GABAergic control of the subthalamic nucleus

Progress in Brain Research

Volumn 160, Issue , 2007, Pages 173-188

  Bevan, Mark D ^a   Hallworth, Nicholas E ^a   Baufreton, Jérôme ^b  

^a NORTHWESTERN UNIVERSITY   (United States)

^b CNRS   (France)

Author keywords

cortex; dopamine; excitation; inhibition; oscillation; Parkinson's disease; synaptic integration

Indexed keywords

4 AMINOBUTYRIC ACID; 4 AMINOBUTYRIC ACID A RECEPTOR; 4 AMINOBUTYRIC ACID B RECEPTOR; CALCIUM CHANNEL; DOPAMINE; POSTSYNAPTIC RECEPTOR; PRESYNAPTIC RECEPTOR; SODIUM CHANNEL;

ACTION POTENTIAL; BRAIN CORTEX; BRAIN NUCLEUS; DOPAMINERGIC TRANSMISSION; ELECTROPHYSIOLOGY; EXCITATORY POSTSYNAPTIC POTENTIAL; GLOBUS PALLIDUS; HYPERPOLARIZATION; INHIBITORY POSTSYNAPTIC POTENTIAL; NEGATIVE FEEDBACK; NERVE CELL; NERVE CELL PLASTICITY; NONHUMAN; PACEMAKER; PARKINSON DISEASE; PRIORITY JOURNAL; REVIEW; SUBTHALAMIC NUCLEUS; SYNAPTIC INHIBITION; VOLUNTARY MOVEMENT;

ACTION POTENTIALS; ANIMALS; BIOLOGICAL CLOCKS; DOPAMINE; GAMMA-AMINOBUTYRIC ACID; HUMANS; NEURAL INHIBITION; NEURAL PATHWAYS; NEURONS; SUBTHALAMIC NUCLEUS; SYNAPTIC TRANSMISSION;

EID: 34247871188     PISSN: 00796123     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0079-6123(06)60010-1     Document Type: Review

References (64)

