Learning and memory is reflected in the responses of reinforcement- related neurons in the primate basal forebrain

Certain basal forebrain neurons encode the learned reinforcement value of objects: they respond differentially to visual stimuli that signal availability of fruit juice (positively reinforcing) or saline (negatively reinforcing) obtained by lick responses in visual discrimination tasks. In this report we describe the rapid, learning- related changes in the responses of these neurons during the acquisition and reversal of the reinforcement contingency of a visual discrimination reversal task. The same neurons also responded differentially to novel and familiar stimuli in 2 recognition memory tasks, in which monkeys applied the learned rule that lick responses to novel stimuli elicited saline and responses to familiar stimuli elicited juice. These differential responses to novel and familiar stimuli thus reflected the reinforcement value of the stimuli. A single presentation of a novel or a familiar stimulus was sufficient to elicit a differential response which was maintained even when the stimulus had not been seen recently. The maintenance of the differential response indicates that these neurons are influenced by a durable memory for the stimuli, estimated to be 30 trials on average. These differential neurons were recorded in the substantia innominata, the diagonal band of Broca, and a periventricular region of the basal forebrain. The responses of the reinforcement-related neurons in these 3 regions were similar in most respects. These results support the conclusion that basal forebrain neurons respond to sensory stimuli that, through learning of different contingencies, signal the availability of reinforcement. We suggest that the properties of learning and memory reflected in these neuronal responses are due to afferent pathways from ventromedial regions of the prefrontal and temporal cortices and the amygdala, and that the responses of these neurons provide an enabling mechanism that facilitates the operation of diverse cortical regions in which specific sensory, motor, or mnemonic functions take place.

[1]  E. Rolls Chapter 6 – NEURONAL ACTIVITY RELATED TO THE CONTROL OF FEEDING , 1986 .

[2]  D. Sparks,et al.  Unitary responses and discrimination learning in the squirrel monkey: The globus pallidus , 1968 .

[3]  D. Amaral,et al.  The afferent connections of the substantia innominata in the monkey, Macaca fascicularis , 1985, The Journal of comparative neurology.

[4]  G K Wilcock,et al.  Anatomical correlates of the distribution of the pathological changes in the neocortex in Alzheimer disease. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[5]  E. T. Rolls,et al.  Hypothalamic neuronal responses associated with the sight of food , 1976, Brain Research.

[6]  M M Mesulam,et al.  Systematic regional differences in the cholinergic innervation of the primate cerebral cortex: Distribution of enzyme activities and some behavioral implications , 1986, Annals of neurology.

[7]  Sweet Wh,et al.  Amnesic syndrome with anterior communicating artery aneurysm. , 1967 .

[8]  G. Rigdon,et al.  Nucleus basalis involvement in conditioned neuronal responses in the rat frontal cortex , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  A. Luria,et al.  Impaired selectivity of mental processes in association with a lesion of the frontal lobe , 1967 .

[10]  W. Scoville,et al.  LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS , 1957, Journal of neurology, neurosurgery, and psychiatry.

[11]  M. Mishkin A memory system in the monkey. , 1982, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[12]  M. Mishkin Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus , 1978, Nature.

[13]  R. Bartus,et al.  Animal Models of Geriatric Cognitive Dysfunction: Evidence for an Important Cholinergic Involvement , 1985 .

[14]  E T Rolls,et al.  Neuronal responses related to visual recognition. , 1982, Brain : a journal of neurology.

[15]  E. Rolls,et al.  Modulation during learning of the responses of neurons in the lateral hypothalamus to the sight of food , 1976, Experimental Neurology.

[16]  M M Mesulam,et al.  Neural inputs into the nucleus basalis of the substantia innominata (Ch4) in the rhesus monkey. , 1984, Brain : a journal of neurology.

[17]  N. Humphrey ‘Interest’ and ‘Pleasure’: Two Determinants of a Monkey's Visual Preferences , 1972, Perception.

[18]  M. Mesulam,et al.  Regional variations in cortical cholinergic innervation: Chemoarchitectonics of acetylcholinesterase-containing fibers in the macaque brain , 1984, Brain Research.

[19]  M Mishkin,et al.  Projections of the amygdala to the thalamus in the cynomolgus monkey , 1984, The Journal of comparative neurology.

[20]  L. Squire,et al.  Dorsal thalamic lesion in a noted case of human memory dysfunction , 1979, Annals of neurology.

[21]  W. Nauta,et al.  Subcortical projections from the temporal neocortex in Macaca mulatta , 1956 .

