Thalamic input to parvalbumin-immunoreactive GABAergic interneurons: Organization in normal striatum and effect of neonatal decortication

Neuroscience

Volumn 88, Issue 4, 1999, Pages 1165-1175

  Rudkin, T M ^a   Sadikot, A F ^a  

^a MCGILL UNIVERSITY   (Canada)

Author keywords

Development; Parvalbumin; Plastic ity; Synaptogenesis; Thalamostriatal; Ultrastructure

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CORPUS STRIATUM; DECORTICATION; ELECTRON MICROSCOPY; GABAERGIC SYSTEM; HISTOCHEMISTRY; IMMUNOHISTOCHEMISTRY; INTERNEURON; NONHUMAN; PRIORITY JOURNAL; RAT; SYNAPTIC TRANSMISSION; THALAMUS NUCLEUS; THALAMUS PARAFASCICULAR NUCLEUS;

ANIMALS; ANIMALS, NEWBORN; BENZIDINES; CEREBRAL CORTEX; CHROMOGENIC COMPOUNDS; COLORING AGENTS; CORPUS STRIATUM; DENERVATION; GAMMA-AMINOBUTYRIC ACID; INTERNEURONS; MICROSCOPY, ELECTRON; P-DIMETHYLAMINOAZOBENZENE; PARVALBUMINS; RATS; RATS, SPRAGUE-DAWLEY; REFERENCE VALUES; SYNAPTIC TRANSMISSION; THALAMUS;

EID: 0032890034     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0306-4522(98)00265-6     Document Type: Article

References (69)