1. Abbott L.F., and Regehr W.G. Synaptic computation. Nature 431 (2004) 796-803
2. Afsharpour S. Topographical projections of the cerebral cortex to the subthalamic nucleus. J. Comp. Neurol. 236 (1985) 14-28
3. Baufreton J., Atherton J.A., and Bevan M.D. Enhancement of excitatory synaptic integration by GABAergic inhibition in the subthalamic nucleus. J. Neurosci. 25 (2005) 8505-8517
4. Baufreton J., Garret M., Dovero S., Dufy B., Bioulac B., and Taupignon A. Activation of GABA(A) receptors in subthalamic neurons in vitro: properties of native receptors and inhibition mechanisms. J. Neurophysiol. 86 (2001) 75-85
5. Baufreton J., Garret M., Rivera A., de la Calle A., Gonon F., Dufy B., Bioulac B., and Taupignon A. D5 (not D1) dopamine receptors potentiate burst-firing in neurons of the subthalamic nucleus by modulating an L-type calcium conductance. J. Neurosci. 23 (2003) 816-825
6. Baufreton J., Zhu Z.T., Garret M., Bioulac B., Johnson S.W., and Taupignon A.I. Dopamine receptors set the pattern of activity generated in subthalamic neurons. FASEB J. 19 (2005) 1771-1777
7. Bergman H., Wichmann T., Karmon B., and DeLong M.R. The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of Parkinsonism. J. Neurophysiol. 72 (1994) 507-520
8. Beurrier C., Bioulac B., and Hammond C. Slowly inactivating sodium current (I(NaP)) underlies single-spike activity in rat subthalamic neurons. J. Neurophysiol. 83 (2000) 1951-1957
9. Beurrier C., Congar P., Bioulac B., and Hammond C. Subthalamic nucleus neurons switch from single-spike activity to burst-firing mode. J. Neurosci. 19 (1999) 599-609
10. Bevan M.D., and Bolam J.P. Cholinergic, GABAergic, and glutamate-enriched inputs from the mesopontine tegmentum to the subthalamic nucleus in the rat. J. Neurosci. 15 (1995) 7105-7120
11. Bevan M.D., Bolam J.P., and Crossman A.R. Convergent synaptic input from the neostriatum and the subthalamus onto identified nigrothalamic neurons in the rat. Eur. J. Neurosci. 6 (1994) 320-334
12. Bevan M.D., Booth P.A., Eaton S.A., and Bolam J.P. Selective innervation of neostriatal interneurons by a subclass of neuron in the globus pallidus of the rat. J. Neurosci. 18 (1998) 9438-9452
13. Bevan M.D., Clark N.P., and Bolam J.P. Synaptic integration of functionally diverse pallidal information in the entopeduncular nucleus and subthalamic nucleus in the rat. J. Neurosci. 17 (1997) 308-324
14. Bevan M.D., Francis C.M., and Bolam J.P. The glutamate-enriched cortical and thalamic input to neurons in the subthalamic nucleus of the rat: convergence with GABA-positive terminals. J. Comp. Neurol. 361 (1995) 491-511
15. Bevan M.D., Magill P.J., Hallworth N.E., Bolam J.P., and Wilson C.J. Regulation of the timing and pattern of action potential generation in rat subthalamic neurons in vitro by GABA-A IPSPs. J. Neurophysiol. 87 (2002) 1348-1362
16. Bevan M.D., and Wilson C.J. Mechanisms underlying spontaneous oscillation and rhythmic firing in rat subthalamic neurons. J. Neurosci. 19 (1999) 7617-7628
17. Bevan M.D., Wilson C.J., Bolam J.P., and Magill P.J. Equilibrium potential of GABA(A) current and implications for rebound burst firing in rat subthalamic neurons in vitro. J. Neurophysiol. 83 (2000) 3169-3172
18. Brown L.L., Markman M.H., Wolfson L.I., Dvorkin B., Warner C., and Katzman R. A direct role of dopamine in the rat subthalamic nucleus and an adjacent intrapeduncular area. Science 206 (1979) 1416-1418
19. Brown P. Oscillatory nature of human basal ganglia activity: relationship to the pathophysiology of Parkinson's disease. Mov. Disord. 18 (2003) 357-363
20. Charara A., Heilman T.C., Levey A.I., and Smith Y. Pre- and postsynaptic localization of GABA(B) receptors in the basal ganglia in monkeys. Neuroscience 95 (2000) 127-140
21. Cragg S., Baufreton J., Xue Y., Bolam P., and Bevan M.D. Synaptic release of dopamine in the subthalamic nucleus. Eur. J. Neurosci. 20 (2004) 1788-1802
22. Degos B., Deniau J.M., Thierry A.M., Glowinski J., Pezard L., and Maurice N. Neuroleptic-induced catalepsy: electrophysiological mechanisms of functional recovery induced by high-frequency stimulation of the subthalamic nucleus. J. Neurosci. 25 (2005) 7687-7696
