Dopamine receptors differentially enhance rule coding in primate prefrontal cortex neurons

Neuron

Volumn 84, Issue 6, 2014, Pages 1317-1328

  Ott, Torben ^a   Jacob, Simon Nikolas ^a,b   Nieder, Andreas ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

DOPAMINE 1 RECEPTOR; DOPAMINE 2 RECEPTOR; 8 CHLORO 2,3,4,5 TETRAHYDRO 3 METHYL 5 PHENYL 1H 3 BENZAZEPIN 7 OL HYDROGEN MALEATE; BENZAZEPINE DERIVATIVE; DOPAMINE RECEPTOR BLOCKING AGENT; DOPAMINE RECEPTOR STIMULATING AGENT; QUINPIROLE; SK&F 81297;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; ASSOCIATION; BRAIN NERVE CELL; CODING; CONTROLLED STUDY; DOPAMINERGIC SYSTEM; EXECUTIVE FUNCTION; FACILITATION; MALE; NERVE CELL EXCITABILITY; NERVE CELL STIMULATION; NEUROMODULATION; NEUROTRANSMISSION; NONHUMAN; PREFRONTAL CORTEX; PRIORITY JOURNAL; RHESUS MONKEY; RIGHT HEMISPHERE; AGONISTS; ANIMAL; ANTAGONISTS AND INHIBITORS; CYTOLOGY; DECISION MAKING; DRUG EFFECTS; IONTOPHORESIS; NERVE CELL; NERVE CELL INHIBITION; PHYSIOLOGY;

ANIMALS; BENZAZEPINES; DECISION MAKING; DOPAMINE AGONISTS; DOPAMINE ANTAGONISTS; EXECUTIVE FUNCTION; IONTOPHORESIS; MACACA MULATTA; MALE; NEURAL INHIBITION; NEURONS; PREFRONTAL CORTEX; QUINPIROLE; RECEPTORS, DOPAMINE D1; RECEPTORS, DOPAMINE D2;

EID: 84926337567     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2014.11.012     Document Type: Article

References (66)

