Neonatal 6-hydroxydopamine treatment affects GABA(A) receptor subunit expression during postnatal development of the rat cerebellum

International Journal of Developmental Neuroscience

Volumn 18, Issue 6, 2000, Pages 565-572

  Podkletnova, I ^a   Alho, H ^b   Makela R ^a   Luddens H ^c   Helen P ^d   Korpi, E R ^e  

^a UNIVERSITY OF TAMPERE MEDICAL SCHOOL   (Finland)

^b NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^c JOHANNES GUTENBERG UNIVERSITY   (Germany)

^d TAMPERE UNIVERSITY HOSPITAL   (Finland)

^e UNIVERSITY OF TURKU   (Finland)

Author keywords

Development; Immunohistochemistry; In situ hybridization; Neuronal plasticity; Neurotoxicity; Noradrenaline depletion

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; MESSENGER RNA; OXIDOPAMINE; RECEPTOR SUBUNIT;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL MIGRATION; CEREBELLUM; CONTROLLED STUDY; FEMALE; GENE EXPRESSION; GRANULE CELL; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MALE; MORPHOMETRICS; NEUROTOXICITY; NEWBORN; NONHUMAN; NORADRENERGIC SYSTEM; OLIGONUCLEOTIDE PROBE; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RAT;

ADRENERGIC AGENTS; ANIMALS; ANIMALS, NEWBORN; CELL COUNT; CEREBELLUM; FEMALE; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; INJECTIONS, SUBCUTANEOUS; MALE; OXIDOPAMINE; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, GABA-A; RNA, MESSENGER;

EID: 0034309845     PISSN: 07365748     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0736-5748(00)00003-4     Document Type: Article

References (37)

