Memory systems in the chick: Regional and temporal control by noradrenaline

Brain Research Bulletin

Volumn 76, Issue 3, 2008, Pages 170-182

  Gibbs, Marie E ^a  

^a MONASH UNIVERSITY   (Australia)

Author keywords

Astrocytes; Bead discrimination learning; Central metabolism; Chick; Memory; Single trial learning

Indexed keywords

4 AMINOBUTYRIC ACID; N METHYL DEXTRO ASPARTIC ACID; NEUROTRANSMITTER; NORADRENALIN;

AROUSAL; ASTROCYTE; BASAL GANGLION; BRAIN REGION; CHICK; CORPUS STRIATUM; DISCRIMINATION LEARNING; ENERGY METABOLISM; EXPERIMENTATION; HIPPOCAMPUS; LEARNING; LOCUS CERULEUS; LONG TERM MEMORY; MEMORY; MEMORY CONSOLIDATION; NEUROPHARMACOLOGY; NONHUMAN; PRIORITY JOURNAL; REINFORCEMENT; REVIEW; REWARD; SHORT TERM MEMORY; TASK PERFORMANCE;

ADRENERGIC AGONISTS; ADRENERGIC ANTAGONISTS; ANIMALS; ASTROCYTES; BEHAVIOR, ANIMAL; BRAIN; CHICKENS; GLUCOSE; LEARNING; MEMORY; NOREPINEPHRINE; RECEPTORS, ADRENERGIC; REWARD;

EID: 43549092256     PISSN: 03619230     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainresbull.2008.02.021     Document Type: Review

References (103)

