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Impaired visual evoked potential and primary axonopathy of the optic nerve in the diabetic BB/W-rat

dc.contributor.authorChakrabarti, Subrataen_US
dc.contributor.authorZhang, Wei-Xianen_US
dc.contributor.authorCherian, P. V.en_US
dc.contributor.authorSima, Anders A. F.en_US
dc.date.accessioned2006-09-11T17:17:22Z
dc.date.available2006-09-11T17:17:22Z
dc.date.issued1992-07en_US
dc.identifier.citationSima, A. A. F.; Zhang, W. -X.; Cherian, P. V.; Chakrabarti, S.; (1992). "Impaired visual evoked potential and primary axonopathy of the optic nerve in the diabetic BB/W-rat." Diabetologia 35(7): 602-607. <http://hdl.handle.net/2027.42/46026>en_US
dc.identifier.issn0012-186Xen_US
dc.identifier.issn1432-0428en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/46026
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=1644237&dopt=citationen_US
dc.description.abstractThe spontaneously diabetic BB/W-rat has emerged as an important model system for somatic and autonomic diabetic polyneuropathy. In this study we examined visual evoked potentials and the presence of morphometric and structural changes in the optic nerve and the retinal ganglion cells and their afferent axons contained in the retinal nerve fibre layer. A six-month duration of diabetes mellitus was associated with significant increases in the latencies of the visual evoked potentials. The latency of the first positive potential showed a 44% increase, and that of the first negative potential was prolonged by 41%. No significant changes were demonstrated at any of the amplitudes. In the optic nerve mean myelinated fibre size was significantly reduced to 82% of control values, which was accounted for by a significant reduction in axonal size. Axo-glial dysjunction, a prominent structural defect of diabetic somato-sensory neuropathy in both man and diabetic rodents, was non-significantly increased in the optic nerve. In diabetic animals retinal ganglion cells displayed dystrophic changes. No such changes were observed in age- and sex-matched control animals. Proximal axons of the retinal nerve fibre layer showed an increase in dystrophic axons in diabetic BB/W-rats. Morphometric analysis of optic nerve capillaries revealed no abnormalities except for basement membrane thickening. The present data suggest that the diabetic BB/W-rat develops a central sensory neuropathy, characterized functionally by prolonged latencies of the visual evoked potentials and structurally by an axonopathy of optic nerve fibres.en_US
dc.format.extent881344 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlagen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherVisual Evoked Potentialen_US
dc.subject.otherOpticnerveen_US
dc.subject.otherHuman Physiologyen_US
dc.subject.otherInternal Medicineen_US
dc.subject.otherMetabolic Diseasesen_US
dc.subject.otherNeuropathyen_US
dc.titleImpaired visual evoked potential and primary axonopathy of the optic nerve in the diabetic BB/W-raten_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartments of Pathology and Internal Medicine and Michigan Diabetes Research and Training Center, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartments of Pathology and Internal Medicine and Michigan Diabetes Research and Training Center, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Manitoba, Winnipeg, Manitoba, Canadaen_US
dc.contributor.affiliationotherDepartment of Pathology, University of Manitoba, Winnipeg, Manitoba, Canadaen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid1644237en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/46026/1/125_2004_Article_BF00400249.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF00400249en_US
dc.identifier.sourceDiabetologiaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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