The Interactions of Temporal and Sensory Representations in the Basal Ganglia.


Journal

Advances in experimental medicine and biology
ISSN: 0065-2598
Titre abrégé: Adv Exp Med Biol
Pays: United States
ID NLM: 0121103

Informations de publication

Date de publication:
2024
Historique:
medline: 26 6 2024
pubmed: 26 6 2024
entrez: 25 6 2024
Statut: ppublish

Résumé

In rodents and primates, interval estimation has been associated with a complex network of cortical and subcortical structures where the dorsal striatum plays a paramount role. Diverse evidence ranging from individual neurons to population activity has demonstrated that this area hosts temporal-related neural representations that may be instrumental for the perception and production of time intervals. However, little is known about how temporal representations interact with other well-known striatal representations, such as kinematic parameters of movements or somatosensory representations. An attractive hypothesis suggests that somatosensory representations may serve as the scaffold for complex representations such as elapsed time. Alternatively, these representations may coexist as independent streams of information that could be integrated into downstream nuclei, such as the substantia nigra or the globus pallidus. In this review, we will revise the available information suggesting an instrumental role of sensory representations in the construction of temporal representations at population and single-neuron levels throughout the basal ganglia.

Identifiants

pubmed: 38918350
doi: 10.1007/978-3-031-60183-5_8
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

141-158

Informations de copyright

© 2024. The Author(s), under exclusive license to Springer Nature Switzerland AG.

