References
Mugnaini, E., and Oertel, W. H. 1985. An atlas of the distribution of GABAergic neurons and terminals in the rat CNS as revealed by GAD immunohistochemistry Pages 436–622in A. Björklund and T. Hökfelt, (eds.), Publ. Elsevier Science Publishers, B. V.Handbook of Chemical Neuroanatomy Vol. 4: GABA and neüropeptides in the CNS. Part 1
Hill, D. R., and Bowery, N. G. 1981.3H-baclofen and3H-GABA bind to bicuculline-insensitive GABAB sites in rat brain. Nature, 290:149–152.
Bowery, N. G. 1989. GABAB receptors and their significance in mammalian pharmacology. Trends in Pharmac. Sci., 10:401–407.
Bormann, J. 1988. Electrophysiology of GABAA and GABAB receptor subtypes, Trends in Neuroscience, 11:112–116.
Bormann, J., Hamill, O. P., Sakmann, B. 1987. Mechanism of anion permeation through channels gated by glycine and gamma aminobutyric acid in mouse cultured spinal neurones. J. Physiol. (Lond.), 385:243–286.
Newberry, N. R. and Nicoll, R. A. 1984. Direct hyperpolarizing action of baclofen on hippocampal pyramidal cells. Nature, 308:450–452.
Newberry, N. R. and Nicoll, R. A. 1985. Comparison of the action of baclofen γ-aminobutyric acid on rat hippocampal pyramidal cells in vitro. J. Physiol. 360:161–185.
Gähwiler, B. H. and Brown, D. A. 1985. GABAB-receptor-activated K+ current in voltage-clamped CA3 pyramidal cells in hippocampal cultures. Proc. Natl. Acad. Sci., USA., 82:1558–1562.
Inoue, M., Matsuo, T. and Ogata, N. 1985a. Baclofen activates voltage-dependent and 4-aminopyridine sensitive K+ conductance in guinea-pig hippocampal pyramidal cells maintained in vitro. Br. J. Pharmacol., 84:833–841.
Inoue, M., Matsuo, T. and Ogata, N. 1985b. Characterization of pre- and postsynaptic actions of (-)baclofen in the guinea-pig hippocampus in vitro. Br. J. Pharmacol., 84:843–851.
Desarmenien, M., Feltz, P., Occhipinti, G., Santangelo, F. and Schlichter, R. 1984. Co-existence of GABAA and GABAB receptors on Aδ and C primary afferents. Br. J. Pharmac., 81:327–333.
Dunlap, K. 1981. Two types of γ-aminobutyric acid receptor on embryonic sensory neurones. Br. J. Pharmac., 74:579–585.
Deisz, R. A. and Lux, H. D. 1985. γ-Aminobutyric acid-induced depression of calcium currents of chick sensory neurons. Neurosci. Lett., 56:205–210.
Dolphin, A. C. 1987. Nucleotide binding proteins in signal transduction and disease. Trends in Neuroscience, 10:53–57.
Dolphin, A. C. and Scott, R. H. 1987. Calcium channel currents and their inhibition by (-)baclofen in rat sensory neurones: Modulation by guanine nucleotides. J. Physiol. (Lond.), 386:1–17.
Holz, G. G., Rane, S. G. and Dunlap, K. 1986. GTP-binding proteins mediate transmitter inhibition of voltage-dependent calcium channels. Nature, 319:670–672.
Andrade, R., Malenka, R. C. and Nicoll, R. A. 1986. A G protein couples serotonin and GABAB receptors to the same channels in hippocampus. Science, 234:1261–1265.
Asano, T., Ui, M. and Ogasawara, N. 1985. Prevention of the agonist binding to γ-aminobutyric acid B receptors by guanine nucleotides and islet-activating protein, pertussis toxin, in bovine cerebral cortex. J. Biol. Chem., 260:12653–12658.
Hill, D. R. 1985. GABAB receptor modulation of adenylate cyclase activity in rat brain slices. Br. J. Pharmacol. 84:249–257.
Innis, R. B., Nestler, E. J. and Aghajanian, G. K. 1988. Evidence for G protein mediation of serotonin-and GABAB induced hyperpolarization of rat dorsal raphe neurons. Brain Res., 459:27–36.
