The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.
Corticostriatal neurons in auditory cortex drive decisions during auditory discrimination
Open accessAbstract
The neural pathways by which information about the acoustic world reaches the auditory cortex are well characterized, but how auditory representations are transformed into motor commands is not known. Here we use a perceptual decision-making task in rats to study this transformation. We demonstrate the role of corticostriatal projection neurons in auditory decisions by manipulating the activity of these neurons in rats performing an auditory frequency-discrimination task. Targeted channelrhodopsin-2 (ChR2)-mediated stimulation of corticostriatal neurons during the task biased decisions in the direction predicted by the frequency tuning of the stimulated neurons, whereas archaerhodopsin-3 (Arch)-mediated inactivation biased decisions in the opposite direction. Striatal projections are widespread in cortex and may provide a general mechanism for the control of motor decisions by sensory cortex.
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Cites
Encoding of conditioned fear in central amygdala inhibitory circuits
Ciocchi, S., Herry, C., Grenier, F., Wolff, S. B. E., Letzkus, J. J., Vlachos, I., Ehrlich, I., Sprengel, R., Deisseroth, K., Stadler, M. B., et al. (2010) · Nature · doi:10.1038/nature09559 · Cited by 924
Cortical microstimulation influences perceptual judgements of motion direction
Salzman, C. D., Britten, K. H., & Newsome, W. T. (1990) · Nature · doi:10.1038/346174a0 · Cited by 881
A cellular mechanism of reward-related learning
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Different time courses of learning-related activity in the prefrontal cortex and striatum.
Pasupathy, A., & Miller, E. K. (2005) · Nature · doi:10.1038/nature03287 · Cited by 712
The effect of stimulus strength on the speed and accuracy of a perceptual decision
Palmer, J., Huk, A. C., & Shadlen, M. N. (2005) · Journal of Vision · doi:10.1167/5.5.1 · Cited by 691
Sparse optical microstimulation in barrel cortex drives learned behaviour in freely moving mice
Huber, D., Petreanu, L., Ghitani, N., Ranade, S., Hromádka, T., Mainen, Z., & Svoboda, K. (2008) · Nature · doi:10.1038/nature06445 · Cited by 539
Cited by
Canales, A., Jia, X., Froriep, U. P., Koppes, R. A., Tringides, C. M., Selvidge, J., Lu, C., Hou, C., Wei, L., Fink, Y., et al. (2015) · Nature Biotechnology · doi:10.1038/nbt.3093 · Cited by 668
Plasticity of Cortical Excitatory-Inhibitory Balance
Froemke, R. C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034002 · Cited by 458
Membrane potential correlates of sensory perception in mouse barrel cortex
Sachidhanandam, S., Sreenivasan, V., Kyriakatos, A., Kremer, Y., & Petersen, C. C. H. (2013) · Nature Neuroscience · doi:10.1038/nn.3532 · Cited by 384
Endocannabinoid Modulation of Orbitostriatal Circuits Gates Habit Formation
Gremel, C. M., Chancey, J. H., Atwood, B. K., Luo, G., Neve, R., Ramakrishnan, C., Deisseroth, K., Lovinger, D. M., & Costa, R. M. (2016) · Neuron · doi:10.1016/j.neuron.2016.04.043 · Cited by 251
Coordinated forms of noradrenergic plasticity in the locus coeruleus and primary auditory cortex
Martins, A. R. O., & Froemke, R. C. (2015) · Nature Neuroscience · doi:10.1038/nn.4090 · Cited by 233
Metadata
- Authors
- Znamenskiy, P., & Zador, A. M.
- Venue
- Nature
- Published
- 2013-05-01
- Volume
- 497
- Issue
- 7450
- Pages
- 482-485
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2051781198
- Cited by
- 348
- References
- 6
- FWCI
- 14.64
- Type
- journal article
- Language
- en
- Open access
- green
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