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Targeted disruption of cocaine-activated nucleus accumbens neurons prevents context-specific sensitization
Open accessAbstract
Learned associations between effects of abused drugs and the drug administration environment are important in drug addiction. Histochemical and electrophysiological studies suggest that these associations are encoded in sparsely distributed nucleus accumbens neurons that are selectively activated by drugs and drug-associated cues. Although correlations have been observed between nucleus accumbens neuronal activity and responsivity to drugs and drug cues, no technique exists for selectively manipulating these activated neurons and establishing their causal role in behavioral effects of drugs and drug cues. Here we describe a new approach, which we term the 'Daun02 inactivation method', that selectively inactivates a minority of neurons previously activated by cocaine in an environment repeatedly paired with cocaine to demonstrate a causal role for these activated neurons in context-specific cocaine-induced psychomotor sensitization in rats. This method provides a new tool for studying the causal roles of selectively activated neurons in behavioral effects of drugs and drug cues and in other learned behaviors.
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Cites
Neural systems of reinforcement for drug addiction: from actions to habits to compulsion
Everitt, B. J., & Robbins, T. W. (2005) · Nature Neuroscience · doi:10.1038/nn1579 · Cited by 3,785
Dopamine, learning and motivation.
Wise, R. A. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1406 · Cited by 3,379
Contributions of the Amygdala to Emotion Processing: From Animal Models to Human Behavior
Phelps, E. A., & LeDoux, J. E. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.025 · Cited by 3,203
Drugs of abuse: anatomy, pharmacology and function of reward pathways
Koob, G. F. (1992) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(92)90060-j · Cited by 2,070
Habits, Rituals, and the Evaluative Brain
Graybiel, A. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112851 · Cited by 1,697 · cited 1×
“Together these studies lead us to speculate that during repeated cocaine injections in a novel environment, the learned association between environment and cocaine effects becomes encoded in specific neuronal ensemble”
Background
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Josselyn, S. A., & Tonegawa, S. (2020) · Science · doi:10.1126/science.aaw4325 · Cited by 1,087
Cell type-specific loss of BDNF signaling mimics optogenetic control of cocaine reward
Lobo, M. K., Covington, H. E., Chaudhury, D., Friedman, A. K., Sun, H., Damez-Werno, D., Dietz, D. M., Zaman, S., Koo, J. W., Kennedy, P. J., et al. (2010) · Science · doi:10.1126/science.1188472 · Cited by 880
Guenthner, C. J., Miyamichi, K., Yang, H. H., Heller, H. C., & Luo, L. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.025 · Cited by 705
Bossert, J. M., Marchant, N. J., Calu, D. J., & Shaham, Y. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3120-y · Cited by 453
Self-citationThe hippocampal-striatal axis in learning, prediction and goal-directed behavior
Pennartz, C. M. A., Ito, R., Verschure, P. F. M. J., Battaglia, F. P., & Robbins, T. W. (2011) · Trends in Neurosciences · doi:10.1016/j.tins.2011.08.001 · Cited by 287
Smith, R. J., Lobo, M. K., Spencer, S., & Kalivas, P. W. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.01.026 · Cited by 272
Telzer, E. H. (2016) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2015.10.010 · Cited by 274
AMPA receptor plasticity in the nucleus accumbens after repeated exposure to cocaine
Wolf, M. E., & Ferrario, C. R. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.01.013 · Cited by 271
A new era for functional labeling of neurons: activity-dependent promoters have come of age
Kawashima, T., Okuno, H., & Bito, H. (2014) · Frontiers in Neural Circuits · doi:10.3389/fncir.2014.00037 · Cited by 165
