Retrograde axonal transport impairment of large- and medium-sized retinal ganglion cells in diabetic rat

References

• Harati Y. Diabetic peripheral neuropathies. Ann Intern Med. 1987;107:546–559.
   PubMed Web of Science ®Google Scholar
• Sharma AK, Thomas PK. Peripheral nerve structure and function in experimental diabetes. J Neurol Sci 1974; 23:1–15.
   PubMed Web of Science ®Google Scholar
• Jefferys JG, Palmano K.P, Sharma AK, Thomas PK. In-fluence of dietary myoinositol on nerve conduction and inositol phospholipids in normal and diabetic rats. J Neurol Neurosurg Psychiatry. 1978;41:333–339.
   PubMed Web of Science ®Google Scholar
• Kador PF. The role of aldose reductase in the develop-ment of diabetic complications. Med Res Rev. 1988,8: 325–352.
   PubMed Web of Science ®Google Scholar
• Yagihashi S, Kamijo M, Watanabe K. Reduced myeli-nated fiber size correlates with loss of axonal neurofila-ments in peripheral nerve of chronically streptozotocin diabetic rats. Am J Pathol. 1990;136:1365–1373.
   Google Scholar
• Sima AAF, Zhang WX, Cherian PV, Chakravorti S. Impaired visual evoked potential and axonopathy of the optic nerve in the diabetic BB/W-rat. Diabetologia 1992;35:602–607.
   PubMed Web of Science ®Google Scholar
• Ino-ue M, Ohgiya N, Yamamoto M. Effect of amino-guanidine on optic nerve involvement in experimental diabetic rats. Brain Res. 1998;800:319–322.
   Google Scholar
• Ino-ue M, Yokogawa H, Yamamoto M, Naka H, Kuriya-ma H. Structural impariments in optic nerve of diabetic rats ameliorated with the aldose reductase inhibitor. Exp Eye Res. 1998;66:397–401.
   Google Scholar
• Puvanendran K, Devathasan G, Wong PK. Visual evoked responses in diabetes. J Neurol Neurosurg Psychiatry. 1983;46:643–647.
   PubMed Web of Science ®Google Scholar
• Prager TC, Garcia CA, Mincher CA, Mishra J, Chu HH. The pattern electroretinogram in diabetes. Am J Ophthal-mol. 1990;109:279–284.
   PubMed Web of Science ®Google Scholar
• Kristensson K, Olsson Y. Diffusion pathways and ret-rograde axonal transport of protein tracers in peripheral nerves. Prog Neurobiol. 1973;1:87–109.
   PubMedGoogle Scholar
• Sidenius P, Jakobsen J. Axonal transport in early experi-mental diabetes. Brain Res. 1979;173:315–330.
   PubMed Web of Science ®Google Scholar
• Jakobsen J, Brimijoin S, Skau K, Sidenius P, Wells D. Retrograde axonal transport of transmitter enzymes, fu-cose-labeled protein, and nerve growth factor in streptozo-tocin-diabetic rats. Diabetes 1981;30:797–803.
   Google Scholar
• Sidenius P, Jakobsen J. Retrograde axonal transport: a possible role in the development of neuropathy. Diabeto-logia 1981;20:110–112.
   PubMed Web of Science ®Google Scholar
• Medori R, Gambetti LA, Monaco S, Gambetti P. Experi-mental diabetic neuropathy: Impairment of slow trans-port with changes in axon cross-sectional area. Pro Natl Acad Sci USA. 1985;82:7716–7720.
   PubMed Web of Science ®Google Scholar
• Medori R, Gambetti LA, Jenich H, Gambetti P. Changes in axon size and slow axonal transport are related in experimental diabetic neuropathy. Neurology 1988;38: 597–601.
   PubMed Web of Science ®Google Scholar
• Karlsson JO, Sjostrand J. Synthesis, migration and turn-over of protein in retinal ganglion cell. J Neurochem. 1971;18:749–767.
   PubMed Web of Science ®Google Scholar
• Chihara E. Impairment of protein synthesis in the reti-nal tissue in diabetic rabbits: Secondary reduction of fast axonal transport. J Neurochem. 1981;37:247–250.
   PubMed Web of Science ®Google Scholar
• Chihara E, Sakugawa M, Entani S. Reduced protein synthesis in diabetic retina and secondary reduction of slow axonal transport. Brain Res. 1982;250:363–366.
