Cognitive processing impairments in a supra-second temporal discrimination task in rats with cerebellar lesion

Neurobiology of Learning and Memory

Volumn 91, Issue 3, 2009, Pages 250-259

  Callu, Delphine ^a   Massioui, Nicole El ^a   Dutrieux, Gérard ^a   Brown, Bruce L ^b   Doyere, Valérie ^a  

^a CNRS   (France)

^b CITY UNIVERSITY OF NEW YORK   (United States)

Author keywords

Bisection; Executive dysfunction; Habit; Interpositus nuclei; Rat; Timing

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BEHAVIOR; CEREBELLUM INJURY; COGNITIVE DEFECT; CONTROLLED STUDY; DECISION MAKING; INTERPOSITUS NUCLEUS; LATENT PERIOD; MALE; NONHUMAN; RAT; TASK PERFORMANCE; TIME PERCEPTION;

ANALYSIS OF VARIANCE; ANIMALS; AUDITORY PERCEPTION; CEREBELLAR DISEASES; CEREBELLUM; CHOICE BEHAVIOR; COGNITION DISORDERS; COLCHICINE; DISCRIMINATION LEARNING; MALE; PSYCHOMOTOR PERFORMANCE; RANDOM ALLOCATION; RATS; RATS, SPRAGUE-DAWLEY; REACTION TIME; REINFORCEMENT (PSYCHOLOGY); TIME PERCEPTION;

EID: 60749129756     PISSN: 10747427     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nlm.2008.12.002     Document Type: Article

References (61)

