Hostname: page-component-cd9895bd7-gxg78 Total loading time: 0 Render date: 2024-12-26T07:28:30.132Z Has data issue: false hasContentIssue false
  • English
  • Français

Neuropeptide Y immunoreactivity of a projection from the lateral thalamic nucleus to the optic tectum of the leopard frog

Published online by Cambridge University Press:  02 June 2009

Angela M. Chapman  and
Elizabeth A. Debski
Angela M. Chapman
Affiliation:
School of Biological Sciences, University of Kentucky, Lexington
Elizabeth A. Debski
Affiliation:
School of Biological Sciences, University of Kentucky, Lexington
Get access Rights & Permissions [Opens in a new window]

Abstract

Using rhodamine-labelled latex beads as a retrograde tracer, we have shown that a subset of the neurons projecting from the lateral thalamic nucleus to the optic tectum of the leopard frog are neuropeptide Y-like immunoreactive (NPY-IR). In juvenile frogs, approximately twice as many lateral thalamic nucleus cells from this area project to the ipsilateral tectum as project to the contralateral tectum. NPY-IR cells make up 25% of the projection to the ipsilateral tectum and 13% of the projection to the contralateral tectum. The ipsilateral NPY-IR projection from the lateral nucleus was present in tadpoles and was similar in its characteristics to that found in the juvenile frog. However, the contralateral tectal projection was virtually nonexistent in these animals. The results of these experiments suggest that NPY from the lateral nucleus is released into the ipsilateral tectal neuropil in both the developing and adult frog.

