The Postnatal Development of the Gaba_a/benzodiazepine Receptor in the Rat Red Nucleus

References

• Stephenson F. A. The GABAA receptors: structure and function. Curr. Asp. Neurosci. 1991; 3: 177–193
   Google Scholar
• Sieghart W. GABAA receptors: ligand‐gated Cl‐ion channels modulated by multiple drug‐binding sites. TIPS 1992; 13: 446–450
   PubMed Web of Science ®Google Scholar
• Casalotti S. O., Stephenson F. A., Barnard E. A. Seperate subunits for agonist and benzodiazepine binding in the GABAA receptor oligomer. J. Biol. Chem. 1986; 261: 15013–15016
   PubMedGoogle Scholar
• Schofield P. R., Darison M. G., Fujita N., Burt D. R., Stephenson F. A., Rodriguez H., Rhee L. M., Ramachandran J., Reale V., Glencorse T. A., Seeburg P. H., Barnard E. A. Sequence and functional expression of GABAA receptor shows a ligand‐gated receptor super‐family. Nature 1987; 328: 221–227
   PubMed Web of Science ®Google Scholar
• Olsen R. W., Towbin A. J. Molecular Biology of GABAA receptors. FASEB J. 1990; 4: 1469–1480
   PubMed Web of Science ®Google Scholar
• Mohler H., Malherbe P., Draguhn A., Richard J. G. GABAA receptors: Structural requirements and sites of gene expression in mammalian brain. Neurochem. Res. 1990; 15: 199–207
   PubMed Web of Science ®Google Scholar
• Vuillon‐Cacciuttolo G., Bosler O., Nieoullon A. GABA neurons in the cat red nucleus: a biochemical and immunohistochemical demonstration. Neurosci. Letters 1984; 52: 129–134
   PubMedGoogle Scholar
• Vuillon‐Cacciuttolo G., Bosler O., Nieoullon A. Immunohistochemical evidence of plasticity of γ‐aminobutyric acid neurons in the red nucleus and adjacent reticular formation after contralateral cerebellectomy in the adult cat. Neurosci. Letters 1986; 70: 308–313
   PubMedGoogle Scholar
• Katsumaru H., Murakami F., Wu J. Y., Tsukahara N. Sprouting of GABAergic synapses in the red nucleus after lesions of the nucleus interpositus in the cat. J. Neurosci. 1986; 6: 2864–2874
   PubMedGoogle Scholar
• Penny J. B., Pan H. S., Young A. B., Frey K. A., Dauth G. W. Quantitative autoradiography of 3H‐muscimol binding in rat brain. Science 1981; 214: 1036–1038
   PubMedGoogle Scholar
• Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein‐dye binding. Anal. Biochem. 1976; 72: 248–254
   PubMed Web of Science ®Google Scholar
• Czajkowski C., Farb D. H. Transmembrane topology and subcellular distribution of the benzodiazepine receptor. J. Neurosci. 1986; 6: 2857–2863
   PubMedGoogle Scholar
• Yin H. S., Fan S. S. Monoclonal antibodies recognizing the benzodiazepine receptor of chick embryo brain. J. Recept. Res. 1990; 10: 249–267
   PubMed Web of Science ®Google Scholar
• Munson P. J., Rodbard D. Ligand: A versatile computerized approach for characterization of ligand‐binding systems. Anal. Biochem. 1980; 107: 220–239
   PubMed Web of Science ®Google Scholar
• Candy J. M., Martin I. L. The postnatal development of the benzodiazepine receptor in the cerebral cortex and cerebellum of the rat. J. Neurochem. 1979; 32: 655–658
   PubMedGoogle Scholar
• Schliebs R., Rothe T., Bigl V. Dark‐rearing affects the development of benzodiazepine receptors in the central visual structures of rat brain. Develop. Brain Res. 1986; 24: 179–185
   Google Scholar
• Eichinger A., Sieghart W. Postnatal development of proteins associated with different benzodiazepine receptors. J. Neurochem. 1986; 46: 173–180
   PubMedGoogle Scholar
• Sieghart W. Comparison of BZDR in cerebellum and inferior colliculus. J. Neurochem. 1986; 47: 920–923
   PubMedGoogle Scholar
• Benke D., Cicin‐Sain A., Mertens S., Mohler H. Immunochemical identification of the α1 and α3 subunits of the GABAA receptor in the rat brain. J. Recept. Res. 1991; 11: 407–424
   PubMed Web of Science ®Google Scholar
• McKernan R. M., Cox P., Gillard N. P., Whiting P. Differential expression of GABAA receptor subunits in rat brain during development. FEBS Letters 1991; 286: 44–46
   PubMedGoogle Scholar
• Zezula J., Fuchs K., Sieghart W. Seperation of α1 α2 and α3 subunits of the GABAA‐benzodiazepine receptor complex by immunoaffinity chromatography. Brain Res. 1991; 563: 325–328
   PubMedGoogle Scholar
• Laurie D. J., Wisden W., Seeburg P. H. The distribution of thirteen GABAA receptor subunit mRNAs in the rat brain. III. Embryonic and postnatal development. J. Neurosci. 1992; 12: 4151–4172
   PubMed Web of Science ®Google Scholar
• Sakaguchi H., Kubota M., Nakamura M., Tsukahara N. Effects of amino acids on cat red nucleus neurons. Exp. Brain Res. 1984; 54: 150–156
   PubMedGoogle Scholar
• Daval J. ‐L., Werck M. ‐C., Nehlig A., de Vasconcelos A. P. Quantitative autoradiographic study of the postnatal development of benzodiazepine binding sites and their coupling to GABA receptors in the rat brain. Int. J. Devl. Neurosci. 1991; 9: 307–320
   PubMedGoogle Scholar
• Desmond J. E., Moore J. W. Single‐unit activity in red nucleus during the classically conditioned rabbit nictitating membrane response. Neurosci. Res. 1991; 10: 260–278
   PubMedGoogle Scholar
• Winters N. K., Webster M. L., Irwin K. B., Bracha V., Bloedel J. R. Involvement of the cerebellar nuclei and the red nucleus in the control of the eyeblink reflex in the rabbit: the role of GABA‐A receptor mediated neurotransmission. Society for Neurosci. Abs. 1993; 19: 1005
   Google Scholar
• Rose S. P. R., Stewart M. G. Transient increase in muscarinic acetylcholine receptor and acetylcholine sterase in visual cortex on first exposure of dark‐reared rats to light. Nature 1978; 271: 169–170
   PubMedGoogle Scholar