Références

Albin, R. L., Young, A. B., & Penney, J. B. (1989). The functional anatomy of basal ganglia disorders. Trends in Neurosciences, 12, 366–375. Available at: https://linkinghub.elsevier.com/retrieve/pii/016622368990074X
pubmed: 2479133 doi: 10.1016/0166-2236(89)90074-X
Alexander, G. E., & DeLong, M. R. (1985). Microstimulation of the primate neostriatum. II. Somatotopic organization of striatal microexcitable zones and their relation to neuronal response properties. Journal of Neurophysiology, 53, 1417–1430. Available at: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=4009227
pubmed: 4009227 doi: 10.1152/jn.1985.53.6.1417
Alexander, G. E., DeLong, M. R., & Delong, R. (1985). Microstimulation of the primate neostriatum. I. Physiological properties of striatal microexcitable zones. Journal of Neurophysiology, 53, 1401–1416. Available at: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=4009226
pubmed: 4009226 doi: 10.1152/jn.1985.53.6.1401
Alloway, K. D., Smith, J. B., Beauchemin, K. J., & Olson, M. L. (2009). Bilateral projections from rat MI whisker cortex to the neostriatum, thalamus, and claustrum: Forebrain circuits for modulating whisking behavior. The Journal of Comparative Neurology, 515, 548–564. Available at: https://onlinelibrary.wiley.com/doi/10.1002/cne.22073
pubmed: 19479997 pmcid: 2696578 doi: 10.1002/cne.22073
Báez-Cordero, A. S., Pimentel-Farfan, A. K., Peña-Rangel, T., & Rueda-Orozco, P. E. (2020). Unbalanced inhibitory/excitatory responses in the substantia Nigra Pars Reticulata underlie cannabinoid-related slowness of movements. The Journal of Neuroscience, 40, 5769–5784. Available at: http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.0045-20.2020
pubmed: 32532888 pmcid: 7380975 doi: 10.1523/JNEUROSCI.0045-20.2020
Bakhurin, K. I., Goudar, V., Shobe, J. L., Claar, L. D., Buonomano, D. V., & Masmanidis, S. C. (2017). Differential encoding of time by prefrontal and striatal network dynamics. The Journal of Neuroscience, 37, 854–870. Available at: http://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.1789-16.2017
pubmed: 28123021 pmcid: 5296780 doi: 10.1523/JNEUROSCI.1789-16.2016
Bakhurin, K. I., Li, X., Friedman, A. D., Lusk, N. A., Watson, G. D. R., Kim, N., & Yin, H. H. (2020). Opponent regulation of action performance and timing by striatonigral and striatopallidal pathways. eLife, 9, 1–25. Available at: https://elifesciences.org/articles/54831
doi: 10.7554/eLife.54831
Barbera, G., Liang, B., Zhang, L., Gerfen, C. R., Culurciello, E., Chen, R., Li, Y., & Lin, D. T. (2016). Spatially compact neural clusters in the dorsal striatum encode locomotion relevant information. Neuron, 92, 202–213. Available at: https://doi.org/10.1016/j.neuron.2016.08.037
pubmed: 27667003 pmcid: 5087607 doi: 10.1016/j.neuron.2016.08.037
Beudel, M., de Geus, C. M., Leenders, K. L., & de Jong, B. M. (2013). Acceleration bias in visually perceived velocity change and effects of Parkinson’s bradykinesia. Neuroreport, 24, 773–778. Available at: https://journals.lww.com/00001756-201310020-00003
pubmed: 23979256 doi: 10.1097/WNR.0b013e328363f739
Bevan, M. (2002). Move to the rhythm: Oscillations in the subthalamic nucleus–external globus pallidus network. Trends in Neurosciences, 25, 525–531. Available at: https://linkinghub.elsevier.com/retrieve/pii/S016622360202235X
pubmed: 12220881 doi: 10.1016/S0166-2236(02)02235-X
Brown, J., Pan, W.-X., & Dudman, J. T. (2014). The inhibitory microcircuit of the substantia nigra provides feedback gain control of the basal ganglia output. eLife, 3, 1–25.
doi: 10.7554/eLife.02397
Buhusi, C. V., & Meck, W. H. (2005). What makes us tick? Functional and neural mechanisms of interval timing. Nature Reviews. Neuroscience, 6, 755–765. Available at: http://www.nature.com/articles/nrn1764
pubmed: 16163383 doi: 10.1038/nrn1764
Buonomano, D. V., & Laje, R. (2010). Population clocks: Motor timing with neural dynamics. Trends in Cognitive Sciences, 14, 520–527. Available at: https://doi.org/10.1016/j.tics.2010.09.002
pubmed: 20889368 pmcid: 2991437 doi: 10.1016/j.tics.2010.09.002
Cadena-Valencia, J., García-Garibay, O., Merchant, H., Jazayeri, M., & de Lafuente, V. (2018). Entrainment and maintenance of an internal metronome in supplementary motor area. eLife, 7, 1–23. Available at: https://elifesciences.org/articles/38983
doi: 10.7554/eLife.38983
Carelli, R. M., & West, M. O. (1991). Representation of the body by single neurons in the dorsolateral striatum of the awake, unrestrained rat. The Journal of Comparative Neurology, 309, 231–249.
pubmed: 1885787 doi: 10.1002/cne.903090205
Carpenter, M. B., Nakano, K., & Kim, R. (1976). Nigrothalamic projections in the monkey demonstrated by autoradiographic technics. The Journal of Comparative Neurology, 165, 401–415. Available at: https://onlinelibrary.wiley.com/doi/10.1002/cne.901650402
pubmed: 57125 doi: 10.1002/cne.901650402
Carrillo-Reid, L., Tecuapetla, F., Tapia, D., Hernandez-Cruz, A., Galarraga, E., Drucker-Colin, R., & Bargas, J. (2008). Encoding network states by striatal cell assemblies. Journal of Neurophysiology, 99, 1435–1450. Available at: http://jn.physiology.org/cgi/doi/10.1152/jn.01131.2007
pubmed: 18184883 doi: 10.1152/jn.01131.2007
Carrillo-Reid, L., Kang Miller, J., Hamm, J. P., Jackson, J., & Yuste, R. (2015a). Endogenous sequential cortical activity evoked by visual stimuli. The Journal of Neuroscience, 35, 8813–8828. Available at: http://www.jneurosci.org/cgi/doi/10.1523/JNEUROSCI.5214-14.2015
pubmed: 26063915 pmcid: 4461687 doi: 10.1523/JNEUROSCI.5214-14.2015
Carrillo-Reid, L., Lopez-Huerta, V. G., Garcia-Munoz, M., Theiss, S., & Arbuthnott, G. W. (2015b). Cell assembly signatures defined by short-term synaptic plasticity in cortical networks. International Journal of Neural Systems, 25, 1550026. Available at: https://www.worldscientific.com/doi/abs/10.1142/S0129065715500264