Keywords

Visual systemThalamusModulationRana pipiens
Type
Research Articles
Information
Visual Neuroscience , Volume 12 , Issue 1 , January 1995 , pp. 1 - 9
Copyright
Copyright © Cambridge University Press 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Antal, M. (1991). Distribution of GABA immunoreactivity in the optic tectum of the frog: A light and electron microscopy study. Neuroscience 42, 879–891.CrossRefGoogle Scholar
Aste, N., Viglietti-Panzica, C., Fasolo, A., Vaudry, H., Pelletier, G. & Panzica, G.C. (1991). Localization of neuropeptide Y-immunoreactive cells and fibres in the brain of the Japanese quail. Cell and Tissue Research 265, 219–230.CrossRefGoogle ScholarPubMed
Bagnoli, P., Fontanesi, G., Alesci, R. & Erichsen, J.T. (1992). Distribution of neuropeptide Y, substance P, and acetyltransferase in the developing visual system of the pigeon and effects of unilateral retina removal. Journal of Comparative Neurology 318, 392–414.CrossRefGoogle ScholarPubMed
Bruun, A., Tornqvist, K. & Ehinger, B. (1986). Neuropeptide Y (NPY) immunoreactive neurons in the retina of different species. Histochemistry 86, 135–140.CrossRefGoogle ScholarPubMed
Danger, J.M., Guy, J., Benyamina, M., Jegou, S., Leboulenger, F., Cote, J., Tonon, M.C., Pelletier, G. & Vaudry, H. (1985). Localization and identification of neuropeptide Y (NPY)-like immunoreactivity in the frog brain. Peptides 6, 1225–1236.CrossRefGoogle ScholarPubMed
Debski, E.A. & Constantine-Paton, M. (1988). The effects of glutamate receptor agonists and antagonists on the evoked tectal potential in Rana pipiens. Society for Neuroscience Abstracts 14, 674.Google Scholar
Debski, E.A. & Constantine-Paton, M. (1993). The development of non-retinal afferent projections to the frog optic tectum and the substance P immunoreactivity of tectal connections. Developmental Brain Research 72, 21–39.CrossRefGoogle Scholar
Desan, P.H., Gruberg, E.R., Grewell, K.M. & Eckenstein, F. (1987). Cholinergic innervation of the optic tectum in the frog Rana pipiens. Brain Research 413, 344–349.CrossRefGoogle ScholarPubMed
Ferriero, D.M. & Sagar, S.M. (1989). Development of neuropeptide Y-immunoreactive neurons in the rat retina. Developmental Brain Research 48, 19–26.CrossRefGoogle ScholarPubMed
Fox, B.E.S. & Fraser, S.E. (1987). Excitatory amino acids in the retinotectal system of Xenopus laevis. Society for Neuroscience Abstracts 13, 766.Google Scholar
Gruberg, E.R., Wallace, M.T. & Waldeck, R.F. (1989). Relationship between isthmotectal fibers and other tectopetal systems in the leopard frog. Journal of Comparative Neurology 288, 39–50.CrossRefGoogle ScholarPubMed
Harrington, M.E., Nance, D.M. & Rusak, B. (1987). Double-labeling of neuropeptide Y-immunoreactive neurons which project from the geniculate to the suprachiasmatic nuclei. Brain Research 410, 275–282.CrossRefGoogle Scholar
Hickmott, P.W. & Constantine-Paton, M. (1993). The contributions of NMDA, non-NMDA, and GABA receptors to postsynaptic responses in neurons of the optic tectum. Journal of Neuroscience 13, 4339–4353.CrossRefGoogle ScholarPubMed
Isayama, T. & Eldred, W.D. (1988). Neuropeptide Y-immunoreactive amacrine cells in the retina of the turtle Pseudemys scripta elegans. Journal of Comparative Neurology 271, 56–66.CrossRefGoogle ScholarPubMed
Katz, L.C., Burkhalter, A. & Dreyer, W.J. (1984). Fluorescent latex microspheres as a retrograde neuronal marker for in vivo and in vitro studies of the visual cortex. Nature 310, 498–500.CrossRefGoogle ScholarPubMed
Lázár, G., Maderdrut, J.L., Trasti, S.L., Liposits, Z., Tóth, P., Kozicz, T. & Merchenthaler, I. (1993). Distribution of proneuropeptide Y-derived peptides in the brain of Rana esculenta and Xenopus laevis. Journal of Comparative Neurology 327, 551–571.CrossRefGoogle ScholarPubMed
McQuiston, A.R. & Colmers, W.F. (1992). Neuropeptide Y does not alter NMDA conductances in CA3 pyramidal neurons: A slice-patch study. Neuroscience Letters 138, 261–264.CrossRefGoogle Scholar
Medina, L., Marti, E., Artero, C., Fasalo, A. & Puelles, L. (1992). Distribution of neuropeptide Y-like immunoreactivity in the brain of the lizard Gallotia galloti. Journal of Comparative Neurology 319, 387–405.CrossRefGoogle ScholarPubMed
Monnet, F.P., Debonnel, G. & De Montigny, C. (1990). Neuropeptide Y selectively potentiates N-methyl-D-aspartate-induced neuronal activation. European Journal of Pharmacology 182, 207–208.CrossRefGoogle ScholarPubMed
Monnet, F.P., Fournier, A., Debonnel, G. & De Montigny, C. (1992). Neuropeptide Y potentiates selectively the N-methyl-D-aspartate response in the rat CA3 dorsal hippocampus. I. Involvement of an atypical neuropeptide Y receptor. Journal of Pharmacology and Experimental Therapeutics 263, 1212–1218.Google ScholarPubMed