1. Aylward R. L., Totterdell S. Neurons in ventral subiculum, amygdala, and entorhinal cortex which project to the nucleus accumbens and their input from somatostatin-immunoreactive boutons. J. chem. Neuroanat. 6:1993;31-42.
2. Bennett B. D., Bolam J. P. Synaptic input and output of parvalbumin-immunoreactive neurons in the neostriatum of the rat. Neuroscience. 62:1994;707-719.
3. Berendse H. W., Groenewegen H. J. Organization of the thalamostriatal projections in the rat, with special emphasis on the ventral striatum. J. comp. Neurol. 299:1990;187-228.
4. Berendse H. W., Groenewegen H. J. Restricted cortical termination fields of the midline and intralaminar thalamic nuclei in the rat. Neuroscience. 42:1991;73-102.
5. Bolam J. P., Clark D. J., Smith A. D., Somogyi P. A type of aspiny neuron in the rat neostriatum accumulates (3H-)GABA: combination of Golgi-staining, autoradiography and electron microscopy. J. comp. Neurol. 213:1983;121-134.
6. Chung J. W., Hassler R., Wagner A. Degeneration of two of nine types of synapses in the putamen after centre median coagulation on the cat. Expl Brain Res. 28:1977;345-361.
7. 1-dependent control of in vivo acetylcholine release in rat striatum. Neuroscience. 71:1996;157-165.
8. Cowan R. L., Wilson C. J., Emson P. C., Heizmann C. W. Parvalbumin-containing GABAergic interneurons in the rat neostriatum. J. comp. Neurol. 302:1990;197-205.
9. Descarries L., Soghomonian J. J., Garcia S., Doucet G., Bruno J. P. Ultrastructural analysis of the serotonin hyperinnervation in adult rat neostriatum following neonatal dopamine denervation with 6-hydroxydopamine. Brain Res. 569:1992;1-13.
10. Deschênes M., Bourassa J., Doan V. D., Parent A. A single-cell study of the axonal projections arising from the posterior intralaminar thalamic nuclei in the rat. Eur. J. Neurosci. 8:1996;329-343.
11. Dimova R., Vuillet J., Nieoullon A., Kerkerian-Le Goff L. Ultrastructural features of the choline acetyltransferase-containing neurons and relationships with nigral dopaminergic and cortical afferent pathways in the rat striatum. Neuroscience. 53:1993;1059-1071.
12. Divac I., Fonnum F., Storm-Mathisen J. High affinity uptake of glutamate in terminals of corticostriatal axons. Nature. 266:1977;377-378.
13. Dubé L., Smith A. D., Bolam J. P. Identification of synaptic terminals of thalamic or cortical origin in contact with distinct medium-size spiny neurons in the rat neostriatum. J. comp. Neurol. 267:1988;455-471.
14. Geneser-Jensen F. A., Blackstad T. W. Distribution of acetyl cholinesterase in the hippocampal region of the guinea pig. I. Entorhinal area, parasubiculum, and presubiculum. Z. Zellforsch. mikrosk. Anat. 114:1971;460-481.
15. Gerfen C. R., Baimbridge K. G., Miller J. J. The neostriatal mosaic: compartmental distribution of calcium binding protein and parvalbumin in the basal ganglia of the rat and monkey. Proc. natn. Acad. Sci. U.S.A. 82:1985;8780-8784.
16. Gerfen C. R. Synaptic organization of the striatum. J. Electron Microsc. Tech. 10:1988;265-281.
17. Groenewegen H. J., Room P., Witter M. P., Lohman A. H. M. Cortical afferents of the nucleus accumbens septi in the cat, studied with anterograde and retrograde transport techniques. Neuroscience. 7:1982;977-996.
18. Hassler R., Haug P., Nitsch C., Kim J. S., Paik K. Effect of motor and premotor cortex ablation on concentrations of amino acids, monoamines, and acetylcholine and on the ultrastructure in rat striatum. A confirmation of glutamate as the specific cortico-striatal transmitter. J. Neurochem. 38:1982;1087-1098.
19. Hattori T., McGeer P. L. Synaptogenesis in the corpus striatum of infant rat. Expl Neurol. 38:1973;70-79.
20. Heimer L., Zahm D. S. and Alheid G. F. (1995) Basal ganglia. In The Rat Nervous System (ed. Paxinos G.), pp. 579-628. Academic, New York.
21. Herkenham M., Pert C. B. Mosaic distribution of opiate receptors, parafascicular projections and acetylcholinesterase in rat striatum. Nature. 291:1981;415-418.
22. Ingham C. A., Hood S. H., van Maldegem B., Weenink A., Arbuthnott G. W. Morphological changes in the rat neostriatum after unilateral 6-hydroxydopamine injections into the nigrostriatal pathway. Expl Brain Res. 93:1993;17-27.