1. Ackermann H., Gräber S., Hertrich I., and Daum I. Cerebellar contributions to the perception of temporal cues within the speech and nonspeech domain. Brain and Language 67 (1999) 228-241
2. Allan L.G. The location and interpretation of the bisection point. The Quarterly Journal of Experimental Psychology B 55 (2002) 43-60
3. Babinski J., and Tournay A. Symptômes des maladies du cervelet. Revue Neurologique 18 (1913) 306-322
4. Balsam P.D., Drew M.R., and Yang C. Timing at the start of associative learning. Learning and Motivation 33 (2002) 141-155
5. Bracha V., Zhao L., Irwin K.B., and Bloedel J.R. The human cerebellum and associative learning: dissociation between the acquisition, retention and extinction of conditioned eyeblinks. Brain Research 860 (2000) 87-94
6. Bracha V., Zhao L., Wunderlich D.A., Morrissy S.J., and Bloedel J.R. Patients with cerebellar lesions cannot acquire but are able to retain conditioned eyeblink reflexes. Brain 120 (1997) 1401-1413
7. Breukelaar J.W.C., and Dalrymple-Alford J.C. Effects of lesions to the cerebellar vermis and hemispheres on timing and counting in rats. Behavioral Neurosciences 113 (1999) 78-90
8. Callu D., Puget S., Faure A., Guegan M., and El Massioui N. Habit learning dissociation in rats with lesions to the vermis and the interpositus of the cerebellum. Neurobiology of Disease 27 (2007) 228-237
9. Canal N.M., Gourevitch R., and Sandner G. Non-monotonic dependency of PPI on temporal parameters: differential alteration by ketamine and MK-801 as opposed to apomorphine and DOI. Psychopharmacology (Berlin) 156 (2001) 169-176
10. Casini L., and Ivry R.B. Effects of divided attention on temporal processing in patients with lesions of the cerebellum or frontal lobe. Neuropsychology 13 (1999) 10-21
11. Christian K.M., Poulos A.M., Lavond D.G., and Thompson R.F. Comment on "Cerebellar LTD and learning-dependent timing of conditioned eyelid responses". Science 304 (2004) 211
12. Christian K.M., and Thompson R.F. Neural substrates of eyeblink conditioning: acquisition and retention. Learning and Memory 10 (2003) 427-455
13. Church R.M., and Deluty M.Z. Bisection of temporal intervals. Journal of Experimental Psychology: Animal Behavior Processes 3 (1977) 216-228
14. Colombel C., Lalonde R., and Caston J. The effects of unilateral removal of the cerebellar hemispheres on spatial learning and memory in rats. Brain Research 1004 (2004) 108-115
15. Courchesne E., and Allen G. Prediction and preparation, fundamental functions of the cerebellum. Learning and Memory 4 (1997) 1-35
16. Doyon J., Penhune V., and Ungerleider L.G. Distinct contribution of the cortico-striatal and cortico-cerebellar systems to motor skill learning. Neuropsychologia 41 (2003) 252-262
17. Fitch R.H., Threlkeld S.W., McClure M.M., and Pfeiffer A.M. Use of a modified prepulse inhibition paradigm to assess complex auditory discrimination in rodents. Brain Research Bulletin 76 (2008) 1-7
18. Gaytan-Tocaven L., and Olvera-Cortés M.E. Bilateral lesion of the cerebellar-dentate nucleus impairs egocentric sequential learning but not egocentric navigation in the rat. Neurobiology of Learning and Memory 82 (2004) 120-127
19. Gibbon J. On the form and location of the psychometric bisection function for time. Journal of Mathematical Psychology 24 (1981) 58-87
20. Goldschmidt R.B., and Steward O. Neurotoxic effects of colchicine: Differential susceptibility of CNS neuronal populations. Neuroscience 7 (1982) 695-714
21. Ito M. Mechanisms of motor learning in the cerebellum. Brain Research 886 (2000) 237-245
22. Ito M. Bases and implications of learning in the cerebellum-adaptative control and internal model mechanism. Progress in Brain Research 148 (2005) 95-109
23. Ivry R.B. The representation of temporal information in perception and motor control. Current Opinion in Neurobiology 6 (1996) 851-857
24. Ivry R.B., and Richardson T.C. Temporal control and coordination: The multiple timer model. Brain and Cognition 48 (2002) 117-132
25. Jahanshahi M., Jones C.R.G., Dirnberger G., and Frith C.D. The Substancia Nigra Pars Compacta and temporal processing. Journal of Neurosciences 26 (2006) 12266-12273
26. Joyal C.C., Strazielle C., and Lalonde R. Effects of dentate nucleus lesions on spatial and postural sensorimotor learning in rats. Behavioural Brain Research 122 (2001) 131-137
27. Jueptner M., Rijntjes M., Weiller C., Faiss J.H., Timmann D., Mueller S.P., et al. Localization of a cerebellar timing process using PET. Neurology 45 (1995) 1540-1545
28. Killeen P.R., Fetterman J.G., and Bizo L.A. Time's causes. In: Bradshaw C.M., and Szabadi E. (Eds). Time and behaviour: Psychological and neurological analyses (1997), Elsevier Science, Amsterdam 79-131
29. Koekkoek S.K.E., Hulscher H.C., Dortland B.R., Hensbroek R.A., Elgersma Y., Ruigrok T.J.H., et al. Cerebellar LTD and learning-dependent timing of conditioned eyelid responses. Science 301 (2003) 1736-1739
30. Lalonde R. The neurobiological basis of spontaneous alternation. Neurosciences and Biobehavioral Reviews 26 (2002) 91-104
31. Leggio M.G., Neri P., Graziano A., Mandolesi L., Molinari M., and Petrosini L. Cerebellar contribution to spatial event processing: Characterization of procedural learning. Experimental Brain Research 127 (1999) 01-11