23. Deschenes M., Bourassa J., Doan V.D., and 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
24. Do M.T., and Bean B.P. Subthreshold sodium currents and pacemaking of subthalamic neurons: modulation by slow inactivation. Neuron 39 (2003) 109-120
25. Francois C., Savy C., Jan C., Tande D., Hirsch E.C., and Yelnik J. Dopaminergic innervation of the subthalamic nucleus in the normal state, in MPTP-treated monkeys, and in Parkinson's disease patients. J. Comp. Neurol. 425 (2000) 121-129
26. Fujimoto K., and Kita H. Response characteristics of subthalamic neurons to the stimulation of the sensorimotor cortex in the rat. Brain Res. 609 (1993) 185-192
27. Galvan A., Charara A., Pare J.F., Levey A.I., and Smith Y. Differential subcellular and subsynaptic distribution of GABA(A) and GABA(B) receptors in the monkey subthalamic nucleus. Neuroscience 127 (2004) 709-721
28. B receptors. J. Neurosci. 25 (2005) 6304-6315
29. Hallworth N.E., Wilson C.J., and Bevan M.D. Apamin-sensitive small conductance calcium-activated potassium channels, through their selective coupling to voltage-gated calcium channels, are critical determinants of the precision, pace, and pattern of action potential generation in rat subthalamic nucleus neurons in vitro. J. Neurosci. 23 (2003) 7525-7542
30. Hanson J.E., Smith Y., and Jaeger D. Sodium channels and dendritic spike initiation at excitatory synapses in globus pallidus neurons. J. Neurosci. 24 (2004) 329-340
31. Hassani O.K., Francois C., Yelnik J., and Feger J. Evidence for a dopaminergic innervation of the subthalamic nucleus in the rat. Brain Res. 749 (1997) 88-94
32. Joel D., and Weiner I. The connections of the primate subthalamic nucleus: indirect pathways and the open-interconnected scheme of basal ganglia-thalamocortical circuitry. Brain Res. Brain Res. Rev. 23 (1997) 62-78
33. Lavoie B., Smith Y., and Parent A. Dopaminergic innervation of the basal ganglia in the squirrel monkey as revealed by tyrosine hydroxylase immunohistochemistry. J. Comp. Neurol. 289 (1989) 36-52
34. Loucif K.C., Wilson C.L., Baig R., Lacey M.G., and Stanford I.M. Functional interconnectivity between the globus pallidus and the subthalamic nucleus in the mouse brain slice. J. Physiol. 567 (2005) 977-987
35. Magill P.J., Bolam J.P., and Bevan M.D. Relationship of activity in the subthalamic nucleus-globus pallidus network to cortical electroencephalogram. J. Neurosci. 20 (2000) 820-833
36. Magill P.J., Bolam J.P., and Bevan M.D. Dopamine regulates the impact of the cerebral cortex on the subthalamic nucleus-globus pallidus network. Neuroscience 106 (2001) 313-330
37. Magill P.J., Sharott A., Bevan M.D., Brown P., and Bolam J.P. Synchronous unit activity and local field potentials evoked in the subthalamic nucleus by cortical stimulation. J. Neurophysiol. 92 (2004) 700-714
38. Maurice N., Deniau J.M., Glowinski J., and Thierry A.M. Relationships between the prefrontal cortex and the basal ganglia in the rat: physiology of the corticosubthalamic circuits. J. Neurosci. 18 (1998) 9539-9546
39. McCormick D.A., and Bal T. Sleep and arousal: thalamocortical mechanisms. Annu. Rev. Neurosci. 20 (1997) 185-215
40. Nakanishi H., Kita H., and Kitai S.T. Intracellular study of rat substantia nigra pars reticulata neurons in an in vitro slice preparation: electrical membrane properties and response characteristics to subthalamic stimulation. Brain Res. 437 (1987) 45-55
41. Nakanishi H., Kita H., and Kitai S.T. Electrical membrane properties of rat subthalamic neurons in an in vitro slice preparation. Brain Res. 437 (1987) 35-44
42. Nambu A., Takada M., Inase M., and Tokuno H. Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplementary motor area. J. Neurosci. 16 (1996) 2671-2683
43. Oorschot D.E. Total number of neurons in the neostriatal, pallidal, subthalamic, and substantia nigral nuclei of the rat basal ganglia: a stereological study using the cavalieri and optical dissector methods. J. Comp. Neurol. 366 (1996) 580-599
