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Regulation of parkinsonian motor behaviours by optogenetic control of basal ganglia circuitry
Open accessAbstract
Neural circuits of the basal ganglia are critical for motor planning and action selection. Two parallel basal ganglia pathways have been described, and have been proposed to exert opposing influences on motor function. According to this classical model, activation of the 'direct' pathway facilitates movement and activation of the 'indirect' pathway inhibits movement. However, more recent anatomical and functional evidence has called into question the validity of this hypothesis. Because this model has never been empirically tested, the specific function of these circuits in behaving animals remains unknown. Here we report direct activation of basal ganglia circuitry in vivo, using optogenetic control of direct- and indirect-pathway medium spiny projection neurons (MSNs), achieved through Cre-dependent viral expression of channelrhodopsin-2 in the striatum of bacterial artificial chromosome transgenic mice expressing Cre recombinase under control of regulatory elements for the dopamine D1 or D2 receptor. Bilateral excitation of indirect-pathway MSNs elicited a parkinsonian state, distinguished by increased freezing, bradykinesia and decreased locomotor initiations. In contrast, activation of direct-pathway MSNs reduced freezing and increased locomotion. In a mouse model of Parkinson's disease, direct-pathway activation completely rescued deficits in freezing, bradykinesia and locomotor initiation. Taken together, our findings establish a critical role for basal ganglia circuitry in the bidirectional regulation of motor behaviour and indicate that modulation of direct-pathway circuitry may represent an effective therapeutic strategy for ameliorating parkinsonian motor deficits.
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“the insula allocates over one-third of its projection to the striatum, particularly the dorsal region, underscoring its pivotal role in motor control and action selection [21][22][23][24].”
From The Insular Cortex: An Interface Between Sensation, Emotion and Cognition (2024) · cites this paper as [21]
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“In a simplified framework, these anatomically distinct pathways have been thought to oppose each other, resulting in net inhibition of thalamus and decrease of movement via activation of the indirect pathway, or net disinhibition (i.e. overall excitation) and increase of movement by activation of the direct pathway (Fig.1) 46,47.”
From DISSECTING OCD CIRCUITS: FROM ANIMAL MODELS TO TARGETED TREATMENTS: Review: Dissecting OCD Circuits: Animals to Treatments (2015) · cites this paper as [46]
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The functional anatomy of basal ganglia disorders
Albin, R. L., Young, A. B., & Penney, J. B. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90074-x · Cited by 5,353
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015
Self-citationFunctional architecture of basal ganglia circuits: neural substrates of parallel processing
Alexander, G. E., & Crutcher, M. D. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90107-l · Cited by 4,131
Primate models of movement disorders of basal ganglia origin
DeLong, M. R. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90110-v · Cited by 3,824
D 1 and D 2 Dopamine Receptor-regulated Gene Expression of Striatonigral and Striatopallidal Neurons
Gerfen, C. R., Engber, T. M., Mahan, L. C., Susel, Z., Chase, T. N., Monsma, F. J., & Sibley, D. R. (1990) · Science · doi:10.1126/science.2147780 · Cited by 2,967
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
Sohal, V. S., Zhang, F., Yizhar, O., & Deisseroth, K. (2009) · Nature · doi:10.1038/nature07991 · Cited by 2,606
Self-citationDriving fast-spiking cells induces gamma rhythm and controls sensory responses
Cardin, J. A., Carlén, M., Meletis, K., Knoblich, U., Zhang, F., Deisseroth, K., Tsai, L.-H., & Moore, C. I. (2009) · Nature · doi:10.1038/nature08002 · Cited by 2,603
Self-citationThe role of the basal ganglia in habit formation
Yin, H. H., & Knowlton, B. J. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1919 · Cited by 2,402
Reversal of experimental parkinsonism by lesions of the subthalamic nucleus.
