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Noninvasive Assessment of Lipid Disposition in Treated and Untreated Atherosclerotic Rabbits

dc.contributor.authorMcConnell, Daniel S.en_US
dc.contributor.authorCounsell, Raymond E.en_US
dc.contributor.authorDegalan, Mark R.en_US
dc.contributor.authorDeForge, Laura E.en_US
dc.date.accessioned2006-09-08T19:21:40Z
dc.date.available2006-09-08T19:21:40Z
dc.date.issued1989-12en_US
dc.identifier.citationDeForge, Laura E.; DeGalan, Mark R.; McConnell, Daniel S.; Counsell, Raymond E.; (1989). "Noninvasive Assessment of Lipid Disposition in Treated and Untreated Atherosclerotic Rabbits." Pharmaceutical Research 6(12): 1011-1016. <http://hdl.handle.net/2027.42/41532>en_US
dc.identifier.issn1573-904Xen_US
dc.identifier.issn0724-8741en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41532
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2622856&dopt=citationen_US
dc.description.abstractIn an effort to visualize whole body cholesteryl ester (CE) deposition using the nuclear medicine imaging technique of gamma camera scintigraphy, 125 I-cholesteryl iopanoate ( 125 I-CI), a nonhydrolyzable CE analogue, was used as a marker for CE deposition in atherosclerotic New Zealand white rabbits. Groups of animals were fed either a cholesterol-enriched diet (2%, w/w) or the same diet supplemented with the hypolipidemic drugs colestipol (1%, w/w) and/or clofibrate (0.3%, w/w). Injections of 125 I-CI were administered biweekly. At the end of 15 weeks, animals were scintigraphically scanned and sacrificed for tissue analysis. The results demonstrated that while drug treatment had no significant effect on plasma lipid levels, it substantially lessened atherosclerotic involvement in the thoracic-abdominal aorta. These differences in aortic lipid accumulation were reflected in the whole-body scans which showed a reduction in tissue accumulation of 125 I-CI in the drug-treated groups. Gamma camera scintigraphy thus represents a rapid means of visualizing tissue CE accumulation which could facilitate the evaluation of lipid-lowering drug efficacy and possible antiatherosclerotic effect.en_US
dc.format.extent1710054 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers-Plenum Publishers; Plenum Publishing Corporation ; Springer Science+Business Mediaen_US
dc.subject.otherBiochemistry, Generalen_US
dc.subject.otherClofibrateen_US
dc.subject.otherPharmacyen_US
dc.subject.otherPharmacology/Toxicologyen_US
dc.subject.otherNoninvasive Imagingen_US
dc.subject.otherBiomedical Engineeringen_US
dc.subject.otherRabbiten_US
dc.subject.otherNonhydrolyzable Cholesteryl Esteren_US
dc.subject.otherBiomedicineen_US
dc.subject.otherColestipolen_US
dc.subject.otherMedical Lawen_US
dc.subject.otherAtherosclerosisen_US
dc.titleNoninvasive Assessment of Lipid Disposition in Treated and Untreated Atherosclerotic Rabbitsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPharmacy and Pharmacologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumInterdepartmental Program in Medicinal Chemistry, University of Michigan, Ann Arbor, Michigan, 48109en_US
dc.contributor.affiliationumDepartment of Pharmacology, University of Michigan Medical School, M6322 Medical Science Building I, Ann Arbor, Michigan, 48109-0626en_US
dc.contributor.affiliationumDepartment of Pharmacology, University of Michigan, Ann Arbor, Michigan, 48109en_US
dc.contributor.affiliationotherUniversity of Miami School of Medicine, Miami, Florida, 33101en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid2622856en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41532/1/11095_2004_Article_306114.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1015918202142en_US
dc.identifier.sourcePharmaceutical Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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