[22]  E. Rolls,et al.  Neuronal responses related to reinforcement in the primate basal forebrain , 1990, Brain Research.

[23]  G. V. Van Hoesen,et al.  Multimodal amnesic syndrome following bilateral temporal and basal forebrain damage. , 1985, Archives of neurology.

[24]  E. Rolls,et al.  The latency of activation of neurones in the lateral hypothalamus and substantia innominata during feeding in the monkey , 1979, Brain Research.

[25]  D. German,et al.  Axonal and transneuronal transport in the transmission of neurological disease: Potential role in system degenerations, including alzheimer's disease , 1987, Neuroscience.

[26]  M. Mishkin,et al.  Visual recognition in monkeys following rhinal cortical ablations combined with either amygdalectomy or hippocampectomy , 1986, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[27]  A R Damasio,et al.  Amnesia following basal forebrain lesions. , 1985, Archives of neurology.

[28]  H. Friedman,et al.  Chronic effects of complete limbic lobe destruction in man , 1969, Neurology.

[29]  H. Groenewegen,et al.  Efferent connections of the prelimbic (area 32) and the infralimbic (area 25) cortices: An anterograde tracing study in the cat , 1985, The Journal of comparative neurology.

[30]  R. Ridley,et al.  Learning impairment following lesion of the basal nucleus of Meynert in the marmoset: Modification by cholinergic drugs , 1986, Brain Research.

[31]  M. Roth,et al.  SELECTIVE LOSS OF NEURONES OF ORIGIN OF ADRENERGIC PROJECTION TO CEREBRAL CORTEX (NUCLEUS LOCUS COERULEUS) IN SENILE DEMENTIA , 1981, The Lancet.

[32]  B. Reisberg,et al.  Cognitive Function in Normal Aging and Early Dementia , 1985 .

[33]  G. Blessed,et al.  NECROPSY EVIDENCE OF CENTRAL CHOLINERGIC DEFICITS IN SENILE DEMENTIA , 1977, The Lancet.

[34]  B. Kintz,et al.  Computational Handbook of Statistics , 1968 .

[35]  E. G. Jones,et al.  Midbrain, diencephalic and cortical relationships of the basal nucleus of meynert and associated structures in primates , 1976, The Journal of comparative neurology.

[36]  M. Voytko Cooling orbital frontal cortex disrupts matching-to-sample and visual discrimination learning in monkeys , 1985 .

[37]  M Mishkin,et al.  An analysis of short-term visual memory in the monkey. , 1975, Journal of experimental psychology. Animal behavior processes.

[38]  J. Coyle,et al.  Alzheimer's disease and senile dementia: loss of neurons in the basal forebrain. , 1982, Science.

[39]  J. A. Horel,et al.  The performance of visual tasks while segments of the inferotemporal cortex are suppressed by cold , 1987, Behavioural Brain Research.

[40]  P. Davies,et al.  SELECTIVE LOSS OF CENTRAL CHOLINERGIC NEURONS IN ALZHEIMER'S DISEASE , 1976, The Lancet.

[41]  D M Bowen,et al.  Neurotransmitter-related enzymes and indices of hypoxia in senile dementia and other abiotrophies. , 1976, Brain : a journal of neurology.

[42]  D. Price,et al.  Topography of the Magnocellular Basal Forebrain System in Human Brain , 1984, Journal of neuropathology and experimental neurology.

[43]  A. Brun,et al.  Regional pattern of degeneration in Alzheimer's disease: neuronal loss and histopathological grading , 1981, Histopathology.

[44]  M. W. Brown,et al.  Neuronal evidence that inferomedial temporal cortex is more important than hippocampus in certain processes underlying recognition memory , 1987, Brain Research.

[45]  G. Leichnetz,et al.  The course of some prefrontal corticofugals to the pallidum, substantia innominata, and amygdaloid complex in monkeys , 1977, Experimental Neurology.

[46]  A. Levey,et al.  Cholinergic innervation of cortex by the basal forebrain: Cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (Substantia innominata), and hypothalamus in the rhesus monkey , 1983, The Journal of comparative neurology.

[47]  Mortimer Mishkin,et al.  Visual recognition impairment follows ventromedial but not dorsolateral prefrontal lesions in monkeys , 1986, Behavioural Brain Research.

[48]  W. Sweet,et al.  AMNESIC SYNDROME WITH ANTERIOR COMMUNICATING ARTERY ANEURYSM , 1967, The Journal of nervous and mental disease.

[49]  T. Powell,et al.  An anatomical study of converging sensory pathways within the cerebral cortex of the monkey. , 1970, Brain : a journal of neurology.