Modification of Receptive Fields of Posteriomedial Barrel Subfield Neocortical Single Units by Known Concentrations of Iontophoresed Noradrenaline in the Rat

References

• Armstrong-James M. NMDA, non-NMDA neurotransmission in the construction of receptive fields of rat barrel-field neurones. Society of Neuroscience Abstracts 1989; 15: 949
   Google Scholar
• Armstrong-James M., Callahan C. A. Thalamo-cortical processing of vibrissal information in the rat. II Saptiotemporal convergence in the thalamic ventroposterior medial nucleus (VPm) and it's relevance to generation of receptive fields of SI cortical barrel neurones. Journal of Comparative Neurology 1988; 303: 211–224
   Google Scholar
• Armstrong-James M., Callahan C. A., Friedman M. A. Thalamo-cortical processing of vibrissal information in the rat. I Intracortical origins of surround, but not center, receptive fields of layer IV neurones in rat SI barrel field cortex. Journal of Comparative Neurology 1988; 303: 193–210
   Google Scholar
• Armstrong-James M., Fox K. Effects of iontophoresed noradrenaline on the spontaneous activity of neurones in rat primary somatosensory cortex. Journal of Physiology 1983; 335: 427–447
   PubMed Web of Science ®Google Scholar
• Armstrong-James M., Fox K. Spatio-temporal diverence and convergence in rat “barrel” cortex. Journal of Comparative Neurology 1987; 263: 265–281
   PubMed Web of Science ®Google Scholar
• Armstrong-James M., Fox K. Evidence for a specific role for cortical NMDA receptors in slow wave sleep. Brain Research 1988; 451: 189–196
   PubMed Web of Science ®Google Scholar
• Armstrong-James M., Fox K., Kruk Z., Millar J. M. Quantitative iontophoresis of cate-cholamines using multi-barrelled carbon fibre microelectrodes. Journal of Neuroscience Methods 1980; 4: 385–406
   Web of Science ®Google Scholar
• Armstrong-James M., George M. J. The influence of anaesthesia on spontaneous activity and receptive field size of single units in rat Sml neocortex. Experimental Neurology 1988; 99: 369–387
   PubMed Web of Science ®Google Scholar
• Armstrong-James M., Millar J. M. Carbon fibre microelectrodes. Journal of Neuroscience Methods 1979; I: 279–287
   Google Scholar
• Armstrong-James M., Welker E., Callahan C. A. The contribution of NMDA receptors to fast and slow transmission of sensory information in the rat SI barrel cortex. Submitted to Journal of Neuroscience 1991
   Google Scholar
• Aston-Jones G., Bloom F. E. Activity of norepinephrine containing locus coeruleus neurons in behaving rats anticipates fluctuations in the sleep-waking cycle. Journal of Neuroscience 1981; 1: 876–886
   PubMed Web of Science ®Google Scholar
• Bradshaw C. M., Stoker M. J., Szabadi E. The effect of microelectrophoretically applied clonidine on single cerebral cortical neurones in the rat: evidence for interaction of α1-adrenore-ceptors. Naunyn-Schmiedebergs Archives of Pharmacology 1982; 320: 230–234
   PubMed Web of Science ®Google Scholar
• Bretag A. H. Synthetic interstitial fluid for isolated mammalian tissue. Life Science 1969; 8: 319–320
   PubMed Web of Science ®Google Scholar
• Donoghue J. P., Carroll K. L. Cholinergic modulation of sensory responses in rat primary somatic sensory cortex. Brain Research 1987; 408: 367–371
   PubMed Web of Science ®Google Scholar
• Foote S. L., Freedman R., Oliver A. P. Effects of putative neurotransmitters on neuronal activity in the monkey auditory cortex. Brain Research 1975; 86: 229–242
   PubMed Web of Science ®Google Scholar
• Fox K., Armstrong-James M. The role of the anterior intralaminar nuclei and N-methyl-D-Aspartate receptors in the generation of spontaneous burst in rat neocortical neurones. Experimental Brain Research 1986; 63: 505–518
   PubMed Web of Science ®Google Scholar
• Fox K., Sato H., Daw N. The location and function of NMDA receptors in cat and kitten visual cortex. Journal of Neuroscience 1989; 9: 2443–2454
   PubMed Web of Science ®Google Scholar
• George M. J., Mridha K. A. Disruption of neocortical lamina V neuronal bursts by serotonin in urethane anaesthetized rats. International Journal of Neuroscience 1989; 45: 111–118
   PubMed Web of Science ®Google Scholar
• Ito M. Some quantitative aspects of vibrissa driven neuronal responses in rat cortex. Journal of Neurophysiology 1981; 46: 705–715
   PubMed Web of Science ®Google Scholar
• Ito M. Processing of vibrissa sensory information within the rat neocortex. Journal of Neurophysiology 1985; 54: 479–490
