Dopamine Modulation of Prefrontal Cortical Interneurons Changes during Adolescence
Open accessAbstract
Adolescence is marked by profound psychological and neuroendocrine changes. Cognitive functions that depend on the prefrontal cortex and dopamine (DA), such as decision making, are acquired or refined during adolescence; yet, little is known about how neural circuits mature in the transition to adulthood. Here, we conducted electrophysiological recordings in rat brain slices, unveiling an enhancement of the excitability of interneurons, which are important for cortical network activity, by D(1) and D(2) DA receptors. The D(2) effect was observed in slices from adult (postnatal day [PD] > 50) but not preadolescent (PD < 36) animals suggesting a possible neural substrate for the maturation of DA-dependent prefrontal cortical functions during or after adolescence and identifying a critical neural population that could be involved in the periadolescent onset of neuropsychiatric disorders, such as schizophrenia.
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Prior to adolescence, D2 stimulation elicits either no effect or only weak inhibition on interneurons; in adult animals, stimulation of D2 receptors is strongly excitatory and results in robust firing of interneurons and potent inhibition of their pyramidal cell targets.
“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 [64]
Split into 2 atoms — 0 confirmed, 2 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredRecent evidence has established that D2 dopamine receptors on interneurons undergo a profound maturational change during adolescence.
“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 [64]
The Abstract and Discussion report that D2-mediated excitation of rat prefrontal interneurons is present in adults but not preadolescent animals, supporting a maturational change in D2 modulation. The Discussion says it remains unclear whether the effect is a direct action on interneurons, so the paper does not establish that the receptors on those cells themselves change during adolescence. (LLM, conf=0.87)
Experimental — accuracy not yet measuredD2 receptors switch from inhibitory to excitatory on parvalbumin interneurons in the mPFC during adolescence.
“D2 receptors switch from inhibitory to excitatory on parvalbumin interneurons in the mPFC during adolescence (Tseng and O'Donnell, 2007).”
From Sensitive periods of substance abuse: Early risk for the transition to dependence (2017) · cites this paper as Tseng and O'Donnell, 2007
In the adult PFC, D2 agonists become strongly excitatory over fast-spiking interneurons.
“In the adult PFC, however, D 2 agonists become strongly excitatory over fast-spiking interneurons, 12”
From Adolescent Onset of Cortical Disinhibition in Schizophrenia: Insights From Animal Models (2011) · cites this paper as [12]
In juvenile rats, D1 agonists increase GABA interneuron firing, whereas D2 agonists have either a weak inhibitory effect or no effect.
“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 [12]
Interneuron recruitment by DA is not efficient in juvenile stages (prior to PD45 in rats).
“As interneuron recruitment by DA is not efficient in juvenile stages (prior to PD45 in rats) 12”
From Adolescent Onset of Cortical Disinhibition in Schizophrenia: Insights From Animal Models (2011) · cites this paper as [12]
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Cites
Shrestha, S., & Offer, S. M. (2016) · Medical Epigenetics · doi:10.1159/000444713 · Cited by 8,949 · see citing works
Brain development during childhood and adolescence: a longitudinal MRI study
Giedd, J. N., Blumenthal, J., Jeffries, N. O., Castellanos, F. X., Liu, H., Zijdenbos, A., Paus, T., Evans, A. C., & Rapoport, J. L. (1999) · Nature Neuroscience · doi:10.1038/13158 · Cited by 5,552 · see citing works
The adolescent brain and age-related behavioral manifestations
Spear, L. P. (2000) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(00)00014-2 · Cited by 5,433 · see citing works
Cortical inhibitory neurons and schizophrenia
Lewis, D. A., Hashimoto, T., & Volk, D. W. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1648 · Cited by 2,297 · see citing works
The principal features and mechanisms of dopamine modulation in the prefrontal cortex
Seamans, J. K., & Yang, C. R. (2004) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2004.05.006 · Cited by 1,592 · see citing works
Structural and functional brain development and its relation to cognitive development
Casey, B. J., Giedd, J. N., & Thomas, K. M. (2000) · Biological Psychology · doi:10.1016/s0301-0511(00)00058-2 · Cited by 1,506 · see citing works
Two networks of electrically coupled inhibitory neurons in neocortex
Gibson, J. R., Beierlein, M., & Connors, B. W. (1999) · Nature · doi:10.1038/47035 · Cited by 1,404 · see citing works
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 · see citing works
