Differential effects of prenatal cocaine exposure on selected subunit mRNAs of the GABAA receptor in rabbit anterior cingulate cortex

Journal of Chemical Neuroanatomy

Volumn 24, Issue 4, 2002, Pages 243-255

  Shumsky, Jed S ^a   Wu, Yunxing ^b   Murphy, E Hazel ^a   Nissanov, Jonathan ^a   O'Brien Jenkins, Ann ^a   Grayson, Dennis R ^c  

^a DREXEL UNIVERSITY COLLEGE OF MEDICINE   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c UNIVERSITY OF ILLINOIS AT CHICAGO   (United States)

Author keywords

Anterior cingulate cortex; Development; In situ hybridization; Rabbit

Indexed keywords

4 AMINOBUTYRIC ACID A RECEPTOR; COCAINE; MESSENGER RNA; RECEPTOR SUBUNIT; SODIUM CHLORIDE;

ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; CINGULATE GYRUS; CONTROLLED STUDY; CYTOARCHITECTURE; DRUG EXPOSURE; IMMUNOREACTIVITY; NISSL SUBSTANCE; NONHUMAN; POSTNATAL DEVELOPMENT; PREGNANCY; PRENATAL CARE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RABBIT; SYNAPSE;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; COCAINE; FEMALE; GYRUS CINGULI; IN SITU HYBRIDIZATION; MOLECULAR SEQUENCE DATA; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RABBITS; RATS; RECEPTORS, GABA-A; RNA, MESSENGER; TIME FACTORS;

EID: 0036842298     PISSN: 08910618     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0891-0618(02)00067-4     Document Type: Article

References (71)