1. Arnsten A.F.T. Catecholamine influences on dorsolateral prefrontal cortical networks. Biol. Psychiatry 2011, 69:e89-e99.
2. Arnsten A.F.T., Cai J.X., Steere J.C., Goldman-Rakic P.S. Dopamine D2 receptor mechanisms contribute to age-related cognitive decline: the effects of quinpirole on memory and motor performance in monkeys. J.Neurosci. 1995, 15:3429-3439.
3. Björklund A., Dunnett S.B. Dopamine neuron systems in the brain: an update. Trends Neurosci. 2007, 30:194-202.
4. Bongard S., Nieder A. Basic mathematical rules are encoded byprimate prefrontal cortex neurons. Proc. Natl. Acad. Sci. USA 2010, 107:2277-2282.
5. Brozoski T.J., Brown R.M., Rosvold H.E., Goldman P.S. Cognitive deficit caused by regional depletion of dopamine in prefrontal cortex of rhesus monkey. Science 1979, 205:929-932.
6. Clark K.L., Noudoost B. The role of prefrontal catecholamines in attention and working memory. Front. Neural Circuits 2014, 8:33.
7. Crofts H.S., Dalley J.W., Collins P., Van Denderen J.C., Everitt B.J., Robbins T.W., Roberts A.C. Differential effects of 6-OHDA lesions of the frontal cortex and caudate nucleus on the ability to acquire an attentional set. Cereb. Cortex 2001, 11:1015-1026.
8. D'Ardenne K., Eshel N., Luka J., Lenartowicz A., Nystrom L.E., Cohen J.D. Role of prefrontal cortex and the midbrain dopamine system in working memory updating. Proc. Natl. Acad. Sci. USA 2012, 109:19900-19909.
9. de Almeida J., Mengod G. D2 and D4 dopamine receptor mRNA distribution in pyramidal neurons and GABAergic subpopulations in monkey prefrontal cortex: implications for schizophrenia treatment. Neuroscience 2010, 170:1133-1139.
10. de Lafuente V., Romo R. Dopamine neurons code subjective sensory experience and uncertainty of perceptual decisions. Proc. Natl. Acad. Sci. USA 2011, 108:19767-19771.
11. de Lafuente V., Romo R. Dopaminergic activity coincides with stimulus detection by the frontal lobe. Neuroscience 2012, 218:181-184.
12. Durstewitz D., Seamans J.K. The dual-state theory of prefrontal cortex dopamine function with relevance to catechol-o-methyltransferase genotypes and schizophrenia. Biol. Psychiatry 2008, 64:739-749.
13. Eiselt A.-K., Nieder A. Representation of abstract quantitative rules applied to spatial and numerical magnitudes in primate prefrontal cortex. J.Neurosci. 2013, 33:7526-7534.
14. Floresco S.B. Prefrontal dopamine and behavioral flexibility: shifting from an "inverted-U" toward a family of functions. Front. Neurosci. 2013, 7:62.
15. Floresco S.B., Magyar O. Mesocortical dopamine modulation of executive functions: beyond working memory. Psychopharmacology (Berl.) 2006, 188:567-585.
16. Floresco S.B., Magyar O., Ghods-Sharifi S., Vexelman C., Tse M.T.L. Multiple dopamine receptor subtypes in the medial prefrontal cortex of the rat regulate set-shifting. Neuropsychopharmacology 2006, 31:297-309.
17. Gao W.J., Krimer L.S., Goldman-Rakic P.S. Presynaptic regulation of recurrent excitation by D1 receptors in prefrontal circuits. Proc. Natl. Acad. Sci. USA 2001, 98:295-300.
18. Green D.M., Swets J.A. Signal Detection Theory and Psychophysics 1966, Wiley, New York.
19. Herrero J.L., Roberts M.J., Delicato L.S., Gieselmann M.A., Dayan P., Thiele A. Acetylcholine contributes through muscarinic receptors to attentional modulation in V1. Nature 2008, 454:1110-1114.
20. Herrero J.L., Gieselmann M.A., Sanayei M., Thiele A. Attention-induced variance and noise correlation reduction in macaque V1 is mediated by NMDA receptors. Neuron 2013, 78:729-739.
21. Herz A., Zieglgänsberger W., Färber G. Microelectrophoretic studies concerning the spread of glutamic acid and GABA in brain tissue. Exp. Brain Res. 1969, 9:221-235.
22. Jacob S.N., Nieder A. Complementary roles for primate frontal and parietal cortex in guarding working memory from distractor stimuli. Neuron 2014, 83:226-237.