44. Otsuka T., Murakami F., and Song W.J. Excitatory postsynaptic potentials trigger a plateau potential in rat subthalamic neurons at hyperpolarized states. J. Neurophysiol. 86 (2001) 1816-1825
45. Paz J.T., Deniau J.M., and Charpier S. Rhythmic bursting in the cortico-subthalamo-pallidal network during spontaneous genetically determined spike and wave discharges. J. Neurosci. 25 (2005) 2092-2101
46. A receptors in central synapses. J. Neurosci. 19 (1999) 578-588
47. Plenz D., and Kitai S.T. A basal ganglia pacemaker formed by the subthalamic nucleus and external globus pallidus. Nature 400 (1999) 677-682
48. Sato F., Lavallee P., Levesque M., and Parent A. A single-axon tracing study of neurons of the external segment of the globus pallidus in primate. J. Comp. Neurol. 417 (2000) 17-31
49. Sharott A., Magill P.J., Harnack D., Kupsch A., Meissner W., and Brown P. Dopamine depletion increases the power and coherence of beta-oscillations in the cerebral cortex and subthalamic nucleus of the awake rat. Eur. J. Neurosci. 21 (2005) 1413-1422
50. Shen K.Z., and Johnson S.W. Presynaptic dopamine D2 and muscarine M3 receptors inhibit excitatory and inhibitory transmission to rat subthalamic neurones in vitro. J. Physiol. 525 (2000) 331-341
51. Shen K.Z., and Johnson S.W. Dopamine depletion alters responses to glutamate and GABA in the rat subthalamic nucleus. Neuroreport 16 (2005) 171-174
52. Shink E., Bevan M.D., Bolam J.P., and Smith Y. The subthalamic nucleus and the external pallidum: two tightly interconnected structures that control the output of the basal ganglia in the monkey. Neuroscience 73 (1996) 335-357
53. Slaght S.J., Paz T., Chavez M., Deniau J.M., Mahon S., and Charpier S. On the activity of the corticostriatal networks during spike-and-wave discharges in a genetic model of absence epilepsy. J. Neurosci. 24 (2004) 6816-6825
54. Smith Y., Bolam J.P., and Von Krosigk M. Topographical and synaptic organization of the GABA-containing pallidosubthalamic projection in the rat. Eur. J. Neurosci. 2 (1990) 500-511
55. Smith Y., and Parent A. Neurons of the subthalamic nucleus in primates display glutamate but not GABA immunoreactivity. Brain Res. 453 (1988) 353-356
56. Song W.J., Baba Y., Otsuka T., and Murakami F. Characterization of Ca(2+) channels in rat subthalamic nucleus neurons. J. Neurophysiol. 84 (2000) 2630-2637
57. Terman D., Rubin J.E., Yew A.C., and Wilson C.J. Activity patterns in a model for the subthalamopallidal network of the basal ganglia. J. Neurosci. 22 (2002) 2963-2976
58. Tseng K.Y., Kasanetz F., Kargieman L., Riquelme L.A., and Murer M.G. Cortical slow oscillatory activity is reflected in the membrane potential and spike trains of striatal neurons in rats with chronic nigrostriatal lesions. J. Neurosci. 21 (2001) 6430-6439
59. Urbain N., Gervasoni D., Souliere F., Lobo L., Rentero N., Windels F., Astier B., Savasta M., Fort P., Renaud B., Luppi P.H., and Chouvet G. Unrelated course of subthalamic nucleus and globus pallidus neuronal activities across vigilance states in the rat. Eur. J. Neurosci. 12 (2000) 3361-3374
60. Urbain N., Rentero N., Gervasoni D., Renaud B., and Chouvet G. The switch of subthalamic neurons from an irregular to a bursting pattern does not solely depend on their GABAergic inputs in the anesthetic-free rat. J. Neurosci. 22 (2002) 8665-8675
61. Wichmann T., Bergman H., and DeLong M.R. The primate subthalamic nucleus. I. Functional properties in intact animals. J. Neurophysiol. 72 (1994) 494-506
62. Wisden W., Laurie D.J., Monyer H., and Seeburg P.H. Distribution of 13 GABAA receptor subunit mRNAs in the brain. I. Telencephalon, diencephalon, mesencephalon. J. Neurosci. 12 (1992) 1040-1062
63. Zhu Z., Bartol M., Shen K., and Johnson S.W. Excitatory effects of dopamine on subthalamic nucleus neurons: in vitro study of rats pretreated with 6-hydroxydopamine and levodopa. Brain Res. 945 (2002) 31-40
64. Zhu Z.T., Shen K.Z., and Johnson S.W. Pharmacological identification of inward current evoked by dopamine in rat subthalamic neurons in vitro. Neuropharmacology 42 (2002) 772-781