Venniro, M., Caprioli, D., Zhang, M., Whitaker, L. R., Zhang, S., Warren, B. L., Cifani, C., Marchant, N. J., Yizhar, O., Bossert, J. M., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.024 · Cited by 162
Self-citationPfarr, S., Meinhardt, M. W., Klee, M. L., Hansson, A. C., Vengeliene, V., Schonig, K., Bartsch, D., Hope, B. T., Spanagel, R., & Sommer, W. H. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.0684-15.2015 · Cited by 143
Self-citationMechanisms of Action and Persistent Neuroplasticity by Drugs of Abuse
Korpi, E. R., den Hollander, B., Farooq, U., Vashchinkina, E., Rajkumar, R., Nutt, D. J., Hyytiä, P., & Dawe, G. S. (2015) · Pharmacological Reviews · doi:10.1124/pr.115.010967 · Cited by 148
Reactivation of recall-induced neurons contributes to remote fear memory attenuation
Khalaf, O., Resch, S., Dixsaut, L., Gorden, V., Glauser, L., & Gräff, J. (2018) · Science · doi:10.1126/science.aas9875 · Cited by 146
Deconstructing behavioral neuropharmacology with cellular specificity
Shields, B. C., Kahuno, E., Kim, C., Apostolides, P. F., Brown, J., Lindo, S., Mensh, B. D., Dudman, J. T., Lavis, L. D., & Tadross, M. R. (2017) · Science · doi:10.1126/science.aaj2161 · Cited by 135
Stimulant-induced dopamine increases are markedly blunted in active cocaine abusers
Volkow, N. D., Tomasi, D., Wang, G.-J., Logan, J., Alexoff, D. L., Jayne, M., Fowler, J. S., Wong, C., Yin, P., & Du, C. (2014) · Molecular Psychiatry · doi:10.1038/mp.2014.58 · Cited by 134
Separate elements of episodic memory subserved by distinct hippocampal-prefrontal connections
Barker, G. R. I., Banks, P. J., Scott, H., Ralph, G. S., Mitrophanous, K. A., Wong, L.-F., Bashir, Z. I., Uney, J. B., & Warburton, E. C. (2017) · Nature Neuroscience · doi:10.1038/nn.4472 · Cited by 124
de Guglielmo, G., Crawford, E., Kim, S., Vendruscolo, L. F., Hope, B. T., Brennan, M., Cole, M., Koob, G. F., & George, O. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1395-16.2016 · Cited by 106
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Funk, D., Coen, K., Tamadon, S., Hope, B. T., Shaham, Y., & Lê, A. D. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1505-16.2016 · Cited by 87
Self-citationClosing the Gate in the Limbic Striatum: Prefrontal Suppression of Hippocampal and Thalamic Inputs
Calhoon, G. G., & O’Donnell, P. (2013) · Neuron · doi:10.1016/j.neuron.2013.01.032 · Cited by 50
Laque, A., L. De Ness, G., Wagner, G. E., Nedelescu, H., Carroll, A., Watry, D., M. Kerr, T., Koya, E., Hope, B. T., Weiss, F., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11799-1 · Cited by 43
Self-citationLiu, Z.-Q., Gu, X.-H., Yang, Y.-J., Yin, X.-P., Xu, L.-J., & Wang, W. (2016) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2016.02.002 · Cited by 23
Dorsolateral caudate nucleus differentiates cocaine from natural reward-associated contextual cues
Liu, H.-S., Chefer, S., Lu, H., Guillem, K., Rea, W., Kurup, P., Yang, Y., Peoples, L., & Stein, E. A. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207531110 · Cited by 23
Neural Circuit Reprogramming: A New Paradigm for Treating Neuropsychiatric Disease?
Tye, K. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.08.022 · Cited by 21
Kim, Y., Kim, K., Lee, Y., Min, H., Ko, Y., Lee, B., Hur, K., Kim, S., Lee, S., & Jang, C. (2024) · British Journal of Pharmacology · doi:10.1111/bph.16427 · Cited by 4
Metadata
- Authors
- Koya, E., Golden, S. A., Harvey, B. K., Guez-Barber, D. H., Berkow, A., Simmons, D. E., Bossert, J. M., Nair, S. G., Uejima, J. L., Marin, M. T., Mitchell, T. B., Farquhar, D., Ghosh, S. C., Mattson, B. J., & Hope, B. T.
- Venue
- Nature Neuroscience
- Published
- 2009-07-20
- Volume
- 12
- Issue
- 8
- Pages
- 1069-1073
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2101640561
- Cited by
- 264
- References
- 5
- FWCI
- 4.77
- Type
- journal article
- Language
- en
- Open access
- green
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