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Typology, distribution and development of the catecholamine-containing neurons in the chicken brain

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Summary

Fluorescence-histochemical investigations by use of the FAGLU method show the presence of several groups of catecholamine (CA)-containing neurons in the chicken brain. The distribution, shape and orientation of the fluorescent perikarya as well as the number and orientation of primary dendrites have been systematically examined. In the chick embryo, the first neurons displaying specific catecholamine fluorescence are identifiable on the 9th day of incubation. The onset of this type of specific fluorescence is consistent with biochemical data reported in the literature for the chick embryo. The main complexes of CA-containing cell bodies, shown at medullary, pontine and mesencephalic levels, display a pattern of distribution that is quite similar in both the chicken and the rat. In the hypothalamus of chick embryos and newly hatched chicks, CA-containing neurons have been localized within the paraventricular organ, and the periventricular and mammillary regions. By the fourth week after hatching, within the hypothalamus the paraventricular organ alone continues to display fluorescent neurons.

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References

  • Bertler Å, Falck B, Gottfries C-G, Ljunggren L, Rosengren E (1964) Some observations on adrenergic connections between the mesencephalon and the cerebral hemispheres. Acta Pharmacol Toxicol 21:283–289

    Google Scholar 

  • Björklund A, Falck B, Ljunggren L (1968) Monoamines in the bird median eminence. Failure of cocaine to block the accumulation of exogenous amines. Z Zellforsch 89:193–200

    Google Scholar 

  • Blessing WW, Chalmers JP, Howe PR (1978) Distribution of catecholamine-containing cell bodies in the rabbit central nervous system. J Comp Neurol 179:407–424

    Google Scholar 

  • Bourne BB (1965) Metabolism of amines in the brain of the chick during embryonic development. Life Sci 4:583–591

    Google Scholar 

  • Calas A (1973) L'innervation monoaminergique de l'éminence médiane. Étude radioautographique et pharmacologique chez le canard, Anas platyrhynchos. Z Zellforsch 138:503–522

    Google Scholar 

  • Calas A (1974) L'innervation peptidergique et monoaminergique de l'éminence médiane. Etude cytophysiologique chez les Oiseaux. Thèse, Académie de Montpellier

  • Calas A, Hartwig H-G, Collin JP (1974) Noradrenergic innervation of the median eminence. Microspectrofluorimetric and pharmacological study in the duck, Anas platyrhynchos. Z Zellforsch 147:491–504

    Google Scholar 

  • Caserta M (1976) The development of noradrenergic and serotonergic innervation of the avian preganglionic sympathetic nucleus (nucleus of Terni). Doctoral dissertation, Cornell University

  • Caserta M, Ross LL (1978) Biochemical and morphological studies of synaptogenesis in the avian sympathetic cell column. Brain Res 144:241–255

    Google Scholar 

  • Chikazawa H, Fujioka T, Watanabe T (1982) Catecholamine-containing neurons in the mesencephalic tegmentum of the chicken. Light, fluorescence and electron microscopic studies. Anat Embryol 164:303–313

    Google Scholar 

  • Chikazawa H, Fujioka T, Watanabe T (1983) Bulbar catecholaminergic neurons projecting to the thoracic spinal cord of the chicken. Evans blue labelling study in combination with catecholamine histofluorescence. Anat Embryol 167:411–423

    Google Scholar 

  • Dahlström A, Fuxe K (1964) Evidence for the existence of monoamine-containing neurons in the central nervous system. I Demonstration of monoamines in the cell bodies of brainstem neurons. Acta Physiol Scand 62 (Suppl 232): 1–55

    Google Scholar 

  • Dubé L, Parent A (1981) The monoamine-containing neurons in avian brain: I. A study of the brain stem of the chicken (Gallus domesticus) by means of fluorescence and acetylcholinesterase histochemistry. J Comp Neurol 196:695–708

    Google Scholar 

  • Eden AR, Correia MJ (1981) Vestibular efferent neurons and catecholamine cell groups in the reticular formation of the pigeon. Neurosci Lett 25:239–242

    Google Scholar 

  • Furness JB, Costa M, Blessing WW (1977) Simultaneous fixation and production of catecholamine fluorescence in central nervous tissue by perfusion with aldehydes. Histochem J 9:745–750

    Google Scholar 

  • Furness JB, Heath JW, Costa M (1978) Aqueous aldehyde (Faglu) methods for the fluorescence histochemical localization of catecholamines and for ultrastructural studies of central nervous system. Histochemistry 57:285–295

