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Studies of Prevention, Treatment and Mechanisms of Heart Failure in the Aging Spontaneously Hypertensive Rat

dc.contributor.authorBing, Oscar H. L.en_US
dc.contributor.authorConrad, Chester H.en_US
dc.contributor.authorBoluyt, Marvin O.en_US
dc.contributor.authorRobinson, Kathleen G.en_US
dc.contributor.authorBrooks, Wesley W.en_US
dc.date.accessioned2006-09-11T16:31:04Z
dc.date.available2006-09-11T16:31:04Z
dc.date.issued2002-01en_US
dc.identifier.citationBing, Oscar H. L.; Conrad, Chester H.; Boluyt, Marvin O.; Robinson, Kathleen G.; Brooks, Wesley W.; (2002). "Studies of Prevention, Treatment and Mechanisms of Heart Failure in the Aging Spontaneously Hypertensive Rat." Heart Failure Reviews 7(1): 71-88. <http://hdl.handle.net/2027.42/45828>en_US
dc.identifier.issn1382-4147en_US
dc.identifier.issn1573-7322en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/45828
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11790924&dopt=citationen_US
dc.description.abstractThe spontaneously hypertensive rat (SHR) is an animal model of genetic hypertension which develops heart failure with aging, similar to man. The consistent pattern of a long period of stable hypertrophy followed by a transition to failure provides a useful model to study mechanisms of heart failure with aging and test treatments at differing phases of the disease process. The transition from compensated hypertrophy to failure is accompanied by changes in cardiac function which are associated with altered active and passive mechanical properties of myocardial tissue; these events define the physiologic basis for cardiac decompensation. In examining the mechanism for myocardial tissue dysfunction, studies have demonstrated a central role for neurohormonal activation, and specifically the renin-angiotensin-aldosterone system. Pharmacologic attenuation of this system at differing points in the course of the process suggests that prevention but not reversal of myocardial tissue dysfunction is possible. The roles of the extracellular matrix, apoptosis, intracellular calcium, beta-adrenergic stimulation, microtubules, and oxygen supply-demand relationships in ultimately mediating myocardial tissue dysfunction are reviewed. Studies suggest that while considerable progress has been made in understanding and treating the transition to failure, our current state of knowledge is limited in scope and we are not yet able to define specific mechanisms responsible for tissue dysfunction. It will be necessary to integrate information on the roles of newly discovered, and as yet undiscovered, genes and pathways to provide a clearer understanding of maladaptive remodeling seen with heart failure. Understanding the mechanism for tissue dysfunction is likely to result in more effective treatments for the prevention and reversal of heart failure with aging. It is anticipated that the SHR model will assist us in reaching these important goals.en_US
dc.format.extent845985 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherCardiologyen_US
dc.subject.otherAgingen_US
dc.subject.otherHypertrophyen_US
dc.subject.otherHeart Failureen_US
dc.subject.otherHeart Failure Preventionen_US
dc.subject.otherMyocardial Functionen_US
dc.subject.otherFibrosisen_US
dc.subject.otherEnergeticsen_US
dc.subject.otherIntracellular Calciumen_US
dc.subject.otherApoptosisen_US
dc.subject.otherMicrotubulesen_US
dc.subject.otherAngiotensin IIen_US
dc.titleStudies of Prevention, Treatment and Mechanisms of Heart Failure in the Aging Spontaneously Hypertensive Raten_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumLaboratory of Molecular Kinesiology, The University of Michigan, Ann Arbor, MI, 48109-2214en_US
dc.contributor.affiliationotherBoston University School of Medicine, Boston, MA, 02130en_US
dc.contributor.affiliationotherBoston University School of Medicine, Boston, MA, 02130en_US
dc.contributor.affiliationotherBoston University School of Medicine, Boston, MA, 02130en_US
dc.contributor.affiliationotherBoston University School of Medicine, Boston, MA, 02130en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid11790924en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/45828/1/10741_2004_Article_391524.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1013753907135en_US
dc.identifier.sourceHeart Failure Reviewsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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