1. 1 receptors stimulates accumulation of γ-aminobutyric acid in slices of the pars reticulata of 6-hydroxydopamine-lesioned rats. Neurosci. Lett. 145:1992;40-42.
2. Beauregard M., Ferron A. Dopamine modulates the inhibition induced by GABA in rat cerebral cortex: an iontophoretic study. Eur. J. Pharmacol. 205:1991;225-231.
3. Ben-Ari Y., Khazipov R., Leinekugel X., Caillard O., Gaiarsa J.-L. GABAA, NMDA and AMPA receptors: a developmentally regulated 'ménage á trois'. Trends Neurosci. 20:1997;523-529.
4. Benes F.M. Relationship of cingulate cortex to schizophrenia and other psychiatric disorders. Vogt B.A., Gabriel M., Neurobiology of Cingulate Cortex and Limbic Thalamus. 1993;581-605 Birkhauser, Boston.
5. A receptors display association of γ2-subunit with α1- and β2/3 subunits. J. Biol. Chem. 266:1991;4478-4483.
6. Bergson C., Mrzljak L., Smiley J.F., Pappy M., Levenson R., Goldman-Rakic P.S. Regional, cellular and subcellular variations in the distribution of D1 and D5 dopamine receptors in primate brain. J. Neurosci. 15:1995;7821-7836.
7. Bernath S., Zigmond M.J. Dopamine may influence GABA release via three separate mechanisms. Brain Res. 476:1989;373-376.
8. A receptor subunit mRNAs in vivo and in vitro. J. Neurochem. 59:1992;62-72.
9. Bureau M., Olsen R.W. Multiple distinct subunits of the γ-aminobutyric acid-A receptor protein show different ligand-binding affinities. Mol. Pharmacol. 37:1990;497-502.
10. 1 receptors facilitate transmitter release. Nature. 366:1993;344-348.
11. Cameron D.L., Williams J.T. Cocaine inhibits GABA release in the VTA through endogenous 5-HT. J. Neurosci. 14:1994;6763-6767.
12. Campbell K., Kalen P., Wictorin K., Lundberg C., Mandel R.J., Bjorklund A. Characterization of GABA release from intrastriatal striatal transplants: dependence on host-derived afferents. Neuroscience. 53:1993;403-415.
13. A receptor subunit mRNAs in rat cerebral cortex: competitive, quantitative reverse transcriptase-polymerase chain reaction analysis. Mol. Pharmacol. 48:1995;861-868.
14. Friedman, E., 1998. D1 dopamine receptor dysfunction in prenatal cocaine exposure. In: Harvey, J.A., Kosofsy, B.E. (Eds.), Cocaine Effects on the Developing Brain, Ann. New York Acad. Sci. 846 238-246.
15. Friedman E., Yadin E., Wang H.-Y. Effect of prenatal cocaine on dopamine receptor-G protein coupling in mesocortical regions of the rabbit brain. Neuroscience. 70:1996;739-747.
16. A-receptor heterogeneity in the adult rat brain: differential regional and cellular distribution of seven major subunits. J. Comp. Neurol. 359:1995;154-194.
17. A-receptor subtypes during postnatal development: an immunohistochemical study. J. Neurosci. 14:1994;5302-5324.
18. Goeders N., Bell V., Guidroz A., McNulty M. Dopaminergic involvement in the cocaine-induced up-regulation of benzodiazepine receptors in the rat caudate nucleus. Brain Res. 515:1990;1-8.
19. Goodman C.S., Shatz C.J. Developmental mechanisms that generate precise patterns of neural connectivity. Cell. 72:1993;77-98.
20. Grayson D.R., Bovolin P., Santi M.R. Absolute quantitation of γ-aminobutyric acid A receptor subunit messenger RNAs by competitive polymerase chain reaction. Methods Neurosci. 12:1993;191-208.
21. Harris B.T., Charlton M.E., Costa E., Grayson D.R. Quantitative changes in α1 and α5 γ-aminobutyric acid type A receptor subunit mRNAs and proteins after a single treatment of cerebellar granule neurons with N-methyl-D-aspartate. Mol. Pharmacol. 45:1994;637-648.
22. Hendry S.H.C., Fuchs J., de Blas A.L., Jones E.G. Distribution and plasticity of immunocytochemically localized GABAA receptors in adult monkey visual cortex. J. Neurosci. 7:1990;1503-1519.
23. Howard C.V., Reed M.G. Unbiased Stereology: Three Dimensional Measurement in Microscopy. 1998;Springer, New York.
24. A receptor subunit mRNAs in monkey visual cortex. J. Neurosci. 14:1994;2236-2259.
25. Jones L., Fischer I., Levitt P. Non-uniform alteration of dendritic development in the cerebral cortex following prenatal cocaine exposure. Cereb. Cortex. 43:1996;439-453.
26. A receptors. Neuron. 3:1989;745-753.
27. Koob G.F. Drugs of abuse: anatomy, pharmacology and function of reward pathways. Trends Pharmacol. Sci. 13:1992;177-184.
28. Land P.W., de Blas A.L., Reddy N. Immunocytochemical localization of GABAA receptors in rat somatosensory cortex and effects of tactile deprivation. Somatosens. Mot. Res. 12:1995;127-141.
29. A receptor subunit mRNAs in the rat brain. III Embryonic and postnatal development. J. Neurosci. 12:1992a;4151-4172.
30. A receptor subunit mRNAs in the rat brain. II. Olfactory bulb and cerebellum. J. Neurosci. 12:1992b;1063-1076.
31. Levitt P., Harvey J.A., Friedman E., Simansky K., Murphy E.H. Prenatal drug exposure: new evidence for neurotransmitter influences on brain development. Trends Neurosci. 20:1997;269-274.
32. Lindefors N. Dopaminergic regulation of glutamic acid decarboxylase mRNA expression and GABA release in the striatum: a review. Prog. Neuropsychopharmacol. Biol. Psychiatry. 17:1993;887-903.
33. A receptor channels. Annu. Rev. Neurosci. 17:1994;569-602.
34. Marlier L.N.J.-L., Zheng T., Tang J., Grayson D.R. Regional distribution in the rat central nervous system of an mRNA encoding a portion of the cardiac sodium/calcium exchanger isolated from cerebellar granule neurons. Mol. Brain Res. 20:1993;21-39.
