Neuronal Ensemble Bursting in the Basal Forebrain Encodes Salience Irrespective of Valence

Neuron

Volumn 59, Issue 1, 2008, Pages 138-149

  Lin, Shih Chieh ^a,b   Nicolelis, Miguel A L ^a,b,c,d  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

^b DUKE UNIVERSITY   (United States)

^c Duke University   (United States)

^d Edmond and Lily Safra International Institute of Neuroscience of Natal   (Brazil)

Author keywords

SYSNEURO

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; ATTENTION; BEHAVIOR; BRAIN CORTEX; FOREBRAIN; MALE; MOTIVATION; NEUROMODULATION; NONHUMAN; PRIORITY JOURNAL; PUNISHMENT; RAT; REINFORCEMENT; REWARD; STIMULUS RESPONSE; TASK PERFORMANCE;

ACOUSTIC STIMULATION; ACTION POTENTIALS; ANIMALS; ATTENTION; BEHAVIOR, ANIMAL; CHOICE BEHAVIOR; CUES; DISCRIMINATION (PSYCHOLOGY); EXTINCTION, PSYCHOLOGICAL; MALE; NEURONS; PHOTIC STIMULATION; PREDICTIVE VALUE OF TESTS; PROSENCEPHALON; RATS; RATS, LONG-EVANS; REINFORCEMENT (PSYCHOLOGY); SPECTRUM ANALYSIS; WATER DEPRIVATION;

EID: 46149098660     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuron.2008.04.031     Document Type: Article

References (54)

