A vulnerable period of colchicine toxicity during goldfish optic nerve regeneration

Brain Research

Volumn 842, Issue 1, 1999, Pages 62-72

  Dybowski, Joseph A ^a   Heacock, Anne M ^b   Agranoff, Bernard W ^b,c  

^a Toxicology Program   (United States)

^b UNIVERSITY OF MICHIGAN   (United States)

^c UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

Axonal transport; Colchicine; Goldfish; Retinal explant; Tubulin; Vision

Indexed keywords

COLCHICINE;

ANIMAL EXPERIMENT; ARTICLE; DRUG EFFECT; GOLDFISH; MICROTUBULE ASSEMBLY; NERVE FIBER GROWTH; NERVE FIBER TRANSPORT; NERVE REGENERATION; NEUROTOXICITY; NONHUMAN; OPTIC NERVE; PRIORITY JOURNAL; PROTEIN SYNTHESIS;

ANIMALS; AXONAL TRANSPORT; BEHAVIOR, ANIMAL; COLCHICINE; EYE; FLUORESCENT DYES; GOLDFISH; INJECTIONS; METHACRYLATES; NERVE CRUSH; NERVE REGENERATION; OPTIC NERVE; PLASTIC EMBEDDING; PROLINE; PYRIDINIUM COMPOUNDS; RETINA; TUBULIN; VISION; VISUAL PATHWAYS;

EID: 0033581347     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(99)01810-7     Document Type: Article

References (48)

