The organization of the striatal output system: A single-cell juxtacellular labeling study in the rat

Neuroscience Research

Volumn 38, Issue 1, 2000, Pages 49-62

  Wu, Ying ^a   Richard, Sandra ^a   Parent, André ^a  

^a UNIVERSITÉ LAVAL   (Canada)

Author keywords

Axonal branching pattern; Basal ganglia; Single cell labeling; Striatofugal system; Striatonigral projections; Striatopallidal projections

Indexed keywords

AMINE; BIOTIN; DEXTRAN;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CAMERA; CELL LABELING; CORPUS STRIATUM; ENTOPEDUNCULAR NUCLEUS; GLOBUS PALLIDUS; MALE; MICROSCOPY; NERVE CELL NETWORK; NERVE FIBER; NERVE PROJECTION; NONHUMAN; PRIORITY JOURNAL; RAT; RETICULAR FORMATION; SUBSTANTIA NIGRA;

ANIMAL; AXONS; BIOTIN; CORPUS STRIATUM; DEXTRANS; ENTOPEDUNCULAR NUCLEUS; GLOBUS PALLIDUS; MALE; NERVE NET; NEURONS; RATS; RATS, SPRAGUE-DAWLEY; SUBSTANTIA NIGRA;

EID: 0034282256     PISSN: 01680102     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-0102(00)00140-1     Document Type: Article

References (38)

