Nitric oxide: what can it compute?

References

• Albus K, Wolf W. Early post-natal development of neuronal function in the kitten's visual cortex: a laminar analysis. J. Physiol. 1984; 348: 153–85
   PubMed Web of Science ®Google Scholar
• Amari S-I. Topographic organization of nerve fields. Bull. Math. Biol. 1980; 42: 339–64
   PubMed Web of Science ®Google Scholar
• Artola A, Singer W. Long term depression of excitatory synaptic transmission and its relationship to long term potentiation. Trends Neurosci. 1993; 16: 480–7
   PubMed Web of Science ®Google Scholar
• Bannerman D, Chapman P, Kelly P, Butcher S, Morris R. Inhibition of nitric oxide synthase does not impair spatial learning. J. Neurosci. 1994; 14: 7404–14
   PubMed Web of Science ®Google Scholar
• Bienenstock E, Cooper L, Munro P. Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex. J. Neurosci. 1982; 2: 32–48
   PubMed Web of Science ®Google Scholar
• Bliss T, Douglas R, Errington M, Lynch M. Correlation between long-term potentiation and release of endogenous amino acids from dentate gyrus of anaesthetized rats. J. Physiol. 1986; 377: 391–408
   PubMed Web of Science ®Google Scholar
• Böhme G A, Bon C, Lemaire M, Reibaud M, Piot O, Stutzmann J-M, Doble A, Blanchard J-C. Altered synaptic plasticity and memory formation in nitric oxide synthase inhibitor-treated rats. Proc. Natl Acad. Sci. USA 1993; 90: 9191–4
   PubMed Web of Science ®Google Scholar
• Bonhoeffer T, Staiger V, Aertsen A. Synaptic plasticity in rat hippocampal slice cultures: Local ‘hebbian’ conjunction of pre and postsynaptic stimulation leads to distributed synaptic enhancement. Proc. Natl Acad. Sci. USA 1989; 86: 8113–7
   PubMed Web of Science ®Google Scholar
• Boulton C L, Irving A J, Southam E, Potier B, Garthwaite J, Collingridge G L. The nitric oxide—cyclic GMP pathway and synaptic depression in rat hippocampal slices. Eur. J. Neurosci. 1994; 6: 1528–35
   PubMed Web of Science ®Google Scholar
• Bredt D S, Snyder S H. Nitric oxide, a novel neuronal messenger. Neuron 1992; 8: 3–11
   PubMed Web of Science ®Google Scholar
• Cummings J A, Nicola S M, Malenka R C. Induction in the rat hippocampus of long-term potentiation (LTP) and long-term depression (LTD) in the presence of a nitric oxide synthase inhibitor. Neurosci. Lett. 1994; 176: 110–4
   PubMed Web of Science ®Google Scholar
• Dermon C, Stamatakis A. Laminar pattern of NDAPH-diaphorase activity in the developing avian cerebellum. Neuroreport 1994; 5: 1941–5
   PubMed Web of Science ®Google Scholar
• Egberongbe Y, Gentleman S, Falkai P, Bogerts B, Polak J, Roberts G. The distribution of nitric oxide synthase immunoreactivity in the human brain. Neurosci. 1994; 59: 561–78
   PubMed Web of Science ®Google Scholar
• Gally J A, Montague P R, Reeke G N, Jr, Edelman G M. The NO hypothesis: possible effects of a short-lived, rapidly diffusing signal in the development and function of the nervous system. Proc. Natl Acad. Sci. USA 1990; 87: 3547–51
   PubMed Web of Science ®Google Scholar
• Garthwaite J, Boulton C. Nitric oxide signalling in the central nervous system. Ann. Rev. Physiol. 1995; 57: 683–706
   PubMed Web of Science ®Google Scholar
• Garthwaite J, Charles S L, Chess-Williams R. Endothelium-derived relaxing factor release on activation of NMDA receptors suggests role as intercellular messenger in the brain. Nature 1988; 336: 385–8
   PubMed Web of Science ®Google Scholar
• Geman S. Some averaging and stability results for random differential equations. SIAM J. Appl. Math. 1979; 36: 86–105
   Web of Science ®Google Scholar
• Hawkins R D. NO honey, I don't remember. Neuron 1996; 16: 465–7
   PubMed Web of Science ®Google Scholar
• Hölscher C, Rose S P. An inhibitor of nitric oxide synthesis prevents memory formation in the chick. Neurosci. Lett. 1992; 145: 165–7
   PubMed Web of Science ®Google Scholar
• Kohonen T. Physiological interpretation of the self-organizing map. Neural Networks 1993; 6: 895–905
   Web of Science ®Google Scholar
• Krekelberg B, Taylor J G (1995) Nitric oxide: a diffusing messenger in a topographic map. Proc. ICANN, Paris, October, 1995, F Fogelman-Soulié, P Gallinari. EC2, Paris, 525–30