pubmed: 26173906 doi: 10.1142/S0129065715500264
Catanese, J., & Jaeger, D. (2021). Premotor ramping of thalamic neuronal activity is modulated by nigral inputs and contributes to control the timing of action release. The Journal of Neuroscience, 41, 1878–1891. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.1204-20.2020
pubmed: 33446518 pmcid: 7939094 doi: 10.1523/JNEUROSCI.1204-20.2020
Chapin, J. K., Waterhouse, B. D., & Woodward, D. J. (1981). Differences in cutaneous sensory response properties of single somatosensory cortical neurons in awake and halothane anesthetized rats. Brain Research Bulletin, 6, 63–70. Available at: https://linkinghub.elsevier.com/retrieve/pii/S036192308180069X
pubmed: 6258757 doi: 10.1016/S0361-9230(81)80069-X
Chen, Z., Zhang, Z.-Y., Zhang, W., Xie, T., Li, Y., Xu, X.-H., & Yao, H. (2021). Direct and indirect pathway neurons in ventrolateral striatum differentially regulate licking movement and nigral responses. Cell Reports, 37, 109847. Available at: https://doi.org/10.1016/j.celrep.2021.109847
pubmed: 34686331 doi: 10.1016/j.celrep.2021.109847
Cheung, T. H. C., Bezzina, G., Hampson, C. L., Body, S., Fone, K. C. F., Bradshaw, C. M., & Szabadi, E. (2007). Effect of quinpirole on timing behaviour in the free-operant psychophysical procedure: Evidence for the involvement of D2 dopamine receptors. Psychopharmacology, 193, 423–436. Available at: https://link.springer.com/10.1007/s00213-007-0798-8
pubmed: 17484066 doi: 10.1007/s00213-007-0798-8
Chiba, A., Oshio, K., & Inase, M. (2015). Neuronal representation of duration discrimination in the monkey striatum. Physiological Reports, 3, e12283. Available at: https://doi.wiley.com/10.14814/phy2.12283
pubmed: 25677545 pmcid: 4393192 doi: 10.14814/phy2.12283
Chuhma, N., Tanaka, K. F., Hen, R., & Rayport, S. (2011). Functional connectome of the striatal medium spiny neuron. The Journal of Neuroscience, 31, 1183–1192. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.3833-10.2011
pubmed: 21273403 pmcid: 3074638 doi: 10.1523/JNEUROSCI.3833-10.2011
Coffey, K. R., Nader, M., & West, M. O. (2016). Single body parts are processed by individual neurons in the mouse dorsolateral striatum. Brain Research, 1636, 200–207. Available at: https://doi.org/10.1016/j.brainres.2016.01.031
pubmed: 26827625 pmcid: 4808626 doi: 10.1016/j.brainres.2016.01.031
Coffey, K. R., Nader, M., Bawa, J., & West, M. O. (2017). Homogeneous processing in the striatal direct and indirect pathways: Single body part sensitive type IIb neurons may express either dopamine receptor D1 or D2. The European Journal of Neuroscience, 46, 2380–2391.
pubmed: 28887882 pmcid: 9004798 doi: 10.1111/ejn.13690
Cook, J. R., Li, H., Nguyen, B., Huang, H., Mahdavian, P., Kirchgessner, M. A., Strassmann, P., Engelhardt, M., Callaway, E. M., & Jin, X. (2022). Secondary auditory cortex mediates a sensorimotor mechanism for action timing. Nature Neuroscience, 25, 330–344. Available at: https://www.nature.com/articles/s41593-022-01025-5
pubmed: 35260862 pmcid: 9288832 doi: 10.1038/s41593-022-01025-5
Coslett, H. B., Wiener, M., & Chatterjee, A. (2010). Dissociable neural systems for timing: Evidence from subjects with basal ganglia lesions Tell F, ed. PLoS One, 5, e10324. Available at: https://dx.plos.org/10.1371/journal.pone.0010324
pubmed: 20428244 pmcid: 2859062 doi: 10.1371/journal.pone.0010324
Cruz, B. F., Guiomar, G., Soares, S., Motiwala, A., Machens, C. K., & Paton, J. J. (2022). Action suppression reveals opponent parallel control via striatal circuits. Nature, 607, 521–526. Available at: https://www.nature.com/articles/s41586-022-04894-9
pubmed: 35794480 doi: 10.1038/s41586-022-04894-9
Cury, K. M., & Uchida, N. (2010). Robust odor coding via inhalation-coupled transient activity in the mammalian olfactory bulb. Neuron, 68, 570–585. Available at: https://doi.org/10.1016/j.neuron.2010.09.040
pubmed: 21040855 doi: 10.1016/j.neuron.2010.09.040
De Corte, B. J., Wagner, L. M., Matell, M. S., & Narayanan, N. S. (2019). Striatal dopamine and the temporal control of behavior. Behavioural Brain Research, 356, 375–379. Available at: https://doi.org/10.1016/j.bbr.2018.08.030
pubmed: 30213664 doi: 10.1016/j.bbr.2018.08.030
DeLong, M. R. (1971). Of pallidal during movement. The Journal of Physiology, 34, 414–427.
Deschênes, M., Takatoh, J., Kurnikova, A., Moore, J. D., Demers, M., Elbaz, M., Furuta, T., Wang, F., & Kleinfeld, D. (2016). Inhibition, not excitation, drives rhythmic whisking. Neuron, 90, 374–387. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0896627316001860
pubmed: 27041498 pmcid: 4929009 doi: 10.1016/j.neuron.2016.03.007
Díaz-Hernández, E., Contreras-López, R., Sánchez-Fuentes, A., Rodríguez-Sibrían, L., Ramírez-Jarquín, J. O., & Tecuapetla, F. (2018). The thalamostriatal projections contribute to the initiation and execution of a sequence of movements. Neuron, 100, 739–752.e5. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0896627318308547
pubmed: 30344045 doi: 10.1016/j.neuron.2018.09.052
Dray, A., Gonye, T. J., & Oakley, N. R. (1976). Caudate stimulation and substantia nigra activity in the rat. The Journal of Physiology, 259, 825–849. Available at: http://doi.wiley.com/10.1113/jphysiol.1976.sp011497
pubmed: 8637 pmcid: 1309066 doi: 10.1113/jphysiol.1976.sp011497
Drew, M. R., Fairhurst, S., Malapani, C., Horvitz, J. C., & Balsam, P. D. (2003). Effects of dopamine antagonists on the timing of two intervals. Pharmacology, Biochemistry, and Behavior, 75, 9–15. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0091305703000364
pubmed: 12759108 doi: 10.1016/S0091-3057(03)00036-4
Dudman, J. T., & Krakauer, J. W. (2016). The basal ganglia: From motor commands to the control of vigor. Current Opinion in Neurobiology, 37, 158–166. Available at: https://doi.org/10.1016/j.conb.2016.02.005
pubmed: 27012960 doi: 10.1016/j.conb.2016.02.005