Montgomery, N.M., Fite, K.V. & Li, Z. (1991). Anatomical evidence for an intergeniculate leaflet in Rana pipiens. Neuroscience Letters 133, 105–108.CrossRefGoogle ScholarPubMed
Neary, T. J. & Northcutt, R.G. (1983). Nuclear organization of the bullfrog diencephalon. Journal of Comparative Neurology 213, 262–278.CrossRefGoogle ScholarPubMed
Nigishi, K., Kiyama, H., Kato, S., Teranishi, T., Hatakenaka, S., Katayama, Y., Miki, N. & Tohyama, M. (1986). An immunohistochemical study of the river lamprey. Brain Research 362, 389–393.CrossRefGoogle Scholar
Nistri, A., Sivilotti, L. & Welsh, D.M. (1990). An electrophysiological study of the action of N-methyl-D-aspartate on excitatory synaptic transmission in the optic tectum of the frog in vitro. Neuropharmacology 29, 681–688.CrossRefGoogle ScholarPubMed
Osborne, N.N., Patel, S., Terenghi, G., Allen, J.M., Polak, J.M. & Bloom, S.R. (1985). Neuropeptide Y (NPY)-like immunoreactive amacrine cells in retinas of frog and goldfish. Cell and Tissue Research 241, 651–656.CrossRefGoogle ScholarPubMed
Perroteau, I., Danger, J.-M., Biffo, S., Pelletier, G., Vaudry, H. & Fasolo, A. (1988). Distribution and characterization of neuropeptide Y-like immunoreactivity in the brain of the crested newt. Journal of Comparative Neurology 275, 309–325.CrossRefGoogle ScholarPubMed
Pontet, A., Danger, J.-M., Dubourg, P., Pelletier, G., Vaudry, G., Calas, H. & Kah, O. (1989). Distribution and characterization of neuropeptide Y-like immunoreactivity in the brain and pituitary of the goldfish. Cell and Tissue Research 255, 529–538.CrossRefGoogle ScholarPubMed
Reh, T.A. & Constantine-Paton, M. (1984). Retinal ganglion cell terminals change their projection sites during larval development of Rana pipiens. Journal of Neuroscience 4, 442–457.CrossRefGoogle ScholarPubMed
Ricciuti, A.J. & Gruberg, E.R. (1985). Nucleus isthmi provides most tectal choline acetyltransferase in the frog Rana pipiens. Brain Research 341, 399–402.CrossRefGoogle ScholarPubMed
Roberts, P.J. & Yates, R.A. (1976). Tectal deafferentation in the frog: Selective loss of L-glutamate and gamma-aminobutyrate. Neuroscience 1, 371–374.CrossRefGoogle ScholarPubMed
Roman, F.J., Pascaud, X., Duffy, O. & Junien, J.L. (1991). N-methyl-D-aspartate receptor complex modulation by neuropeptide Y and peptide YY in rat hippocampus in vitro. Neuroscience Letters 122, 202–204.CrossRefGoogle ScholarPubMed
Scalia, F. (1976). The optic pathway of the frog: Nuclear organization and connections. In Frog Neurobiology, ed. Llinás, R. & Precht, W., pp. 386–406. New York: Springer.CrossRefGoogle Scholar
Singman, E.L. & Scalia, F. (1990). Quantitative study of the tectally projecting retinal ganglion cells in the adult frog: I. The size of the contralateral and ipsilateral projections. Journal of Comparative Neurology 302, 792–809.CrossRefGoogle ScholarPubMed
Smolen, A.J., Wright, L.L. & Cunningham, T.J. (1983). Neuron numbers in the superior cervical sympathetic ganglion of the rat: A critical comparison of methods for cell counting. Journal of Neurocytology 12, 739–750.CrossRefGoogle Scholar
Székely, A.D., Csillag, A. & Gorcs, T. (1992). Neuropeptide Y innervation of retinorecipient layers of chick optic tectum. Journal of Neurocytology 21, 148–156.CrossRefGoogle Scholar
Székely, G., Setalo, G. & Lázár, G. (1973). Fine structure of the frog's optic tectum: Optic fibre termination layers. Journal of Hirnforsch 14, 189–225.Google ScholarPubMed
Székely, G. & Lázár, G. (1976). Cellular and synaptic architecture of the optic tectum. In Frog Neurobiology, ed. Llinás, R. & Precht, W., pp. 407–434. New York: Springer.CrossRefGoogle Scholar
Tam, S.W. & Mitchell, K.N. (1991). Neuropeptide Y and peptide YY do not bind to brain sigma and phencyclidine binding sites. European Journal of Pharmacology 193, 121–122.Google Scholar
Taylor, A.C. & Kollros, J.J. (1946). Stages in the development of Rana pipiens larvae. Anatomical Record 94, 7–23.CrossRefGoogle ScholarPubMed
Vecino, E. & Ekström, P. (1990). Distribution of met-enkephalin, leuenkephalin, substance P, neuropeptide Y, FMRFamide, and serotonin immunoreactivities in the optic tectum of the atlantic salmon (Salmo salar L.). Journal of Comparative Neurology 299, 229–241.CrossRefGoogle ScholarPubMed
Verstappen, A., Van Reeth, O., Vaudry, H., Pelletier, G. & Vanderhaeghen, J.J. (1986). Demonstration of a neuropeptide Y (NPY)-like immunoreactivity in the pigeon retina. Neuroscience Letters 70, 193–197.CrossRefGoogle ScholarPubMed
Wilczynski, W. & Northcutt, R.G. (1977). Afferents to the optic tectum of the leopard frog: An HRP study. Journal of Comparative Neurology 173, 219–230.CrossRefGoogle Scholar