   Google Scholar
• Farid Ahmed AKM, Dong K, Yamadori T. A retrograde double-labeling study of retinal ganglion cells that project ipsilaterally to vLGN and LPN rather than dLGN and SC in albino rat. Brain Res. 1995;674:275–282.
   Google Scholar
• Perry VH. The ganglion layer of retina of the rat: a Golgi study. Proc R Soc Lond B Biol Sci. 1979;204:363–375.
   PubMed Web of Science ®Google Scholar
• Schmued LC, Fallon JH. Fluoro-Gold: a new fluorescent retrograde axonal tracer with numerous unique proper-ties. Brain Res. 1986;377:147–154.
   PubMed Web of Science ®Google Scholar
• Sidenius P, Jakobsen J. Reduced perikaryal volume of lower motor and primary sensory neurons in early ex-perimental diabetes. Diabetes 1980;29:182–186.
   PubMed Web of Science ®Google Scholar
• Hellweg R, Hartung HD. Endogenous levels of nerve growth factor (NGF) are altered in experimental diabetes mellitus: a possible role for NGF in the pathogenesis of diabetic neuropathy. J Neurosci Res. 1990;26:258–267.
   PubMed Web of Science ®Google Scholar
• Jakobson J. Axonal dwindling in early experimental dia- betes. I. A study of cross-sectioned nerves. Diabetologia 1976;12:539–546.
   PubMedGoogle Scholar
• Sharma AK, Bajada S, Thomas PK. Influence of strepto-zotocin-induced diabetes on myelinated nerve fiber maturation and on body growth in the rat. Acta Neuro-pathol. 1981;53:257–265.
   Google Scholar
• Boycott BB, Wassle H. The morphological types of ganglion cells of the domestic cat's retina. J Physiol (Lon-don). 1974;240:397–419.
   PubMed Web of Science ®Google Scholar
• Di Leo MAS, Falsini B, Caputo S, Ghirlanda G, Porciatti V, Greco AV. Spatial Frequency-selective losses with pattern electroretinogram in type 1 (insulin-dependent) diabetic patients without retinopathy. Diabetologia 1990; 33:726–730.
   PubMed Web of Science ®Google Scholar
• Louzada-Junior P, Dias JJ, Santos WF, Lachat JJ, Bradford HF, Coutinho-Netto J. Glutamate release in ex-perimental ischaemia of the retina: an approach using microdialysis. J Neurochem. 1992;59:358–363.
   Google Scholar
• Neal MJ, Cunningham JR, Hutson PH, Hogg J. Effects of ischaemia on neurotransmitter release from the iso-lated retina. J Neurochem. 1994;62:1025–1033.
   PubMed Web of Science ®Google Scholar
• Ambati J, Chalam KV, Chawla DK, D'Angio CT, Guillet EG, Rose SJ, Vanderlinde RE, Ambati BK. Elevated gamma aminobutyric acid, glutamate, and vascular en-dothelial growth factor levels in vitreous of patients with proliferative diabetic retinopathy. Arch Ophthalmol. 1997; 115:1161–1166.
   Google Scholar
• Caprioli J, Kitano S. Large retinal ganglion cell are more susceptible to excitotoxic and hypoxic injury than small cells. Invest Ophthalmol Vis Sci. 1993;34(Suppl):1429.
   Google Scholar
• Dreyer EB, Pan ZH, Storm S, Lipton SA. Greater sensi-tivity of larger retinal ganglion cell to NMDA-mediated cell death. Neuroreport 1994;5:629–631.
   PubMed Web of Science ®Google Scholar
• Glovinsky Y, Quigley HA, Dunkelberger GR. Retinal ganglion cell loss is size dependent in experimental glau-coma. Invest Ophthalmol Vis Sci. 1991;32:484–491.
   PubMed Web of Science ®Google Scholar
• Quigley HA, Dunkelberger GR, Green WR. Chronic hu-man glaucoma causing selectively greater loss of large optic nerve fibers. Ophthalmology 1988;95:357–363.
   Google Scholar
• Sadun AA, Bassi CJ. Optic nerve damage in Alzheimer's disease. Ophthalmology 1990;97:9–17.
   PubMed Web of Science ®Google Scholar