Erro, M. E., Lanciego, J. L., Arribas, J., & Gimenez-Amaya, J. M. (2001). Striatal input from the ventrobasal complex of the rat thalamus. Histochemistry and Cell Biology, 115, 447–454.
pubmed: 11455444 doi: 10.1007/s004180100273
Erro, M. E., Lanciego, J. L., & Giménez-Amaya, J. M. (2002). Re-examination of the thalamostriatal projections in the rat with retrograde tracers. Neuroscience Research, 42, 45–55. Available at: http://linkinghub.elsevier.com/retrieve/pii/S0168010201003029
doi: 10.1016/S0168-0102(01)00302-9
Frederick, D. (1996). Effects of selective dopamine D1- and D2-agonists and antagonists on timing performance in rats. Pharmacology, Biochemistry, and Behavior, 53, 759–764. Available at: https://linkinghub.elsevier.com/retrieve/pii/0091305795021035
pubmed: 8801575 doi: 10.1016/0091-3057(95)02103-5
Gaidica, M., Hurst, A., Cyr, C., & Leventhal, D. K. (2018). Distinct populations of motor thalamic neurons encode action initiation, action selection, and movement vigor. The Journal of Neuroscience, 38, 6563–6573. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.0463-18.2018
pubmed: 29934350 pmcid: 6052244 doi: 10.1523/JNEUROSCI.0463-18.2018
Gámez, J., Mendoza, G., Prado, L., Betancourt, A., & Merchant, H. (2019). The amplitude in periodic neural state trajectories underlies the tempo of rhythmic tapping Zatorre R, ed. PLoS Biology, 17, e3000054. Available at: https://dx.plos.org/10.1371/journal.pbio.3000054
pubmed: 30958818 pmcid: 6472824 doi: 10.1371/journal.pbio.3000054
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990). D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. Science (80- ), 250, 1429–1432. Available at: https://www.science.org/doi/10.1126/science.2147780
doi: 10.1126/science.2147780
Goel, A., & Buonomano, D. V. (2014). Timing as an intrinsic property of neural networks: Evidence from in vivo and in vitro experiments. Philosophical Transactions of the Royal Society, B: Biological Sciences, 369, 20120460. Available at: https://royalsocietypublishing.org/doi/10.1098/rstb.2012.0460
pmcid: 3895985 doi: 10.1098/rstb.2012.0460
Goel, A., & Buonomano, D. V. (2016). Temporal interval learning in cortical cultures is encoded in intrinsic network dynamics. Neuron, 91, 320–327. Available at: https://doi.org/10.1016/j.neuron.2016.05.042
pubmed: 27346530 pmcid: 4969202 doi: 10.1016/j.neuron.2016.05.042
Gouvêa, T. S., Monteiro, T., Motiwala, A., Soares, S., Machens, C., & Paton, J. J. (2015). Striatal dynamics explain duration judgments. eLife, 4, 1–14. Available at: https://elifesciences.org/articles/11386
doi: 10.7554/eLife.11386
Graybiel, A. M. (2008). Habits, rituals, and the evaluative brain. Annual Review of Neuroscience, 31, 359–387. Available at: http://www.annualreviews.org/doi/10.1146/annurev.neuro.29.051605.112851
pubmed: 18558860 doi: 10.1146/annurev.neuro.29.051605.112851
Guo, Z. V., Inagaki, H. K., Daie, K., Druckmann, S., Gerfen, C. R., & Svoboda, K. (2017). Maintenance of persistent activity in a frontal thalamocortical loop. Nature, 545, 181–186. Available at: http://www.nature.com/articles/nature22324
pubmed: 28467817 pmcid: 6431254 doi: 10.1038/nature22324
Hegeman, D. J., Hong, E. S., Hernández, V. M., & Chan, C. S. (2016). The external globus pallidus: Progress and perspectives Bolam P, ed. The European Journal of Neuroscience, 43, 1239–1265. Available at: https://onlinelibrary.wiley.com/doi/10.1111/ejn.13196
pubmed: 26841063 pmcid: 4874844 doi: 10.1111/ejn.13196
Henke, J., Bunk, D., von Werder, D., Häusler, S., Flanagin, V. L., & Thurley, K. (2021). Distributed coding of duration in rodent prefrontal cortex during time reproduction. eLife, 10, 1–24. Available at: https://elifesciences.org/articles/71612
doi: 10.7554/eLife.71612
Hidalgo-Balbuena, A. E., Luma, A. Y., Pimentel-Farfan, A. K., Peña-Rangel, T., & Rueda-Orozco, P. E. (2019). Sensory representations in the striatum provide a temporal reference for learning and executing motor habits. Nature Communications, 10, 4074. Available at: https://doi.org/10.1038/s41467-019-12075-y
pubmed: 31501436 pmcid: 6733846 doi: 10.1038/s41467-019-12075-y
Hikosaka, O. (2007). GABAergic output of the basal ganglia. Progress in Brain Research, 209–226. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0079612306600125
Hikosaka, O., & Wurtz, R. H. (1983). Visual and oculomotor functions of monkey substantia nigra pars reticulata. III. Memory-contingent visual and saccade responses. Journal of Neurophysiology, 49, 1268–1284. Available at: http://www.physiology.org/doi/10.1152/jn.1983.49.5.1268
pubmed: 6864250 doi: 10.1152/jn.1983.49.5.1268
Hintiryan, H., Foster, N. N., Bowman, I., Bay, M., Song, M. Y., Gou, L., Yamashita, S., Bienkowski, M. S., Zingg, B., Zhu, M., Yang, X. W., Shih, J. C., Toga, A. W., & Dong, H. W. (2016). The mouse cortico-striatal projectome. Nature Neuroscience, 19, 1100–1114.
pubmed: 27322419 pmcid: 5564682 doi: 10.1038/nn.4332
Honma, M., Kuroda, T., Futamura, A., Shiromaru, A., & Kawamura, M. (2016). Dysfunctional counting of mental time in Parkinson’s disease. Scientific Reports, 6, 25421. Available at: http://www.nature.com/articles/srep25421
pubmed: 27146904 pmcid: 4857080 doi: 10.1038/srep25421
Honma, M., Masaoka, Y., Koyama, S., Kuroda, T., Futamura, A., Shiromaru, A., Terao, Y., Ono, K., & Kawamura, M. (2018). Impaired cognitive modification for estimating time duration in Parkinson’s disease Ginsberg SD, ed. PLoS One, 13, e0208956. Available at: https://dx.plos.org/10.1371/journal.pone.0208956
pubmed: 30543694 pmcid: 6292599 doi: 10.1371/journal.pone.0208956
Hoover, J. E., Hoffer, Z. S., & Alloway, K. D. (2003). Projections from primary somatosensory cortex to the neostriatum: The role of somatotopic continuity in corticostriatal convergence. Journal of Neurophysiology, 89, 1576–1587. Available at: http://jn.physiology.org/cgi/doi/10.1152/jn.01009.2002
