Distribution and developmental change in [3H]MK-801 binding within zebra finch song nuclei.

In many songbirds, vocal learning depends upon appropriate auditory experience during a sensitive period that coincides with the formation and reorganization of song-related neural pathways. Because some effects of early sensory experience on neural organization and early learning have been linked to activation of N-methyl-D-aspartate (NMDA) receptors, we measured binding to this receptor within the neural system controlling song behavior in zebra finches. Quantitative autoradiography was used to measure binding of the noncompetitive antagonist [3H]MK-801 (dizocilpine) in the brains of both adult and juvenile male zebra finches, focusing on four telencephalic regions implicated in song learning and production. Overall, the pattern of MK-801 binding in zebra finches was similar to the pattern found in rats (Monaghan and Cotman, 1985, J. Neurosci. 5:2909-2919; Sakurai, Cha, Penney, and Young, 1991, Neuroscience 40:533-543). That is, binding was highest in the telencephalon, intermediate in thalamic regions, and virtually absent from the brain stem and cerebellum. The telencephalic song areas exhibited intermediate levels of binding, and binding in the juveniles was not significantly different from adult levels in most song nuclei. However, in the lateral magnocellular nucleus of the anterior neostriatum (IMAN), binding at 30 days of age was significantly higher than binding in adults. Given the established role of NMDA receptors in other developing neural systems, both their presence in song control nuclei and their developmental regulation within a region implicated in song learning suggest that NMDA receptors play a role in mediating effects of auditory experience on the development of song behavior.

[1]  R. Dingledine,et al.  Requirement for glycine in activation of NMDA-receptors expressed in Xenopus oocytes. , 1988, Science.

[2]  K. Immelmann Song development in the zebra finch and other estrildid finches , 1969 .

[3]  A. Doupe,et al.  Song-selective auditory circuits in the vocal control system of the zebra finch. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[4]  C. Hudson,et al.  Evidence for transient perinatal glutamatergic innervation of globus pallidus , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[5]  EJ Nordeen,et al.  Sex and regional differences in the incorporation of neurons born during song learning in zebra finches , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[6]  E. Nordeen,et al.  Projection neurons within a vocal motor pathway are born during song learning in zebra finches , 1988, Nature.

[7]  F. Nottebohm,et al.  Central control of song in the canary, Serinus canarius , 1976, The Journal of comparative neurology.

[8]  A. Arnold,et al.  The development of afferent projections to the robust archistriatal nucleus in male zebra finches: a quantitative electron microscopic study , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  C. Cotman,et al.  Distribution of N-methyl-D-aspartate-sensitive L-[3H]glutamate-binding sites in rat brain , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  A. Young,et al.  Differential ontogenic development of three receptors comprising the NMDA receptor/channel complex in the rat hippocampus , 1990, Experimental Neurology.

[11]  W Singer,et al.  The development of N-methyl-D-aspartate receptors in cat visual cortex. , 1989, Brain research. Developmental brain research.

[12]  E. Nordeen,et al.  Selective impairment of song learning following lesions of a forebrain nucleus in the juvenile zebra finch. , 1990, Behavioral and neural biology.

[13]  L. A. Eales Song learning in zebra finches: some effects of song model availability on what is learnt and when , 1985, Animal Behaviour.

[14]  F. Nottebohm,et al.  Effect of testosterone on input received by an identified neuron type of the canary song system: a Golgi/electron microscopy/degeneration study , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  G. Lynch,et al.  The biochemistry of memory: a new and specific hypothesis. , 1984, Science.

[16]  A. Arnold,et al.  Forebrain lesions disrupt development but not maintenance of song in passerine birds. , 1984, Science.

[17]  P. Marler A comparative approach to vocal learning: Song development in white-crowned sparrows. , 1970 .

[18]  Y. Ben‐Ari,et al.  Developmental study of [3H]TCP and [3H]glycine binding sites in the rat hippocampus. , 1990, Brain research. Developmental brain research.

[19]  Philip H. Price Developmental determinants of structure in zebra finch song. , 1979 .

[20]  P. Marler,et al.  Selective Vocal Learning in a Sparrow , 1977, Science.

[21]  A. Arnold,et al.  Sexual dimorphism in vocal control areas of the songbird brain. , 1976, Science.

[22]  F. Nottebohm,et al.  Birth of projection neurons in adult avian brain may be related to perceptual or motor learning. , 1990, Science.

[23]  L. Iversen,et al.  The anticonvulsant MK-801 is a potent N-methyl-D-aspartate antagonist. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[24]  Sandra A. Brown,et al.  Axonal connections of a forebrain nucleus involved with vocal learning in zebra finches , 1989, The Journal of comparative neurology.

[25]  F. Nottebohm,et al.  Production and survival of projection neurons in a forebrain vocal center of adult male canaries , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[26]  M. Kennedy,et al.  Regulation of brain Type II Ca 2+ calmodulin -dependent protein kinase by autophosphorylation: A Ca2+-triggered molecular switch , 1986, Cell.

[27]  J. Penney,et al.  Regional distribution and properties of [3H]MK-801 binding sites determined by quantitative autoradiography in rat brain , 1991, Neuroscience.

[28]  F. Nottebohm,et al.  A comparative study of the behavioral deficits following lesions of various parts of the zebra finch song system: implications for vocal learning , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[29]  E. Nordeen,et al.  Sex-dependent loss of projection neurons involved in avian song learning. , 1992, Journal of neurobiology.

[30]  M. Kuhar,et al.  Quantitative receptor mapping by autoradiography: some current technical problems , 1985, Trends in Neurosciences.

[31]  A. Arnold,et al.  Ontogeny of brain nuclei controlling song learning and behavior in zebra finches , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[32]  A. Arnold,et al.  The Ontogeny of Vocal Learning in Songbirds , 1986 .

[33]  D. Vicario,et al.  Brain pathways for learned and unlearned vocalizations differ in zebra finches , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[34]  Nozomu Saito,et al.  NMDA receptors participate differentially in two different synaptic inputs in neurons of the zebra finch robust nucleus of the archistriatum in vitro , 1991, Neuroscience Letters.

[35]  C. Cotman,et al.  NMDA receptor activation and early olfactory learning. , 1988, Brain research.

[36]  R. Mooney,et al.  Two distinct inputs to an avian song nucleus activate different glutamate receptor subtypes on individual neurons. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[37]  Masakazu Konishi,et al.  Neuronal growth, atrophy and death in a sexually dimorphic song nucleus in the zebra finch brain , 1985, Nature.

[38]  W. Singer,et al.  Blockade of "NMDA" receptors disrupts experience-dependent plasticity of kitten striate cortex. , 1987, Science.

[39]  D. Sengelaub,et al.  Cell death during development of a forebrain nucleus involved with vocal learning in zebra finches. , 1989, Journal of neurobiology.

[40]  N. Daw,et al.  The location and function of NMDA receptors in cat and kitten visual cortex , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  C. Honey,et al.  Ketamine and phencyclidine cause a voltage-dependent block of responses to l-aspartic acid , 1985, Neuroscience Letters.