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Mechanisms of Dopamine Activation of Fast-Spiking Interneurons That Exert Inhibition in Rat Prefrontal Cortex
Abstract
Prefrontal cortical dopamine (DA) modulates pyramidal cell excitability directly and indirectly by way of its actions on local circuit GABAergic interneurons. DA modulation of interneuronal functions is implicated in the computational properties of prefrontal networks during cognitive processes and in schizophrenia. Morphologically and electrophysiologically distinct classes of putative GABAergic interneurons are found in layers II-V of rat prefrontal cortex. Our whole cell patch-clamp study shows that DA induced a direct, TTX-insensitive, reversible membrane depolarization, and increased the excitability of fast-spiking (FS) interneurons. The DA-induced membrane depolarization was reduced significantly by D1/D5 receptor antagonist SCH 23390, but not by the D2 receptor antagonist (−)sulpiride, D4 receptor antagonists U101958 or L-745870, α1-adrenoreceptor antagonist prazosin, or serotoninergic receptor antagonist mianserin. The D1/5 agonists SKF81297 or dihydrexidine, but not D2 agonist quinpirole, also induced a prolonged membrane depolarization. Voltage-clamp analyses of the voltage-dependence of DA-sensitive currents, and the effects of changing [K+]O on reversal potentials of DA responses, revealed that DA suppressed a Cs+-sensitive inward rectifier K+current and a resting leak K+current. D1/D5, but not D2 agonists mimicked the suppressive effects of DA on the leak current, but the DA effects on the inward rectifier K+current were not mimicked by either agonist. In a subgroup of FS interneurons, the slowly inactivating membrane outward rectification evoked by depolarizing voltage steps was also attenuated by DA. Collectively, these data showed that DA depolarizes FS interneurons by suppressing a voltage-independent ‘leak’ K+current (via D1/D5 receptor mechanism) and an inwardly rectifying K+current (via unknown DA mechanisms). Additional suppression of a slowly inactivating K+current led to increase in repetitive firing in response to depolarizing inputs. This D1-induced increase in interneuron excitability enhances GABAergic transmission to PFC pyramidal neurons and could represent a mechanism via which DA suppresses persistent firing of pyramidal neurons in vivo.
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“Prior to adolescence, D2 stimulation elicits either no effect or only weak inhibition on interneurons. However, in adult animals stimulation of D2 receptors is strongly excitatory and therefore results in robust firing of interneurons and potent inhibition of their pyramidal cell targets.”
From A role for synaptic plasticity in the adolescent development of executive function (2013) · cites this paper as [62]
In the citing paper
“recent evidence has established that D2 dopamine receptors on interneurons undergo a profound maturational change during adolescence.62, 63, 64”
From A role for synaptic plasticity in the adolescent development of executive function (2013) · cites this paper as [62]
In the citing paper
“In juvenile rats, D 1 agonists increase GABA interneuron firing, whereas D 2 agonists have either a weak inhibitory effect or no effect.12,13”
From Adolescent Onset of Cortical Disinhibition in Schizophrenia: Insights From Animal Models (2011) · cites this paper as [13]
Citations
Cites
The Rat Brain in Stereotaxic Coordinates
Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585
Cellular basis of working memory
Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
The cognitive neuropsychology of schizophrenia
(1993) · Choice Reviews Online · doi:10.5860/choice.31-0601 · Cited by 1,901
Whittington, M. A., Traub, R. D., & Jefferys, J. G. R. (1995) · Nature · doi:10.1038/373612a0 · Cited by 1,613
Modulation of memory fields by dopamine Dl receptors in prefrontal cortex
Williams, G. V., & Goldman-Rakic, P. S. (1995) · Nature · doi:10.1038/376572a0 · Cited by 1,593
Synchronization of neuronal activity in hippocampus by individual GABAergic interneurons
Cobb, S. R., Buhl, E. H., Halasy, K., Paulsen, O., & Somogyi, P. (1995) · Nature · doi:10.1038/378075a0 · Cited by 1,498
GABAergic cell subtypes and their synaptic connections in rat frontal cortex
Kawaguchi, Y. (1997) · Cerebral Cortex · doi:10.1093/cercor/7.6.476 · Cited by 1,416
D1 Dopamine Receptors in Prefrontal Cortex: Involvement in Working Memory
Sawaguchi, T., & Goldman-Rakic, P. S. (1991) · Science · doi:10.1126/science.1825731 · Cited by 1,364
Neuropsychological Function in Schizophrenia
Saykin, A. J. (1991) · Archives of General Psychiatry · doi:10.1001/archpsyc.1991.01810310036007 · Cited by 1,160
GABAergic Interneurons Implications for Understanding Schizophrenia and Bipolar Disorder
Benes, F. (2001) · Neuropsychopharmacology · doi:10.1016/s0893-133x(01)00225-1 · Cited by 1,082
Research works printed but not linked: 6
- Ahn S, 2000, Soc Neurosci Abst, 366, 6
- Björklund A, 1984, Handbook of Chemical Neuroanatomy: Classical Transmitter In The Rat, 2, 55
- Godbout R, 1991, J Pharmacol Exp Ther, 258, 728
- Gorelova N, 1998, Soc Neurosci Abstr, 24, 350
- Merchant KM, 1996, J Pharmacol Exp Ther, 279, 1392
- Sesack SR, 1989, J Pharmacol Exp Ther, 248, 1323