1. Alonso G. Effects of colchicine on the intraneuronal transport of secretory material prior to the axon: a morphofunctional study in hypothalamic neurosecretory neurons of the rat. Brain Res. 453:1988;191-203.
2. B.W. Agranoff, T.S. Ford-Holevinski, Biochemical aspects of the regenerating goldfish visual system, in: J.S. Elam, P. Cancalon (Eds.), B.W. Agranoff, M.H. Aprison (Series Eds.), Advances in Neurochemistry, Vol. 6, Axonal Transport in Neuronal Growth and Regeneration, Plenum, New York, 1984, pp. 69-86.
3. Benowitz L.I., Jing Y., Tabibiazar R., Jo S.A., Petrausch B., Stuermer C.A.O., Rosenberg P.A., Irwin N. Axon outgrowth is regulated by an intracellular purine-sensitive mechanism in retinal ganglion cells. J. Biol. Chem. 273:1998;29626-29634.
4. L.I. Benowitz, N.I. Perrone-Bizzozero, R.I. Neve, W. Rodriguez, GAP-43 as a marker for structural plasticity in the mature CNS, in: P. Coleman, G. Higgins, C. Phelps (Eds.), Progress in Brain Research, Vol. 86, Elsevier, Amsterdam, 1990, pp. 309-320.
5. Bisby M.A., Tetzlaff W. Changes in cytoskeletal protein synthesis following axon injury and during axon regeneration. Mol. Neurobiol. 6:1992;107-123.
6. A receptors independently of microtubule depolymerization. Neuropharmacology. 37:1998;383-390.
7. Burrell H.R., Heacock A.M., Water R.D., Agranoff B.W. Increased tubulin messenger mRNA in the goldfish during optic nerve regeneration. Brain Res. 168:1979;628-632.
8. Cleveland D.W., Lopata M.A., Sherline P., Kirshner M.W. Unpolymerized tubulin modulates the level of tubulin mRNA's. Cell. 24:1981;537-546.
9. Downing K.H., Nogales E. New insights into microtubule structure and function from the atomic model of tubulin. Eur. Biophys. J. 27:1998;431-436.
10. Davis R.E. A method of restraining goldfish during conditioning of electric-shock-induced suppression of breathing movements. Behav. Res. Methods Instrum. 13:1981;650-652.
11. Davis R.E. Effect of optic nerve lesions and intraocular colchicine on cell proliferation in the germinal zone of the optic tectum and in the torus longitudinalis in the goldfish. Brain Res. 512:1990;46-53.
12. Davis R.E., Schlumpf B.E., Klinger P.D. Comparative neurotoxicity of tubulin-binding drugs: inhibition of goldfish optic nerve regeneration. Toxicol. Appl. Pharmacol. 80:1985;308-315.
13. Dybowski J., Klinger P., Blaivis M., Agranoff B.W. Increased vulnerability to the toxic effects of colchicine during optic nerve regeneration in goldfish. Toxicologist. 30:1996;125.
14. Edwards D.L., Alpert R.M., Grafstein B. Recovery of vision in regeneration of goldfish optic axons: enhancement of axonal outgrowth by a conditioning lesion. Exp. Neuro. 72:1981;672-686.
15. Eitan S., Solomon A., Lavie V., Yoles E., Hirschberg D.L., Belkin M., Schwartz M. Recovery of visual response of injured adult rat optic nerves treated with transglutaminase. Science. 264:1994;1764-1768.
16. Elam J.S., Agranoff B.W. Rapid transport of protein in the optic system of the goldfish. J. Neurochem. 18:1971;375-387.
17. Feldman E., Axelrod D., Schwartz M., Heacock A.M., Agranoff B.W. Studies on the localization of newly added membrane in growing neurites. J. Neurobiol. 12:1981;591-598.
18. Ford-Holevinski T.S., Dahlberg T.A., Agranoff B.W. A microcomputer-based image analyzer for quantitating neurite outgrowth. Brain Res. 368:1986;339-346.
19. Gay D.A., Sisodia S.S., Cleveland D.W. Autoregulatory control of β-tubulin mRNA stability is linked to translation elongation. Proc. Natl. Acad. Sci. U.S.A. 86:1989;5763-5767.
20. P. Gomez-Ramos, D. Chaverri Rada, Ultrastructural effects of colchicine on perikarya and intitial segment of rat retinal ganglion cells, Vol. 15, Cell Biol. Int. Rep. (1991) 511-515.
21. Gonzalez-Garay M.L., Cabral F. alpha-Tubulin limits its own synthesis: evidence for a mechanism involving translational repression. J. Cell Biol. 135:1996;1525-1534.
22. B. Grafstein, The goldfish visual system as a model for the study of regeneration in the central nervous system, in: J.R. Cronly-Dillon (Ed.), Development and Plasticity of the Visual System, Vision and Visual Dysfunction, Vol. 11, Macmillan, London, 1991, pp. 190-205.
23. Grafstein B., Murray M. Transport of protein in goldfish optic nerve regeneration. Exp. Neuro. 25:1969;494-508.
24. Hall C.M. Differential regulation of two classes of neuronal intermediate filament proteins during optic nerve crush. J. Neurochem. 63:1994;2307-2313.
25. 2 during goldfish optic nerve regeneration: effect of tectal ablation. Neuroscience. 41:1991;695-701.
26. Heacock A.M., Agranoff B.W. Enhanced labeling of a retinal protein during regeneration of optic nerve in goldfish. Proc. Natl. Acad. Sci. U.S.A. 73:1976;828-832.
27. Heacock A.M., Agranoff B.W. Protein synthesis and transport in the regenerating goldfish visual system. Neurochem. Res. 7:1982;771-788.
28. Hieber V., Agranoff B.W., Goldman D. Target-dependent regulation of retinal nicotinic acetylcholine receptor and tubulin RNAs during optic nerve regeneration in goldfish. J. Neurochem. 58:1992;1009-1015.
29. Hitchcock P.F., Raymond P.A. Retinal regeneration. Trends Neurosci. 15:1992;103-108.
30. Landreth G.E., Agranoff B.W. Explant culture of adult goldfish retina: a model for the study of CNS regeneration. Brain Res. 161:1979;39-53.
31. Machu T.K. Colchicine competitively antagonizes glycine receptors expressed in Xenopus oocytes. Neuropharmacology. 37:1998;391-396.
32. Murray M., Grafstein B. Changes in the morphology and amino acid incorporation of regenerating goldfish optic neurons. Exp. Neurol. 23:1969;544-560.
33. Neumann D., Scherson T., Ginzburg I., Littauer U.Z., Schwartz M. Regulation of mRNA levels for microtubule proteins during nerve regeneration. FEBS. 162:1983;270-276.
34. Northmore D.P.M. Neural activity in the regenerating optic nerve of the goldfish. J. Physiol. 391:1987;299-312.
35. Oh D.J., Northmore D.P.M. Functional properties of retinal ganglion cells during optic nerve regeneration in the goldfish. Visual Neurosci. 15:1998;1145-1155.
36. Pachter J.S., Yen T.J., Cleveland D.W. Autoregulation of tubulin expression is achieved through specific degradation of polysomal tubulin mRNAs. Cell. 51:1987;283-292.
37. Panda D., Daijo J.E., Wilson M.A.J.L. Kinetic stabilization of microtubule dynamics at steady state in vitro by substoichiometric concentrations of tubulin-colchicine complex. Biochemistry. 34:1995;9921-9929.
38. J.C. Paulson, W.O. McClure, Inhibition of axoplasmic transport by colchicine, podophyllotoxin, and vinblastine: an effect on microtubules, Ann. N.Y. Acad. Sci. (1975) 517-527.
39. Reich J.B., Burmeister D.W., Schmidt J.T., Grafstein B. Effects of conditioning lesion on regeneration of goldfish optic axon: time course of the cell body reaction to axotomy. Brain Res. 515:1990;256-260.
40. Salles F.J., Schechter N., Strickland S. A plasminogen activator is induced during goldfish optic nerve regeneration. EMBO J. 9:1990;2471-2477.
41. Schwalb J.M., Boulis N.M., Gu M., Winickoff J., Jackson P.S., Irwin N., Benowitz L.I. Two factors secreted by the goldfish optic nerve induced retinal ganglion cells to regenerate axons in culture. J. Neurosci. 15:1995;5514-5525.
42. Springer A.D., Agranoff B.W. Effect of temperature on rate of goldfish optic nerve regeneration: a radioautographic and behavioral study. Brain Res. 128:1977;405-415.
43. Stuermer C.A.O., Bastmeyer M., Bahr M., Strobel G., Paschke K. Trying to understand axonal regeneration in the CNS of fish. J. Neurobiol. 23:1992;537-550.
44. Takano M., Horie H. Critical period of degradation of adult rat retinal ganglion cells and their regeneration capability after axotomy. Neurosci. Lett. 175:1994;129-132.
45. Tesser P., Jones P.S., Schechter N. Elevated levels of retinal neurofilament mRNA accompany optic nerve regeneration. J. Neurochem. 47:1986;1235-1243.
46. Thanos S., Kacza J., Seeger J., Mey J. Old dyes for new scopes: the phagocytosis-dependent long-term fluorescence labelling of microglial cells in vivo. Trends Neurosci. 17:1994;177-182.
47. N.G. Theodorakis, D.W. Cleveland, Physical evidence for cotranslational regulation of β-tubulin mRNA degradation, Mol. Cell. Biol. (1992) 791-799.
48. Vandecandelaere A., Martin S.R., Schilstra M.J., Bayley P.M. Effects of the tubulin-colchicine complex on microtubule dynamic instability. Biochemistry. 33:1994;2792-2801.