Bergman, H., Wichmann, T., & Delong, M. (1990) · Science · doi:10.1126/science.2402638 · Cited by 2,003
The primate subthalamic nucleus. II. Neuronal activity in the MPTP model of parkinsonism
Bergman, H., Wichmann, T., Karmon, B., & DeLong, M. R. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.2.507 · Cited by 1,366
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LRRK2 mutant knock-in mouse models: therapeutic relevance in Parkinson's disease
Chang, E. E. S., Ho, P. W., Liu, H., Pang, S. Y.-Y., Leung, C.-T., Malki, Y., Choi, Z. Y.-K., Ramsden, D. B., & Ho, S. (2022) · Translational Neurodegeneration · doi:10.1186/s40035-022-00285-2 · Cited by 45
Lucas, E. K., Dougherty, S., McMeekin, L. J., Trinh, A. T., Reid, C. S., & Cowell, R. M. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042878 · Cited by 44
Varin, C., Cornil, A., Houtteman, D., Bonnavion, P., & d’Exaerde, A. D. K. (2023) · Nature Communications · doi:10.1038/s41467-023-40677-0 · Cited by 43
Oeckl, P., Hengerer, B., & Ferger, B. (2014) · Experimental Neurology · doi:10.1016/j.expneurol.2014.04.010 · Cited by 43
Tools, methods, and applications for optophysiology in neuroscience
Smedemark-Margulies, N., & Trapani, J. G. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00018 · Cited by 43
Ena, S., Backer, J. D., Schiffmann, S. N., & d’Exaerde, A. D. K. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2989-12.2013 · Cited by 43
Genetic manipulation for inherited neurodegenerative diseases: myth or reality?
Yu‐Wai‐Man, P. (2016) · British Journal of Ophthalmology · doi:10.1136/bjophthalmol-2015-308329 · Cited by 43
Neuronal firing patterns outweigh circuitry oscillations in parkinsonian motor control
Pan, M., Kuo, S., Tai, C., Liou, J.-Y., Pei, J.-C., Chang, C., Wang, Y., Liu, W.-C., Wang, T.-R., Lai, W., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci88170 · Cited by 46
Nigral Glutamatergic Neurons Control the Speed of Locomotion
Ryczko, D., Grätsch, S., Schläger, L., Keuyalian, A., Boukhatem, Z., Garcia, C., Auclair, F., Büschges, A., & Dubuc, R. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1810-17.2017 · Cited by 43
The subcortical belly of sleep: New possibilities in neuromodulation of basal ganglia?
Hasegawa, H., Selway, R., Gnoni, V., Beniczky, S., Williams, S., Kryger, M. H., Ferini‐Strambi, L., Goadsby, P. J., Leschziner, G. D., Ashkan, K., et al. (2020) · Sleep Medicine Reviews · doi:10.1016/j.smrv.2020.101317 · Cited by 43
Mahato, A. K., & Sidorova, Y. A. (2020) · Cell and Tissue Research · doi:10.1007/s00441-020-03227-4 · Cited by 43
Shin, J. H., Song, M. J., Paik, S., & Jung, M. W. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2010361117 · Cited by 43
Bidirectional Modulation of Substantia Nigra Activity by Motivational State
Rossi, M. A., Fan, D., Barter, J. W., & Yin, H. H. (2013) · PLoS ONE · doi:10.1371/journal.pone.0071598 · Cited by 43
Maps of the adult human hypothalamus
Lemaire, J., Nezzar, H., Sakka, L. J., Boirie, Y., Fontaine, D., Coste, A., Coll, G., Sontheimer, A., Sarret, C., Gabrillargues, J., et al. (2013) · Surgical Neurology International · doi:10.4103/2152-7806.110667 · Cited by 43
Chen, Z., Zhang, Z., Zhang, W., Xie, T., Li, Y., Xu, X., & Yao, H. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109847 · Cited by 42
Airy-beam holographic sonogenetics for advancing neuromodulation precision and flexibility
Hu, Z., Yang, Y., Yang, L., Gong, Y., Chukwu, C., Ye, D., Yue, Y., Yuan, J., Kravitz, A. V., & Chen, H. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2402200121 · Cited by 42
Self-citationDeranged NMDAergic cortico-subthalamic transmission underlies parkinsonian motor deficits
Pan, M., Tai, C., Liu, W.-C., Pei, J.-C., Lai, W., & Kuo, C. (2014) · Journal of Clinical Investigation · doi:10.1172/jci75587 · Cited by 42
