Effects of acute prenatal ethanol exposure on Bergmann glia cells early postnatal development

Brain Research

Volumn 746, Issue 1-2, 1997, Pages 305-308

  Pérez Torrero, Esther ^a   Durán, Pilar ^a   Granados, Leticia ^a   Gutiérrez Ospina, Gabriel ^a   Cintra, Léon ^a   Díaz Cintra, Sofía ^a  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

Author keywords

Bergmann glial cell; Cerebellum; Development; Ethanol exposure; Wistar rat

Indexed keywords

ALCOHOL;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CELL STRUCTURE; CONTROLLED STUDY; FETUS; GLIA CELL; HISTOLOGY; NEWBORN; NONHUMAN; PRENATAL EXPOSURE; PRIORITY JOURNAL; RAT;

ANIMALS; CELL SIZE; CENTRAL NERVOUS SYSTEM DEPRESSANTS; CEREBELLUM; ETHANOL; FEMALE; NEUROGLIA; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RATS; RATS, WISTAR;

EID: 0342547119     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(96)01235-8     Document Type: Article

References (24)

1. Anton, E.S., Cameron, R.S. and Rakic, P., Role of neuron-glial junctional domain proteins in the maintenance and termination of neuronal migration across the embryonic cerebral wall, J. Neurosci., 17 (1996) 2283-2293.
2. Brodie, C. and Vernadakis, A., Ethanol increases cholinergic and decreases GABAergic neuronal expression in cultures derived from 8-day-old chick embryo hemispheres: interaction of ethanol and growth factors, Dev. Brain Res., 65 (1992) 253-157.
3. Del Cerro, M. and Swarz, J.R., Prenatal development of Bergmann glial fibers in rodent cerebellum, J. Neurocytol., 5 (1976) 669-676.
4. Diana, M., Pistis, M., Carboni, S., Gessa, G.L. and Rossetti, Z.L., Profound decrement of mesolimbic dopaminergic neuronal activity during ethanol withdrawal syndrome in rats: electrophysiological and biochemical evidence, Proc. Natl. Acad. Sci. USA, 90 (1993) 7966-7969.
5. Díaz-Cintra, S., García-Ruiz, M., Corkidi, G. and Cintra, L., Effects of prenatal malnutrition and postnatal nutritional rehabilitation on CA3 hippocampal pyramidal cells in rats of four ages, Brain Res., 662 (1994) 117-126.
6. Ghandour, M.S., Labourdette, G., Vincendon, G. and Gombos, G., A biochemical and immunohistological study of S100 protein in the developing rat cerebellum, Dev. Neurosci., 4 (1981) 98-109.
7. Heaton, M.B., Paiva, M., Swanson, D.J. and Walker, D.W., Alterations in responsiveness to ethanol and neurotrophic substances in fetal septohippocampal neurons following chronic prenatal ethanol exposure, Dev. Brain Res., 85 (1995) 1-13.
8. Jacobsen, S., Rich, J. and Tovsky, N.J., Delayed myelination and lamination in the cerebral cortex of the albino rat as a result of fetal alcohol syndrome, Curr. Alcohol, 6 (1979) 123-133.
9. Jensen, K.F. and Killackey, H.P., Terminal arbors of axons projecting to the somatosensory cortex of the adult rat. II. The altered morphology of thalamocortical afferents following neonatal infraorbital nerve cut, J. Neurosci., 7 (1987) 3544-3553.
10. Lokhorst, D.K. and Druse, M.J., Effects of ethanol on cultured fetal astroglia, Alcohol Clin. Exp. Res., 17 (1993) 810-815.
11. Majewski, F., Two teratogens of major importance: Alcohol and anticonvulsants. In M. Arima, Y. Susuki and H. Yabuuchi (Eds.), The Developing Brain and its Disorders, Karger, Basel, 1985, pp. 223-246.
12. Milner, R.J., Randolph, L., Bohr, D., Cappello, M., Lenoir, D., Miller, F. and Bloom, F.E., Molecular biological approaches to the brain and their application to the study of alcoholism. In H.W. Goedde and D.P. Agarwall (Eds.), Genetics and Alcoholism, Alan R. Liss, Inc., New York, 1987, pp. 291-302.
13. Miller, M.W. and Robertson, S., Prenatal exposure to ethanol alters the postnatal development and transformation of radial glia to astrocytes in the cortex, J. Comp. Neurol., 337 (1993) 253-266.
14. Miller, M.W., Effects of alcohol on the generation and migration of cerebral cortical neurons, Science, 233 (1986) 1308-1311.
15. Miller, M.W., Migration of cortical neurons is altered by gestational exposure to ethanol, Alcohol Clin. Exp. Res., 17 (1993) 304-314.
16. Mocsary, Z. and Bradberry, C.W., Effect of ethanol on extracellular dopamine in nucleus accumbens: comparison between Lewis and Fischer 344 rat strains, Brain Res., 706 (1996) 194-198.
17. Naus, C.G. and Bechberger, J.F., Effects of prenatal ethanol exposure on postnatal neural gene expression in the rat, Dev. Gen., 12 (1991) 293-298.
18. 3 receptors but not by N-methyl-D-aspartate receptor complex, Brain Res., 706 (1996) 227-232.
19. Rakic, P. and Sidman, R.L., Weaver mutant mouse cerebellum: Defective neuronal migration secondary to abnormality of Bergmann Glia, Proc. Natl. Acad. Sci. USA, 70 (1973) 240-244.
20. Shen, R. and Chioto, L.A., The effects of in utero ethanol administration on the electrophysiological activity of rat nigrostriatal dopaminergic neurons, Brain Res., 624 (1993) 216-222.
21. Shetty, A.K. and Phillips, D.E., Effects of prenatal ethanol exposure on the development of Bergmann Glia and astrocytes in the rat cerebellum: An Immnuhistochemical study, Comp. Neurol., 321 (1992) 19-32.
22. Shetty, A.K., Burrows, R.C. and Phillips, D.E., Alterations in neuronal development in the substantia nigra pars compacta following in utero ethanol exposure: Immunohistochemical and Golgi studies, Neuroscience, 52 (1993) 311-322.
23. Shetty, A.K., Burrows, R.C., Wall, K.A. and Phillips, D.E., Combined pre- and postnatal ethanol exposure alters the development of Bergmann glia in rat cerebellum, Int. J. Dev. Neurosci., 12 (1994) 641-649.
24. Spoerry, P.E., Srivastava, N. and Vernadakis, A., GABA attenuates the neurotoxic effects of ethanol in neuron-enriched cultures from 8-day-old chick embryo cerebral hemispheres, Dev. Brain Res., 86 (1995) 94-100.