‘Paigen’ diet develop occlusive, atherosclerotic coronary arterial disease (CHD), myocardial infarctions (MI), and heart dysfunction and die prematurely (50% mortality ~40 days after initiation of this diet). Because few murine models share with HypoE mice these cardinal, human-like, features of CHD, HypoE mice represent a novel, small animal, diet-inducible and genetically tractable model for CHD. To better describe the properties of this model, we have explored the effects of varying the composition and timing of administration of atherogenic diets, as well as social isolation vs. group housing, on these animals. Methodology/Principal Findings: HypoE mice were maintained on a standard lab chow diet (control) until two months of age. Subsequently they received one of three atherogenic diets (Paigen, Paigen without cholate, Western) or control diet for varying times and were housed in groups or singly, and we determined the plasma cholesterol levels, extent of cardiomegaly and/or survival. The rate of disease progression could be reduced by lowering the severity of the atherogenic diet and accelerated by social isolation. Disease could be induced by Paigen diets either containing or free of cholate. We also established conditions under which CHD could be initiated by an atherogenic diet and then subsequently, by replacing this diet with standard lab chow, hypercholesterolemia could be reduced and progression to early death prevented. Conclusions/Significance: HypoE mice provide a powerful, surgery-free, diet-‘titratable’ small animal model that can be used to study the onset of recovery from occlusive, atherosclerotic CHD and heart failure due to MI. HypoE mice can be used for the analysis of the effects of environment (diet, social isolation) on a variety of features of cardiovascular disease.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.)en_US
dc.description.sponsorshipNational Heart, Lung, and Blood Instituteen_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0047965en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleDietary Manipulation and Social Isolation Alter Disease Progression in a Murine Model of Coronary Heart Diseaseen_US
dc.typeArticleen_US
dc.identifier.citationNakagawa-Toyama, Yumiko, Songwen Zhang, and Monty Krieger. “Dietary Manipulation and Social Isolation Alter Disease Progression in a Murine Model of Coronary Heart Disease.” Ed. Massimo Federici. PLoS ONE 7.10 (2012): e47965. Web.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorNakagawa-Toyama, Yumiko
dc.contributor.mitauthorZhang, Songwen
dc.contributor.mitauthorKrieger, Monty
dc.relation.journalPLoS Oneen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsNakagawa-Toyama, Yumiko; Zhang, Songwen; Krieger, Montyen
dc.identifier.orcidhttps://orcid.org/0000-0003-4541-5181
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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