pubmed: 12611938 doi: 10.1152/jn.01009.2002
Inagaki, H. K., Chen, S., Ridder, M. C., Sah, P., Li, N., Yang, Z., Hasanbegovic, H., Gao, Z., Gerfen, C. R., & Svoboda, K. (2022). A midbrain-thalamus-cortex circuit reorganizes cortical dynamics to initiate movement. Cell, 185, 1065–1081.e23. Available at: https://doi.org/10.1016/j.cell.2022.02.006
pubmed: 35245431 pmcid: 8990337 doi: 10.1016/j.cell.2022.02.006
Iwamuro, H., Tachibana, Y., Ugawa, Y., Saito, N., & Nambu, A. (2017). Information processing from the motor cortices to the subthalamic nucleus and globus pallidus and their somatotopic organizations revealed electrophysiologically in monkeys. The European Journal of Neuroscience, 46, 2684–2701. Available at: https://onlinelibrary.wiley.com/doi/10.1111/ejn.13738
pubmed: 29044874 pmcid: 5725726 doi: 10.1111/ejn.13738
Jaeger, D., & Kita, H. (2011). Functional connectivity and integrative properties of globus pallidus neurons. Neuroscience, 198, 44–53. Available at: https://doi.org/10.1016/j.neuroscience.2011.07.050
pubmed: 21835227 doi: 10.1016/j.neuroscience.2011.07.050
Jin, D. Z., Fujii, N., & Graybiel, A. M. (2009). Neural representation of time in cortico-basal ganglia circuits. Proceedings of the National Academy of Sciences, 106, 19156–19161. Available at: https://pnas.org/doi/full/10.1073/pnas.0909881106
doi: 10.1073/pnas.0909881106
Johansson, Y., & Silberberg, G. (2020). The functional organization of cortical and thalamic inputs onto five types of striatal neurons is determined by source and target cell identities. Cell Reports, 30, 1178–1194.e3. Available at: https://doi.org/10.1016/j.celrep.2019.12.095
pubmed: 31995757 doi: 10.1016/j.celrep.2019.12.095
Junek, S., Kludt, E., Wolf, F., & Schild, D. (2010). Olfactory coding with patterns of response latencies. Neuron, 67, 872–884. Available at: https://doi.org/10.1016/j.neuron.2010.08.005
pubmed: 20826317 doi: 10.1016/j.neuron.2010.08.005
Jurado-Parras, M.-T., Safaie, M., Sarno, S., Louis, J., Karoutchi, C., Berret, B., & Robbe, D. (2020). The dorsal striatum energizes motor routines. Current Biology, 30, 4362–4372.e6. Available at: https://doi.org/10.1016/j.cub.2020.08.049
pubmed: 32946750 doi: 10.1016/j.cub.2020.08.049
Kamada, T., & Hata, T. (2021). Striatal dopamine D1 receptors control motivation to respond, but not interval timing, during the timing task. Learning & Memory, 28, 24–29. Available at: http://learnmem.cshlp.org/lookup/doi/10.1101/lm.052266.120
doi: 10.1101/lm.052266.120
Karalis, N., & Sirota, A. (2022). Breathing coordinates cortico-hippocampal dynamics in mice during offline states. Nature Communications, 13, 467. Available at: https://www.nature.com/articles/s41467-022-28090-5
pubmed: 35075139 pmcid: 8786964 doi: 10.1038/s41467-022-28090-5
Ketzef, M., Spigolon, G., Johansson, Y., Bonito-Oliva, A., Fisone, G., & Silberberg, G. (2017). Dopamine depletion impairs bilateral sensory processing in the striatum in a pathway-dependent manner. Neuron, 94, 855–865.e5. Available at: https://doi.org/10.1016/j.neuron.2017.05.004
pubmed: 28521136 doi: 10.1016/j.neuron.2017.05.004
Kim, J., Ghim, J.-W., Lee, J. H., & Jung, M. W. (2013). Neural correlates of interval timing in rodent prefrontal cortex. The Journal of Neuroscience, 33, 13834–13847. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.1443-13.2013
pubmed: 23966703 pmcid: 6618661 doi: 10.1523/JNEUROSCI.1443-13.2013
Kita, H., & Jaeger, D. (2016). Organization of the globus pallidus. In Handbook of behavioral neuroscience (pp. 259–276). Available at: https://linkinghub.elsevier.com/retrieve/pii/B9780128022061000131
Kravitz, A. V., Freeze, B. S., Parker, P. R. L., Kay, K., Thwin, M. T., Deisseroth, K., & Kreitzer, A. C. (2010). Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry. Nature, 466, 622–626. Available at: http://www.nature.com/articles/nature09159
pubmed: 20613723 pmcid: 3552484 doi: 10.1038/nature09159
Kunimatsu, J., Suzuki, T. W., Ohmae, S., & Tanaka, M. (2018). Different contributions of preparatory activity in the basal ganglia and cerebellum for self-timing. eLife, 7, 1–19. Available at: https://elifesciences.org/articles/35676
doi: 10.7554/eLife.35676
Lee, C. R., Yonk, A. J., Wiskerke, J., Paradiso, K. G., Tepper, J. M., & Margolis, D. J. (2019). Opposing influence of sensory and motor cortical input on striatal circuitry and choice behavior. Current Biology, 29, 1313–1323.e5. Available at: https://doi.org/10.1016/j.cub.2019.03.028
pubmed: 30982651 doi: 10.1016/j.cub.2019.03.028
Luczak, A., Barthó, P., Marguet, S. L., Buzsáki, G., & Harris, K. D. (2007). Sequential structure of neocortical spontaneous activity in vivo. Proceedings of the National Academy of Sciences, 104, 347–352. Available at: https://pnas.org/doi/full/10.1073/pnas.0605643104
doi: 10.1073/pnas.0605643104
Luczak, A., Barthó, P., & Harris, K. D. (2009). Spontaneous events outline the realm of possible sensory responses in neocortical populations. Neuron, 62, 413–425. Available at: https://doi.org/10.1016/j.neuron.2009.03.014
pubmed: 19447096 pmcid: 2696272 doi: 10.1016/j.neuron.2009.03.014
Luczak, A., McNaughton, B. L., & Harris, K. D. (2015). Packet-based communication in the cortex. Nature Reviews. Neuroscience, 16, 745–755. Available at: https://doi.org/10.1038/nrn4026
pubmed: 26507295 doi: 10.1038/nrn4026
Matell, M. S., Meck, W. H., & Nicolelis, M. A. L. (2003). Interval timing and the encoding of signal duration by ensembles of cortical and striatal neurons. Behavioral Neuroscience, 117, 760–773. Available at: http://doi.apa.org/getdoi.cfm?doi=10.1037/0735-7044.117.4.760
pubmed: 12931961 doi: 10.1037/0735-7044.117.4.760
Matsuyama, K., & Tanaka, M. (2021). Temporal prediction signals for periodic sensory events in the primate central thalamus. The Journal of Neuroscience, 41, 1917–1927. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.2151-20.2021