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Xing, B., Li, Y.-C., & Gao, W.-J. (2016) · Brain Research · doi:10.1016/j.brainres.2016.01.005 · Cited by 196
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Gamo, N. J., Lur, G., Higley, M. J., Wang, M., Paspalas, C. D., Vijayraghavan, S., Yang, Y., Ramos, B. P., Peng, K., Kata, A., et al. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.01.009 · Cited by 97
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Auksztulewicz, R., Schwiedrzik, C. M., Thesen, T., Doyle, W., Devinsky, O., Nobre, A. C., Schroeder, C. E., Friston, K. J., & Melloni, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0369-18.2018 · Cited by 83
Imeraj, L., Sonuga-Barke, E. J. S., Antrop, I., Roeyers, H., Wiersema, R., Bal, S., & Deboutte, D. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.04.007 · Cited by 90
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Park, J., Wood, J. T., Bondi, C. O., Arco, A. D., & Moghaddam, B. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.4250-15.2016 · Cited by 78
López-Gil, X., Artigas, F., & Adell, A. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210790361416 · Cited by 80
Tanaka, S. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.08.070 · Cited by 79
Zvara, Á., Szekeres, G., Janka, Z., Kelemen, J. Z., Cimmer, C., Sántha, M., & Puskás, L. G. (2005) · Disease Markers · doi:10.1155/2005/275318 · Cited by 76
Soltani, A., Noudoost, B., & Moore, T. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221236110 · Cited by 73
Wang, H., Luo, B., Huang, Y., Zhou, K., & Chen, L. (2008) · Hearing Research · doi:10.1016/j.heares.2007.11.015 · Cited by 75
Glutamatergic modulatory therapy for Tourette syndrome
Singer, H. S., Morris, C. M., & Grados, M. A. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2009.11.028 · Cited by 74
Eytan, D., Minerbi, A., Ziv, N. E., & Marom, S. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00202.2004 · Cited by 72
Visual Cue-Discriminative Dopaminergic Control of Visuomotor Transformation and Behavior Selection
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Dopamine, cognitive function, and gamma oscillations: role of D4 receptors
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Lin, S., Pan, W. H. T., & Yeh, P.-H. (2006) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2006.10.001 · Cited by 69
Cholinergic modulation of dopamine pathways through nicotinic acetylcholine receptors
de Kloet, S. F., Mansvelder, H. D., & De Vries, T. J. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.07.014 · Cited by 69
Dopaminergic Modulation of Motor Maps in Rat Motor Cortex: An In Vivo Study
Hosp, J. A., Molina-Luna, K., Hertler, B., Atiemo, C. O., & Luft, A. R. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2008.12.056 · Cited by 67
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Rioult-Pedotti, M.-S., Pekanovic, A., Atiemo, C. O., Marshall, J. J., & Luft, A. R. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124986 · Cited by 68
Lauzon, N. M., Bishop, S. F., & Laviolette, S. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0178-09.2009 · Cited by 71
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Function and developmental origin of a mesocortical inhibitory circuit
Kabanova, A., Pabst, M., Lorkowski, M., Braganza, O., Boehlen, A., Nikbakht, N., Pothmann, L., Vaswani, A. R., Musgrove, R., Di Monte, D. A., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4020 · Cited by 61
Park, B., Kebets, V., Larivière, S., Hettwer, M. D., Paquola, C., van Rooij, D., Buitelaar, J. K., Franke, B., Hoogman, M., Schmaal, L., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03963-z · Cited by 65
Spoleti, E., Barbera, L. L., Cauzzi, E., Paolis, M. L. D., Saba, L., Marino, R., Sciamanna, G., Lazzaro, V. D., Keller, F., Nobili, A., et al. (2024) · Molecular Psychiatry · doi:10.1038/s41380-024-02408-9 · Cited by 63
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Metadata
- Authors
- Gorelova, N., Seamans, J. K., & Yang, C. R.
- Affiliations
- University of British Columbia (CA)
- Medical University of South Carolina (US)
- Eli Lilly (United States) (US)
- ORCID
- Seamans, Jeremy K.
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 2002-12-01
- Volume
- 88
- Issue
- 6
- Pages
- 3150-3166
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W2033043582
- Cited by
- 302
- References
- 99
- Citations by year
- 2026: 7 · 2025: 5 · 2024: 9 · 2023: 6 · 2022: 15 · 2021: 8 · 2020: 4 · 2019: 6 · 2018: 14 · 2017: 13 · 2016: 15 · 2015: 12 · 2014: 8 · 2013: 14 · 2012: 10
- FWCI
- 4.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Keywords
- dopamine, fast-spiking interneurons, prefrontal cortex, GABAergic interneurons, dopamine D1/D5 receptors, interneuron excitability, membrane depolarization, inward rectifier potassium current, dopamine D2 receptor, repetitive firing, schizophrenia
- MeSH terms
- Action Potentials, Animals, Dopamine, Electrophysiology, Interneurons, Male, Neural Inhibition, Reaction Time, Potassium Channels, Rats, Sprague-Dawley, Prefrontal Cortex, Receptors, Dopamine D1, Patch-Clamp Techniques, Potassium Channels, Inwardly Rectifying, Receptors, Dopamine D5, Rats, In Vitro Techniques
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