1. Anderson C.M., and Nedergaard M. Astrocyte-mediated control of cerebral microcirculation. Trends Neurosci. 26 (2003) 340-344
2. Anokhin K.V., Tiunova A.A., and Rose S.P. Reminder effects-reconsolidation or retrieval deficit? Pharmacological dissection with protein synthesis inhibitors following reminder for a passive-avoidance task in young chicks. Eur. J. Neurosci. 15 (2002) 1759-1765
3. Araque A., Parpura V., Sanzgiri R.P., and Haydon P.G. Tripartite synapses: glia, the unacknowledged partner. Trends Neurosci. 22 (1999) 208-215
4. Arnsten A.F.T. Through the looking glass: differential noradrenergic modulation of prefrontal cortical function. Neural Plast. 7 (2000) 133-146
5. Aston-Jones G., and Cohen J.D. An integrative theory of locus coeruleus-norepinephrine function: adaptive gain and optimal performance. Annu. Rev. Neurosci. 28 (2005) 403-450
6. Atallah H.E., Frank M.J., and O'Reilly R.C. Hippocampus, cortex, and basal ganglia: insights from computational models of complementary learning systems. Neurobiol. Learn. Mem. 82 (2004) 253-267
7. Berridge C.W., and Abercrombie E.D. Relationship between locus coeruleus discharge rates and rates of noradrenaline release within neocortex as assessed by in vivo microdialysis. Neuroscience 93 (1999) 1263-1270
8. Berridge C.W., and Waterhouse B.D. The locus coeruleus-noradrenergic system: modulation of behavioral state and state-dependent cognitive processes. Brain Res. Rev. 42 (2003) 33-84
9. Bouret S., Duvel A., Onat S., and Sara S.J. Phasic activation of locus ceruleus neurons by the central nucleus of the amygdala. J. Neurosci. 23 (2003) 3491-3497
10. Bouret S., and Sara S.J. Network reset: a simplified overarching theory of locus coeruleus noradrenaline function. Trends Neurosci. 28 (2005) 574-582
11. Cherkin A. Kinetics of memory consolidation: role of amnesic treatment parameters. Proc. Natl. Acad. Sci. U.S.A. 63 (1969) 1094-1101
12. Clark R.E., Broadbent N.J., and Squire L.R. The hippocampus and spatial memory: findings with a novel modification of the water maze. J. Neurosci. 27 (2007) 6647-6654
13. Colombo M., and Broadbent N. Is the avian hippocampus a functional homologue of the mammalian hippocampus?. Neurosci. Biobehav. Rev. 24 (2000) 465-484
14. Colombo P.J., and Gold P.E. Multiple memory systems. Neurobiol. Learn. Mem. 82 (2004) 169-170
15. Crow T.J., and Arbuthnott G.W. Function of catecholamine-containing neurones in mammalian central nervous system. Nature 238 (1972) 245-246
16. Crowe S.F., Ng K.T., and Gibbs M.E. Forebrain noradrenaline concentration following weakly reinforced training. Pharmacol. Biochem. Behav. 40 (1991) 173-176
17. Csillag A. Striato-telencephalic and striato-tegmental circuits: relevance to learning in domestic chicks. Behav. Brain Res. 98 (1999) 227-236
18. Daisley J.N., Gruss M., Rose S.P.R., and Braun K. Passive avoidance training and recall are associated with increased glutamate levels in the intermediate medial hyperstriatum ventrale of the day-old chick. Neural Plast. 6 (1998) 53-61
19. Daisley J.N., and Rose S.P.R. Amino acid release from the intermediate medial hyperstriatum ventrale (IMHV) of day-old chicks following a one-trial passive avoidance task. Neurobiol. Learn. Mem 77 (2002) 185-201
20. Devoto P., Flore G., Saba P., Fa M., and Gessa G.L. Stimulation of the locus coeruleus elicits noradrenaline and dopamine release in the medial prefrontal and parietal cortex. J. Neurochem. 92 (2005) 368-374
21. Fellin T., and Carmignoto G. Neurone-to-astrocyte signalling in the brain represents a distinct multifunctional unit. J. Physiol. 559 (2004) 3-15
22. Foote S.L., Berridge C.W., Adams L.M., and Pineda J.A. Electrophysiological evidence for the involvement of the locus coeruleus in alerting, orienting, and attending. Prog. Brain Res. 88 (1991) 521-532
23. Gibbs M.E. Memory and behaviour: birds and their memories. Bird Behav. 4 (1983) 93-107
24. Gibbs M.E. Behavioral and pharmacological unravelling of memory formation. Neurochem. Res. 16 (1991) 715-726
25. Gibbs M.E., Anderson D.G., and Hertz L. Inhibition of glycogenolysis in astrocytes interrupts memory consolidation in young chicks. Glia 54 (2006) 214-222
26. Gibbs M.E., and Barnett J.M. Drug effects on succesive discrimination learning in young chickens. Brain Res. Bull. 1 (1976) 295-299
