R. L. Albin, A. B. Young, and J. B. Penny, The functional anatomy of basal ganglia disorders, Trends Neurosci, vol.12, pp.366-375, 1989.

A. M. Graybiel, Neurotransmitters and neuromodulators in the basal ganglia, Trends Neurosci, vol.13, pp.244-254, 1990.

C. R. Gerfen, T. M. Engber, and L. C. Mahan, D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons, Science, vol.250, pp.1429-1432, 1990.

M. R. Delong, Primate models of movement disorders of basal ganglia origin, Trends Neurosci, vol.13, pp.281-285, 1990.

Y. Kawaguchi, C. J. Wilson, and P. C. Emson, Projection subtypes of rat neostriatal matrix cells revealed by intracellular injection of biocytin, J Neurosci, vol.10, pp.3421-3438, 1990.

Y. Wu, S. Richard, and A. Parent, The organization of the striatal output system: a single-cell juxtacellular labeling study in the rat, Neurosci Res, vol.38, pp.49-62, 2000.

F. Fujiyama, J. Sohn, and T. Nakano, Exclusive and common targets of neostriatofugal projections of rat striosome neurons: a single neuron-tracing study using a viral vector, Eur J Neurosci, vol.33, pp.668-677, 2011.

M. Levesque and A. Parent, The striatofugal fiber system in primates: a reevaluation of its organization based on single-axon tracing studies, Proc Natl Acad Sci USA, vol.102, pp.11888-11893, 2005.

A. Nadjar, J. M. Brotchie, and C. Guigoni, Phenotype of striatofugal medium spiny neurons in parkinsonian and dyskinetic nonhuman primates: a call for a reappraisal of the functional organization of the basal ganglia, J Neurosci, vol.26, pp.8653-8661, 2006.

A. Parent, A. Charara, and D. Pinault, Single striatofugal axons arborizing in both pallidal segments and in the substantia nigra in primates, Brain Res, vol.698, pp.280-284, 1995.

G. Cui, S. B. Jun, and X. Jin, Concurrent activation of striatal direct and indirect pathways during action initiation, Nature, vol.494, pp.238-242, 2013.

M. Cazorla, F. D. De-carvalho, and M. O. Chohan, Dopamine D2 receptors regulate the anatomical and functional balance of basal ganglia circuitry, Neuron, vol.81, pp.153-164, 2014.
URL : https://hal.archives-ouvertes.fr/inserm-02438087

A. V. Kravitz, B. S. Freeze, and P. R. Parker, Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry, Nature, vol.466, pp.622-626, 2010.

E. Valjent, J. Bertran-gonzalez, D. Herve, G. Fisone, and J. A. Girault, Looking BAC at striatal signaling: cell-specific analysis in new transgenic mice, Trends Neurosci, vol.32, pp.538-547, 2009.

C. R. Gerfen and D. J. Surmeier, Modulation of striatal projection systems by dopamine, Annu Rev Neurosci, vol.34, pp.441-466, 2011.

N. Mallet, B. R. Micklem, and P. Henny, Dichotomous organization of the external globus pallidus, Neuron, vol.74, pp.1075-1086, 2012.

A. H. Gittis, J. D. Berke, and M. D. Bevan, New roles for the external globus pallidus in basal ganglia circuits and behavior, J Neurosci, vol.34, pp.15178-15183, 2014.

K. J. Mastro, R. S. Bouchard, H. A. Holt, and A. H. Gittis, Transgenic mouse lines subdivide external segment of the globus pallidus (GPe) neurons and reveal distinct GPe output pathways, J Neurosci, vol.34, pp.2087-2099, 2014.

M. D. Bevan, P. A. Booth, S. A. Eaton, and J. P. Bolam, Selective innervation of neostriatal interneurons by a subclass of neuron in the globus pallidus of the rat, J Neurosci, vol.18, pp.9438-9452, 1998.

N. Chuhma, K. F. Tanaka, R. Hen, and S. Rayport, Functional connectome of the striatal medium spiny neuron, J Neurosci, vol.31, pp.1183-1192, 2011.