23. Ingham C. A., Hood S. H., Taggart P. and Arbuthnott G. W. (1996) Synaptic plasticity in the rat neostriatum after unilateral 6-hydroxydopamine lesion of the nigrostriatal dopaminergic pathway. In Advances in Behavioural Biology, The Basal Ganglia (eds Ohye V. C. et al.), Vol. 47, pp. 157-164. Plenum, New York.
24. Johnson L. R., Aylward R. L. M., Hussain Z., Totterdell S. Input from the amygdala to the rat nucleus accumbens: its relationship with tyrosine hydroxylase immunoreactivity and identified neurons. Neuroscience. 61:1994;851-865.
25. Kachidian P., Vuillet J., Nieoullon A., Lafaille G., Kerkerian-Le Goff L. Striatal neuropeptide Y neurones are not a target for thalamic afferent fibres. NeuroReport. 7:1996;1665-1669.
26. Katz L. C., Shatz C. J. Synaptic activity and the construction of cortical circuits. Science. 274:1996;1133-1138.
27. Kawaguchi Y. Physiological, morphological, and histochemical characterization of three classes of interneurons in rat neostriatum. J. Neurosci. 13:1993;4908-4923.
28. Kelley A. E., Domesick V. B., Nauta W. J. H. The amygdalostriatal projection in the rat - An anatomical study by anterograde and retrograde tracing methods. Neuroscience. 7:1982;615-630.
29. Kemp D. E., Powell J. F. The termination of fibers from the cerebral cortex and thalamus upon dendritic spines in the caudate nucleus: a study with the Golgi method. Phil. Trans. R. Soc. 262:1971;429-439.
30. Kita H., Kitai S. T. Amygdaloid projections to the frontal cortex and striatum in the rat. J. comp. Neurol. 298:1990;40-49.
31. Kita H., Kosaka T., Heizmann C. W. Parvalbumin-immunoreactive neurons in the rat neostriatum: a light and electron microscopic study. Brain Res. 536:1990;1-15.
32. Kitai S. T., Kocsis J. D., Preston R. J., Sugimori M. Monosynaptic inputs to caudate neurons identified by intracellular injection of horseradish peroxidase. Brain Res. 109:1976;601-606.
33. Kolb B., Gibb R., van der Kooy D. Cortical and striatal structure and connectivity are altered by neonatal hemidecortication in rats. J. comp. Neurol. 322:1992;311-324.
34. Kubota Y., Mikawa S., Kawaguchi Y. Neostriatal GABAergic interneurones contain NOS, calretinin or parvalbumin. NeuroReport. 5:1993;205-208.
35. Lapper S. R., Smith Y., Sadikot A. F., Parent A., Bolam J. P. Cortical input to parvalbumin-immunoreactive neurones in the putamen of the squirrel monkey. Brain Res. 580:1992;215-224.
36. Lapper S. R., Bolam J. P. Input from the frontal cortex and the parafascicular nucleus to cholinergic interneurons in the dorsal striatum of the rat. Neuroscience. 51:1992;533-545.
37. Llewellyn-Smith I. J., Pilowsky P., Minson J. B. The tungstate-stabilized tetramethylbenzidine reaction for light and electron microscopic immunocytochemistry and for revealing biocytin-filled neurons. J. Neurosci. Meth. 46:1993;27-40.
38. McGeer P. L., McGeer E. G., Scherer U., Singh K. A glutamatergic corticostriatal path? Brain Res. 128:1977;369-373.
39. McGeorge A. J., Faull R. L. M. The organization of the projection from the cerebral cortex to the striatum in the rat. Neuroscience. 29:1989;503-537.
40. Mensah P. L. An electron microscopical study of neuronal cell clustering in postnatal mouse striatum, with special emphasis on neuronal cell death. Anat. Embryol. 164:1982;387-401.
41. Meredith G. E., Chang H. T. Synaptic relationships of enkephalinergic and cholinergic neurons in the nucleus accumbens of the rat. Brain Res. 667:1994;67-76.
42. Meredith G. E., Wouterlood F. G. Hippocampal and midline thalamic fibers and terminals in relation to the choline acetyltransferase neurons in nucleus accumbens of the rat: a light and electron microscopic study. J. comp. Neurol. 296:1990;204-221.
43. Misgeld U., Dodt H. U., Frotscher M. Late development of intrinsic excitation in the rat neostriatum: an in vitro study. Brain Res. 392:1986;59-67.
44. Paré D., Smith Y. Thalamic collaterals of corticostriatal axons: their termination field and synaptic targets in cats. J. comp. Neurol. 372:1996;551-567.
45. Parent A. (1996) The basal ganglia. In Carpenter's Human Neuroanatomy (ed. Parent A.), pp. 795-863. Williams and Wilkins, Philadelphia.
46. Paxinos G. and Watson C. (1986) The Rat Brain in Stereotaxic Coordinates. Academic, New York.
47. Pennartz C. M., Kitai S. T. Hippocampal inputs to identified neurons in an in vitro slice preparation of the rat nucleus accumbens: evidence for feed-forward inhibition. J. Neurosci. 11:1991;2838-2847.