Karbon, E. W. and Enna, S. J. 1985. Characterization of the relationship between γ-aminobutyric acid B agonists and transmitter-coupled cyclic nucleotide-generating systems in rat brain. Mol. Pharmacol., 27:53–59.
Thalmann, R. H. 1988. Evidence that guanosine triphosphate (GTP) binding proteins control a synaptic response in brain. effect of pertussis toxin and GTPγS on the late inhibitory postsynaptic potential of hippocampal CA3 neurons. J. Neuroscience, 8:4589–4602.
Wojcik, W. J., and Neff, N. H. 1984. γ-Aminobutyric acid B receptors are negatively coupled to adenylate cyclase in brain, and in the cerebellum these receptors may be associated with granule cells. Mol. Pharmac., 25:24–28.
Xu, J. and Wojcik, W. J. 1986. Gamma aminobutyric acid B receptor-mediated inhibition of adenylate cyclase in cultured cerebellar granule cells: blockade by islet-activating protein. J. Pharmac. Exp. Ther., 239:568–573.
Wilkin, G. P., Hudson, A. L. Hill, D. R. and Bowery, N. G. 1981. Autoradiographic localization of GABAB receptors in rat cerebellum. Nature, 294:584–587.
Price, G. W., Kelly, J. S. and Bowery, N. G. 1987. The location of GABAB receptor binding sites in mammalian spinal cord. Synapse, 1:530–538.
Bowery, N.G., Hudson, A. L., and Price, G. W. 1987. GABAA and GABAB receptor site distribution in the rat central nervous system. Neuroscience, 20:365–383.
Chu, D. C. M., Albin, R. L., Young, A. B., and Penney, J. B. 1990. Distribution of kinetics of GABAB binding sites in rat central nervous system: a quantitative autoradiographic study. Neuroscience, 34:341–357.
Barber, R.P., Vaughn, J. E., Saito, K., McLaughlin, B. J. and Roberts, E. 1978. GABAergic terminals are presynaptic to primary afferent terminals in the substantia gelatinosa of the rat spinal cord. Brain Res, 141:35–55.
Curtis, D. R. 1978. Pre- and non-synaptic activities of GABA and related amino acids in the mammalian nervous system. In:Amino Acids As Chemical Transmitters (Ed. F. Fonnum, Publ. Plenum Press, New York) pp. 55–86.
Bowery, N. G., Doble, A., Hill, D. R., Hudson, A. L., Shaw, J. S., Turnbull, M. J. and Warrington, R. 1981. Bicuculline-insensitive GABA receptors on peripheral autonomic nerve terminals. Eur. J. Pharmacol., 71:53–70.
Bowery, N. G., Hill, D. R., Hudson, A. L., Doble, A., Middlemiss, D. N., Shaw, J., and Turnbull, M. J. 1980. Baclofen decreases neurotransmitter release in the mammalian CNS by an action at a novel GABA receptor. Nature, 283:92–94.
Lanthorn, T. H. and Cotman, C. W. 1981. Baclofen selectively inhibits excitatory synaptic transmission in the hippocampus. Brain Res. 225:171–178.
Ault, B., and Nadler, J. V. 1982. Baclofen selectively inhibits transmission at synapses made by axons of CA3 pyramidal cells in the hippocampal slice. J. Pharm. Exp. Ther., 223:291–297.
Olpe, H-R., Baudry, M., Fagni, L. and Lynch, G. 1982. The blocking action of baclofen on excitatory transmission in the rat hippocampal slice. J. Neurosci., 2:698–703.
Kato, K., Goto, M. and Fukuda, H. 1982. Baclofen: Inhibition of the release of L-[3H]glutamate and L-[3H]aspartate from rat whole brain synaptosomes. Gen. Pharmacol., 13:445–447.
Collins, G. G. S., Anson, J., and Kelly, E. P. 1982. Baclofen: Effects on evoked field potentials and amino acid transmitter release in the rat olfactory cortex. Brain Res., 238:371–383.
Collins, G. G. S. and Howlett, S. J. 1988. The pharmacology of excitatory transmission in the rat olfactory cortex slice. Neuropharmacology, 27:697–705.
Burke, S. P. and Nadler, J. V. 1988. Regulation of glutamate and aspartate release from slices of the hippocampal CA1 area: Effects of adenosine and baclofen. J. Neurochem., 51:1541–1551.