pubmed: 33452224 pmcid: 7939086 doi: 10.1523/JNEUROSCI.2151-20.2021
Meck, W. H. (2006). Neuroanatomical localization of an internal clock: A functional link between mesolimbic, nigrostriatal, and mesocortical dopaminergic systems. Brain Research, 1109, 93–107. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0006899306017203
pubmed: 16890210 doi: 10.1016/j.brainres.2006.06.031
Mello, G. B. M., Soares, S., & Paton, J. J. (2015). A scalable population code for time in the striatum. Current Biology, 25, 1113–1122. Available at: https://doi.org/10.1016/j.cub.2015.02.036
pubmed: 25913405 doi: 10.1016/j.cub.2015.02.036
Merchant, H., Zarco, W., Bartolo, R., Perez, O., & Prado, L. (2011). Measuring time with different neural chronometers during a synchronization-continuation task. Proceedings of the National Academy of Sciences, 108, 19784–19789.
doi: 10.1073/pnas.1112933108
Merchant, H., Harrington, D. L., & Meck, W. H. (2013). Neural basis of the perception and estimation of time. Annual Review of Neuroscience, 36, 313–336. Available at: https://www.annualreviews.org/doi/10.1146/annurev-neuro-062012-170349
pubmed: 23725000 doi: 10.1146/annurev-neuro-062012-170349
Mochol, G., Hermoso-Mendizabal, A., Sakata, S., Harris, K. D., & de la Rocha, J. (2015). Stochastic transitions into silence cause noise correlations in cortical circuits. Proceedings of the National Academy of Sciences, 112, 3529–3534. Available at: http://www.pnas.org/lookup/doi/10.1073/pnas.1410509112
doi: 10.1073/pnas.1410509112
Mole, J., Winegardner, J., Malley, D., & Fish, J. (2018). Time perception impairment following thalamic stroke: A case study. Neuropsychological Rehabilitation, 28, 208–222. Available at: https://doi.org/10.1080/09602011.2017.1383273
pubmed: 29108479 doi: 10.1080/09602011.2017.1383273
Monteiro, T., Rodrigues, F. S., Pexirra, M., Cruz, B. F., Rueda-Orozco, P. E., & Paton, J. J. (2021). Using temperature to analyse the neural basis of a latent temporal decision. bioRxiv. Available at: https://doi.org/10.1101/2020.08.24.251827
Monteiro, T., Rodrigues, F. S., Pexirra, M., Cruz, B. F., Gonçalves, A. I., Rueda-Orozco, P. E., & Paton, J. J. (2023). Using temperature to analyze the neural basis of a time-based decision. Nature Neuroscience. Available at: https://doi.org/10.1038/s41593-023-01378-5
Nagy, A., Paróczy, Z., Norita, M., & Benedek, G. (2005). Multisensory responses and receptive field properties of neurons in the substantia nigra and in the caudate nucleus. The European Journal of Neuroscience, 22, 419–424. Available at: http://doi.wiley.com/10.1111/j.1460-9568.2005.04211.x
pubmed: 16045495 doi: 10.1111/j.1460-9568.2005.04211.x
Nambu, A. (2011). Somatotopic organization of the primate basal ganglia. Frontiers in Neuroanatomy, 5, 1–9. Available at: http://journal.frontiersin.org/article/10.3389/fnana.2011.00026/abstract
doi: 10.3389/fnana.2011.00026
Nozaradan, S., Schwartze, M., Obermeier, C., & Kotz, S. A. (2017). Specific contributions of basal ganglia and cerebellum to the neural tracking of rhythm. Cortex, 95, 156–168. Available at: https://doi.org/10.1016/j.cortex.2017.08.015
pubmed: 28910668 doi: 10.1016/j.cortex.2017.08.015
Pare, D., Steriade, M., Deschenes, M., & Oakson, G. (1987). Physiological characteristics of anterior thalamic nuclei, a group devoid of inputs from reticular thalamic nucleus. Journal of Neurophysiology, 57, 1669–1685. Available at: https://www.physiology.org/doi/10.1152/jn.1987.57.6.1669
pubmed: 3037038 doi: 10.1152/jn.1987.57.6.1669
Parent, A., Mackey, A., Smith, Y., & Boucher, R. (1983). The output organization of the substantia nigra in primate as revealed by a retrograde double labeling method. Brain Research Bulletin, 10, 529–537. Available at: https://linkinghub.elsevier.com/retrieve/pii/036192308390151X
pubmed: 6305462 doi: 10.1016/0361-9230(83)90151-X
Parent, A., Bouchard, C., & Smith, Y. (1984). The striatopallidal and striatonigral projections: Two distinct fiber systems in primate. Brain Research, 303, 385–390. Available at: https://linkinghub.elsevier.com/retrieve/pii/0006899384912241
pubmed: 6744030 doi: 10.1016/0006-8993(84)91224-1
Paton, J. J., & Lau, B. (2015). Tread softly and carry a clock’s tick. Nature Neuroscience, 18, 329–330. Available at: https://doi.org/10.1038/nn.3959
pubmed: 25710833 doi: 10.1038/nn.3959
Peña-Rangel, T. M., Lugo-Picos, P. I., Báez-Cordero, A. S., Hidalgo-Balbuena, A. E., Luma, A. Y., Pimentel-Farfan, A. K., & Rueda-Orozco, P. E. (2021). Altered sensory representations in parkinsonian cortical and basal ganglia networks. Neuroscience, 466, 10–25. Available at: http://www.ncbi.nlm.nih.gov/pubmed/33965505
pubmed: 33965505 doi: 10.1016/j.neuroscience.2021.04.031
Peters, A. J., Fabre, J. M. J., Steinmetz, N. A., Harris, K. D., & Carandini, M. (2021). Striatal activity topographically reflects cortical activity. Nature, 591, 420–425. Available at: https://doi.org/10.1038/s41586-020-03166-8
pubmed: 33473213 pmcid: 7612253 doi: 10.1038/s41586-020-03166-8
Pidoux, M., Mahon, S., Deniau, J. M., & Charpier, S. (2011). Integration and propagation of somatosensory responses in the corticostriatal pathway: An intracellular study in vivo. The Journal of Physiology, 589, 263–281.
pubmed: 21059765 doi: 10.1113/jphysiol.2010.199646
Pimentel-Farfan, A. K., Báez-Cordero, A. S., Peña-Rangel, T. M., & Rueda-Orozco, P. E. (2022). Cortico-striatal circuits for bilaterally coordinated movements. Science Advances, 8, 1–19. Available at: https://www.science.org/doi/10.1126/sciadv.abk2241
doi: 10.1126/sciadv.abk2241
Rao, S. M., Harrington, D. L., Haaland, K. Y., Bobholz, J. A., Cox, R. W., & Binder, J. R. (1997). Distributed neural systems underlying the timing of movements. The Journal of Neuroscience, 17, 5528–5535. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.17-14-05528.1997
