Hormone-induced changes in identified cell populations of the higher vocal center in male canaries.

Male canaries revise their vocal repertoire every year. Early work indicated that the volume and neuron number of the song-control nucleus HVC (Higher Vocal Center) declined in late-summer/fall as birds added and deleted syllables from their repertoire, and increased in spring as the set of song syllables stabilized to a fixed number. Seasonal variation in serum testosterone levels suggested that these changes in brain and behavior were regulated by testosterone (T). However, although initial studies describing growth and regression of HVC used Nissl-staining to define its borders, recent experiments that have measured the distribution of identified populations of HVC cells (projection neurons, hormone target cells) suggest that there are no seasonal changes in HVC volume or neuron number. In order to clarify the role of T in the regulation of HVC morphology, we castrated male canaries, maintained them on short (fall-like) days, and treated them with either T, antisteroid drugs, or nothing. After 1 month of treatment, we used a double-labeling technique to characterize HVC projection neurons and androgen target cells. The results showed that hormonal manipulation influenced HVC volume, the density and size of HVC cells, and the absolute number and percentage of androgen target cells in HVC. Hormonal manipulation did not influence the absolute number of cells in HVC. Moreover, the distribution of projection neurons, androgen target cells, and the Nissl-defined borders of HVC were closely aligned in all experimental groups, indicating that exposure to T and/or its metabolites (estradiol and dihydrotestosterone) regulates the overall size of HVC by affecting the distributions of both projection neurons and androgen target cells. Analysis of double-labeling results suggests that T specifically influences both cell size and the ability to accumulate androgen among HVC neurons that project to the robust nucleus of the archistriatum (RA). The results of this study show that steroid hormones exert potent effects on HVC morphology in male canaries, but differences between our results and studies of seasonal males suggest there may be additional factors that can regulate HVC morphology.

[1]  M. Gahr,et al.  Delineation of a brain nucleus: Comparisons of cytochemical, hodological, and cytoarchitectural views of the song control nucleus HVC of the adult canary , 1990, The Journal of comparative neurology.

[2]  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.

[3]  F. Johnson,et al.  Neurogenesis in adult canary telencephalon is independent of gonadal hormone levels , 1993, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[4]  M. Gahr Localization of androgen receptors and estrogen receptors in the same cells of the songbird brain. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[5]  R. Neri,et al.  On the Mechanism of the Anti-androgenic Action ofFlutamide (α-α-α-Trifluoro-2-methyl-4'-nitro-m-propionotoluidide)in the Rat , 1974 .

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

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

[8]  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.

[9]  E. Nordeen,et al.  Projections of androgen-accumulating neurons in a nucleus controlling avian song , 1989, Brain Research.

[10]  J. Davidson,et al.  Chapter 9 – Hormone Administration: Peripheral and Intracranial Implants1 , 1977 .

[11]  E. Adkins-Regan,et al.  Sex steroid levels in developing and adult male and female zebra finches (Poephila guttata). , 1990, General and comparative endocrinology.

[12]  J. Wingfield,et al.  Seasonal changes in gonadal hormone levels of adult male canaries and their relation to song. , 1987, Behavioral and neural biology.

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

[14]  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.

[15]  C. Harding,et al.  The effects of an aromatization inhibitor on the reproductive behavior of male zebra finches , 1988, Hormones and Behavior.

[16]  F. Nottebohm,et al.  Birth of projection neurons in the higher vocal center of the canary forebrain before, during, and after song learning. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Eliot A. Brenowitz,et al.  The effects of systemic androgen treatment on androgen accumulation in song control regions of the adult female canary brain. , 1990, Journal of neurobiology.

[18]  S. Bottjer,et al.  Testosterone and the incidence of hormone target cells in song-control nuclei of adult canaries. , 1991, Journal of neurobiology.

[19]  E. Nordeen,et al.  Estrogen accumulation in zebra finch song control nuclei: implications for sexual differentiation and adult activation of song behavior. , 1987, Journal of neurobiology.

[20]  F. Nottebohm,et al.  Ultrastructural characterization of synaptic terminals formed on newly generated neurons in a song control nucleus of the adult canary forebrain , 1985, The Journal of comparative neurology.

[21]  Peter Marler,et al.  The role of sex steroids in the acquisition and production of birdsong , 1988, Nature.

[22]  Eliot A. Brenowitz,et al.  Hormone accumulation in song regions of the canary brain. , 1992, Journal of neurobiology.

[23]  Fernando Nottebohm,et al.  Testosterone triggers growth of brain vocal control nuclei in adult female canaries , 1980, Brain Research.

[24]  B. McEwen,et al.  The effects of an inhibitor of aromatization (1,4,6-androstatriene-3,17-dione) and an anti-estrogen (Cl-628) on in vivo formed testosterone metabolites recovered from neonatal rat brain tissues and purified cell nuclei. Implications for sexual differentiation of the rat brain , 1977, Brain Research.

[25]  S. Bottjer,et al.  Joint hormonal and sensory stimulation modulate neuronal number in adult canary brains. , 1988, Journal of neurobiology.

[26]  R. Clower,et al.  Song-related brain regions in the red-winged blackbird are affected by sex and season but not repertoire size. , 1989, Journal of neurobiology.

[27]  K. Carlström,et al.  Flutamide has no effect on adrenal androgen response to acute ACTH stimulation in patients with prostatic cancer , 1990, The Prostate.

[28]  A. Arnold,et al.  Brain is the major site of estrogen synthesis in a male songbird. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[29]  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.

[30]  F. Nottebohm,et al.  Synaptogenesis and changes in synaptic morphology related to acquisition of a new behavior , 1985, Brain Research.

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

[32]  F. Nottebohm,et al.  Neurons generated in the adult brain are recruited into functional circuits. , 1984, Science.

[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]  F. Nottebohm A brain for all seasons: cyclical anatomical changes in song control nuclei of the canary brain. , 1981, Science.

[35]  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.

[36]  Gregory F Ball,et al.  Immunocytochemical localization of androgen receptors in the male songbird and quail brain , 1992, The Journal of comparative neurology.

[37]  S. Bottjer,et al.  Castration and antisteroid treatment impair vocal learning in male zebra finches. , 1992, Journal of neurobiology.

[38]  F. Nottebohm,et al.  Developmental and seasonal changes in canary song and their relation to changes in the anatomy of song-control nuclei. , 1986, Behavioral and neural biology.