   PubMed Web of Science ®Google Scholar
• Jensen K. F., Killackey H. P. Terminal arbors of axons projecting to the somatosensory cortex of adult rats. 1. The normal morphology of specific thalamocortical afferents. Journal of Neuroscience 1987; 7: 3529–3543
   PubMed Web of Science ®Google Scholar
• Killackey H. P. Anatomical evidence for cortical sub-divisions based on vertically discrete thalamic projections from the ventral posterior nucleus to cortical to cortical barrels in the rat. Brain Research 1973; 51: 326–331
   PubMed Web of Science ®Google Scholar
• Levitt P., Moore R. Y. Noradrenaline neuron innervation of the neocortex in the rat. Brain Research 1979; 139: 219–231
   Web of Science ®Google Scholar
• Lidov H. G. W., Rice F. L., Molliver M. E. The organisation of the catecholamine innervation of somatosensory cortex: the barrel field of the mouse. Brain Research 1978; 153: 577–584
   PubMed Web of Science ®Google Scholar
• Millar J. M. A ‘wavegate’ spike discriminator for sorting extracellular nerve action potentials. Journal of Neuroscience Methods 1983; 7: 157–164
   PubMed Web of Science ®Google Scholar
• Millar J., Todd A. A method for marking extracellular recording sites in the CNS using carbon fibre microelectrodes. Journal of Physiology 1982; 328: 6P
   Web of Science ®Google Scholar
• Moises H. C., Woodward D. J. Potentiation of GABA inhibitory action in cerebellum by locus coeruleus stimulation. Brain Research 1980; 182: 327–344
   PubMed Web of Science ®Google Scholar
• Moises H. C., Woodward D. J., Hoffer B. J., Freedman R. Interactions of Norepinephrine with Purkinje cell responses to putative amino acid neurotransmitters applied by microiontopho-resis. Experimental Neurology 1979; 64: 493–515
   PubMed Web of Science ®Google Scholar
• Monaghan D. T., Cotman C. W. Distribution of N-methyl-D-Aspartate L-[3H] glutamate binding sites in rat brain. Journal of Neuroscience 1985; 5: 2909–2919
   PubMed Web of Science ®Google Scholar
• Morrison J. H., Foote S. L., Molliver M. E., Bloom F. E., Lidov H. G. W. Noradrenergic and Serotinergic fibres innervate complementary layers in monkey primary visual cortex; an im-munohistochemical study. Proceedings of the National Academy of Science USA 1982; 79: 2401–2405
   PubMed Web of Science ®Google Scholar
• Morrison J. H., Grzanna R., Molliver M. E., Coyle J. T. The distribution and orientation of noradrenergic fibres in neocortex of the rat; an immunoflurescence study. Journal of Comparative Neurology 1978; 181: 17–40
   PubMed Web of Science ®Google Scholar
• Morriset R. A., Mott D. A., Lewis D. V., Swartzwelder H. S., Wilson W. A. GABA B Receptor mediated inhibition of the N-Methyl-D-Aspartate component of synaptic transmission in the rat hippocampus. Journal of Neuroscience 1991; 11: 203–209
   PubMed Web of Science ®Google Scholar
• Mountcastle V. B. Some functional properties of the somatic afferent system. Sensory Communication, W. Rosenblith. MIT Press, Cambridge, MA 1961; 403–436
   Google Scholar
• Simons D. J. Response properties of vibrissa units in rat SI somatosensory neocortex. Journal of Neurophysiology 1978; 41: 798–820
   PubMed Web of Science ®Google Scholar
• Simons D. J. Multi-whisker stimulation and its effects on vibrissa units in rat Sm 1 barrel cortex. Brain Research 1983; 276: 172–182
   Web of Science ®Google Scholar
• Szabadi E. Adrenoreceptors on central neurones: microelectrophoretic studies. Neuropharmacology 1979; 18: 831–843
   PubMedGoogle Scholar
• Videen T. D., Daw N., Rader R. K. The effect of norepinephrine on visual cortical neurones in kittens and adult cats. Journal of Neuroscience 1984; 4: 1607–1617
   PubMed Web of Science ®Google Scholar
• Waterhouse B. D., Moises H. C., Woodward D. J. Noradrenergic modulation of somatosensory cortical neuronal responses to iontophoretically applied putative neurotransmitters. Experimental Neurology 1980; 69: 30–49
   PubMed Web of Science ®Google Scholar
• Waterhouse B. D., Sessler F. M., Cheng J-T., Woodward D. J., Azizi S. A., Moises H. C. New evidence for a gating action of norepinephrine in central neuronal circuits of mam-malian brain. Brain Research Bulletin 1988; 21: 425–432
   PubMed Web of Science ®Google Scholar
• Welker C. Receptive fields of barrels in the somatosensory neocortex of the rat. Journal of Comparative Neurology 1976; 166: 173–190
   PubMed Web of Science ®Google Scholar