A model for experience-dependent changes in the responses of inferotemporal neurons

References

• Amit D J. What is and what is not a theory of context correlations. Network: Comput. Neural Syst. 1999; 10: 273
   PubMed Web of Science ®Google Scholar
• Barkai E, Hasselmo M E. Modulation of the input/output function of rat piriform cortex pyramidal cells. J. Neurophysiol. 1994; 72: 644–58
   PubMed Web of Science ®Google Scholar
• Bear M B, Press W A, Connors B W. Long-term potentiation in slices of kitten visual cortex and the effects of NMDA receptor blockade. J. Neurophysiol. 1992; 67: 841–51
   PubMed Web of Science ®Google Scholar
• Blitzer R D, Gil O, Landau E M. Cholinergic stimulation enhances long-term potentiation in the CA1 region of rat hippocampus. Neurosci. Lett. 1990; 119: 207–10
   PubMed Web of Science ®Google Scholar
• Brown M W, Wilson F A, Riches I P. Neuronal evidence that inferomedial temporal cortex is more important than hippocampus in certain processes underlying recognition memory. Brain Res. 1987; 409: 158–62
   PubMed Web of Science ®Google Scholar
• Brunel N. Hebbian learning of context in recurrent neural networks. Neural Comput. 1996; 8: 1677–710
   PubMed Web of Science ®Google Scholar
• Burgard E C, Sarvey J M. Muscarinic receptor activation facilitates the induction of long-term potentiation (LTP) in the rat dentate gyrus. Neurosci. Lett. 1990; 116: 34–9
   PubMed Web of Science ®Google Scholar
• Carpenter G A, Grossberg S. Normal and amnesic learning, recognition and memory by a neural model of cortico-hippocampal interactions. Trends Neurosci. 1993; 16: 131–7
   PubMed Web of Science ®Google Scholar
• Cauller L J, Connors B W. Synaptic physiology of horizontal afferents to layer I in slices of rat SI neocortex. J. Neurosci. 1994; 14: 751–62
   PubMed Web of Science ®Google Scholar
• Delacour J. Cortex inférotemporal et mémoire visuelle á court terme chez le singe: Nouvelles domnnées. Exp. Brain Res. 1977; 28: 301–10
   PubMedGoogle Scholar
• Desimone R, Miller E K, Chelazzi L. The interaction of neural systems for attention and memory. Large Scale Neuronal Theories of the Brain, C Koch, J Davis. MIT Press, Cambridge, MA 1994
   Google Scholar
• Dudkin K N, Kruchinin V K, Chueva I V. Participation of cholinergic structures of the prefrontal and inferotemporal cortex in the processes of visual recognition in monkeys. Neurosci. Behav. Physiol. 1994; 24: 341–50
   PubMedGoogle Scholar
• Dykes R W. Mechanisms controlling neuronal plasticity in somatosensory cortex. Can J. Physiol. Pharmacol. 1997; 75: 535–45
   PubMed Web of Science ®Google Scholar
• Fuster J M. Inferotemporal units in selective visual attention and short-term memory. J. Neurophysiol. 1990; 64: 681–97
   PubMed Web of Science ®Google Scholar
• Fuster J M, Jervey J P. Inferotemporal neurons distinguish and retain behaviourally relevant features of visual stimuli. Science 1981; 212: 952–5
   PubMed Web of Science ®Google Scholar
• Fuster J M, Jervey J P. Neuronal firing in the inferotemporal cortex of the monkey in a visual memory task. J. Neurosci. 1982; 2: 361–75
   PubMed Web of Science ®Google Scholar
• Gaffan D, Weiskrantz L. Recency effects and lesion effects in delayed nonmatching to randomly baited samples by monkeys Macaca mulatta. Brain Res. 1980; 196: 373–86
   PubMed Web of Science ®Google Scholar
• Gil Z, Connors B W, Amitay Y. Differential regulation of neocortical synapses by neuromodulators and activity. Neuron 1997; 19: 679–86
   PubMed Web of Science ®Google Scholar
• Gross C G, Bender D G, Rocha-Miranda C E. Visual receptive fields of neurons in inferotemporal cortex of the monkey. Science 1969; 166: 1303–6
   PubMed Web of Science ®Google Scholar
• Grossberg S. On the development of feature detectors in the visual cortex with applications to learning and reaction-diffusion systems. Biol. Cybernet. 1976; 21: 145–59
   PubMed Web of Science ®Google Scholar
• Gustafsson B, Wigstrom H. Physiological mechanisms underlying long-term potentiation. Trends Neurosci. 1988; 11: 156–62
   PubMed Web of Science ®Google Scholar
• Hasselmo M E. The representation and storage of visual information in the temporal lobe. Oxford University. 1988, PhD Thesis
   Google Scholar
• Hasselmo M E, Barkai E. Cholinergic modulation of activity-dependent synaptic plasticity in the piriform cortex and associative memory function in a network biophysical simulation. J. Neurosci. 1995; 15: 6592–604