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 · see citing works
Turning on and off recurrent balanced cortical activity
Shu, Y., Hasenstaub, A., & McCormick, D. A. (2003) · Nature · doi:10.1038/nature01616 · Cited by 1,054 · see citing works
Molecular and Physiological Diversity of Cortical Nonpyramidal Cells
Cauli, B., Audinat, E., Lambolez, B., Angulo, M. C., Ropert, N., Tsuzuki, K., Hestrin, S., & Rossier, J. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03894.1997 · Cited by 738 · see citing works
Development of the dopaminergic innervation in the prefrontal cortex of the rat
Kalsbeek, A., Voorn, P., Buijs, R. M., Pool, C. W., & Uylings, H. B. M. (1988) · Journal of Comparative Neurology · doi:10.1002/cne.902690105 · Cited by 545 · see citing works
Bidirectional dopamine modulation of GABAergic inhibition in prefrontal cortical pyramidal neurons
Seamans, J. K., Gorelova, N., Durstewitz, D., & Yang, C. R. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03628.2001 · Cited by 507 · see citing works
Tseng, K. Y., & O'Donnell, P. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1021-04.2004 · Cited by 402 · see citing works
Self-citationKawaguchi, Y., & Kondo, S. (2002) · Journal of Neurocytology · doi:10.1023/a:1024126110356 · Cited by 395 · see citing works
Neuronal correlates of goal-based motor selection in the prefrontal cortex.
Matsumoto, K., Suzuki, W., & Tanaka, K. (2003) · Science · doi:10.1126/science.1084204 · Cited by 384 · see citing works
Tarazi, F. I., & Baldessarini, R. J. (2000) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(99)00108-2 · Cited by 327 · see citing works
Gaspar, P., Bloch, B., & Le Moine, C. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01092.x · Cited by 323 · see citing works
Selective D2 receptor actions on the functional circuitry of working memory
Wang, M., Vijayraghavan, S., & Goldman-Rakic, P. S. (2004) · Science · doi:10.1126/science.1091162 · Cited by 319 · see citing works
Gorelova, N., Seamans, J. K., & Yang, C. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00335.2002 · Cited by 302 · see citing works
Lewis, B. L. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.12.1168 · Cited by 287 · see citing works
Benes, F. M. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.10.1014 · Cited by 268 · see citing works
Charting the maturation of the frontal lobe: An electrophysiological strategy
Segalowitz, S. J., & Davies, P. L. (2004) · Brain and Cognition · doi:10.1016/s0278-2626(03)00283-5 · Cited by 246 · see citing works
Sesack, S. R., Snyder, C. L., & Lewis, D. A. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903630208 · Cited by 226 · see citing works
Cellular distribution of dopamine D1 and D2 receptors in rat medial prefrontal cortex
Vincent, S. L., Khan, Y., & Benes, F. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-06-02551.1993 · Cited by 223 · see citing works
Rosenberg, D. R., & Lewis, D. A. (1994) · Biological Psychiatry · doi:10.1016/0006-3223(94)90610-6 · Cited by 174 · see citing works
Post-pubertal Emergence of Prefrontal Cortical Up States Induced by D1-NMDA Co-activation
Tseng, K. Y. (2004) · Cerebral Cortex · doi:10.1093/cercor/bhh107 · Cited by 169 · see citing works
Self-citationFrequency Dependence of Spike Timing Reliability in Cortical Pyramidal Cells and Interneurons
Fellous, J., Houweling, A. R., Modi, R. H., Rao, R. P. N., Tiesinga, P. H. E., & B, T. J. S. A. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.4.1782 · Cited by 151 · see citing works
Verney, C., Berger, B., Adrien, J., Vigny, A., & Gay, M. (1982) · Developmental Brain Research · doi:10.1016/0165-3806(82)90111-0 · Cited by 147 · see citing works
Tarazi, F. I., Tomasini, E. C., & Baldessarini, R. J. (1998) · Developmental Brain Research · doi:10.1016/s0165-3806(98)00111-4 · Cited by 141 · see citing works
Grobin, A. C., & Deutch, A. Y. (1998) · PubMed · Cited by 141 · see citing works
Dendritic Branch Typing and Spine Expression Patterns in Cortical Nonpyramidal Cells
Kawaguchi, Y., Karube, F., & Kubota, Y. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj015 · Cited by 125 · see citing works
Zhu, Y., Stornetta, R. L., & Zhu, J. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0544-04.2004 · Cited by 125 · see citing works
Distinct Firing Patterns of Neuronal Subtypes in Cortical Synchronized Activities
Kawaguchi, Y. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07261.2001 · Cited by 123 · see citing works
Tseng, K. Y., Mallet, N. P., Toreson, K. L., Moine, C. L., Gonon, F., & O’Donnell, P. (2006) · Synapse · doi:10.1002/syn.20255 · Cited by 119 · see citing works
Self-citationMoine, C. L., & Gaspar, P. (1998) · Molecular Brain Research · doi:10.1016/s0169-328x(98)00118-1 · Cited by 117 · see citing works
Cortical localization of dopamine D4 receptors in the rat brain--immunocytochemical study.