23. Jacob S.N., Ott T., Nieder A. Dopamine regulates two classes of primate prefrontal neurons that represent sensory signals. J.Neurosci. 2013, 33:13724-13734.
24. Lidow M.S., Wang F., Cao Y., Goldman-Rakic P.S. Layer V neurons bear the majority of mRNAs encoding the five distinct dopamine receptor subtypes in the primate prefrontal cortex. Synapse 1998, 28:10-20.
25. Matsumoto M., Hikosaka O. Two types of dopamine neuron distinctly convey positive and negative motivational signals. Nature 2009, 459:837-841.
26. Matsumoto M., Takada M. Distinct representations of cognitive and motivational signals in midbrain dopamine neurons. Neuron 2013, 79:1011-1024.
27. McNab F., Varrone A., Farde L., Jucaite A., Bystritsky P., Forssberg H., Klingberg T. Changes in cortical dopamine D1 receptor binding associated with cognitive training. Science 2009, 323:800-802.
28. Mehta M.A., Sahakian B.J., McKenna P.J., Robbins T.W. Systemic sulpiride in young adult volunteers simulates the profile of cognitive deficits in Parkinson's disease. Psychopharmacology (Berl.) 1999, 146:162-174.
29. Miller E.K., Cohen J.D. An integrative theory of prefrontal cortex function. Annu. Rev. Neurosci. 2001, 24:167-202.
30. Müller U., von Cramon D.Y., Pollmann S. D1- versus D2-receptor modulation of visuospatial working memory in humans. J.Neurosci. 1998, 18:2720-2728.
31. Nawrot M.P., Boucsein C., Rodriguez Molina V., Riehle A., Aertsen A., Rotter S. Measurement of variability dynamics in cortical spike trains. J.Neurosci. Methods 2008, 169:374-390.
32. Nieder A. Supramodal numerosity selectivity of neurons in primate prefrontal and posterior parietal cortices. Proc. Natl. Acad. Sci. USA 2012, 109:11860-11865.
33. Nieder A. Coding of abstract quantity by 'number neurons' of the primate brain. J.Comp. Physiol. A Neuroethol. Sens. Neural Behav. Physiol. 2013, 199:1-16.
34. Nieder A., Miller E.K. Coding of cognitive magnitude: compressed scaling of numerical information in the primate prefrontal cortex. Neuron 2003, 37:149-157.
35. Nieder A., Freedman D.J., Miller E.K. Representation of the quantity of visual items in the primate prefrontal cortex. Science 2002, 297:1708-1711.
36. Noudoost B., Moore T. Control of visual cortical signals by prefrontal dopamine. Nature 2011, 474:372-375.
37. Noudoost B., Moore T. The role of neuromodulators in selective attention. Trends Cogn. Sci. 2011, 15:585-591.
38. Puig M.V., Miller E.K. The role of prefrontal dopamine D1 receptors in the neural mechanisms of associative learning. Neuron 2012, 74:874-886.
39. Puig M.V., Miller E.K. Neural substrates of dopamine D2 receptor modulated executive functions in the monkey prefrontal cortex. Cerebral Cortex 2014, Published online May 9, 2014. 10.1093/cercor/bhu096.
40. Ragozzino M.E. The effects of dopamine D(1) receptor blockade in the prelimbic-infralimbic areas on behavioral flexibility. Learn. Mem. 2002, 9:18-28.
41. Redgrave P., Gurney K., Reynolds J. What is reinforced by phasic dopamine signals?. Brain Res. Brain Res. Rev. 2008, 58:322-339.
42. Robbins T.W., Arnsten A.F.T. The neuropsychopharmacology of fronto-executive function: monoaminergic modulation. Annu. Rev. Neurosci. 2009, 32:267-287.
43. Sawaguchi T. The effects of dopamine and its antagonists on directional delay-period activity of prefrontal neurons in monkeys during an oculomotor delayed-response task. Neurosci. Res. 2001, 41:115-128.
44. Sawaguchi T., Goldman-Rakic P.S. D1 dopamine receptors in prefrontal cortex: involvement in working memory. Science 1991, 251:947-950.
45. Sawaguchi T., Goldman-Rakic P.S. The role of D1-dopamine receptor in working memory: local injections of dopamine antagonists into the prefrontal cortex of rhesus monkeys performing an oculomotor delayed-response task. J.Neurophysiol. 1994, 71:515-528.