   PubMed Web of Science ®Google Scholar
• Hasselmo M E, Bower J M. Cholinergic suppression specific to intrinsic not afferent fibre synapses in rat piriform (olafactory) cortex. J. Neurophysiol. 1992; 67: 1222–9
   PubMed Web of Science ®Google Scholar
• Hasselmo M E, Cekic M. Cholinergic suppression of synaptic transmission may allow combination of associative feedback and self-organizing feedforward connections in the neocortex. Behav. Brain Res. 1996; 79: 153–61
   PubMed Web of Science ®Google Scholar
• Hasselmo M E, Rolls E T, Baylis G C. The role of expression and identity in the face-selective responses of neurons in the temporal visual cortex of the monkey. Behav. Brain Res. 1989a; 32: 203–18
   PubMed Web of Science ®Google Scholar
• Hasselmo M E, Rolls E T, Baylis G C, Nalwa V. Object-centered encoding by face-selective neurons in the cortex in the superior temporal sulcus of the monkey. Exp. Brain Res. 1989b; 75: 417–29
   PubMed Web of Science ®Google Scholar
• Hasselmo M E, Schnell E, Barkai E. Dynamics of learning and recall at excitatory recurrent synapses and cholinergic modulation in rat hippocampal region CA3. J. Neurosci. 1995; 15: 5249–62
   PubMed Web of Science ®Google Scholar
• Hsieh C Y, Cruikshank S J, Metherate R. Cholinergic agonist differentially suppresses auditory thalamocortical and intracortical transmission. Soc. Neurosci. Abstr. 1998; 24: 1879
   Google Scholar
• Lancaster B, Adams P R. Calcium dependent current generating the afterhyperpolarization of of hippocampal neurons. J. Physiol. 1986; 387: 519–48
   Google Scholar
• Levy W B. A computational approach to the hippocampal formation. Computational Models of Learning in Simple Neural Systems, R D Hawkins, G H Bower. Academic, Orlando, FL 1989
   Google Scholar
• Li L, Miller E K, Desimone R. The representation of stimulus familiarity in anterior inferior temporal cortex. J. Neurophysiol. 1993; 69: 1918–29
   PubMed Web of Science ®Google Scholar
• McCormick D A, Prince D A. Post-natal development of electrophysiological properties of rat cerebral cortical pyramidal neurons. J. Physiol. 1987; 393: 743–62
   PubMed Web of Science ®Google Scholar
• Mesulam M M, Mufson E J. Neural inputs into the nucleus basalis of the substantia innominata (Ch4) in the rhesus monkey. Brain 1984; 104: 253–74
   Web of Science ®Google Scholar
• Mesulam M M, Mufson E J, Wainer B H, Levey A I. Central cholinergic pathways in the rat: an overview based on an alternative nomenclature. Neuroscience 1983; 10: 1185–201
   PubMed Web of Science ®Google Scholar
• Metherate R, Ashe J H, Weinberger N M. Acetylcholine modifies neuronal acoustic rate-level functions in guinea pig auditory cortex by an action at muscarinic receptors. Synapse 1990; 6: 364–8
   PubMed Web of Science ®Google Scholar
• Metherate R, Weinberger N M. Acetylcholine produces stimulus-specific receptive field alterations in cat auditory cortex. Brain Res. 1989; 480: 372–7
   PubMed Web of Science ®Google Scholar
• Miller E K, Desimone R. Scopolamine affects short-term memory but not inferior temporal neurons. Neuro Rep. 1993; 4: 81–4
   PubMed Web of Science ®Google Scholar
• Miller E K, Desimone R. Parallel neuronal mechanisms for short-term memory. Science 1994; 263: 520–2
   PubMed Web of Science ®Google Scholar
• Miller E K, Gochin P M, Gross C G. Habituation-like decrease in the responses of neurons in inferior temporal cortex of the macaque. Visual Neurosci. 1991a; 7: 357–62
   PubMed Web of Science ®Google Scholar
• Miller E K, Li L, Desimone R. A neural mechanism for working and recognition memory in inferior temporal cortex. Science 1991b; 254: 1377–9
   PubMed Web of Science ®Google Scholar
• Miller E K, Li L, Desimone R. Activity of neurons in anterior inferior temporal cortex during a short-term memory task. J. Neurosci. 1993; 13: 1460–78
   PubMed Web of Science ®Google Scholar
• Mishkin M. A memory system in the monkey. Phil. Trans. R. Soc. B 1982; 298: 83–95
   PubMed Web of Science ®Google Scholar
• Mishkin M, Delacour J. An analysis of short-term visual memory in the monkey. J. Exp. Psychol. 1975; 1: 326–34
   Google Scholar
• Miyashita Y. Neuronal correlate of visual associative long-term memory in the primate temporal cortex. Nature 1988; 335: 817–20