Dutar, P. and Nicoll, R. A. 1988a. Pre- and post-synaptic GABAB receptors in the hippocampus have different pharmacological properties. Neuron, 1:585–598.
Harrison, N. L. 1990. On the presynaptic action of baclofen at inhibitory synapses between cultured rat hippocampal neurones. J. Physiol., 422:433–446.
Pittaluga, A., Asaro, D., Pellegrini, G. and Raiteri, M. 1987. Studies on3H-GABA and endogenous GABA release in rat cerebral cortex suggest the presence of autoreceptors of the GABAB type. Eur. J. Pharmacol., 144:45–52.
Harrison, N. L., Lange, G. D. and Barker, J. L. 1988. (-)Baclofen activates presynaptic GABAB receptors on GABAergic inhibitory neurons from embryonic rat hippocampus. Neurosci. Leters, 85:105–109.
Waldmeier, P. C., Wicki, P., Feldtauer, J. J., and Baumann, P. A. 1988. Potential involvement of a baclofen-sensitive autoreceptor in the modulation of the release of endogenous GABA from rat brain slices in vitro. Naunyn-Schmiedeberg's Arch. Pharmacol., 237:289–295.
Potashner, S. J. 1979. Baclofen: Effects on amino release and metabolism in slices of the guinea-pig cerebral cortex. J. Neurochem. 32:103–109.
Kilpatrick, G. J., Muhyaddin, M. S., Roberts, P. J. and Woodruff, G. N. 1983. GABAB binding sites on rat striatal synptic membranes. Br. J. Pharmacol., 78: suppl., 6P.
Reimann, W., Zum, D. and Starke, K. 1982. γ-Aminobutyric acid can both inhibit and facilitate dopamine release in the caudate nucleus of the rabbit. J. Neurochem., 39:961–969.
Moratalla, R., Barth, T. and Bowery, N. G. 1989. Benzodiazepine receptor autoradiography in corpus striatum of rat after large frontal cortex lesions and chronic treatment with diazepam. Neuropharmacology, 28:893–900.
Flamm, E. S., Demopoulos, H. B., Seligman, M. L., Tomasula, J. J., DeCrescito, V. and Ransohoff, J. 1977. Ethanol potentiation of central nervous system trauma. J. Neurosurg., 46:328–335.
Unnerstall, J. R., Niehoff, D. L., Kuhar, M. J. and Palacios, J. M. 1982. Quantitative receptor autoradiography using tritiated Ultrofilm: application to multiple benzodiazepine receptors. J. Neuroscience Methods, 6:59–73.
Stephenson, G. A. 1988. Understanding the GABAA receptor: a chemically gated ion channel. Biochem. J., 249:21–32.
Olsen, R. W. and Tobin, A. J. 1990. Molecular biology of GABAA receptors. FASEB J., 4:1469–1480.
Gobbi, M. & Mennini, T. (personal communication).
Grimm, V. E. and Hershkowitz, M. 1981. The effect of chronic diazepam treatment on discrimination performance and3H-flunitrazepam binding in the brains of shocked and non-shocked rats. Psychopharmachology (Berlin), 74:132–136.
Chu, D. C. M., Penney, J. B., and Young, A. B. 1987. Autoradiographic evidence for postsynaptic GABAB receptors in rat striatum and hippocampus. Soc. Neurosci. Abstract, 13:952.
Moratalla, R. and Bowery, N. G. 1988. Autoradiographic measurement of GABAA and GABAB binding sites in rat caudate putamen after denervation of neuronal inputs. Br. J. Pharmacol., 95:476P.
Bowery, N. G., Knott, C., Moratalla, R. and Pratt, G. D. 1990. GABAB receptors and their heterogeneity. In:GABA and benzodiazepine receptor subtypes: from molecular biology to clinical practice: (Eds. G. Biggio and E. Costa); Publ. Raven Press, New York; (in press).
Author information
Authors and Affiliations
Additional information
Special issue dedicated to Dr. Eugene Roberts.
Rights and permissions
About this article
Cite this article
Moratalla, R., Bowery, N.G. Chronic lesion of corticostriatal fibers reduces GABAB but not GABAA binding in rat caudate putamen: An autoradiographic study. Neurochem Res 16, 309–315 (1991). https://doi.org/10.1007/BF00966094
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00966094