1. Aizman O., Brismar H., Uhlén P., Zettergren E., Levey A.I., Forssberg H., Greengard P., Aperia A. Anatomical and physiological evidence for D1 and D2 dopamine receptor colocalization in neostriatal neurons. Nat. Neurosci. 3:2000;226-230.
2. Albin R.L., Young A.B., Penney J.B. The functional anatomy of basal ganglia disorders. Trends Neurosci. 12:1989;366-375.
3. Beckstead R.M., Cruz C.J. Striatal axons to the globus pallidus, entopeduncular nucleus and substania nigra come mainly from separate cell populations in cat. Neuroscience. 19:1986;147-158.
4. Bishop G.A., Chang H.T., Kitai S.T. Morphological and physiological properties of neurons: an intracellular horseradish peroxidase study in the rat. Neuroscience. 7:1982;179-191.
5. Chang H.T., Wilson C.J., Kitai S.T. Single neostriatal efferent axons in the globus pallidus: a light and electron microscopic study. Science. 213:1981;915-918.
6. Chesselet M.F., Delfs J.M. Basal ganglia and movement disorders: an update. Trends Neurosci. 19:1996;417-422.
7. Danner H., Pfister C. Untersuchugen zur Struktur des Neostriatum der Ratte. J. Hirnforsch. 20:1979;285-301.
8. DeLong M.R. Primate models of movement disorders of basal ganglia origin. Trends Neurosci. 13:1990;281-859.
9. DiFiglia M., Pasik P., Pasik T. A Golgi study of neuronal types in the neostriatum of monkeys. Brain Res. 114:1976;245-256.
10. Dimova R., Vuillet J., Seite R. Study of the rat neostriatum using a combined Golgi-electron microscope technique and serial sections. Neuroscience. 5:1980;1581-1596.
11. Féger J., Crossman A.R. Identification of different subpopulations of neostriatal neurones projecting to globus pallidus or substantia nigra in the monkey: a retrograde fluorescence double-labelling study. Neurosci. Lett. 49:1984;7-12.
12. Flaherty A.W., Graybiel A.M. Corticostriatal transformations in the primate somatosensory system. Projections from physiologically mapped body-part representations. J. Neurosci. 66:1991;1249-1263.
13. Fox C.A., Andrade A.N., Hillman D.E., Schwyn R.C. The spiny neurons in the primate striatum: a Golgi and electron microscopic study. J. Hirnforsch. 13:1971/1972;181-201.
14. Gerfen C.R., Wilson C.J. The basal ganglia. Swanson L.W., Björkulnd A., Hökfelt T. Handbook of Chemical Anatomy, Integrated Systems in the CNS, Part III. 1996;371-468 Elsevier, Amsterdam.
15. Haber S.N., Nauta W.J.H. Ramifications of the globus pallidus in the rat as indicated by patterns of immunohistochemistry. Neuroscience. 9:1983;245-260.
16. Johnston J.G., Gerfen C.R., Haber S.N., van der Kooy D. Mechanisms of striatal pattern formation: conservation of mammalian compartmentalization. Brain Res. Dev. Brain Res. 57:1990;93-102.
17. Kawaguchi Y., Wilson C.J., Emson P.C. Projection subtypes of rat neostriatal matrix cells revealed by intracellular injection of biocytin. J. Neurosci. 10:1990;3421-3438.
18. Kemp J.M., Powell T.P.S. The connexions of the striatum and globus pallidus: synthesis and speculation. Phil. Trans. R. Soc. Lond. B. Biol. Sci. 262:1971;441-457.
19. Loopuijt L.D., van der Kooy D. Organization of the striatum: collateralization of its efferent axons. Brain Res. 348:1985;86-99.
20. 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.
21. Parent A. Extrinsic connections of the basal ganglia. Trends Neurosci. 13:1990;254-258.
22. Parent A., Bouchard C., Smith Y. The striatopallidal and striatonigral projections: two distinct fiber systems in primate. Brain Res. 303:1984;385-390.
23. Parent A., Charara A., Pinault D. Single striatofugal axons arborizing in the both pallidal segments and in the substantia nigra in primates. Brain Res. 698:1985;280-284.
24. Paxinos G., Watson C. The rat brain in stereotaxic coordinates. second ed. 1986;Academic Press, Sydney.
25. Pinault D. A novel single-cell staining procedure performed in vivo under electrophysiological control: morpho-functional features of juxtacellulary labeled thalamic cells and other central neurons with biocytin or Neurobiotin. J. Neurosci. Methods. 65:1996;113-136.
26. Preston R.J., Bishop G.A., Kitai S.T. Medium spiny neuron projection from the rat striatum: an intracellular horseradish peroxidase study. Brain Res. 183:1980;253-263.
27. Sato F., Lavallée P., Lévesque M., Parent A. Single-axon tracing study of neurons of the external segment of the globus pallidus in primate. J. Comp. Neurol. 417:2000a;17-31.
28. Sato, F., Parent, M., Lévesque, M., Parent, A., 2000b. Axonal branching pattern of neurons of the subthalamic nucleus in primates. J. Comp. Neurol., in press.
29. 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.
30. Smith Y., Bevan M.D., Shink E., Bolam J.P. Microcircuitryo of the direct and indirect pathways of the basal ganglia. Neuroscience. 86:1998;353-387.
31. Wichmann T., DeLong M.R. Functional and pathophysiological models of the basal ganglia. Curr. Opin. Neurobiol. 6:1996;751-758.
32. Wilson C.J., Groves P.M. Spontaneous firing patterns of identified spiny neurons in the rat neostriatum. Brain Res. 220:1981;67-80.
33. Wilson C.J., Phelan K.D. Dual topographic representation of neostriatum in the globus pallidus of rats. Brain Res. 243:1982;354-359.
34. Wong-Riley M.T.T. Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry. Brain Res. 171:1979;11-28.
35. Wu Y., Parent A. A single cell labeling study of the striatal output system in the rat. Soc. Neurosci. Abstr. 25:1999;1299.
36. Yelnik J., François C., Percheron G., Tande D. Morphological taxonomy of the neurons of the primate striatum. J. Comp. Neurol. 313:1991;273-294.
37. Yoshida M., Rabin A., Anderson M.E. Monosynaptic inhibition of pallidal neurons by axon collaterals of caudato-nigral fibers. Exp. Brain Res. 15:1972;337-347.
38. Yung K.K., Smith A.D., Levey A.I., Bolam J.P. Synaptic connections between spiny neurons of the direct and indirect pathways in the neostriatum of the rat: evidence from dopamine receptor and neuropeptide immunostaining. Eur. J. Neurosci. 8:1996;861-869.