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Inhibition of aortic wall calcification in bioprosthetic heart valves by ethanol pretreatment: Biochemical and biophysical mechanisms

dc.contributor.authorLee, Chi-Hyunen_US
dc.contributor.authorVyavahare, Narendra R.en_US
dc.contributor.authorZand, Roberten_US
dc.contributor.authorKruth, Howarden_US
dc.contributor.authorSchoen, Frederick J.en_US
dc.contributor.authorBianco, Richarden_US
dc.contributor.authorLevy, Robert J.en_US
dc.date.accessioned2006-04-28T16:36:12Z
dc.date.available2006-04-28T16:36:12Z
dc.date.issued1998-10en_US
dc.identifier.citationLee, Chi-Hyun; Vyavahare, Narendra; Zand, Robert; Kruth, Howard; Schoen, Frederick J.; Bianco, Richard; Levy, Robert J. (1998)."Inhibition of aortic wall calcification in bioprosthetic heart valves by ethanol pretreatment: Biochemical and biophysical mechanisms." Journal of Biomedical Materials Research 42(1): 30-37. <http://hdl.handle.net/2027.42/38020>en_US
dc.identifier.issn0021-9304en_US
dc.identifier.issn1097-4636en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/38020
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9740004&dopt=citationen_US
dc.description.abstractThe effectiveness of ethanol pretreatment on preventing calcification of glutaraldehyde-fixed porcine aortic bioprosthetic heart valve (BPHV) cusps was previously demonstrated, and the mechanism of action of ethanol was attributed in part to both lipid removal and a specific collagen conformational change. In the present work, the effect of ethanol pretreatment on BPHV aortic wall calcification was investigated using both rat subdermal and sheep circulatory implants. Ethanol pretreatment significantly inhibited calcification of BPHV aortic wall, but with less than complete inhibition. The maximum inhibition of calcification of BPHV aortic wall was achieved using an 80% ethanol pretreatment; calcium levels were 71.80 ± 8.45 Μg/mg with 80% ethanol pretreatment compared to the control calcium level of 129.90 ± 7.24 Μg/mg ( p = 0.001). Increasing the duration of ethanol exposure did not significantly improve the inhibitory effect of ethanol on aortic wall calcification. In the sheep circulatory implants, ethanol pretreatment partly prevented BPHV aortic wall calcification with a calcium level of 28.02 ± 4.42 Μg/mg compared to the control calcium level of 56.35 ± 6.14 Μg/mg ( p = 0.004). Infrared spectroscopy (ATR-FTIR) studies of ethanol-pretreated BPHV aortic wall (vs. control) demonstrated a significant change in protein structure due to ethanol pretreatment. The water content of the aortic wall tissue and the spin-lattice relaxation times ( T 1 ) as assessed by proton nuclear magnetic resonance spectroscopy did not change significantly owing to ethanol pretreatment. The optimum condition of 80% ethanol pretreatment almost completely extracted both phospholipids and cholesterol from the aortic wall; despite this, significant calcification occurred. In conclusion, these results clearly demonstrate that ethanol pretreatment is significantly but only partially effective for inhibition of calcification of BPHV aortic wall and this effect may be due in part to lipid extraction and protein structure changes caused by ethanol. It is hypothesized that ethanol pretreatment may be of benefit for preventing bioprosthetic aortic wall calcification only in synergistic combination with another agent. © 1998 John Wiley & Sons, Inc. J. Biomed Mater Res, 42, 30–37, 1998.en_US
dc.format.extent185456 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherChemistryen_US
dc.subject.otherPolymer and Materials Scienceen_US
dc.titleInhibition of aortic wall calcification in bioprosthetic heart valves by ethanol pretreatment: Biochemical and biophysical mechanismsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbsecondlevelBiomedical Engineeringen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, The University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationumDepartment of Biochemistry and Biophysics, University of Michigan, Ann Arbor, Michigan 48109en_US
dc.contributor.affiliationotherThe Joseph Stokes, Jr., Research Institute, Children's Hospital of Philadelphia, Abramson Pediatric Research Center, 1107B, 34th Street and Civic Center Blvd., Philadelphia, Pennsylvania 19104en_US
dc.contributor.affiliationotherNHLBI, Bethesda, Marylanden_US
dc.contributor.affiliationotherBrigham and Women's Hospital and Harvard Medical School, Boston, Massachusettsen_US
dc.contributor.affiliationotherDepartment of Surgery, University of Minnesota Medical School, Minnesotaen_US
dc.contributor.affiliationotherThe Joseph Stokes, Jr., Research Institute, Children's Hospital of Philadelphia, Abramson Pediatric Research Center, 1107B, 34th Street and Civic Center Blvd., Philadelphia, Pennsylvania 19104 ; The Joseph Stokes, Jr., Research Institute, Children's Hospital of Philadelphia, Abramson Pediatric Research Center, 1107B, 34th Street and Civic Center Blvd., Philadelphia, Pennsylvania 19104en_US
dc.identifier.pmid9740004en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/38020/1/5_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-4636(199810)42:1<30::AID-JBM5>3.0.CO;2-Pen_US
dc.identifier.sourceJournal of Biomedical Materials Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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