Projection neurons within a vocal motor pathway are born during song learning in zebra finches

Many birds learn song during a restricted 'sensitive' period1. Juveniles memorize a song model, and then learn the pattern of muscle contractions necessary to reproduce the song. Of the neural changes accompanying avian song learning, perhaps the most remarkable is the production of new neurons which are inserted into the hyperstriatum ventralis pars caudalis (HVc)2, a region critical for song production3. We report here that in young male zebra finches many of the new neurons incorporated into the HVc innervate the robust nucleus of the archistriatum (RA) which projects to motor neurons controlling the vocal musculature3. Furthermore, far fewer of these new neurons are incorporated into the HVc of either adult males that are beyond the sensitive learning period, or young females (who do not develop song). Thus, a major portion of the vocal motor pathway is actually created during song learning. This may enable early sensory experience and vocal practice to not only modify existing neuronal circuits, but also shape the insertion and initial synaptic contacts of neurons controlling adult song.

[1]  F. Nottebohm Neuronal Replacement in Adulthood , 1985, Annals of the New York Academy of Sciences.

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

[3]  D. Purves,et al.  Elimination of synapses in the developing nervous system. , 1980, Science.

[4]  J. Rauschecker,et al.  Imprinting and cortical plasticity. Comparative aspects of sensitive periods Edited by J. P. Rauschecker and P. Nader. Wiley Series in Neuroscience. 1987, 377 pages, £57.50. , 1988, Neuropsychologia.

[5]  F. Nottebohm Birdsong as a Model in Which to Study Brain Processes Related to Learning , 1984 .

[6]  E. Nordeen,et al.  Sexual differentiation of androgen accumulation within the zebra finch brain through selective cell loss and addition , 1987, The Journal of comparative neurology.

[7]  A. Arnold,et al.  Changes in neuronal number, density and size account for increases in volume of song-control nuclei during song development in zebra finches , 1986, Neuroscience Letters.

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

[9]  L. C. Katz,et al.  Auditory responses in the zebra finch's motor system for song , 1981, Brain Research.

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

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

[12]  J. Rauschecker,et al.  Imprinting and cortical plasticity , 1987 .

[13]  F. Nottebohm,et al.  Cells born in adult canary forebrain are local interneurons , 1985, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[14]  F. Nottebohm Hope for a new neurology. , 1985, Annals of the New York Academy of Sciences.

[15]  F. Nottebohm,et al.  Neuronal production, migration, and differentiation in a vocal control nucleus of the adult female canary brain. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[16]  E. Blass Handbook of behavioral neurobiology , 1988 .

[17]  J. Nicholls From neuron to brain , 1976 .