27. M.E. Gibbs, D.N. Bowser, D.S. Hutchinson, R.E. Loiacono, R.J. Summers, Memory processing in the avian hippocampus involves interactions between b-adrenoceptors, glutamate receptors and metabolism, Neuropsychopharmacology, 2008, doi:10.1038/npp.2008.5.
28. Gibbs M.E., and Hertz L. Importance of glutamate-generating metabolic pathways for memory consolidation in chick. J. Neurosci. Res. 81 (2005) 293-300
29. Gibbs M.E., Hertz L., and Ng K.T. Inhibition of short-term memory formation in the chick by blockade of extracellular glutamate uptake. Learn. Mem. 81 (2004) 115-119
30. M.E. Gibbs, D.S. Hutchinson, R.J. Summers, Role of (-adrenoceptors in memory consolidation: (3-adrenoceptors act on glucose uptake and (2-adrenoceptors on glycogenolysis, Neuropsychopharmacol (2007), doi:10.1038/sj.npp.1301629 (advanced online publication, 28 November, 2007).
31. C receptors in short-term memory formation in young chicks. Neuroscience 131 (2005) 567-576
32. Gibbs M.E., Lloyd H.G.E., Santa T., and Hertz L. Glycogen is a preferred glutamate precursor during learning in 1-day-old chick: biochemical and behavioral evidence. J. Neurosci. Res. 85 (2007) 3326-3333
33. Gibbs M.E., and Ng K.T. Diphenylhydantoin facilitation of labile, protein-independent memory. Brain Res. Bull. 1 (1976) 203-208
34. Gibbs M.E., and Ng K.T. Psychobiology of memory: towards a model of memory formation. Biobehav. Rev. 1 (1977) 113-136
35. Gibbs M.E., and Ng K.T. Neuronal depolarization and the inhibition of short-term memory formation. Physiol. Behav. 23 (1979) 369-375
36. Gibbs M.E., and Ng K.T. Dual action of cycloheximide on memory formation in day-old chicks. Behav. Brain Res. 12 (1984) 21-27
37. Gibbs M.E., Ng K.T., and Crowe S.F. Hormones and the timing of phases of memory formation. In: Andrew R.J. (Ed). Neural and Behavioural Plasticity: The Use of the Domestic Chick as a Model (1991), Oxford University Press, New York 440-455
38. Gibbs M.E., O'Dowd B.S., Hertz E., and Hertz L. Astrocytic energy metabolism consolidates memory in young chicks. Neuroscience 141 (2006) 9-13
39. Gibbs M.E., O'Dowd B.S., Hertz L., Robinson S.R., Sedman G.L., and Ng K.T. Inhibition of glutamine synthetase activity prevents memory consolidation. Cogn. Brain Res. 4 (1996) 57-64
40. 3-adrenoceptors in memory consolidation. Neuroscience 95 (2000) 913-922
41. Gibbs M.E., and Summers R.J. Role of adrenoceptor subtypes in memory consolidation. Prog. Neurobiol. 67 (2002) 345-391
42. 3-adrenoceptor agonists. Neuroscience 114 (2002) 69-79
43. Gibbs M.E., and Summers R.J. Locus coeruleus involvement in memory formation. Proc. Aust. Neurosci. Soc. 14 (2003) 8
44. 2-Adrenoceptors in the basal ganglia have a role in memory consolidation and reinforcement. Neuropharmacology 45 (2003) 355-367
45. Gibbs M.E., and Summers R.J. Principle neurotransmitters. Adrenaline and noradrenaline. In: Riedel G., and Platt B. (Eds). From Messengers to Molecules: Memories are Made of These (2004), Kluwer Academic/Plenum Publishers, New York 155-173
46. 3-adrenoceptors in memory formation in the chick. Neuroscience 131 (2005) 31-42
47. Gilbert D.B., Patterson T.A., and Rose S.P.R. Dissociation of brain sites necessary for registration and storage of memory for a one-trial passive avoidance task in the chick. Behav. Neurosci. 105 (1991) 553-561
48. Gold P.E., and McGaugh J.L. A single-trace, two-process view of memory storage processes. In: Deutsch D., and Deutsch J.A. (Eds). Short-term Memory (1975), Academic Press, New York 355-378
49. Halassa M.M., Fellin T., Takano H., Dong J.H., and Haydon P.G. Synaptic islands defined by the territory of a single astrocyte. J. Neurosci. 27 (2007) 6473-6477
50. Haydon P.G., and Carmignoto G. Astrocyte control of synaptic transmission and neurovascular coupling. Physiol. Rev. 86 (2006) 1009-1031
51. Hebb D.O. The Organization of Behavior (1949), Wiley, New York
52. Hertz L., O'Dowd B.S., Ng K.T., and Gibbs M.E. Reciprocal changes in forebrain contents of glycogen and of glutamate/glutamine during early memory consolidation in the day-old chick. Brain Res. 994 (2003) 226-233
53. Hertz L., Peng L., and Dienel G.A. Energy metabolism in astrocytes: high rate of oxidative metabolism and spatiotemporal dependence on glycolysis/glycogenolysis. J. Cereb. Blood Flow Metab. 27 (2007) 219-249