pubmed: 9204934 pmcid: 6793838 doi: 10.1523/JNEUROSCI.17-14-05528.1997
Redgrave, P., Rodriguez, M., Smith, Y., Rodriguez-Oroz, M. C., Lehericy, S., Bergman, H., Agid, Y., Delong, M. R., & Obeso, J. A. (2010). Goal-directed and habitual control in the basal ganglia: Implications for Parkinson’s disease. Nature Reviews. Neuroscience, 11, 760–772. Available at: https://doi.org/10.1038/nrn2915
pubmed: 20944662 pmcid: 3124757 doi: 10.1038/nrn2915
Reig, R., & Silberberg, G. (2014). Multisensory integration in the mouse striatum. Neuron, 83, 1200–1212. Available at: https://doi.org/10.1016/j.neuron.2014.07.033
pubmed: 25155959 pmcid: 4157575 doi: 10.1016/j.neuron.2014.07.033
Reig, R., & Silberberg, G. (2016). Distinct corticostriatal and intracortical pathways mediate bilateral sensory responses in the striatum. Cerebral Cortex, 26, 4405–4415. Available at: https://academic.oup.com/cercor/article-lookup/doi/10.1093/cercor/bhw268
pubmed: 27664965 pmcid: 5193142 doi: 10.1093/cercor/bhw268
Reiner, A., Jiao, Y., Del Mar, N., Laverghetta, A. V., & Lei, W. L. (2003). Differential morphology of pyramidal tract-type and intratelencephalically projecting-type corticostriatal neurons and their intrastriatal terminals in rats. The Journal of Comparative Neurology, 457, 420–440.
pubmed: 12561080 doi: 10.1002/cne.10541
Robbe, D. (2018). To move or to sense? Incorporating somatosensory representation into striatal functions. Current Opinion in Neurobiology, 52, 123–130. Available at: https://doi.org/10.1016/j.conb.2018.04.009
pubmed: 29860150 doi: 10.1016/j.conb.2018.04.009
Rowe, K. C., Paulsen, J. S., Langbehn, D. R., Duff, K., Beglinger, L. J., Wang, C., O’Rourke, J. J. F., Stout, J. C., & Moser, D. J. (2010). Self-paced timing detects and tracks change in prodromal Huntington disease. Neuropsychology, 24, 435–442. Available at: http://doi.apa.org/getdoi.cfm?doi=10.1037/a0018905
pubmed: 20604618 pmcid: 2900808 doi: 10.1037/a0018905
Rueda-Orozco, P. E., & Robbe, D. (2015). The striatum multiplexes contextual and kinematic information to constrain motor habits execution. Nature Neuroscience, 18, 435–460.
doi: 10.1038/nn.3924
Schmidt, R., Leventhal, D. K., Mallet, N., Chen, F., & Berke, J. D. (2013). Canceling actions involves a race between basal ganglia pathways. Nature Neuroscience, 16, 1118–1124. Available at: http://www.nature.com/articles/nn.3456
pubmed: 23852117 pmcid: 3733500 doi: 10.1038/nn.3456
Schultz, W. (1986). Activity of pars reticulata neurons of monkey substantia nigra in relation to motor, sensory, and complex events. Journal of Neurophysiology, 55, 660–677. Available at: https://www.physiology.org/doi/10.1152/jn.1986.55.4.660
pubmed: 3701399 doi: 10.1152/jn.1986.55.4.660
Schwartze, M., Stockert, A., & Kotz, S. A. (2015). Striatal contributions to sensory timing: Voxel-based lesion mapping of electrophysiological markers. Cortex, 71, 332–340. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0010945215002610
pubmed: 26298502 doi: 10.1016/j.cortex.2015.07.016
Sheng, M., Lu, D., Shen, Z., & Poo, M. (2019). Emergence of stable striatal D1R and D2R neuronal ensembles with distinct firing sequence during motor learning. Proceedings of the National Academy of Sciences, 116, 11038–11047. Available at: https://pnas.org/doi/full/10.1073/pnas.1901712116
doi: 10.1073/pnas.1901712116
Shi, L. H., Luo, F., Woodward, D. J., & Chang, J. Y. (2004). Neural responses in multiple basal ganglia regions during spontaneous and treadmill locomotion tasks in rats. Experimental Brain Research, 157, 303–314. Available at: http://link.springer.com/10.1007/s00221-004-1844-y
pubmed: 15067433 doi: 10.1007/s00221-004-1844-y
Shi, L. H., Luo, F., Woodward, D. J., & Chang, J. Y. (2005). Dose and behavioral context dependent inhibition of movement and basal ganglia neural activity by delta-9-tetrahydrocannabinol during spontaneous and treadmill locomotion tasks in rats. Synapse, 55, 1–16. Available at: http://doi.wiley.com/10.1002/syn.20088
pubmed: 15499609 doi: 10.1002/syn.20088
Sippy, T., Lapray, D., Crochet, S., & Petersen, C. C. H. (2015). Cell-type-specific sensorimotor processing in striatal projection neurons during goal-directed behavior. Neuron, 88, 298–305. Available at: https://doi.org/10.1016/j.neuron.2015.08.039
pubmed: 26439527 pmcid: 4622932 doi: 10.1016/j.neuron.2015.08.039
Smith, J. B., Mowery, T. M., & Alloway, K. D. (2012). Thalamic POm projections to the dorsolateral striatum of rats: Potential pathway for mediating stimulus-response associations for sensorimotor habits. Journal of Neurophysiology, 108, 160–174. Available at: http://jn.physiology.org/cgi/doi/10.1152/jn.00142.2012
pubmed: 22496533 pmcid: 3434604 doi: 10.1152/jn.00142.2012
Smith, Y., Galvan, A., Ellender, T. J., Doig, N., Villalba, R. M., Huerta-Ocampo, I., Wichmann, T., & Bolam, J. P. (2014). The thalamostriatal system in normal and diseased states. Frontiers in Systems Neuroscience, 8, 1–18. Available at: http://journal.frontiersin.org/article/10.3389/fnsys.2014.00005/abstract
doi: 10.3389/fnsys.2014.00005
Soares, S., Atallah, B. V., & Paton, J. J. (2016). Midbrain dopamine neurons control judgment of time. Science (80- ), 354, 1273–1277. Available at: https://www.science.org/doi/10.1126/science.aah5234
doi: 10.1126/science.aah5234
Sommer, M. A. (2003). The role of the thalamus in motor control. Current Opinion in Neurobiology, 13, 663–670. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0959438803001697
pubmed: 14662366 doi: 10.1016/j.conb.2003.10.014
Sreenivasan, V., & Petersen, C. C. H. (2016). Inhibition patterns the whisking rhythm. Neuron, 90, 211–213. Available at: https://doi.org/10.1016/j.neuron.2016.04.012
pubmed: 27100193 doi: 10.1016/j.neuron.2016.04.012
Stevens, M. C., Kiehl, K. A., Pearlson, G., & Calhoun, V. D. (2007). Functional neural circuits for mental timekeeping. Human Brain Mapping, 28, 394–408. Available at: https://onlinelibrary.wiley.com/doi/10.1002/hbm.20285