    Google Scholar 

  • Fuxe K, Ljunggren L (1965) Cellular localization of monoamines in the upper brain stem of the pigeon. J Comp Neurol 125:355–382

    Google Scholar 

  • Gérard-Ivanoff A (1974) Histogenèse des neurones aminergiques du diencéphale chez le poulet, Gallus gallus. Arch Anat Histol Embryol (Strasb) 57:115–134

    Google Scholar 

  • Guglielmone R, Panzica GC (1982) Topographic, morphologic and developmental characterization of the nucleus loci coerulei in the chicken. A Golgi and fluorescence-histochemical study. Cell Tissue Res 225:95–110

    Google Scholar 

  • Guglielmone R, Panzica GC (1983) Localization of catecholaminecontaining cell bodies in the posterior hypothalamus of chickens. Neurosci Lett Suppl 14:147 (Abstract)

    Google Scholar 

  • Hartwig H-G (1981) Hypothalamic distribution of monoaminecontaining neurons in homeothermic vertebrates. In: Farner DS, Lederis K (eds) Neurosecretion. Molecules, cells, systems. Plenum Press, New York London, pp 93–103

    Google Scholar 

  • Ikeda H, Gotoh J (1971) Distribution of monoamine-containing cells in the central nervous system of the chicken. Jpn J Pharmacol 21:763–784

    Google Scholar 

  • Karten HJ, Hodos W (1967) A stereotaxic atlas of the brain of the pigeon (Columba livia). The Johns Hopkins Press, Baltimore, pp

    Google Scholar 

  • Katz DM, Karten HJ (1979) The discrete anatomical localization of vagal aortic afferents within a catecholamine-containing cell group in the nucleus solitarius. Brain Res 171:187–195

    Google Scholar 

  • Kuenzel WJ, van Tienhoven A (1982) Nomenclature and location of avian hypothalamic nuclei and associated circumventricular organs. J Comp Neurol 206:293–313

    Google Scholar 

  • Lewis JW, Ryan SM, Arnold AP, Butcher LL (1981) Evidence for a catecholaminergic projection to area X in the zebra finch. J Comp Neurol 196:347–354

    Google Scholar 

  • Moore RY, Bloom FE (1978) Central catecholamine neuron systems: anatomy and physiology of the dopamine systems. Ann Rev Neurosci 1:129–169

    Google Scholar 

  • Moore RY, Bloom FE (1979) Central catecholamine neuron systems: anatomy and physiology of the norepinephrine and epinephrine systems. Ann Rev Neurosci 2:113–168

    Google Scholar 

  • Mugnaini E, Dahl AL (1975) Mode of distribution of aminergic fibers in the cerebellar cortex of the chicken. J Comp Neurol 162:417–432

    Google Scholar 

  • Nobin A, Björklund A (1973) Topography of monoamine neuron systems in the human brain as revealed in fetuses. Acta Physiol Scand 88 (Suppl 388):1–40

    Google Scholar 

  • Oksche A, Farner DS (1974) Neurohistological studies of the hypothalamo-hypophysial system of Zonotrichia leucophrys gambelii (Aves, Passeriformes). With special attention to its role in the control of reproduction. Adv Anat Embryol Cell Biol 48:1–136

    Google Scholar 

  • Olson L, Seiger A (1972) Early prenatal ontogeny of central monoamine neurons in the rat: fluorescence histochemical observations. Z Anat Entwicklungsgesch 137:301–316

    Google Scholar 

  • Parent A (1979) Anatomical organization of monoamineand acetylcholinesterase-containing neuronal systems in the vertebrate hypothalamus. In: Morgane PJ, Panksepp J (eds) Handbook of the hypothalamus. Vol I Anatomy of the hypothalamus. Marcel Dekker, Inc, New York, Basel, pp 247–285

    Google Scholar 

  • Pearson R (1972) The avian brain. Acad Press, London New York, pp 1–658

    Google Scholar 

  • Prozialeck WC, Pylypiw A, Ross L (1982) Development of β-adrenergic receptors and the in vitro accumulation of cyclic AMP in the chick spinal cord. Dev Brain Res 3:49–63

    Google Scholar 

  • Reiner A, Karten HJ, Solina AR (1983) Substance P: localization within paleostriatal-tegmental pathways in the pigeon. Neuroscience 9:61–85

    Google Scholar 

  • Sharp PJ, Follett BK (1968) The distribution of monoamines in the hypothalamus of the Japanese quail, Coturnix coturnix japonica. Z Zellforsch 90:245–262