54. Hertz L., and Zielke H.R. Astrocytic control of glutamatergic activity: astrocytes as stars of the show. Trends Neurosci. 27 (2004) 735-743
55. Horn G., and Johnson M.H. Memory systems in the chick: dissociations and neuronal analysis. Neuropsychologia 27 (1989) 1-22 (Special Issue: Memory)
56. Horridge G.A. Interneurones: Their Origin, Action, Specificity, Growth and Plasticity (1968), Freeman, San Francisco
57. 3-adrenoceptors activate glucose uptake in chick astrocytes by distinct mechanisms: a mechanism for memory enhancement?. J. Neurochem. 103 (2007) 997-1008
58. Izawa E., Zachar G., Yanagihara S., and Matsushima T. Localized lesion of caudal part of lobus parolfactorius caused impulsive choice in the domestic chick: evolutionarily conserved function of ventral striatum. J. Neurosci. 23 (2003) 1894-1902
59. Izawa E.-I., Yanagihara S., Atsumi T., and Matsushima T. The role of basal ganglia in reinforcement learning and imprinting in domestic chicks. Neuroreport 12 (2001) 1743-1747
60. Jarvis E.D., Gunturkun O., et al. Opinion: avian brains and a new understanding of vertebrate brain evolution. Nat. Rev. Neurosci. 6 (2005) 151-159
61. Jeffrey P.L., and Gibbs M.E. Biochemical actions of sympathomimetic drugs which overcome cycloheximide-induced amnesia. Pharmacol. Biochem. Behav. 5 (1976) 571-575
62. Kabai P., Stewart M.G., Tarcali J., and Csillag A. Inhibiting effect of D1, but not D2 antagonist administered to the striatum on retention of passive avoidance in the chick. Neurobiol. Learn. Mem. 81 (2004) 155-158
63. Kety S.S. The biogenic amines in the central nervous system: their possible roles in arousal, emotion, and learning. In: Schmitt F.O. (Ed). The Neurosciences: Second Study Program (1970), The Rockefeller University Press, New York 324-336
64. Kim J.J., and Baxter M.G. Multiple brain-memory systems: the whole does not equal the sum of its parts. Trends Neurosci. 24 (2001) 324-330
65. Kiss J.P., Zsilla G., Mike A., Zelles T., Toth E., Lajtha A., and Vizi E.S. Subtype-specificity of the presynaptic alpha 2-adrenoceptors modulating hippocampal norepinephrine release in rat. Brain Res. 674 (1995) 238-244
66. Li J.S., and Chao Y.S. Electrolytic lesions of dorsal CA3 impair episodic-like memory in rats. Neurobiol. Learn. Mem. 89 (2008) 192-198
67. Magistretti P.J., and Pellerin L. Cellular mechanisms of brain energy metabolism and their relevance to functional brain imaging. Phil. Trans. R. Soc. Lond. B 354 (1999) 1155-1163
68. Mark R.F., and Watts M.E. Drug inhibition of memory formation in chickens. I. Long-term memory. Proc. R. Soc. Lond. B: Biol. Sci. 178 (1971) 439-454
69. Martineau M., Baux G., and Mothet J.P. Gliotransmission at central glutamatergic synapses: d-serine on stage. J. Physiol. (Paris) 99 (2006) 103-110
70. Matsushima T., Izawa E., Aoki N., and Yanagihara S. The mind through chick eyes: memory, cognition and anticipation. Zool. Sci. 20 (2003) 395-408
71. McCormick D.A., Pape H.-C., and Williamson A. Actions of norepinephrine in the cerebral cortex and thalamus: implications for function of the central noradrenergic system. Prog. Brain Res. 88 (1991) 293-305
72. McKittrick C.R., and Abercrombie E.D. Catecholamine mapping within nucleus accumbens: differences in basal and amphetamine-stimulated efflux of norepinephrine and dopamine in shell and core. J. Neurochem. 100 (2007) 1247-1256
73. Metea M.R., and Newman E.A. Glial cells dilate and constrict blood vessels: a mechanism of neurovascular coupling. J. Neurosci. 26 (2006) 2862-2870
74. Nedergaard M., Ransom B., and Goldman S.A. New roles for astrocytes: redefining the functional architecture of the brain. Trends Neurosci 26 (2003) 523-530
75. Newman E.A. New roles for astrocytes: regulation of synaptic transmission. Trends Neurosci. 26 (2003) 536-542
76. Ng K.T., O'Dowd B.S., Rickard N.S., Robinson S.R., Gibbs M.E., Rainey C., Zhao W.Q., Sedman G.L., and Hertz L. Complex roles of glutamate in the Gibbs-Ng model of one-trial aversive learning in the new-born chick. Neurosci. Biobehav. Rev. 21 (1997) 45-54
77. O'Dowd B.S., Gibbs M.E., Ng K.T., Hertz E., and Hertz L. Astrocytic glycogenolysis energizes memory processes in neonate chicks. Dev. Brain Res. 78 (1994) 137-141
78. O'Dowd B.S., Gibbs M.E., Sedman G.L., and Ng K.T. Astrocytes implicated in the energizing of intermediate memory processes in neonate chicks. Cogn. Brain Res. 2 (1994) 93-102