Wędzony, K., Chocyk, A., Maćkowiak, M., Fijał, K., & Czyrak, A. (2000) · PubMed · Cited by 105 · see citing works
Funahashi, S. (2000) · Cerebral Cortex · doi:10.1093/cercor/10.6.535 · Cited by 76 · see citing works
Maturational increases in c‐fos expression in the ascending dopamine systems
Andersen, S. L., Leblanc, C. J., & Lyss, P. J. (2001) · Synapse · doi:10.1002/syn.1091 · Cited by 55 · see citing works
Neurotensin Activates GABAergic Interneurons in the Prefrontal Cortex
Petrie, K. A., Schmidt, D. E., Bubser, M., Fadel, J. R., Carraway, R. E., & Deutch, A. Y. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3579-04.2005 · Cited by 48 · see citing works
Flagged first, then by citations
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Sorted by citations
Why do many psychiatric disorders emerge during adolescence?
Paus, T., Keshavan, M., & Giedd, J. N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2513 · Cited by 3,123 · see citing works
Adolescence as a neurobiological critical period for the development of higher-order cognition
Larsen, B., & Luna, B. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.005 · Cited by 853 · see citing works
Beyond simple models of self-control to circuit-based accounts of adolescent behavior
Casey, B. J. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015156 · Cited by 742 · see citing works
The dynamic effects of nicotine on the developing brain
Dwyer, J. B., McQuown, S. C., & Leslie, F. M. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.02.003 · Cited by 559 · see citing works
Uhlhaas, P. J., & Singer, W. (2012) · Neuron · doi:10.1016/j.neuron.2012.09.004 · Cited by 512 · see citing works
Sensitive periods of substance abuse: Early risk for the transition to dependence
Jordan, C. J., & Andersen, S. L. (2017) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2016.10.004 · Cited by 455 · see citing works
“For example, D2 receptors switch from inhibitory to excitatory on parvalbumin interneurons in the mPFC during adolescence (Tseng and O'Donnell, 2007).”
A role for synaptic plasticity in the adolescent development of executive function
Selemon, L. D. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.7 · Cited by 439 · see citing works
Doremus-Fitzwater, T. L., Varlinskaya, E. I., & Spear, L. P. (2010) · Brain and Cognition · doi:10.1016/j.bandc.2009.08.008 · Cited by 397 · see citing works
Mechanisms contributing to prefrontal cortex maturation during adolescence
Caballero, A., Granberg, R., & Tseng, K. Y. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.013 · Cited by 357 · see citing works
Self-citationSpear, L. P. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.08.001 · Cited by 292 · see citing works
Adolescence: what do transmission, transition and translation have to do with it?