R. R. Lalchandani, M. S. Van-der-goes, J. G. Partridge, and S. Vicini, Dopamine D2 receptors regulate collateral inhibition between striatal medium spiny neurons, J Neurosci, vol.33, pp.14075-14086, 2013.

O. Hikosaka, Y. Takikawa, and R. Kawagoe, Role of the basal ganglia in the control of purposive saccadic eye movements, Physiol Rev, vol.80, pp.953-978, 2000.

J. W. Mink, The Basal Ganglia and involuntary movements: impaired inhibition of competing motor patterns, Arch Neurol, vol.60, pp.1365-1368, 2003.

A. Nambu, Seven problems on the basal ganglia, Curr Opin Neurobiol, vol.18, pp.595-604, 2008.

P. F. Durieux, B. Bearzatto, and S. Guiducci, D2R striatopallidal neurons inhibit both locomotor and drug reward processes, Nat Neurosci, vol.12, pp.393-395, 2009.

T. Hikida, K. Kimura, N. Wada, K. Funabiki, and S. Nakanishi, Distinct roles of synaptic transmission in direct and indirect striatal pathways to reward and aversive behavior, Neuron, vol.66, pp.896-907, 2010.

A. V. Kravitz, L. D. Tye, and A. C. Kreitzer, Distinct roles for direct and indirect pathway striatal neurons in reinforcement, Nat Neurosci, vol.15, pp.816-818, 2012.

M. K. Lobo, . Covington-he-3rd, and D. Chaudhury, Cell type-specific loss of BDNF signaling mimics optogenetic control of cocaine reward, Science, vol.330, pp.385-390, 2010.

L. H. Tai, A. M. Lee, N. Benavidez, A. Bonci, and L. Wilbrecht, Transient stimulation of distinct subpopulations of striatal neurons mimics changes in action value, Nat Neurosci, vol.15, pp.1281-1289, 2012.

T. V. Maia and M. J. Frank, From reinforcement learning models to psychiatric and neurological disorders, Nat Neurosci, vol.14, pp.154-162, 2011.

B. S. Freeze, A. V. Kravitz, N. Hammack, J. D. Berke, and A. C. Kreitzer, Control of basal ganglia output by direct and indirect pathway projection neurons, J Neurosci, vol.33, pp.18531-18539, 2013.

S. M. Catalano and C. J. Shatz, Activity-dependent cortical target selection by thalamic axons, Science, vol.281, pp.559-562, 1998.

N. V. De-marco-garcia, T. Karayannis, and G. Fishell, Neuronal activity is required for the development of specific cortical interneuron subtypes, Nature, vol.472, pp.351-355, 2011.

J. Y. Hua, M. C. Smear, H. Baier, and S. J. Smith, Regulation of axon growth in vivo by activity-based competition, Nature, vol.434, pp.1022-1026, 2005.

M. Cazorla, M. Shegda, R. B. Harrison, N. L. Kellendonk, and C. , Striatal D2 receptors regulate dendritic morphology of medium spiny neurons via Kir2 channels, J Neurosci, vol.32, pp.2398-2409, 2012.
URL : https://hal.archives-ouvertes.fr/inserm-02472212

C. J. Wilson and Y. Kawaguchi, The origins of two-state spontaneous membrane potential fluctuations of neostriatal spiny neurons, J Neurosci, vol.16, pp.2397-2410, 1996.

T. H. Mcneill, S. A. Brown, J. A. Rafols, and I. Shoulson, Atrophy of medium spiny I striatal dendrites in advanced Parkinson's disease, Brain Res, vol.455, pp.148-152, 1988.

K. Y. Tseng, F. Kasanetz, L. Kargieman, L. A. Riquelme, and M. G. Murer, Cortical slow oscillatory activity is reflected in the membrane potential and spike trains of striatal neurons in rats with chronic nigrostriatal lesions, J Neurosci, vol.21, pp.6430-6439, 2001.

S. Zaja-milatovic, D. Milatovic, and A. M. Schantz, Dendritic degeneration in neostriatal medium spiny neurons in Parkinson disease, Neurology, vol.64, pp.545-547, 2005.