79. Perea G., and Araque A. Communication between astrocytes and neurons: a complex language. J. Physiol. (Paris) 96 (2002) 199-207
80. Pfaff D. Parsimonious biological models of memory and reinforcement. Psychol. Rev. 76 (1969) 70-81
81. Pfaff D.W., Martin E.M., and Ribeiro A.C. Relations between mechanisms of CNS arousal and mechanisms of stress. Stress 10 (2007) 316-325
82. Puelles L., Kuwana E., Puelles E., Bulfone A., Shimamura K., Keleher J., Smiga S., and Rubenstein J.L. Pallial and subpallial derivatives in the embryonic chick and mouse telencephalon, traced by the expression of the genes Dlx-2, Emx-1, Nkx-2.1, Pax-6, and Tbr-1. J. Comp. Neurol. 424 (2000) 409-438
83. Reiner A., Perkel D.J., Bruce L.L., et al. Revised nomenclature for avian telencephalon and some related brainstem nuclei. J. Comp. Neurol. 473 (2004) 377-414
84. Riedel G., Platt B., and Micheau J. Glutamate receptor function in learning and memory. Brain Res. Rev. 140 (2003) 1-47
85. Rose S.P.R. How chicks make memories: the cellular cascade from c-fos to dendritic remodelling. Trends Neurosci. 14 (1991) 390-397
86. Saigusa T., Tuinstra T., Koshikawa N., and Cools A.R. High and low responders to novelty effects: effects of a catecholamine synthesis inhibitor on novelty-induced changes in behaviour and release of accumbal dopamine. Neuroscience 88 (1999) 1153-1163
87. Sandi C., Rose S.P., and Patterson T.A. Unilateral hippocampal lesions prevent recall of a passive avoidance task in day-old chicks. Neurosci. Lett. 141 (1992) 255-258
88. Sara S.J. Retrieval and reconsolidation: toward a neurobiology of remembering. Learn. Mem. 7 (2000) 73-84
89. Schnabel R., Metzger M., Jiang S., Hemmings Jr. H.C., Greengard P., and Braun K. Localization of dopamine D1 receptors and dopaminoceptive neurons in the chick forebrain. J. Comp. Neurol. 388 (1997) 146-168
90. Segal M. The action of norepinephrine in the rat hippocampus: intracellular studies in the slice preparation. Brain Res. 206 (1981) 107-128
91. Singewald N., and Philippu A. Release of neurotransmitters in the locus coeruleus. Prog. Neurobiol. 56 (1998) 237-267
92. Stewart M.G., Kabai P., Harrison E., Steele R.J., Kossut M., Gierdalski M., and Csillag A. The involvement of dopamine in the striatum in passive avoidance training in the chick. Neuroscience 70 (1996) 7-14
93. Summers C. Mechanisms for quick and variable responses. Brain Behav. Evol. 57 (2001) 283
94. Summers M.J., Crowe S.F., and Ng K.T. Memory retrieval in the day-old chick: a psychobiological approach. Neurosci. Biobehav. Rev. 27 (2003) 219-231
95. Tuinstra T., and Cools A.R. High and low responders to novelty: effects of adrenergic agents on the regulation of accumbal dopamine under challenged and non-challenged conditions. Neuroscience 99 (2000) 55-64
96. Tuinstra T., and Cools A.R. Newly synthesized dopamine in the nucleus accumbens is regulated by β-adrenergic, but not α-adrenergic, receptors. Neuroscience 98 (2000) 743-747
97. Valentino R.J., and Aston-Jones G. Physiological and anatomical determinants of locus coeruleus discharge. In: Bloom F.E., and Kupfer D.J. (Eds). Psychopharmacology: The Fourth Generation of Progress (1995), Raven Press, Ltd, New York 373-385
98. Ventura R., Morrone C., and Puglisi-Allegra S. Prefrontal/accumbal catecholamine system determines motivational salience attribution to both reward- and aversion-related stimuli. Proc. Natl. Acad. Sci. U.S.A. 104 (2007) 5181-5186
99. Watts M.E., and Mark R.F. Drug inhibition of memory formation in chickens. II. Short-term memory. Proc. R. Soc. Lond. B: Biol. Sci. 178 (1971) 455-464
100. Watts M.E., and Mark R.F. Separate actions of ouabain and cycloheximide on memory. Brain Res. 25 (1971) 420-423
101. Woolf N.J. Global and serial neurons form A hierarchically arranged interface proposed to underlie memory and cognition. Neuroscience 74 (1996) 625-651
102. Yanagihara S., Izawa E.-I., Koga K., and Matsushima T. Reward-related neuronal activities in basal ganglia of domestic chicks. Neuroreport 12 (2001) 1431-1435
103. Zonta M., Angulo M.C., Gobbo S., Rosengarten B., Hossmann K.A., Pozzan T., and Carmignoto G. Neuron-to-astrocyte signaling is central to the dynamic control of brain microcirculation. Nat. Neurosci. 6 (2003) 43-50