Changes in the structure of synapses associated with learning

Two experiments were conducted to investigate the effects of training on a region of the chick brain known to be critically involved in imprinting, the intermediate and medial extent of the hyperstriatum ventrale (IMHV). In the first experiment, three groups of chicks were used: (i) dark-reared (n = 9), (ii) trained for 20 min (n = 17), and (iii) trained for 140 min (n = 7). Chicks were trained by exposing them when they were approximately 21 hr old to a flashing red light. Chicks were killed when they were approximately 30 hr old and blocks of tissue were removed from the right and left IMHV. Stereological techniques were used to measure from electron micrographs the numerical density of dendritic spine and shaft synapses and the length of the postsynaptic density of these synaptic junctions. There was a significant effect of training only in the left IMHV and on only one measure, the overall mean length of the postsynaptic density of spine synapses, SPL. This measure was significantly greater by 17.2% in chicks trained for 140 min than in dark-reared controls. There was no significant effect of training for 20 min. In the second experiment one group of chicks (n = 15) was exposed to a rotating red box for a total of 3 hr. Another group of chicks was dark-reared (n = 15). The chicks were killed when they were approximately 46 hr old. Samples from the hyperstriatum accessorium and IMHV of the right and left sides were analyzed. Training was associated with a significant change, an increase, only of SPL in the left IMHV.(ABSTRACT TRUNCATED AT 250 WORDS)

[1]  William G. Cochran,et al.  Experimental Designs, 2nd Edition , 1950 .

[2]  I. Freiman Conditioned Reflexes and Neuron Organization , 1950 .

[3]  H. T. Chang,et al.  Cortical neurons with particular reference to the apical dendrites. , 1952, Cold Spring Harbor symposia on quantitative biology.

[4]  Gray Eg Axo-somatic and axo-dendritic synapses of the cerebral cortex: An electron microscope study , 1959 .

[5]  J. Eccles The Physiology of Synapses , 1964, Springer Berlin Heidelberg.

[6]  E. Weibel Stereological principles for morphometry in electron microscopic cytology. , 1969, International review of cytology.

[7]  G. Gottlieb,et al.  Auditory versus visual flicker in directing the approach response of domestic chicks. , 1969, Journal of comparative and physiological psychology.

[8]  P. Bateson,et al.  The effects of prior exposure to light on the imprinting process in domestic chicks. , 1972, Behaviour.

[9]  S. Hunt,et al.  Thalamo-hyperstriate interrelations in the pigeon. , 1972, Brain research.

[10]  G Horn,et al.  Experience and plasticity in the central nervous system. , 1973, Science.

[11]  M. L. Simner The development of visual flicker rate preference in the newly hatched chick. , 1973, Developmental psychobiology.

[12]  W Hodos,et al.  Neural connections of the “visual wulst” of the avian telencephalon. Experimental studies in the pigeon (Columba livia) and owl (Speotyto cunicularia) , 1973, The Journal of comparative neurology.

[13]  S. Rose,et al.  Imprinting: Lasting Effects on Uracil Incorporation into Chick Brain , 1973, Science.

[14]  P. Bateson,et al.  Imprinting: Correlations between activities of chicks during training and testing. , 1974, Animal behaviour.

[15]  D. Gaffan,et al.  Recognition impaired and association intact in the memory of monkeys after transection of the fornix. , 1974, Journal of comparative and physiological psychology.

[16]  S. Rose,et al.  Imprinting: Correlations between behaviour and incorporation of [14C]uracil into chick brain , 1975, Brain Research.

[17]  D. Miceli,et al.  The retino-thalamo-hyperstriatal pathway in the pigeon (Columba livia) , 1975, Brain Research.

[18]  Synaptogenesis in the cerebral hemisphere (accessory hyperstriatum) of the chick embryo , 1977, Neuroscience Letters.

[19]  J. Cherfas Simultaneous colour discrimination in chicks is improved by brief exposure to light , 1978, Animal Behaviour.

[20]  P. Bateson,et al.  An autoradiographic study of the chick brain after imprinting , 1979, Brain Research.

[21]  P. Bateson Brief exposure to a novel stimulus during imprinting in chicks and its influence on subsequent preferences , 1979 .

[22]  T M Mayhew,et al.  Stereological approach to the study of synapse morphometry with particular regard to estimating number in a volume and on a surface , 1979, Journal of neurocytology.

[23]  G. Horn,et al.  Neuronal plasticity in the chick brain: morphological effects of visual experience on neurones in hyperstriatum accessorium , 1979, Brain Research.

[24]  M. W. Brown,et al.  Neuronal plasticity in the chick brain: electrophysiological effects of visual experience on hyperstriatal neurones , 1979, Brain Research.

[25]  E. Weibel Stereological Methods. Practical methods for biological morphometry , 1979 .

[26]  T. Lentz,et al.  Localization of acetylcholine receptors by means of horseradish peroxidase-alpha-bungarotoxin during formation and development of the neuromuscular junction in the chick embryo , 1979, The Journal of cell biology.

[27]  L. Rogers,et al.  Functional lateralization of the chicken forebrain revealed by use of intracranial glutamate , 1980, Brain Research.

[28]  M. Cohen Development of an amphibian neuromuscular junction in vivo and in culture. , 1980, The Journal of experimental biology.

[29]  Gabriel Horn,et al.  Effects of restricted lesions of the chick forebrain on the acquisition of filial preferences during imprinting , 1981, Brain Research.

[30]  L. Weiskrantz Comparative aspects of studies of amnesia. , 1982, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[31]  M. Mishkin,et al.  Visual recognition impairment following medial thalamic lesions in monkeys , 1983, Neuropsychologia.

[32]  R. Andrew,et al.  The lateralization of fear behaviour in the male domestic chick: A developmental study , 1983, Animal Behaviour.

[33]  M. W. Brown,et al.  Modifiability of responsiveness in a visual projection area of the chick brain: Visual experience is only one of several factors involved , 1984, Behavioural Brain Research.

[34]  S. Rose,et al.  Hemispheric asymmetry of synapses in chick medial hyperstriatum ventrale following passive avoidance training: a stereological investigation. , 1984, Brain research.

[35]  L. Squire,et al.  Preserved learning in monkeys with medial temporal lesions: sparing of motor and cognitive skills , 1984, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  G. Horn,et al.  Predispositions and preferences. Effects on imprinting of lesions to the chick brain , 1984, Animal Behaviour.

[37]  G. Horn,et al.  Long-term consequences of exposure to an imprinting stimulus on ‘spontaneous’ impulse activity in the chick brain , 1984, Behavioural Brain Research.

[38]  J. Rostas,et al.  The maturation of post-synaptic densities in chicken forebrain , 1984, Neuroscience Letters.

[39]  S. Rose,et al.  Differential 2-deoxyglucose uptake into chick brain structures during passive avoidance training , 1984, Neuroscience.

[40]  G. Horn,et al.  Memory, Imprinting and the Brain , 1985 .

[41]  G Horn,et al.  Noradrenaline and learning: effects of the noradrenergic neurotoxin DSP4 on imprinting in the domestic chick. , 1985, Behavioral neuroscience.

[42]  M. Colonnier,et al.  An empirical assessment of stereological formulae applied to the counting of synaptic disks in the cerebral cortex , 1985, The Journal of comparative neurology.

[43]  M. Johnson,et al.  Dissociation of recognition memory and associative learning by a restricted lesion of the chick forebrain , 1986, Neuropsychologia.