Bergamini, G., Sigrist, H., Ferger, B., Singewald, N., Seifritz, E., & Pryce, C. R. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.03.048 · Cited by 48
Grosenick, L., Shi, T. C., Gunning, F. M., Dubin, M. J., Downar, J. H., & Liston, C. M. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2019.04.013 · Cited by 43
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Striatal circuit development and its alterations in Huntington's disease
Lebouc, M., Richard, Q., Garret, M., & Baufreton, J. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105076 · Cited by 45
On the role of subsecond dopamine release in conditioned avoidance
Oleson, E. B., & Cheer, J. F. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00096 · Cited by 44
Wood, J., LaPalombara, Z., & Ahmari, S. E. (2018) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2017.0023 · Cited by 41
Implantable Micro-Light-Emitting Diode (µLED)-based optogenetic interfaces toward human applications
Lee, J. H., Lee, S., Kim, D., & Lee, K. J. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114399 · Cited by 43
Haleem, D. J. (2014) · Behavioural Pharmacology · doi:10.1097/fbp.0000000000000123 · Cited by 41
Neural circuitry for behavioural arrest
Roseberry, T. K., & Kreitzer, A. C. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0197 · Cited by 44
Self-citationHo, H., Both, M. D. D., Siniard, A. L., Sharma, S., Notwell, J. H., Wallace, M., Leone, D. P., Nguyen, A., Zhao, E., Lee, H., et al. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00159 · Cited by 41
Cheng, Y., Wang, X., Wei, X., Xie, X., Melo, S., Miranda, R. C., & Wang, J. (2018) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.13806 · Cited by 41
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Wilson, R. S., & Nairn, A. C. (2018) · Proteomes · doi:10.3390/proteomes6040051 · Cited by 41
Ruud, J., Alber, J., Tokarska, A., Engström, L., Nolte, H., Biglari, N., Lippert, R. N., Lautenschlager, Ä., Cieślak, P. E., Szumiec, Ł., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.05.037 · Cited by 42
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Kwak, S., & Jung, M. W. (2019) · eLife · doi:10.7554/elife.46050 · Cited by 41
Stefanescu, R. A., Shivakeshavan, R. G., Khargonekar, P. P., & Talathi, S. S. (2013) · Bulletin of Mathematical Biology · doi:10.1007/s11538-013-9888-4 · Cited by 41
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Konur, O. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818305-2.00026-7 · Cited by 40
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Zhang, T., Azghadi, M. R., Lammie, C., Amirsoleimani, A., & Genov, R. (2023) · Journal of Neural Engineering · doi:10.1088/1741-2552/acc7cc · Cited by 42
Recent advances in organic solar cells: materials, design, and performance
Mahdi, A. S., Shaker, L. M., & Al‐Amiery, A. A. (2023) · Journal of Optics · doi:10.1007/s12596-023-01262-2 · Cited by 40
Ding, S., Li, L., & Zhou, F.-M. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00752.2014 · Cited by 40
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Meirsman, A. C., Robé, A., d’Exaerde, A. D. K., & Kieffer, B. L. (2016) · eNeuro · doi:10.1523/eneuro.0202-16.2016 · Cited by 42
Drive and Reinforcement Circuitry in the Brain: Origins, Neurotransmitters, and Projection Fields
Wise, R. A., & McDevitt, R. A. (2017) · Neuropsychopharmacology · doi:10.1038/npp.2017.228 · Cited by 43
Baimel, C., McGarry, L. M., & Carter, A. G. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.07.074 · Cited by 40
Progress in Brain‐Compatible Interfaces with Soft Nanomaterials
Jeong, Y., Lee, H. E., Shin, A., Kim, D., Lee, K. J., & Kim, D. (2020) · Advanced Materials · doi:10.1002/adma.201907522 · Cited by 40
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Mimura, K., Nagai, Y., Inoue, K., Matsumoto, J., Hori, Y., Sato, C., Kimura, K., Okauchi, T., Hirabayashi, T., Nishijo, H., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103066 · Cited by 40