   Google Scholar
• Krekelberg B, Taylor J G. Nitric oxide and the development of long-range horizontal connectivity. Neural Networks World 1996; 6: 185–9
   Google Scholar
• Krekelberg B, Taylor J G. Nitric oxide in cortical map formation. J. Chem. Neuroanat. 1996; 10(3/4)
   PubMed Web of Science ®Google Scholar
• Krekelberg B, Taylor J G. Non-linear learning dynamics of a diffusing messenger. Mathematics of Neural Networks: Models, Algorithms and Applications, S W Ellacott, J C Mason, I J Anderson. Kluwer Academic, Dordrecht 1997
   Google Scholar
• Krekelberg B, Taylor J G (1996) Temporal self-organization with a diffusing messenger. Proc. Computational Neuroscience, Boston, 1996, J Bower. Plenum, New York
   Google Scholar
• Madison D V. Commentary: Pass the nitric oxide. Proc. Natl Acad. Sci. USA 1993; 90: 4329–31
   PubMed Web of Science ®Google Scholar
• Maren S, Baudry M. Properties and mechanisms of long-term synaptic plasticity in the mammalian brain: Relationships to learning and memory. Neurobiol. Learn. Mem. 1995; 63: 1–18
   PubMed Web of Science ®Google Scholar
• Meulemans A. Diffusion coefficients and half-lives of nitric oxide and n-nitroso-l-arginine in rat cortex. Neurosci. Lett. 1994; 171: 89–93
   PubMed Web of Science ®Google Scholar
• Montague P R, Gally J A, Edelman G M. Spatial signalling in the development of neural connections. Cereb. Cortex 1991; 1: 199–220
   PubMed Web of Science ®Google Scholar
• O'dell T, Hawkins R, Kandel E, Arancio O. Tests of the roles of two diffusable substances in long-term potentiation: evidence for nitric oxide as a possibly early retrograde messenger. Proc. Natl Acad. Sci. USA 1991; 88: 11285–9
   PubMed Web of Science ®Google Scholar
• Schuman E M, Madison D V. A requirement for the intercellular messenger nitric oxide in long-term potentiation. Science 1991; 254: 1503–6
   PubMed Web of Science ®Google Scholar
• Schuman E M, Madison D V. Locally distributed synaptic potentiation in the hippocampus. Science 1994; 263: 532–6
   PubMed Web of Science ®Google Scholar
• Takeuchi A, Amari S-I. Formation of topographic maps and columnar microstructures in nerve fields. Biol. Cybern. 1979; 35: 63–72
   PubMed Web of Science ®Google Scholar
• Vanderkooi J M, Wright W W, Erecinska M. Nitric oxide diffusion coefficients in solutions, proteins and membranes determined by phosphorescence. Biochem. Biophys. Acta 1994; 1207: 249–54
   PubMed Web of Science ®Google Scholar
• Williams C V, Nordquist D, Mcloon S. Correlation of nitric oxide synthase expression with changing patterns of axonal projections in the developing visual system. J. Neurosci. 1994; 14: 1746–55
   PubMed Web of Science ®Google Scholar
• Williams J, Li Y-G, Nayak A, Errington M, Murphy K, Bliss T. The suppression of long-term potentiation in rat hippocampus by inhibitors of nitric oxide synthase is temperature and age dependent. Neuron 1993; 11: 877–84
   PubMed Web of Science ®Google Scholar
• Willshaw D, von der Malsburg C. How patterned neural connections can be set up by self-organization. Proc. R. Soc. B 1976; 194: 431–45
   PubMed Web of Science ®Google Scholar
• Wood J, Garthwaite J. Models of the diffusional spread of nitric oxide: implications for neural nitric oxide signalling and its pharmacological properties. Neuropharm. 1994; 33: 1235–44
   PubMed Web of Science ®Google Scholar
• Wu H H, Williams C V, McLoon S. Involvement of nitric oxide in the elimination of a transient retinotectal projection in development. Science 1994; 265: 1593–6
   PubMed Web of Science ®Google Scholar
• Zhuo M, Kandel E, Hawkins R. Nitric oxide and cGMP can produce either synaptic depression or potentiation depending on the frequency of presynaptic stimulation in the hippocampus. Neuroreport 1994; 5: 1033–6
   PubMed Web of Science ®Google Scholar
• Zhuo M, Small S A, Kandel E R, Hawkins R D. Nitric oxide and carbon monoxide produce activity-dependent long-term synaptic enhancement in hippocampus. Science 1993; 260: 1946–50
   PubMed Web of Science ®Google Scholar