Effects of Dark Rearing and Light Exposure on Memory for a Passive Avoidance Task in Day-Old Chicks

Light exposure during embryogenesis is necessary for functional and morphological maturation in the domestic chick. In the present study, dark incubation was demonstrated to induce a weak amnestic effect on retention for a passive avoidance task and a diminution in discriminative memory ability in day-old chicks. Putative explanations based on possible motor, attentional, or visual impairment were excluded. Light exposure of dark-reared eggs, specifically during embryonic days E19 to E20, alleviated the retention and discrimination deficits. The processes which might mediate between prehatch light stimulation and posthatch behavioral effects are discussed.

[1]  J. Truman,et al.  Steroid receptors and nervous system metamorphosis in insects. , 1996, Developmental neuroscience.

[2]  Weiqin Zhao,et al.  The impairment of long-term memory formation by the phosphatase inhibitor okadaic acid , 1995, Brain Research Bulletin.

[3]  E. Zee,et al.  Distribution of AVP and Ca2+-dependent PKC-isozymes in the suprachiasmatic nucleus of the mouse and rabbit , 1995, Brain Research.

[4]  S. Rose Cell-adhesion molecules, glucocorticoids and long-term-memory formation , 1995, Trends in Neurosciences.

[5]  B. McEwen,et al.  Stress and cognitive function , 1995, Current Opinion in Neurobiology.

[6]  Lesley J. Rogers,et al.  Development of Brain and Behaviour in the Chicken , 1995 .

[7]  Carmen Sandi,et al.  Corticosterone enhances long-term retention in one-day-old chicks trained in a weak passive avoidance learning paradigm , 1994, Brain Research.

[8]  G. Horn,et al.  Learning‐dependent Changes in the Responses to Visual Stimuli of Neurons in a Recognition Memory System , 1992, The European journal of neuroscience.

[9]  A. Azimi-Zonooz,et al.  The developing chick brain shows a dramatic increase in the ω-conotoxin binding sites around the hatching period , 1992, International Journal of Developmental Neuroscience.

[10]  L. Rogers,et al.  Structural asymmetry in the thalamofugal visual projections in 2-day-old chick is correlated with a hemispheric difference in synaptic density in the hyperstriatum accessorium , 1992, Brain Research.

[11]  S. Rose,et al.  Memory in the chick: multiple cues, distinct brain locations. , 1992, Behavioral neuroscience.

[12]  L. Rogers,et al.  Hemispheric specialization for the control of copulation in the young chick and effects of 5α-dihydrotestosterone and 17β-oestradiol , 1992, Behavioural Brain Research.

[13]  S. F. Plazas,et al.  Effect of a simple visual pattern on the early postnatal development oF GABA Receptor sites in the chick optic lobe , 1991, International Journal of Developmental Neuroscience.

[14]  A. C. Webb,et al.  The effects of age and visual experience on potentiation of responses in slices from the chick forebrain , 1991, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[15]  L. Rogers,et al.  Light-dependent development and asymmetry of visual projections , 1991, Neuroscience Letters.

[16]  L. Rogers Light input and the reversal of functional lateralization in the chicken brain , 1990, Behavioural Brain Research.

[17]  R. Andrew,et al.  The development of visual lateralization in the domestic chick , 1988, Behavioural Brain Research.

[18]  T. Petit,et al.  Synaptic structural changes during development and aging. , 1987, Brain research.

[19]  R. Phillips,et al.  Unilateral kainic acid lesions reveal dominance of right archistriatum in avian fear behavior , 1986, Brain Research.

[20]  P. Savard,et al.  Serotonin, 5-hydroxyindoleacetic acid and substance P content of discrete brain nuclei in rats made hypo- or hyperthyroid in the neonatal period: effect of growth hormone treatment. , 1984, Brain research.

[21]  L. Rogers,et al.  Light experience during development affects asymmetry of forebrain function in chickens. , 1983, Brain research.

[22]  S. Rose,et al.  Passive Avoidance Training Increases Fucokinase Activity in Right Forebrain Base of Day‐Old Chicks , 1983, Journal of neurochemistry.

[23]  V. Denenberg Hemispheric laterality in animals and the effects of early experience , 1981, Behavioral and Brain Sciences.

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

[25]  G. Horn,et al.  Effects of visual experience on photically evoked potentials recorded in the chick forebrain , 1978, Brain Research.

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

[27]  J. Cherfas Visual system activation in the chick: one-trial avoidance learning affected by duration and patterning of light exposure. , 1977, Behavioral biology.

[28]  M. Vince,et al.  Sensitivity to odours in the embryo of the domestic fowl , 1976, Animal Behaviour.

[29]  G. F. Cooper,et al.  Development of the Brain depends on the Visual Environment , 1970, Nature.

[30]  R. Andrew,et al.  Precocious adult behaviour in the young chick. , 1966, Animal behaviour.

[31]  V. Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1951, Journal of morphology.

[32]  G. Robinson,et al.  Juvenile hormone, behavioral maturation, and brain structure in the honey bee. , 1996, Developmental neuroscience.

[33]  C. Cotman,et al.  The excitatory amino acid receptors: their classes, pharmacology, and distinct properties in the function of the central nervous system. , 1989, Annual review of pharmacology and toxicology.

[34]  J. Wolff Evidence for a dual role of GABA as a synaptic transmitter and a promoter of synaptogenesis. , 1981, Advances in biochemical psychopharmacology.

[35]  F. V. Defeudis,et al.  Amino acid neurotransmitters , 1981 .

[36]  M. Vince,et al.  Development of the Avian Embryo , 1974 .