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Tai, C. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.11.044 · Cited by 39
Wang, W., Xie, X., Zhuang, X., Huang, Y., Tan, T., Gangal, H., Huang, Z., Purvines, W., Wang, X., Stefanov, A., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112089 · Cited by 39
Hyperactivity of indirect pathway-projecting spiny projection neurons promotes compulsive behavior
Piantadosi, S. C., Manning, E. E., Chamberlain, B. L., Hyde, J., LaPalombara, Z., Bannon, N. M., Pierson, J. L., Namboodiri, V. M. K., & Ahmari, S. E. (2024) · Nature Communications · doi:10.1038/s41467-024-48331-z · Cited by 42
Neurophysiological markers of motor compensatory mechanisms in early Parkinson’s disease
Passaretti, M., Cilia, R., Rinaldo, S., Sebastiano, D. R., Orunesu, E., Devigili, G., Braccia, A., Paparella, G., Riggi, M. D., van Eimeren, T., et al. (2024) · Brain · doi:10.1093/brain/awae210 · Cited by 39
Bentley, J. N., Chestek, C. A., Stacey, W. C., & Patil, P. G. (2013) · Neurosurgical FOCUS · doi:10.3171/2013.3.focus1364 · Cited by 42
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Bologna, M., Suppa, A., Conte, A., Latorre, A., Rothwell, J. C., & Berardelli, A. (2015) · Clinical Neurophysiology · doi:10.1016/j.clinph.2015.02.009 · Cited by 39
Gentry, R. N., Schuweiler, D. R., & Roesch, M. R. (2018) · Brain Research · doi:10.1016/j.brainres.2018.10.008 · Cited by 41
Suryanarayana, S. M., Kotaleski, J. H., Grillner, S. E., & GURNEY, K. N. (2018) · Neural Networks · doi:10.1016/j.neunet.2018.10.003 · Cited by 39
Salery, M., Trifilieff, P., Caboche, J., & Vanhoutte, P. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.11.001 · Cited by 47
Kovaleski, R. F., Callahan, J. W., Chazalon, M., Wokosin, D. L., Baufreton, J., & Bevan, M. D. (2020) · The Journal of Physiology · doi:10.1113/jp279232 · Cited by 39
Vicente, A. M., Martins, G. J., & Costa, R. M. (2020) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2020.05.042 · Cited by 41
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Allichon, M., Ortiz, V., Pousinha, P. A., Andrianarivelo, A., Petitbon, A., Heck, N., Trifilieff, P., Barik, J., & Vanhoutte, P. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.799274 · Cited by 43
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Skirzewski, M., Princz‐Lebel, O., German‐Castelan, L., Crooks, A. M., Kim, K., Tarnow, S. H., Reichelt, A. C., Memar, S., Palmer, D. D., Li, Y., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35601-x · Cited by 41
Cheung, T. H. C., Ding, Y., Zhuang, X., & Kang, U. J. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2213093120 · Cited by 38
Contemporary approaches to neural circuit manipulation and mapping: focus on reward and addiction
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Optogenetic tools for modulating and probing the epileptic network
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Robertson, B., Huerta-Ocampo, I., Ericsson, J., Stephenson‐Jones, M., Pérez‐Fernández, J., Bolam, J. P., Heijtz, R. D., & Grillner, S. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0035642 · Cited by 39
Reiner, A., Lafferty, D., Wang, H. B., Mar, N. D., & Deng, Y. P. (2012) · Neurobiology of Disease · doi:10.1016/j.nbd.2012.03.025 · Cited by 38
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Gangarossa, G., Castell, L., Castro, L. R., Tarot, P., Veyrunes, F., Vincent, P., Bertaso, F., & Valjent, E. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14804 · Cited by 41
Brice, N., Schiffer, H. H., Monenschein, H., Mulligan, V. J., Page, K. J., Powell, J., Xu, X., Cheung, T., Burley, J. R., Sun, H., et al. (2021) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.120.000438 · Cited by 38
