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Neuroregulation of protein synthesis in odontoblasts of the first molar of the rat after wounding

dc.contributor.authorChiego, Daniel J.en_US
dc.contributor.authorAvery, James K.en_US
dc.contributor.authorKlein, Robert M.en_US
dc.date.accessioned2006-09-11T19:16:23Z
dc.date.available2006-09-11T19:16:23Z
dc.date.issued1987-04en_US
dc.identifier.citationChiego, Daniel J.; Avery, James K.; Klein, Robert M.; (1987). "Neuroregulation of protein synthesis in odontoblasts of the first molar of the rat after wounding." Cell and Tissue Research 248(1): 119-123. <http://hdl.handle.net/2027.42/47683>en_US
dc.identifier.issn1432-0878en_US
dc.identifier.issn0302-766Xen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/47683
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=3568111&dopt=citationen_US
dc.description.abstractOdontoblasts respond to occlusal trauma by increased elaboration of a matrix which is subsequently calcified to form reparative dentin. The purpose of the present study was to analyze quantitatively and compare the ability of odontoblasts to synthesize collagen after wounding in rats with an intact innervation (baseline) and in rats with sensory (inferior alveolar nerve, IAN) and/or sympathetic (superior cervical ganglion, SCG) surgical denervation. Surgery was performed 7 days prior to wounding. All rats had 1 mm of enamel and dentin removed from the occlusal surface of the first mandibular molar (resected side) with the contralateral tooth serving as a control. Rats were killed 1 h after injection with 3 H-proline on days 0, 5, 10 or 15 after wounding, and mandibles were removed and processed for autoradiography. Grain counts were performed over odontoblasts throughout the pulp horns for each time period and for control and experimental molars in intact (baseline) and denervated groups. When compared to the control baseline, the experimental baseline data showed increased 3 -proline uptake throughout the study with a peak at 5 days. When compared to the baseline data, IAN and SCG results demonstrated a delay or attenuation of the protein synthetic response. The results indicate that the sensory and sympathetic neural components may regulate odontoblastic response to wounding.en_US
dc.format.extent567918 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherNeurosciencesen_US
dc.subject.otherDenervationen_US
dc.subject.otherNeurologyen_US
dc.subject.otherEndocrinologyen_US
dc.subject.otherProtein Synthesisen_US
dc.subject.otherWound Healingen_US
dc.subject.otherNeural Regulationen_US
dc.subject.otherAutoradiographyen_US
dc.subject.otherBiomedicineen_US
dc.subject.otherOdontoblastsen_US
dc.subject.otherCell Biologyen_US
dc.subject.otherRaten_US
dc.titleNeuroregulation of protein synthesis in odontoblasts of the first molar of the rat after woundingen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Oral Biology, University of Michigan, School of Dentistry, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Oral Biology, University of Michigan, School of Dentistry, Ann Arbor, Michigan, USA; Department of Oral Biology, University of Michigan, School of Dentistry, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Anatomy/Division of Cell Biology, University of Kansas, College of Health Sciences and Hospital, Kansas City, Kansas, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid3568111en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/47683/1/441_2005_Article_BF01239971.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01239971en_US
dc.identifier.sourceCell and Tissue Researchen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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