1. Alonso A., Khateb A., Fort P., Jones B.E., and Muhlethaler M. Differential oscillatory properties of cholinergic and noncholinergic nucleus basalis neurons in guinea pig brain slice. Eur. J. Neurosci. 8 (1996) 169-182
2. 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
3. Belova M.A., Paton J.J., Morrison S.E., and Salzman C.D. Expectation modulates neural responses to pleasant and aversive stimuli in primate amygdala. Neuron 55 (2007) 970-984
4. Burk J.A., and Sarter M. Dissociation between the attentional functions mediated via basal forebrain cholinergic and GABAergic neurons. Neuroscience 105 (2001) 899-909
5. Buzsaki G., Bickford R., Ponomareff G., Thal L., Mandel R., and Gage F. Nucleus basalis and thalamic control of neocortical activity in the freely moving rat. J. Neurosci. 8 (1988) 4007-4026
6. Daw N.D., Kakade S., and Dayan P. Opponent interactions between serotonin and dopamine. Neural Netw. 15 (2002) 603-616
7. Dykes R.W. Mechanisms controlling neuronal plasticity in somatosensory cortex. Can. J. Physiol. Pharmacol. 75 (1997) 535-545
8. Engel A.K., Fries P., and Singer W. Dynamic predictions: oscillations and synchrony in top-down processing. Nat. Rev. Neurosci. 2 (2001) 704-716
9. Everitt B.J., and Robbins T.W. Central cholinergic systems and cognition. Annu. Rev. Psychol. 48 (1997) 649-684
10. Folstein J.R., and Van Petten C. Influence of cognitive control and mismatch on the N2 component of the ERP: a review. Psychophysiology 45 (2008) 152-170
11. Freund T.F., and Meskenaite V. gamma-Aminobutyric acid-containing basal forebrain neurons innervate inhibitory interneurons in the neocortex. Proc. Natl. Acad. Sci. USA 89 (1992) 738-742
12. Gervasoni D., Lin S.C., Ribeiro S., Soares E.S., Pantoja J., and Nicolelis M.A. Global forebrain dynamics predict rat behavioral states and their transitions. J. Neurosci. 24 (2004) 11137-11147
13. Green D.M., and Swets J.A. Signal Detection Theory and Psychophysics (1966), John Wiley, New York
14. Gritti I., Mainville L., Mancia M., and Jones B.E. GABAergic and other noncholinergic basal forebrain neurons, together with cholinergic neurons, project to the mesocortex and isocortex in the rat. J. Comp. Neurol. 383 (1997) 163-177
15. Herrmann C.S., and Knight R.T. Mechanisms of human attention: event-related potentials and oscillations. Neurosci. Biobehav. Rev. 25 (2001) 465-476
16. Holland P.C. Disconnection of the amygdala central nucleus and the substantia innominata/nucleus basalis magnocellularis disrupts performance in a sustained attention task. Behav. Neurosci. 121 (2007) 80-89
17. Holland P.C., and Gallagher M. Amygdala circuitry in attentional and representational processes. Trends Cogn. Sci. 3 (1999) 65-73
18. Jolkkonen E., Miettinen R., Pikkarainen M., and Pitkanen A. Projections from the amygdaloid complex to the magnocellular cholinergic basal forebrain in rat. Neuroscience 111 (2002) 133-149
19. Kaczmarek L.K., and Levitan I.B. Neuromodulation: The Biochemical Control of Neuronal Excitability (1987), Oxford University Press, New York
20. Kilgard M.P., and Merzenich M.M. Cortical map reorganization enabled by nucleus basalis activity. Science 279 (1998) 1714-1718
21. Lang P.J., and Davis M. Emotion, motivation, and the brain: reflex foundations in animal and human research. Prog. Brain Res. 156 (2006) 3-29
22. Lee M.G., Manns I.D., Alonso A., and Jones B.E. Sleep-wake related discharge properties of basal forebrain neurons recorded with micropipettes in head-fixed rats. J. Neurophysiol. 92 (2004) 1182-1198
23. Lee M.G., Hassani O.K., Alonso A., and Jones B.E. Cholinergic basal forebrain neurons burst with theta during waking and paradoxical sleep. J. Neurosci. 25 (2005) 4365-4369
24. Lin S.C., Gervasoni D., and Nicolelis M.A. Fast modulation of prefrontal cortex activity by basal forebrain noncholinergic neuronal ensembles. J. Neurophysiol. 96 (2006) 3209-3219
25. Maddux J.M., Kerfoot E.C., Chatterjee S., and Holland P.C. Dissociation of attention in learning and action: effects of lesions of the amygdala central nucleus, medial prefrontal cortex, and posterior parietal cortex. Behav. Neurosci. 121 (2007) 63-79
26. Matsumoto M., and Hikosaka O. Lateral habenula as a source of negative reward signals in dopamine neurons. Nature 447 (2007) 1111-1115
27. McGaughy J., Dalley J.W., Morrison C.H., Everitt B.J., and Robbins T.W. Selective behavioral and neurochemical effects of cholinergic lesions produced by intrabasalis infusions of 192 IgG-Saporin on attentional performance in a five-choice serial reaction time task. J. Neurosci. 22 (2002) 1905-1913
28. Muir J.L., Everitt B., and Robbins T. AMPA-induced excitotoxic lesions of the basal forebrain: a significant role for the cortical cholinergic system in attentional function. J. Neurosci. 14 (1994) 2313-2326