W. Shen, X. Tian, and M. Day, Cholinergic modulation of Kir2 channels selectively elevates dendritic excitability in striatopallidal neurons, Nat Neurosci, vol.10, pp.1458-1466, 2007.

K. Azdad, M. Chavez, D. Bischop, and P. , Homeostatic plasticity of striatal neurons intrinsic excitability following dopamine depletion, PLoS One, vol.4, p.6908, 2009.

M. Day, Z. Wang, and J. Ding, Selective elimination of glutamatergic synapses on striatopallidal neurons in Parkinson disease models, Nat Neurosci, vol.9, pp.251-259, 2006.

T. Fieblinger, S. M. Graves, and L. E. Sebel, Cell type-specific plasticity of striatal projection neurons in parkinsonism and L-DOPA-induced dyskinesia, Nat Commun, vol.5, p.5316, 2014.

E. Fino, J. Glowinski, and L. Venance, Effects of acute dopamine depletion on the electrophysiological properties of striatal neurons, Neurosci Res, vol.58, pp.305-316, 2007.

M. D. Bevan, P. J. Magill, D. Terman, J. P. Bolam, and C. J. Wilson, Move to the rhythm: oscillations in the subthalamic nucleus-external globus pallidus network, Trends Neurosci, vol.25, pp.525-531, 2002.

H. Bergman, T. Wichmann, B. Karmon, and M. R. Delong, The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism, J Neurophysiol, vol.72, pp.507-520, 1994.

J. Best, C. Park, D. Terman, and C. Wilson, Transitions between irregular and rhythmic firing patterns in excitatory-inhibitory neuronal networks, J Comput Neurosci, vol.23, pp.217-235, 2007.

C. Dejean, G. Arbuthnott, J. R. Wickens, L. Moine, C. Boraud et al., Power fluctuations in beta and gamma frequencies in rat globus pallidus:association with specific phases of slow oscillations and differential modulation by dopamine D1 and D2 receptors, J Neurosci, vol.31, pp.6098-6107, 2011.
URL : https://hal.archives-ouvertes.fr/hal-01160418

O. D. Howes, J. Kambeitz, and E. Kim, The nature of dopamine dysfunction in schizophrenia and what this means for treatment, Arch Gen Psychiatry, vol.69, pp.776-786, 2012.

A. Abi-dargham, J. Rodenhiser, and D. Printz, Increased baseline occupancy of D2 receptors by dopamine in schizophrenia, Proc Natl Acad Sci USA, vol.97, pp.8104-8109, 2000.

A. Meyer-lindenberg, R. S. Miletich, and P. D. Kohn, Reduced pre-frontal activity predicts exaggerated striatal dopaminergic function in schizophrenia, Nat Neurosci, vol.5, pp.267-271, 2002.

A. Abi-dargham, E. Van-de-giessen, M. Slifstein, L. S. Kegeles, and M. Laruelle, Baseline and amphetamine-stimulated dopamine activity are related in drug-naive schizophrenic subjects, Biol Psychiatry, vol.65, pp.1091-1093, 2009.

Y. Kumakura, P. Cumming, and I. Vernaleken, Elevated [18F]fluorodopamine turnover in brain of patients with schizophrenia:an [18F]fluorodopa/positron emission tomography study, J Neurosci, vol.27, pp.8080-8087, 2007.

O. D. Howes, A. J. Montgomery, and M. C. Asselin, Elevated striatal dopamine function linked to prodromal signs of schizophrenia, Arch Gen Psychiatry, vol.66, pp.13-20, 2009.

M. Sherwood, A. E. Thornton, and W. G. Honer, A meta-analysis of profile and time-course of symptom change in acute schizophrenia treated with atypical antipsychotics, Int J Neuropsychopharmacol, vol.9, pp.357-366, 2006.

R. G. , Tardive dyskinesia:eliminated, forgotten, or overshadowed?, Curr Opin Psychiatry, vol.20, pp.131-137, 2007.