Casey, B. J., Duhoux, S., & Cohen, M. M. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.033 · Cited by 297 · see citing works
Brenhouse, H. C., Sonntag, K. C., & Andersen, S. L. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5064-07.2008 · Cited by 287 · see citing works
Steullet, P., Cabungcal, J. H., Monin, A., Dwir, D., O'Donnell, P., Cuenod, M., & Do, K. Q. (2016) · Schizophrenia Research · doi:10.1016/j.schres.2014.06.021 · Cited by 262 · see citing works
Self-citationUhlhaas, P. J., & Singer, W. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.11.019 · Cited by 243 · see citing works
Koss, W. A., Belden, C. E., Hristov, A. D., & Juraska, J. M. (2014) · Synapse · doi:10.1002/syn.21716 · Cited by 228 · see citing works
Cabungcal, J.-H., Steullet, P., Kraftsik, R., Cuenod, M., & Do, K. Q. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2012.09.020 · Cited by 232 · see citing works
McCormick, C. M., & Mathews, I. Z. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.09.019 · Cited by 230 · see citing works
Santana, N., Mengod, G., & Artigas, F. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhn134 · Cited by 231 · see citing works
Circular inferences in schizophrenia
Jardri, R., & Denève, S. (2013) · Brain · doi:10.1093/brain/awt257 · Cited by 201 · see citing works
Parallel maturation of goal-directed behavior and dopaminergic systems during adolescence
Naneix, F., Marchand, A. R., Di Scala, G., Pape, J.-R., & Coutureau, E. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.3080-12.2012 · Cited by 209 · see citing works
Caballero, A., Flores-Barrera, E., Cass, D. K., & Tseng, K. Y. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0508-8 · Cited by 178 · see citing works
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Kilb, W. (2012) · The Neuroscientist · doi:10.1177/1073858411422114 · Cited by 190 · see citing works
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Mukherjee, A., Carvalho, F., Eliez, S., & Caroni, P. (2019) · Cell · doi:10.1016/j.cell.2019.07.023 · Cited by 169 · see citing works
Alvaro, P. K., Roberts, R. M., & Harris, J. K. (2014) · Sleep Medicine · doi:10.1016/j.sleep.2014.03.019 · Cited by 183 · see citing works
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Piekarski, D. J., Johnson, C. M., Boivin, J. R., Thomas, A. W., Lin, W. C., Delevich, K., M. Galarce, E., & Wilbrecht, L. (2017) · Brain Research · doi:10.1016/j.brainres.2016.08.042 · Cited by 175 · see citing works
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More Is Less: A Disinhibited Prefrontal Cortex Impairs Cognitive Flexibility
Gruber, A. J., Calhoon, G. G., Shusterman, I., Schoenbaum, G., Roesch, M. R., & O'Donnell, P. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4623-10.2010 · Cited by 160 · see citing works
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Kim, J. H., Li, S., & Richardson, R. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq116 · Cited by 149 · see citing works
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Harris, J. J., Reynell, C., & Attwell, D. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.04.001 · Cited by 142 · see citing works
Adolescent Onset of Cortical Disinhibition in Schizophrenia: Insights From Animal Models
O'Donnell, P. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr028 · Cited by 145 · see citing works
Self-citationTseng, K. Y., Lewis, B. L., Hashimoto, T., Sesack, S. R., Kloc, M., Lewis, D. A., & O'Donnell, P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4166-08.2008 · Cited by 144 · see citing works
Self-citationTseng, K. Y., & O'Donnell, P. (2007) · Synapse · doi:10.1002/syn.20432 · Cited by 141 · see citing works
Self-citationMesocorticolimbic Dopamine Pathways Across Adolescence: Diversity in Development
Reynolds, L. M., & Flores, C. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.735625 · Cited by 137 · see citing works
Tseng, K.-Y., Lewis, B. L., Lipska, B. K., & O’Donnell, P. (2007) · Biological Psychiatry · doi:10.1016/j.biopsych.2006.10.012 · Cited by 132 · see citing works
Self-citationDoremus-Fitzwater, T. L., & Spear, L. P. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.08.015 · Cited by 125 · see citing works
The emergence of gonadal hormone influences on dopaminergic function during puberty
Kuhn, C., Johnson, M., Thomae, A., Luo, B., Simon, S. A., Zhou, G., & Walker, Q. D. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2009.10.015 · Cited by 113 · see citing works
Zhang, Y., Behrens, M. M., & Lisman, J. E. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00079.2008 · Cited by 107 · see citing works
Adolescent Maturation of Cortical Dopamine
O’Donnell, P. (2010) · Neurotoxicity Research · doi:10.1007/s12640-010-9157-3 · Cited by 107 · see citing works
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Reichelt, A. C., & Rank, M. M. (2017) · Birth Defects Research · doi:10.1002/bdr2.1173 · Cited by 102 · see citing works
Developmental imaging genetics: Linking dopamine function to adolescent behavior
Padmanabhan, A., & Luna, B. (2014) · Brain and Cognition · doi:10.1016/j.bandc.2013.09.011 · Cited by 87 · see citing works
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Reynolds, L. M., Yetnikoff, L., Pokinko, M., Wodzinski, M., Epelbaum, J. G., Lambert, L. C., Cossette, M.-P., Arvanitogiannis, A., & Flores, C. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhy247 · Cited by 75 · see citing works
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Sullivan, E. M., & O'Donnell, P. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs052 · Cited by 71 · see citing works
Self-citationSturman, D. A., & Moghaddam, B. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4210-10.2011 · Cited by 69 · see citing works
Brenhouse, H., Lukkes, J., & Andersen, S. (2013) · Brain Sciences · doi:10.3390/brainsci3010143 · Cited by 68 · see citing works
Cass, D. K., Thomases, D. R., Caballero, A., & Tseng, K. Y. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.02.021 · Cited by 63 · see citing works
“Thus, the acquisition of an increased prefrontal GABAergic function during the normal adolescent period (19, 20) is thought to be associated with the maturation of cognitive abilities such as working memory, decision making and impulse control (21, 22).”