35. A receptors. Brain Res. Rev. 29:1999;196-217.
36. Meier E., Hertz L., Schousboe A. Neurotransmitters as developmental signals. Neurochem. Int. 19:1991;1-15.
37. Memo M., Bovolin P., Costa E., Grayson D.R. Regulation of γ-aminobutyric acidA receptor subunit expression by activation of N-methyl-D-aspartate-selective glutamate receptors. Mol. Pharmacol. 39:1991;599-603.
38. Mhatre M., Ticku M.K. Chronic ethanol treatment upregulates the GABA receptor beta subunit expression. Brain Res. Mol. Brain Res. 23:1994;246-252.
39. Micheva K.D., Beaulieu C. Development and plasticity of the inhibitory neocortical circuitry with an emphasis on the rodent barrel field cortex: a review. Can. J. Physiol. Pharmacol. 75:1997;470-478.
40. Murphy E.H. Critical periods and the development of the rabbit visual cortex. Stone J., Rappaport E., Development of Visual Pathways in Mammals. 1984;439-462 Alan Liss, New York.
41. Murphy E.H., Hammer J.G., Schumann M.D., Groce M.Y., Wang X.-H., Jones L., Romano A.G., Harvey J.A. The rabbit as a model for studies of in utero cocaine exposure. Lab. Anim. Sci. 45:1995;163-168.
42. Murphy E.H., Chon J., Darvish-Sefat F., Diven K., Schumann M., Shumsky J.S. Effects of cocaine-induced seizures during pregnancy in the rabbit. Physiol. Behav. 62:1997a;597-604.
43. Murphy E.H., Fischer I., Friedman E., Grayson D., Jones L., Levitt P., O'Brien-Jenkins A., Wang H.-Y., Wang X.-H. Cocaine administration in pregnant rabbits alters cortical structure and function in their progeny in the absence of maternal seizures. Exp. Brain Res. 114:1997b;433-441.
44. Nissanov J., McEachron D.L. Advances in image processing for autoradiography. J. Chem. Neuroanat. 4:1991;329-342.
45. A receptor α subunit mRNAs in the developing rat CNS. J. Neurosci. 12:1992;2888-2900.
46. Pritchett D.B., Seeburg P.H. γ-aminobutyric acidA receptor α5 subunit creates novel Type II benzodiazepine receptor pharmacology. J. Neurochem. 54:1990;1802-1804.
47. A- benzodiazepine receptors produced in transfected cells. Science. 245:1989a;1389-1392.
48. A receptor subunit for benzodiazepine pharmacology. Nature. 338:1989b;582-585.
49. - currents. Mol. Pharmacol. 39:1991;691-696.
50. A receptor research. Synapse. 21:1995;189-274.
51. Rakic P. Mode of cell migration to the superficial layers of fetal monkey neocortex. J. Comp. Neurol. 145:1972;61-84.
52. Rakic P. Prenatal development of the visual system in the rhesus monkey. Philos. Trans. R. Soc. London (Biol.). 278:1977;245-260.
53. 3H]GABA in the rat prefrontal cortex. Neuroscience. 43:1991;323-329.
54. Rogers A.W. Techniques of Autoradiography. 1979;Elsevier, New York.
55. A receptor diversity in the human genome. Gene. 227:1999;213-222.
56. B receptor agonists and antagonists. Brain Res. 630:1993;28-31.
57. Schousboe A., Redburn D.A. Modulatory actions of gamma aminobutyric acid (GABA) on GABA Type A receptor subunit expression and function. J. Neurosci. Res. 41:1995;1-7.
58. A receptor subunits exist in distinct neuronal subpopulations. Neuron. 3:1989;327-337.
59. A receptor subunit mRNA expression in rabbit visual cortex. Ann. New York Acad. Sci. 846:1998;371-374.
60. A receptors on channel function. Neuron. 5:1990;703-711.
61. Stanwood G.D., Washington R.A., Shumsky J.S., Levitt P. Prenatal cocaine exposure produces consistent developmental alterations in dopamine-rich regions of cerebral cortex. Neuroscience. 106:2001;5-14.
62. Verney C., . Alvarez C., Geffard M., Berger B. Ultrastructural double-labelling study of dopamine terminals and GABA-containing neurons in rat anteromedial cerebral cortex. Eur. J. Neurosci. 2:1990;960-972.
63. Vincent S.L., Sorenson I., Benes F.M. Localization and high resolution imaging of cortical neurotransmitter compartments using confocal laser scanning microscopy: GABA and glutamate interactions in rat cortex. Biotechniques. 11:1991;628-633.
64. Vogt B.A., Sikes R.W., Vogt L.J. Anterior cingulate cortex and the medial pain system. Vogt B.A., Gabriel M., Neurobiology of Cingulate Cortex and Limbic Thalamus. 1993;313-344 Birkhauser, Boston.
65. Wang H.-Y., Runyan S., Yadin E., Friedman E. Prenatal exposure to cocaine selectively reduces D1 dopamine receptor-mediated activation of striatal Gs proteins. J. Pharmacol. Exp. Ther. 273:1995;492-498.
66. Wang X.-H., Levitt P., Grayson D.R., Murphy E.H. Intrauterine cocaine exposure of rabbits: persistent elevation of GABA-immunoreactive neurons in anterior cingulate cortex but not visual cortex. Brain Res. 689:1995;32-46.
67. Wang X.-H., O'Brien-Jenkins A., Choi L., Murphy E.H. Altered neuronal distribution of parvalbumin in anterior cingulate cortex of rabbits exposed in utero to cocaine. Exp. Brain Res. 112:1996;359-371.
68. A receptor maturation in cerebellar granule neurons in vitro. J. Neurochem. 71:1998;693-704.
69. A receptor α subunit mRNAs show differential patterns of expression in bovine brain. Neuron. 1:1988;937-947.
70. A receptor β subunit heterogeneity: functional expression of cloned cDNAs. EMBO J. 8:1989;1665-1670.
71. A receptor function in cerebellar granule neurons. J. Neurosci. 15:1995;7692-7701.