46. Schultz W. Predictive reward signal of dopamine neurons. J.Neurophysiol. 1998, 80:1-27.
47. Schultz W. Multiple dopamine functions at different time courses. Annu. Rev. Neurosci. 2007, 30:259-288.
48. Seamans J.K., Yang C.R. The principal features and mechanisms of dopamine modulation in the prefrontal cortex. Prog. Neurobiol. 2004, 74:1-58.
49. Seamans J.K., Durstewitz D., Christie B.R., Stevens C.F., Sejnowski T.J. Dopamine D1/D5 receptor modulation of excitatory synaptic inputs to layer V prefrontal cortex neurons. Proc. Natl. Acad. Sci. USA 2001, 98:301-306.
50. Stefani M.R., Moghaddam B. Rule learning and reward contingency are associated with dissociable patterns of dopamine activation in the rat prefrontal cortex, nucleus accumbens, and dorsal striatum. J.Neurosci. 2006, 26:8810-8818.
51. Stelzel C., Fiebach C.J., Cools R., Tafazoli S., D'Esposito M. Dissociable fronto-striatal effects of dopamine D2 receptor stimulation on cognitive versus motor flexibility. Cortex 2013, 49:2799-2811.
52. Stoet G., Snyder L.H. Neural correlates of executive control functions in the monkey. Trends Cogn. Sci. 2009, 13:228-234.
53. Takahashi H., Kato M., Takano H., Arakawa R., Okumura M., Otsuka T., Kodaka F., Hayashi M., Okubo Y., Ito H., Suhara T. Differential contributions of prefrontal and hippocampal dopamine D(1) and D(2) receptors in human cognitive functions. J.Neurosci. 2008, 28:12032-12038.
54. Takahashi H., Yamada M., Suhara T. Functional significance of central D1 receptors in cognition: beyond working memory. J.Cereb. Blood Flow Metab. 2012, 32:1248-1258.
55. Thiele A., Delicato L.S., Roberts M.J., Gieselmann M.A. A novel electrode-pipette design for simultaneous recording of extracellular spikes and iontophoretic drug application in awake behaving monkeys. J.Neurosci. Methods 2006, 158:207-211.
56. Trantham-Davidson H., Neely L.C., Lavin A., Seamans J.K. Mechanisms underlying differential D1 versus D2 dopamine receptor regulation of inhibition in prefrontal cortex. J.Neurosci. 2004, 24:10652-10659.
57. Tseng K.Y., O'Donnell P. Dopamine-glutamate interactions controlling prefrontal cortical pyramidal cell excitability involve multiple signaling mechanisms. J.Neurosci. 2004, 24:5131-5139.
58. Vallentin D., Bongard S., Nieder A. Numerical rule coding in the prefrontal, premotor, and posterior parietal cortices of macaques. J.Neurosci. 2012, 32:6621-6630.
59. Vijayraghavan S., Wang M., Birnbaum S.G., Williams G.V., Arnsten A.F.T. Inverted-U dopamine D1 receptor actions on prefrontal neurons engaged in working memory. Nat. Neurosci. 2007, 10:376-384.
60. Viswanathan P., Nieder A. Neuronal correlates of a visual "sense of number" in primate parietal and prefrontal cortices. Proc. Natl. Acad. Sci. USA 2013, 110:11187-11192.
61. Wallis J.D., Anderson K.C., Miller E.K. Single neurons in prefrontal cortex encode abstract rules. Nature 2001, 411:953-956.
62. Wang Y., Goldman-Rakic P.S. D2 receptor regulation of synaptic burst firing in prefrontal cortical pyramidal neurons. Proc. Natl. Acad. Sci. USA 2004, 101:5093-5098.
63. Wang M., Vijayraghavan S., Goldman-Rakic P.S. Selective D2 receptor actions on the functional circuitry of working memory. Science 2004, 303:853-856.
64. Wang M., Yang Y., Wang C.-J., Gamo N.J., Jin L.E., Mazer J.A., Morrison J.H., Wang X.-J., Arnsten A.F.T. NMDA receptors subserve persistent neuronal firing during working memory in dorsolateral prefrontal cortex. Neuron 2013, 77:736-749.
65. Williams G.V., Goldman-Rakic P.S. Modulation of memory fields by dopamine D1 receptors in prefrontal cortex. Nature 1995, 376:572-575.
66. Winterer G., Weinberger D.R. Genes, dopamine and cortical signal-to-noise ratio in schizophrenia. Trends Neurosci. 2004, 27:683-690.