   PubMed Web of Science ®Google Scholar
• Pitler T A, Alger B E. Cholinergic excitation of GABAergic interneurons in the rat hippocampal slice. J. Physiol. 1992; 450: 127–42
   PubMed Web of Science ®Google Scholar
• Richardson R T, DeLong M R. Functional implications of tonic and phasic activity changes in nucleus basalis neurons. Activation to Acquisition: Functional Aspects of the Basal Forebrain Cholinergic System, R T Richardson. Birkhäuser, Boston, MA 1991
   Google Scholar
• Riches I P, Wilson F A, Brown M W. The effects of visual stimulion and memory on neurons of the hippocampal formation and the neighbouring parahippocampal gyrus and inferior temporal cortex of the primate. J. Neurosci. 1991; 11: 1763–79
   PubMed Web of Science ®Google Scholar
• Riesenhuber M, Poggio T. Hierarchical models of object recognition in cortex. Nature Neurosci. 1999; 2: 1019–25
   PubMed Web of Science ®Google Scholar
• Rolls E T, Baylis G C, Hasselmo M E, Nalwa V. The effect of learning on the face selective responses of neurons in the cortex in the superior temproal sulcus of the monkey. Exp. Brain Res. 1989; 76: 153–64
   PubMed Web of Science ®Google Scholar
• Rumelhart D E, Zipser D. Feature discovery by competitive learning Foundations. Parallel Distributed Processing: Explorations in the Microstructure of Cognition vol 1. MIT Press, Cambridge 1986
   Google Scholar
• Russchen F T, Amaral D J, Price J L. The afferent connections of the substantia innominata in the monkey Macaca fascicularis. J. Comput. Neurol. 1985; 242: 1–27
   PubMed Web of Science ®Google Scholar
• Schwindt P C, Spain W J, Crill W E. Calcium-dependent potassium currents in neurons from cat sensorimotor cortex. J. Neurophysiol. 1992; 67: 216–26
   PubMed Web of Science ®Google Scholar
• Schwindt P C, Spain W J, Foehring R C, Stafstrom C E, Chubb M C, Crill W E. Slow conductances in neurons from cat sensorimotor cortex and their role in slow excitability changes. J. Neurophysiol. 1988; 59: 450–67
   PubMed Web of Science ®Google Scholar
• Sillito A M, Kemp J A. Cholinergic modulation of the functional organization of the cat visual cortex. Brain Res. 1983; 289: 143–55
   PubMed Web of Science ®Google Scholar
• Stanton P K, Sejnowski T J. Associative long-term depression in the hippocampus induced by Hebbian covariance. Nature 1989; 339: 215–8
   PubMed Web of Science ®Google Scholar
• Stern C E, Corkin S, Gonzalez R G, Guimaraes A R, Baker J R, Jennings P J, Carr C A, Sugiura R M, Vedantham V, Rosen B R. The hippocampal formation participates in novel picture encoding: evidence from function magnetic resonance imaging. Proc. Natl Acad. Sci. USA 1996; 93: 8660–5
   PubMed Web of Science ®Google Scholar
• Tremblay N, Warren R A, Dykes R W. Electrophysiological studies of acetylcholine and the role of the basal forebrain in the somatosensory cortex of the cat II. Cortical neurons excited by somatic stimuli. J. Neurophysiol. 1990; 64: 1212–22
   PubMed Web of Science ®Google Scholar
• von der Malsburg C. Self-organization of orientation sensitive cells in the striate cortex. Kybernetik 1973; 14: 85–100
   PubMed Web of Science ®Google Scholar
• Wallis G. Spatio-temporal influences at the neural level of object recognition. Network: Comput. Neural Syst. 1998; 9: 265
   PubMed Web of Science ®Google Scholar
• Whitlock D G, Nauta W J H. Subcortical projections from the temporal neocortex Macaca mulatta. J. Comput. Neurol. 1956; 106: 184–207
   Web of Science ®Google Scholar
• Wilson F A W, Rolls E T. Neuronal responses related to the novelty and familiarity of visual stimuli in the substantia innominata, diagonal band of Broca and periventricular region of the primate basal forebrain. Exp. Brain Res. 1990; 80: 104–20
   PubMed Web of Science ®Google Scholar
• Wilson H R, Cowan J D. Excitatory and inhibitory interactions in localized populations of model neurons. Biophys. J. 1972; 12: 1–24
   PubMed Web of Science ®Google Scholar
• Woody C D, Gruen E. Acetylcholine reduces net outward currents measured in vivo with single electrode voltage clamp techniques in neurons of the motor cortex of cats. Brain Res. 1987; 424: 193–8
   PubMed Web of Science ®Google Scholar
• Zipser D, Kehoe B, Littlewort G, Fuster J. A spiking network model of short-term active memory. J. Neurosci. 1993; 13: 3406–20
   PubMed Web of Science ®Google Scholar