48. Purpura D. P., Malliani A. I. Synaptic potentials and discharge characteristics of caudate neurons activated by thalamic stimulation. Brain Res. 6:1967;325-340.
49. Rajakumar N., Elisevich K., Flumerfelt B. A. Biotinylated dextran: a versatile anterograde and retrograde neuronal tracer. Brain Res. 607:1993;47-53.
50. Royce G. J., Mourey R. J. Efferent connections of the centromedian and parafascicular thalamic nuclei: an autoradiographic investigation in the cat. J. comp. Neurol. 235:1985;277-300.
51. Sadikot A. F., Parent A., François C. The centre median and parafascicular thalamic nuclei project respectively to the sensorimotor and associative-limbic striatal territories in the squirrel monkey. Brain Res. 510:1990;161-165.
52. Sadikot A. F., Parent A., François C. Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: a PHA-L study of subcortical projections. J. comp. Neurol. 315:1992;137-159.
53. Sadikot A. F., Parent A., Smith Y., Bolam J. P. Efferent connections of the centromedian and parafascicular thalamic nuclei in the squirrel monkey: a light and electron microscopic study of the thalamostriatal projection in relation to striatal heterogeneity. J. comp. Neurol. 320:1992;228-242.
54. Sadikot A. F. and Rudkin T. M. (1996) The amygdalostriatal projection: an analysis of synaptic inputs to GABAergic interneuron subtypes. In Advances in Behavioural Biology, The Basal Ganglia (eds Ohye V. C. et al.), Vol. 47, pp. 33-42. Plenum, New York.
55. Smith A. D., Bolam J. P. The neural network of the basal ganglia as revealed by the study of synaptic connections of identified neurons. Trends Neurosci. 13:1990;259-265.
56. Smith Y., Bennett B. D., Bolam J. P., Parent A., Sadikot A. F. Synaptic relationships between dopaminergic afferents and cortical or thalamic input in the sensorimotor territory of the striatum in monkey. J. comp. Neurol. 344:1994;1-19.
57. Soghomonian J. J., Descarries L., Watkins K. C. Serotonin innervation in adult rat neostriatum. II. Ultrastructural features and a radioautographic and immunohistochemical study. Brain Res. 481:1989;67-86.
58. Somogyi P., Bolam J. P., Smith A. D. Monosynaptic cortical input and local axon collaterals of identified striatonigral neurons. A light and electron microscopic study using the Golgi-peroxidase transport-degeneration procedure. J. comp. Neurol. 195:1981;567-584.
59. Sterio D. C. Estimating numbers, mean sizes and variations in size of particles in 3-D specimens using dissectors. J. Microsc. 134:1984;127-136.
60. Tepper J. M., Trent F. In vivo studies of the postnatal development of rat neostriatal neurons. Prog. Brain Res. 99:1993;35-50.
61. Tessier-Lavigne M., Goodman C. S. The molecular biology of axon guidance. Science. 274:1996;1123-1133.
62. Totterdell S., Smith A. D. Convergence of hippocampal and dopaminergic input onto identified neurons in the nucleus accumbens in the rat neostriatum. J. chem. Neuroanat. 2:1989;285-298.
63. Veenman C. L., Reiner A., Honig M. G. Biotinylated dextran amine as an anterograde tracer for single- and double-labeling studies. J. Neurosci. Meth. 41:1992;239-254.
64. Vuillet J., Kerkerian L., Kachidian P., Bosler O., Nieoullon A. Ultrastructural correlates of functional relationships between nigral dopaminergic or cortical afferent fibers and neuropeptide Y-containing neurons in the rat striatum. Neurosci. Lett. 100:1989;99-104.
65. Wouterlood F. G., Bol J. G., Steinbusch H. W. Double-label immunocytochemistry: combination of anterograde neuroanatomical tracing with Phaseolus vulgaris-leucoagglutinin and enzyme immunocytochemistry of target neurons. J. Histochem. Cytochem. 35:1987;817-823.
66. Wouterlood F. G., Jorritsma-Byham B. The anterograde neuroanatomical tracer biotinylated dextran-amine: comparison with the tracer Phaseolus vulgaris-leucoagglutinin in preparations for electron microscopy. J. Neurosci. Meth. 48:1993;75-87.
67. Xu Z. C., Wilson C. J., Emson P. C. Restoration of thalamostriatal projections in rat neostriatal grafts: an electron microscopic analysis. J. comp. Neurol. 303:1991;22-34.
68. Yelnik J., François C., Percheron G., Tande D. Morphological taxonomy of the neurons of the primate striatum. J. comp. Neurol. 313:1991;273-294.
69. Zilles K. (1985) The Cortex of the Rat. A Stereotaxic Atlas. Springer-Verlag, Berlin.