Self-citationBergstrom, H. C., McDonald, C. G., French, H. T., & Smith, R. F. (2008) · Synapse · doi:10.1002/syn.20467 · Cited by 60 · see citing works
Parr, A. C., Calabro, F., Larsen, B., Tervo-Clemmens, B., Elliot, S., Foran, W., Olafsson, V., & Luna, B. (2021) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2021.101997 · Cited by 60 · see citing works
Milstein, J. A., Elnabawi, A., Vinish, M., Swanson, T., Enos, J. K., Bailey, A. M., Kolb, B., & Frost, D. O. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057308 · Cited by 57 · see citing works
Feleder, C., Tseng, K. Y., Calhoon, G. G., & O'Donnell, P. (2010) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.09.028 · Cited by 57 · see citing works
Self-citationSteullet, P., Cabungcal, J.-H., Cuénod, M., & Do, K. Q. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00244 · Cited by 49 · see citing works
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Bernheim, A., Halfon, O., & Boutrel, B. (2013) · Frontiers in Pharmacology · doi:10.3389/fphar.2013.00118 · Cited by 49 · see citing works
Protracted maturation of forebrain afferent connections of the ventral tegmental area in the rat
Yetnikoff, L., Reichard, R. A., Schwartz, Z. M., Parsely, K. P., & Zahm, D. S. (2014) · Journal of Comparative Neurology · doi:10.1002/cne.23459 · Cited by 30 · see citing works
Seemiller, L. R., & Gould, T. J. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107234 · Cited by 23 · see citing works
Adolescence: a time of transition for the phenotype of dcc heterozygous mice
Yetnikoff, L., Pokinko, M., Arvanitogiannis, A., & Flores, C. (2014) · Psychopharmacology · doi:10.1007/s00213-013-3083-z · Cited by 18 · see citing works
- Authors
- Tseng, K.-Y., & O'Donnell, P.
- Affiliations
- Rosalind Franklin University of Medicine and Science (US)
- Venue
- Cerebral Cortex
- Publisher
- Oxford University Press (OUP)
- Published
- 2006-06-13
- Volume
- 17
- Issue
- 5
- Pages
- 1235-1240
- ISSN
- 1047-3211 (ISSN-L)
- 1460-2199
- PMC
- PMC2204087
- OpenAlex
- W2128508619
- Cited by
- 339
- References
- 40
- Citations by year
- 2026: 8 · 2025: 12 · 2024: 8 · 2023: 21 · 2022: 12 · 2021: 19 · 2020: 11 · 2019: 10 · 2018: 24 · 2017: 15 · 2016: 31 · 2015: 13 · 2014: 18 · 2013: 36 · 2012: 16
- FWCI
- 5.31
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cerebral Cortex (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Mental Health (MH57683, R56MH057683, R01MH057683)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- dopamine, prefrontal cortex, cortical interneurons, adolescence, dopamine D1 receptor, dopamine D2 receptor, neuronal excitability, neural circuit maturation, decision-making, schizophrenia, neuropsychiatric disorders, rat brain slices
- MeSH terms
- Adaptation, Physiological, Aging, Animals, Cells, Cultured, Dopamine, Interneurons, Nerve Net, Neuronal Plasticity, Receptors, Dopamine, Prefrontal Cortex, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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