1. A receptor subunit mRNAs in rat cerebellar granule neurons: importance of environmental cues. J. Neurochem. 66:1996;1347-1353.
2. Glinka Y., Tipton K.F., Youdim M.B.H. Nature of inhibition of mitochondrial respiratory complex I by 6-hydroxydopamine. J. Neurochem. 66:1996;2004-2010.
3. Gustafson E.L., Moore R.Y. Noradrenaline neuron plasticity in developing rat brain: effects of neonatal 6-hydroxydopamine demonstrated by dopamine-β-hydroxylase immunocytochemistry. Dev. Brain Res. 37:1987;143-155.
4. Jacobson M. Developmental Neurobiology. 1978;Plenum Press, New York and London.
5. Hatten M.E. Riding the glial monorail: a common mechanism for glial-guided neuronal migration in different regions of the developing mammalian brain. Trends Neurosci. 13:(5):1990;179-184.
6. A receptor α subunit is expressed only in cerebellar granule cells. J. Molec. Biol. 214:1990;619-624.
7. A receptor subtypes in developing hippocampal neurons. Neuron. 7:1991;927-936.
8. A receptor function. J. Neurochem. 63:1994;1167-1170.
9. A receptor. Nature. 361:1993;356-359.
10. 3H]RO 15-4513 binding sites. Neuroscience. 53:1993;483-488.
11. Lauder J.M. Roles for neurotransmitters in development: possible interaction with drugs during the fetal and neonatal periods. Marois M. Prevention of Physical and Mental Congenital Defect. 1985;375-380 Alan R. Liss, New York.
12. A receptor subunit mRNAs in the rat brain. III. Embryonic and postnatal development. J. Neurosci. 12:1992;4151-4172.
13. Lidov H.G., Molliver M.E. The structure of cerebral cortex in the rat following prenatal administration of 6-hydroxydopamine. Brain Res. 255:(1):1982;81-108.
14. Lovell K.L. Effects of 6-hydroxydopamine-induced norepinephrine depletion on cerebellar development. Dev. Neurosci. 5:1982;359-368.
15. Mangold U., Sievers J., Berry M. 6-Hydroxydopamine-induced ectopia of external granule cells in the subarachnoid space covering the cerebellum. II. Differentiation of granule cells: a scanning and transmission electron microscopic study. J. Comp. Neurol. 227:1984;267-284.
16. A receptor complex in an inhibitory synaptic circuit in the rat cerebellum. Dev. Brain Res. 55:1990;73-86.
17. Molina-Holgado E., Dewar K.M., Grondin L., van Gelder N.M., Reader T.A. Amino acid levels and γ-aminobutyric acidA receptors in rat neostriatum, cortex, and thalamus after neonatal 6-hydroxydopamine lesion. J. Neurochem. 60:(3):1993;936-945.
18. A receptors in ANT rats selectively bred for high alcohol sensitivity. Neuropharmacology. 35:1996;1493-1502.
19. 14C-2-Deoxyglucose uptake revealed by exposure to novel stimulation. Dev. Psychobiol. 25:1992;183-198.
20. Pehlemann F.W., Sievers J., Berry M. Meningeal cells are involved in foliation, lamination, and neurogenesis of the cerebellum: evidence from 6-hydroxydopamine-induced destruction of meningeal cells. Dev. Biol. 110:(1):1985;136-146.
21. Podkletonova I., Raevsky V., Alho H. Reduction of GABAergic transmission and alterations in behavior after 6-OHDA treatment of rats. Dev. Brain Res. 94:1996;197-204.
22. Podkletnova I., Alho H. Neonatal noradrenaline depletion prevents the transition of Bergmann glia in the developing cerebellum. J. Chem. Neuroanat. 14:1998;167-173.
23. Rakis P. Neuronal-glial interaction during drain development. TINS. 4:1981;184-187.
24. Robain O., Lanfumey L., Adrien J., Farkas E. Developmental changes in the cerebellar cortex after locus ceruleus lesion with 6-hydroxydopamine in the rat. Exp. Neurol. 88:(1):1985;150-164.
25. Rowe S.J., Messenger N.J., Warner A.E. The role of noradrenaline in the differentiation of amphibian embryonic neurons. Development. 119:(4):1993;1343-1357.
26. Sachs C., Jonsson G. Effects of 6-hydroxydopamine on central noradrenaline neurons during ontogeny. Brain Res. 99:1975;277-291.
27. Seidler F.J., Temple S.W., McCook E.C., Slotkin T.A. Cocaine inhibits central noradrenergic and dopaminergic activity during the critical developmental period in which catecholamines influence cell development. Dev. Brain Res. 85:1995;48-53.
28. Sievers J., Pehlemann F.W., Gude S., Berry M. A time course study of the alterations in the development of the hamster cerebellar cortex after destruction of the overlying meningeal cells with 6-hydroxydopamine on the day of birth. J. Neurocytol. 23:1994;117-134.
29. Super H., Martinez A., Soriano E. Degeneration of Cajal-Retzius cells in the developing cerebral cortex of the mouse after ablation of meningeal cells by 6-hydroxydopamine. Dev. Brain Res. 98:1997;5-20.
30. Verney C., Grzanna R., Farkas E. Distribution of dopamine-β-hydroxylase-like immunoreactive fibers in the rat cerebellar cortex during ontogeny. Dev. Neurosci. 5:1982;369-374.
31. Wagner J.P., Seidler R.J., Lappi S.E., McCook E.C., Slotkin T.A. Role of presynaptic input in the ontogeny of adrenergic cell signaling in rat brain: beta receptors, adenylate cyclase and c-fos protooncogene expression. J. Pharmacol. Exp. Ther. 273:1995;415-426.
32. Watson M., McElligott J.G. Cerebellar norepinephrine depletion and impaired acquisition of specific locomotor tasks in rats. Brain Res. 296:(1):1984;129-138.
33. Wendlandt S., Crow T.J., Stirling R.V. The involvement of the noradrenegic system arising from the locus coeruleus in the postnatal development of the cortex in rat brain. Brain Res. 125:(1):1977;1-9.
34. Whittaker-Azmitia P.M. Role of serotonin and other neurotransmitter receptors in brain development: basis for developmental pharmacology. Pharmacol. Rev. 43:1991;553-561.
35. Wisden W., Korpi E.R., Bahn S. The cerebellum: a model system for studying GABA receptor diversity. Neuropharmacology. 35:1996;1139-1160.
36. A receptor subunit mRNAs in the rat brain. I. Telencephalon, diencephalon, mesencephalon. J. Neurosci. 12:1992;1040-1082.
37. A receptor subunit mRNA occurs only after cerebellar granule cell migration. Dev. Brain Res. 75:1993;91-103.