pubmed: 16944489 doi: 10.1002/hbm.20285
Tanaka, M. (2006). Inactivation of the central thalamus delays self-timed saccades. Nature Neuroscience, 9, 20–22. Available at: http://www.nature.com/articles/nn1617
pubmed: 16341209 doi: 10.1038/nn1617
Tanaka, M. (2007). Cognitive signals in the primate motor thalamus predict saccade timing. The Journal of Neuroscience, 27, 12109–12118. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.1873-07.2007
pubmed: 17978052 pmcid: 6673367 doi: 10.1523/JNEUROSCI.1873-07.2007
Taverna, S., Ilijic, E., & Surmeier, D. J. (2008). Recurrent collateral connections of striatal medium spiny neurons are disrupted in models of Parkinson’s disease. The Journal of Neuroscience, 28, 5504–5512. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.5493-07.2008
pubmed: 18495884 pmcid: 3235738 doi: 10.1523/JNEUROSCI.5493-07.2008
Teki, S., Grube, M., Kumar, S., & Griffiths, T. D. (2011). Distinct neural substrates of duration-based and beat-based auditory timing. The Journal of Neuroscience, 31, 3805–3812. Available at: https://www.jneurosci.org/lookup/doi/10.1523/JNEUROSCI.5561-10.2011
pubmed: 21389235 pmcid: 3074096 doi: 10.1523/JNEUROSCI.5561-10.2011
Toda, K., Lusk, N. A., Watson, G. D. R., Kim, N., Lu, D., Li, H. E., Meck, W. H., & Yin, H. H. (2017). Nigrotectal stimulation stops interval timing in mice. Current Biology, 27, 3763–3770.e3. Available at: https://doi.org/10.1016/j.cub.2017.11.003
pubmed: 29199075 doi: 10.1016/j.cub.2017.11.003
Toso, A., Reinartz, S., Pulecchi, F., & Diamond, M. E. (2021). Time coding in rat dorsolateral striatum. Neuron, 109, 3663–3673.e6. Available at: https://doi.org/10.1016/j.neuron.2021.08.020
pubmed: 34508666 doi: 10.1016/j.neuron.2021.08.020
Turner, R. S., & Desmurget, M. (2010). Basal ganglia contributions to motor control: A vigorous tutor. Current Opinion in Neurobiology, 20, 704–716. Available at: https://doi.org/10.1016/j.conb.2010.08.022
pubmed: 20850966 pmcid: 3025075 doi: 10.1016/j.conb.2010.08.022
Wang, J., Narain, D., Hosseini, E. A., & Jazayeri, M. (2018). Flexible timing by temporal scaling of cortical responses. Nature Neuroscience, 21, 102–110. Available at: https://doi.org/10.1038/s41593-017-0028-6
pubmed: 29203897 doi: 10.1038/s41593-017-0028-6
Weder, B. J., Leenders, K. L., Vontobel, P., Nienhusmeier, M., Keel, A., Zaunbauer, W., Vonesch, T., & Ludin, H.-P. (1999). Impaired somatosensory discrimination of shape in Parkinson’s disease: Association with caudate nucleus dopaminergic function. Human Brain Mapping, 8, 1–12. Available at: https://onlinelibrary.wiley.com/doi/10.1002/(SICI)1097-0193(1999)8:1%3C1::AID-HBM1%3E3.0.CO;2-E
pubmed: 10432178 pmcid: 6873336 doi: 10.1002/(SICI)1097-0193(1999)8:1<1::AID-HBM1>3.0.CO;2-E
Weder, B., Azari, N. P., Knorr, U., Seitz, R. J., Keel, A., Nienhusmeier, M., Maguire, R. P., Leenders, K. L., & Ludin, H.-P. (2000). Disturbed functional brain interactions underlying deficient tactile object discrimination in Parkinson’s disease. Human Brain Mapping, 11, 131–145. Available at: https://onlinelibrary.wiley.com/doi/10.1002/1097-0193(200011)11:3%3C131::AID-HBM10%3E3.0.CO;2-M
pubmed: 11098793 pmcid: 6871839 doi: 10.1002/1097-0193(200011)11:3<131::AID-HBM10>3.0.CO;2-M
West, M. O. (1998). Anesthetics eliminate somatosensory-evoked discharges of neurons in the somatotopically organized sensorimotor striatum of the rat. The Journal of Neuroscience, 18, 9055–9068.
pubmed: 9787009 pmcid: 6793534 doi: 10.1523/JNEUROSCI.18-21-09055.1998
West, M. O., Carelli, R. M., Pomerantz, M., Cohen, S. M., Gardner, J. P., Chapin, J. K., & Woodward, D. J. (1990). A region in the dorsolateral striatum of the rat exhibiting single-unit correlations with specific locomotor limb movements. Journal of Neurophysiology, 64, 1233–1246. Available at: http://www.physiology.org/doi/10.1152/jn.1990.64.4.1233
pubmed: 2258744 doi: 10.1152/jn.1990.64.4.1233
Wurtz, R. H., & Hikosaka, O. (1986). Role of the basal ganglia in the initiation of saccadic eye movements. Progress in Brain Research, 64, 175–190. Available at: https://linkinghub.elsevier.com/retrieve/pii/S0079612308634123
pubmed: 3523602 doi: 10.1016/S0079-6123(08)63412-3
Xu, M., Zhang, S., Dan, Y., & Poo, M. (2014). Representation of interval timing by temporally scalable firing patterns in rat prefrontal cortex. Proceedings of the National Academy of Sciences, 111, 480–485. Available at: https://pnas.org/doi/full/10.1073/pnas.1321314111
doi: 10.1073/pnas.1321314111
Yin, H. H. (2017). The basal ganglia in action. Neuroscience, 23, 299–313. Available at: http://journals.sagepub.com/doi/10.1177/1073858416654115
Yoshida, M., & Precht, W. (1971). Monosynaptic inhibition of neurons of the substantia nigra by caudatonigral fibers. Brain Research, 32, 225–228. Available at: https://linkinghub.elsevier.com/retrieve/pii/0006899371901703
pubmed: 4329651 doi: 10.1016/0006-8993(71)90170-3
Zhou, S., Masmanidis, S. C., & Buonomano, D. V. (2020). Neural sequences as an optimal dynamical regime for the readout of time. Neuron, 108, 651–658.e5. Available at: https://doi.org/10.1016/j.neuron.2020.08.020
pubmed: 32946745 pmcid: 7825362 doi: 10.1016/j.neuron.2020.08.020

Auteurs

Pavel E Rueda-Orozco (PE)

Institute of Neurobiology, National Autonomous University of México, Querétaro, Mexico. ruedap@unam.mx.

Ana E Hidalgo-Balbuena (AE)

Institute of Neurobiology, National Autonomous University of México, Querétaro, Mexico.

Perla González-Pereyra (P)

Institute of Neurobiology, National Autonomous University of México, Querétaro, Mexico.

Mario G Martinez-Montalvo (MG)

Institute of Neurobiology, National Autonomous University of México, Querétaro, Mexico.

Ana S Báez-Cordero (AS)

Institute of Neurobiology, National Autonomous University of México, Querétaro, Mexico.

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