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Dupuis, J. P., Feyder, M. T., Miguélez, C., García, L., Morin, S., Choquet, D., Hosy, E., Bézard, E., Fisone, G., Bioulac, B. H., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1681-13.2013 · Cited by 38
Salem, G. H., Dennis, J. U., Krynitsky, J., Garmendia‐Cedillos, M., Swaroop, K., Malley, J. D., Pajevic, S., Abuhatzira, L., Bustin, M., Gillet, J., et al. (2014) · Behavior Research Methods · doi:10.3758/s13428-014-0451-5 · Cited by 38
Mouse Models of Neurodevelopmental Disease of the Basal Ganglia and Associated Circuits
Pappas, S. S., Leventhal, D., Albin, R. L., & Dauer, W. T. (2014) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-397920-9.00001-9 · Cited by 41
Lee, A. M., Tai, L.-H., Zador, A., & Wilbrecht, L. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2014.12.042 · Cited by 37
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Walters, J. L., Lansdell, T. A., Lookingland, K. J., & Baker, L. E. (2015) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2015.09.026 · Cited by 37
Horstmann, A. (2017) · Physiology & Behavior · doi:10.1016/j.physbeh.2017.04.001 · Cited by 37
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Grimm, C., Frässle, S., Steger, C., von Ziegler, L., Sturman, O., Shemesh, N., Peleg‐Raibstein, D., Burdakov, D., Bohacek, J., Stephan, K. E., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.110161 · Cited by 38
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Dib, P. B., Gnägi, B., Daly, F., Sabado, V., Tas, D., Glauser, D. A., Meister, P., & Nagoshi, E. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004718 · Cited by 37
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Yang, X. W., & Lu, X.-H. (2011) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32834451fb · Cited by 36
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Metadata
- Authors
- Kravitz, A. V., Freeze, B. S., Parker, P. R. L., Kay, K., Thwin, M. T., Deisseroth, K., & Kreitzer, A. C.
- Affiliations
- Gladstone Institutes (US)
- Stanford University (US)
- Corresponding author
- Kreitzer, Anatol C.
- ORCID
- Venue
- Nature
- Published
- 2010-07
- Volume
- 466
- Issue
- 7306
- Pages
- 622-626
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3552484
- OpenAlex
- W1971797700
- Cited by
- 1,885
- References
- 28
- Citations by year
- 2026: 76 · 2025: 110 · 2024: 138 · 2023: 110 · 2022: 96 · 2021: 120 · 2020: 118 · 2019: 119 · 2018: 137 · 2017: 133 · 2016: 128 · 2015: 138 · 2014: 133 · 2013: 112 · 2012: 100
- FWCI
- 62.12
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- W. M. Keck Foundation
- McKnight Foundation
- National Institutes of Health
- University of California, San Francisco
- National Institute of Neurological Disorders and Stroke (R01NS064984)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Deep Brain Stimulation and Movement Disorders
- Health Sciences › Medicine › Clinical Neurology › Parkinson's Disease Mechanisms and Treatments
- Life Sciences › Neuroscience › Cognitive Neuroscience › Motor Control and Adaptation
- Keywords
- basal ganglia, Parkinson's disease, direct pathway, indirect pathway, medium spiny neurons, striatum, optogenetics, channelrhodopsin-2, dopamine D1 receptor, dopamine D2 receptor, locomotion, bradykinesia, freezing behavior, motor control, functional connectivity, mouse model of Parkinson's disease, viral gene expression, Cre recombinase
- MeSH terms
- Channelrhodopsins, Animals, Basal Ganglia, Disease Models, Animal, Gait, Mice, Transgenic, Models, Neurological, Motor Activity, Neural Pathways, Neurons, Parkinson Disease, Psychomotor Performance, Receptors, Dopamine, Oxidopamine, Neostriatum, Hypokinesia, Integrases, Chromosomes, Artificial, Bacterial, Mice
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