    Google Scholar 

  • Sharp PJ, Follett BK (1970) The adrenergic supply within the avian hypothalamus. In: Bargmann W, Scharrer B (eds) Aspects of neuroendocrinology. Springer Verlag, Berlin Heidelberg New York, pp 95–103

    Google Scholar 

  • Shiosaka S, Takatsuki K, Inagaki S, Sakanaka M, Takagi H, Senba E, Matsuzaki T, Tohyama M (1981) Topographic atlas of somatostatin-containing neuron system in the avian brain in relation to catecholamine-containing neuron system. II Mesencephalon, rhomboencephalon and spinal cord. J Comp Neurol 202:115–124

    Google Scholar 

  • Singer HS, Coyle JT, Vernon N, Kallman CH, Price DL (1980) The development of catecholaminergic innervation in the chick spinal cord. Brain Res 191:417–428

    Google Scholar 

  • Smolen AJ, Glazer EJ, Ross LL (1979) Horseradish peroxidase histochemistry combined with glyoxylic acid-induced fluorescence used to identify brain stem catecholaminergic neurons which project to the chick thoracic spinal cord. Brain Res 160:353–357

    Google Scholar 

  • Specht LA, Pickel VM, Joh TH, Reis DJ (1981) Light-microscopic immunocytochemical localization of tyrosine hydroxylase in prenatal rat brain. I Early ontogeny. J Comp Neurol 199:233–253

    Google Scholar 

  • Takatsuki K, Shiosaka S, Inagaki S, Sakanaka M, Takagi H, Senba E, Matsuzaki T, Tohyama M (1981) Topographic atlas of somatostatin-containing neuron system in the avian brain in relation to catecholamine-containing neuron system. I Telencephalon and diencephalon. J Comp Neurol 202:103–113

    Google Scholar 

  • Tohyama M, Maeda T, Hashimoto J, Shresta GR, Tamura O, Shimizu N (1974) Comparative anatomy of the locus coeruleus. I. Organization and ascending projections of the catecholamine containing neurons in the pontine region of the bird, Melopsittacus undulatus. J Hirnforsch 15:319–330

    Google Scholar 

  • Vigh B, Tar E, Teichmann I (1968) The development of the paraventricular organ in the white leghorn chicken. Acta Biol Acad Sci Hung 19:215–225

    Google Scholar 

  • Warren SP (1968) Primary catecholamine fibres in the ventral hypothalamus of the white-crowned sparrow, Zonotrichia leucophrys gambelii. Master's Thesis, University of Washington (cited by Sharp and Follett 1970)

  • Warren Soest S, Farner DS, Oksche A (1973) Fluorescence microscopy of neurons containing primary catecholamines in the ventral hypothalamus of the white-crowned sparrow, Zonotrichia leucophrys gambelii. Z Zellforsch 141:1–17

    Google Scholar 

  • Wiklund L, Leger L, Persson M (1981) Monoamine cell distribution in the cat brainstem. A fluorescence histochemical study with quantification of indolaminergic and locus coeruleus cell groups. J Comp Neurol 203:613–647

    CAS  PubMed  Google Scholar 

  • Wild JM, Zeigler P (1980) Central representation and somatotopic organization of the jaw muscles within the facial and trigeminal nuclei of the pigeon (Columba livia). J Comp Neurol 192:175–201

    Google Scholar 

  • Yurkewicz L, Lauder JM, Giacobini E, Marchi M (1979) 3H-thymidine autoradiography as a method for dating the time of origin in the chick embryo: development of the locus coeruleuscerebellar system. Soc Neurosci Abstr 5:186

    Google Scholar 

  • Yurkewicz L, Lauder JM, Marchi M, Giacobini E (1981 a) 3H-thymidine long survival autoradiography as a method for dating the time of neuronal origin in the chick embryo: the locus coeruleus and cerebellar Purkinje cells. J Comp Neurol 203:257–267

    Google Scholar 

  • Yurkewicz L, Marchi M, Lauder JM, Giacobini E (1981 b) Development and aging of noradrenergic cell bodies and axon terminals in the chicken. J Neurosci Res 6:638–647

    Google Scholar 

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This investigation was supported by grants from the Italian National Research Council (CNR) No 82.02079.04 (R.G.), No 83.00492.04 (G.C.P.) and MPI (40%).

Part of this study was previously presented at the 7th ENA meeting, Hamburg, FRG, September 1983 (Guglielmone and Panzica 1983).

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Guglielmone, R., Panzica, G.C. Typology, distribution and development of the catecholamine-containing neurons in the chicken brain. Cell Tissue Res. 237, 67–79 (1984). https://doi.org/10.1007/BF00229201

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