29. Nicolelis M.A., Ghazanfar A.A., Faggin B.M., Votaw S., and Oliveira L.M. Reconstructing the engram: simultaneous, multisite, many single neuron recordings. Neuron 18 (1997) 529-537
30. Nicolelis M.A., Dimitrov D., Carmena J.M., Crist R., Lehew G., Kralik J.D., and Wise S.P. Chronic, multisite, multielectrode recordings in macaque monkeys. Proc. Natl. Acad. Sci. USA 100 (2003) 11041-11046
31. Page K.J., Everitt B.J., Robbins T.W., Marston H.M., and Wilkinson L.S. Dissociable effects on spatial maze and passive avoidance acquisition and retention following AMPA- and ibotenic acid-induced excitotoxic lesions of the basal forebrain in rats: differential dependence on cholinergic neuronal loss. Neuroscience 43 (1991) 457-472
32. Pang K., Williams M.J., Egeth H., and Olton D.S. Nucleus basalis magnocellularis and attention: effects of muscimol infusions. Behav. Neurosci. 107 (1993) 1031-1038
33. Parikh V., Kozak R., Martinez V., and Sarter M. Prefrontal acetylcholine release controls cue detection on multiple timescales. Neuron 56 (2007) 141-154
34. Paton J.J., Belova M.A., Morrison S.E., and Salzman C.D. The primate amygdala represents the positive and negative value of visual stimuli during learning. Nature 439 (2006) 865-870
35. Paxinos G., and Watson C. The Rat Brain in Stereotaxic Coordinates. 5th Edition (2005), Academic Press, San Diego, CA
36. Pessiglione M., Schmidt L., Draganski B., Kalisch R., Lau H., Dolan R.J., and Frith C.D. How the brain translates money into force: a neuroimaging study of subliminal motivation. Science 316 (2007) 904-906
37. Richardson R.T., and DeLong M. Context-dependent responses of primate nucleus basalis neurons in a go/no-go task. J. Neurosci. 10 (1990) 2528-2540
38. Riekkinen Jr. P., Sirvio J., Riekkinen M., and Riekkinen P. EEG changes induced by acute and chronic quisqualic or ibotenic acid nucleus basalis lesions are stabilized by tacridine. Brain Res. 559 (1991) 304-308
39. Roesch M.R., and Olson C.R. Neuronal activity related to reward value and motivation in primate frontal cortex. Science 304 (2004) 307-310
40. Roitman M.F., Wheeler R.A., and Carelli R.M. Nucleus accumbens neurons are innately tuned for rewarding and aversive taste stimuli, encode their predictors, and are linked to motor output. Neuron 45 (2005) 587-597
41. Sambeth A., Maes J.H., Van Luijtelaar G., Molenkamp I.B., Jongsma M.L., and Van Rijn C.M. Auditory event-related potentials in humans and rats: effects of task manipulation. Psychophysiology 40 (2003) 60-68
42. Sarter M., and Bruno J.P. The neglected constituent of the basal forebrain corticopetal projection system: GABAergic projections. Eur. J. Neurosci. 15 (2002) 1867-1873
43. Schultz W., Dayan P., and Montague P.R. A neural substrate of prediction and reward. Science 275 (1997) 1593-1599
44. Semba K. Multiple output pathways of the basal forebrain: organization, chemical heterogeneity, and roles in vigilance. Behav. Brain Res. 115 (2000) 117-141
45. Seymour B., O'Doherty J.P., Koltzenburg M., Wiech K., Frackowiak R., Friston K., and Dolan R. Opponent appetitive-aversive neural processes underlie predictive learning of pain relief. Nat. Neurosci. 8 (2005) 1234-1240
46. Voytko M.L., Olton D.S., Richardson R.T., Gorman L.K., Tobin J.R., and Price D.L. Basal forebrain lesions in monkeys disrupt attention but not learning and memory. J. Neurosci. 14 (1994) 167-186
47. Ward L.M. Synchronous neural oscillations and cognitive processes. Trends Cogn. Sci. 7 (2003) 553-559
48. Weinberger N.M. The nucleus basalis and memory codes: auditory cortical plasticity and the induction of specific, associative behavioral memory. Neurobiol. Learn. Mem. 80 (2003) 268-284
49. Wenk G.L. The nucleus basalis magnocellularis cholinergic system: one hundred years of progress. Neurobiol. Learn. Mem. 67 (1997) 85-95
50. Whalen P.J., Kapp B., and Pascoe J. Neuronal activity within the nucleus basalis and conditioned neocortical electroencephalographic activation. J. Neurosci. 14 (1994) 1623-1633
51. Wiest M.C., Bentley N., and Nicolelis M.A. Heterogeneous integration of bilateral whisker signals by neurons in primary somatosensory cortex of awake rats. J. Neurophysiol. 93 (2005) 2966-2973
52. Wilson F.A., and Rolls E.T. Learning and memory is reflected in the responses of reinforcement-related neurons in the primate basal forebrain. J. Neurosci. 10 (1990) 1254-1267
53. Yacubian J., Glascher J., Schroeder K., Sommer T., Braus D.F., and Buchel C. Dissociable systems for gain- and loss-related value predictions and errors of prediction in the human brain. J. Neurosci. 26 (2006) 9530-9537
54. Zaborszky L., and Duque A. Sleep-wake mechanisms and basal forebrain circuitry. Front. Biosci. 8 (2003) d1146-d1169