32. Livesey A.C., Wall M.B., and Smith A.T. Time perception: Manipulation of task difficulty dissociates clock functions from other cognitive demands. Neuropsychologia 45 (2007) 321-331
33. Malapani C., Dubois B., Rancurel G., and Gibbon J. Cerebellar dysfunctions of temporal processing in the seconds range in humans. Neuroreport 9 (1998) 3907-3912
34. Mangels J.A., Ivry R.B., and Shimizu N. Dissociable contributions of the prefrontal and neocerebellar cortex to time perception. Brain Research Cognitive Brain Research 7 (1998) 15-39
35. Maquet P., Lejeune H., Pouthas V., Bonnet M., Casini L., Macar F., et al. Brain activation induced by estimation of duration: A PET study. Neuroimage 3 (1996) 119-126
36. Maricq A.V., and Church R.M. The differential effects of haloperidol and methamphetamine on time estimation in the rat. Psychopharmacology 79 (1983) 10-15
37. Maricq A.V., Roberts S., and Church R.M. Methamphetamine and time estimation. Journal of Experimental Psychology: Animal Behavior Processes 7 (1981) 18-30
38. Meck W.H. Neuropsychology of timing and time perception. Brain and Cognition 58 (2005) 1-8
39. Melgire M., Ragot R., Samson S., Penney T.B., Meck W.H., and Pouthas V. Auditory/visual duration bisection in patients with left or right medial-temporal lobe resection. Brain and Cognition 58 (2005) 119-124
40. Montoya C.P., Campbell-Hope L.J., Pemberton K.D., and Dunett S.B. The "staircase test": A measure of independent forelimb reaching and grasping abilities in rats. Journal of Neurosciences methods 36 (1991) 219-228
41. Monzée J., Drew T., and Smith A.M. Effects of muscimol inactivation of the cerebellar nuclei on precision grip. Journal of Neurophysiology 91 (2004) 1240-1249
42. Monzée J., and Smith A.M. Responses of cerebellar interpositus neurons to predictable perturbations applied to an object held in a precision grip. Journal of Neurophysiology 91 (2004) 1230-1239
43. Nixon P.D. The role of the cerebellum in preparing responses to predictable sensory events. Cerebellum 2 (2003) 114-122
44. Nixon P.D., and Passingham R.E. The cerebellum and cognition: Cerebellar lesions impair sequence learning but not conditional visuomotor learning in monkeys. Neuropsychologia 38 (2000) 1054-1072
45. Ohyama T., and Mauk M.D. Latent acquisition of timed responses in cerebellar cortex. Journal of Neurosciences 21 (2001) 682-690
46. O'Reilly J.X., Mesulmam M.M., and Nobre A.C. The cerebellum predicts the timing of perceptual events. Journal of Neurosciences 28 (2008) 2252-2260
47. Palmer S.L., Goloubeva O., Reddick W.E., Glass J.O., Gajjar A., Kun L., et al. Patterns of intellectual development among survivors of pediatric medulloblastoma: A longitudinal analysis. Journal of Clinical Oncology 19 (2001) 2302-2308
48. Paxinos G., and Watson C. The rat brain in stereotaxic coordinates. 2nd ed. (1986), Academic Press, Sydney
49. Perrett S.P., Ruiz B.P., and Mauk M.D. Cerebellar cortex lesions disrupt learning-dependant timing of conditioned eyelid responses. Journal of Neurosciences 13 (1993) 1708-1718
50. Petrosini L., Leggio M.G., and Molinari M. The cerebellum in the spatial problem solving: A co-star or a guest star?. Progress in Neurobiology 56 (1998) 191-210
51. Rao S.M., Mayer A.R., and Harrington D.L. The evolution of brain activation during temporal processing. Nature Neurosciences 4 (2001) 317-323
52. Rodríguez-Gironés M.A., and Kacelnik A. Response latencies in temporal bisection: Implications for timing models. In: De Keyser V., d'Ydewalle G., and Vandierendonck A. (Eds). Time and the dynamic control of behavior (1998), Hogrefe & Huber, Seattle 51-70
53. Rouanet H., Bernard J.M., and Leroux B. Statistiques en sciences humaines: Analyse inductive des données (1990), Dunod, Paris
54. Schiffrin R.N., and Schneider W. Controlled and automatic human information processing: II Perceptual learning, automatic attending and a general theory. Psychological Review 84 (1997) 127-190
55. Schneider W., and Shiffrin R.M. Controlled and automatic human information processing: I. Detection, search and attention. Psychological Review 84 (1977) 1-66
56. Steward O., Goldschmidt R.B., and Sutula T. IV Neurotoxicity of colchicines and other tubulin-binding agents: A selective vulnerability of certain neurons to the disruption of microtubules. Life Sciences 35 (1984) 43-51
57. Ungerleider L.G., Doyon J., and Karni A. Imaging brain plasticity during motor skill learning. Neurobiology of Learning and Memory 78 (2002) 553-564
58. Vajnerova O., Zhuravin I.A., and Brozek G. Functional ablation of deep cerebellar nuclei temporarily impairs learned coordination of forepaw and tongue movements. Behavioural Brain Research 108 (2000) 189-195
59. Voogd J. The human cerebellum. Journal of Chemical Neuroanatomy 26 (2003) 243-252
60. Wang J.J., Shimansky Y., Bracha V., and Bloedel J.R. Effects of cerebellar nuclear inactivation on the learning of a complex forelimb movement in cats. Journal of Neurophysiology 79 (1998) 2447-2459
61. Wearden J.H. Human performance on an analogue of an interval bisection task. The Quarterly Journal of Experimental Psychology B 43 (1991) 59-81