Touchscreen tasks in mice to demonstrate differences between hippocampal and striatal functions

[1]  Melissa J. Green,et al.  Corticostriatal Control of Goal-Directed Action Is Impaired in Schizophrenia , 2015, Biological Psychiatry.

[2]  Jean-Christophe Cassel,et al.  Optimization of Touchscreen-Based Behavioral Paradigms in Mice: Implications for Building a Battery of Tasks Taxing Learning and Memory Functions , 2014, PloS one.

[3]  B. Balleine,et al.  Translational studies of goal-directed action as a framework for classifying deficits across psychiatric disorders , 2014, Front. Syst. Neurosci..

[4]  B. Balleine,et al.  Dorsal and ventral streams: The distinct role of striatal subregions in the acquisition and performance of goal-directed actions , 2014, Neurobiology of Learning and Memory.

[5]  T. Bussey,et al.  Neuroscience and Biobehavioral Reviews Testing Long-term Memory in Animal Models of Schizophrenia: Suggestions from Cntrics , 2022 .

[6]  Timothy J Bussey,et al.  The touchscreen operant platform for testing learning and memory in rats and mice , 2013, Nature Protocols.

[7]  Lisa M. Saksida,et al.  A touch screen-automated cognitive test battery reveals impaired attention, memory abnormalities, and increased response inhibition in the TgCRND8 mouse model of Alzheimer's disease , 2013, Neurobiology of Aging.

[8]  Andrea Brovelli,et al.  Advanced Parkinson's disease effect on goal-directed and habitual processes involved in visuomotor associative learning , 2013, Front. Hum. Neurosci..

[9]  Richard D Emes,et al.  Synaptic scaffold evolution generated components of vertebrate cognitive complexity , 2012, Nature Neuroscience.

[10]  L. Saksida,et al.  TNiK Is Required for Postsynaptic and Nuclear Signaling Pathways and Cognitive Function , 2012, The Journal of Neuroscience.

[11]  M. Jahanshahi,et al.  Probabilistic classification learning with corrective feedback is selectively impaired in early Huntington’s disease—Evidence for the role of the striatum in learning with feedback , 2012, Neuropsychologia.

[12]  L. Saksida,et al.  New translational assays for preclinical modelling of cognition in schizophrenia: The touchscreen testing method for mice and rats , 2012, Neuropharmacology.

[13]  Inah Lee,et al.  Hippocampus is required for paired associate memory with neither delay nor trial uniqueness. , 2011, Learning & memory.

[14]  R. J. McDonald,et al.  Parallel associative processing in the dorsal striatum: Segregation of stimulus–response and cognitive control subregions , 2011, Neurobiology of Learning and Memory.

[15]  G. Barker,et al.  When Is the Hippocampus Involved in Recognition Memory? , 2011, The Journal of Neuroscience.

[16]  T. Robbins,et al.  Hippocampal dysfunction in patients with mild cognitive impairment: A functional neuroimaging study of a visuospatial paired associates learning task , 2011, Neuropsychologia.

[17]  L. Saksida,et al.  A computer-automated touchscreen paired-associates learning (PAL) task for mice: impairments following administration of scopolamine or dicyclomine and improvements following donepezil , 2011, Psychopharmacology.

[18]  Emma R. Wood,et al.  The role of hippocampal subregions in memory for stimulus associations , 2010, Behavioural Brain Research.

[19]  L. Saksida,et al.  Trial-unique, delayed nonmatching-to-location (TUNL): A novel, highly hippocampus-dependent automated touchscreen test of location memory and pattern separation , 2010, Neurobiology of Learning and Memory.

[20]  C. Paul,et al.  Spatial memory: Theoretical basis and comparative review on experimental methods in rodents , 2009, Behavioural Brain Research.

[21]  L. Saksida,et al.  A new touchscreen test of pattern separation: effect of hippocampal lesions , 2009, Neuroreport.

[22]  B. Balleine,et al.  The integrative function of the basal ganglia in instrumental conditioning , 2009, Behavioural Brain Research.

[23]  L. Saksida,et al.  A novel touchscreen-automated paired-associate learning (PAL) task sensitive to pharmacological manipulation of the hippocampus: a translational rodent model of cognitive impairments in neurodegenerative disease , 2009, Psychopharmacology.

[24]  R. D'Hooge,et al.  Hippocampal involvement in the acquisition of relational associations, but not in the expression of a transitive inference task in mice. , 2009, Behavioral neuroscience.

[25]  Michael R. Hunsaker,et al.  The CA3 subregion of the hippocampus is critical for episodic memory processing by means of relational encoding in rats. , 2008, Behavioral neuroscience.

[26]  J. Waltz,et al.  Reward processing in schizophrenia: a deficit in the representation of value. , 2008, Schizophrenia bulletin.

[27]  Inah Lee,et al.  The roles of the medial prefrontal cortex and hippocampus in a spatial paired-association task. , 2008, Learning & memory.

[28]  Glen T Prusky,et al.  Retrograde amnesia for visual memories after hippocampal damage in rats. , 2008, Learning & memory.

[29]  R. J. McDonald,et al.  A complex associative structure formed in the mammalian brain during acquisition of a simple visual discrimination task: Dorsolateral striatum, amygdala, and hippocampus , 2007, Hippocampus.

[30]  B. Balleine,et al.  The Role of the Dorsal Striatum in Reward and Decision-Making , 2007, The Journal of Neuroscience.

[31]  R. Clark,et al.  Rats depend on habit memory for discrimination learning and retention. , 2007, Learning & memory.

[32]  R. D'Hooge,et al.  Differences in behavioural test battery performance between mice with hippocampal and cerebellar lesions , 2006, Behavioural Brain Research.

[33]  M. Good,et al.  Double dissociation between hippocampal and prefrontal lesions on an operant delayed matching task and a water maze reference memory task , 2006, Behavioural Brain Research.

[34]  H. Yin,et al.  The role of the basal ganglia in habit formation , 2006, Nature Reviews Neuroscience.

[35]  Howard Eichenbaum,et al.  The Role of CA3 Hippocampal NMDA Receptors in Paired Associate Learning , 2006, The Journal of Neuroscience.

[36]  R. J. McDonald,et al.  Lesions of the dorsolateral striatum impair the acquisition of a simplified stimulus-response dependent conditional discrimination task , 2005, Neuroscience.

[37]  B. Balleine,et al.  Lesions of Medial Prefrontal Cortex Disrupt the Acquisition But Not the Expression of Goal-Directed Learning , 2005, The Journal of Neuroscience.

[38]  L. Squire.  Memory systems of the brain: A brief history and current perspective , 2004, Neurobiology of Learning and Memory.

[39]  F. J. Staay,et al.  The T-maze continuous alternation task for assessing the effects of putative cognition enhancers in the mouse , 2004, Behavioural Brain Research.

[40]  L. Gold,et al.  Modeling a task that is sensitive to dementia of the Alzheimer’s type: individual differences in acquisition of a visuo-spatial paired-associate learning task in rhesus monkeys , 2004, Behavioural Brain Research.

[41]  Raymond P. Kesner,et al.  Memory for objects and their locations: The role of the hippocampus in retention of object–place associations , 2004, Neurobiology of Learning and Memory.

[42]  S. Killcross,et al.  Inactivation of the infralimbic prefrontal cortex reinstates goal-directed responding in overtrained rats , 2003, Behavioural Brain Research.

[43]  R. Morris,et al.  Glutamate-receptor-mediated encoding and retrieval of paired-associate learning , 2003, Nature.

[44]  H. Eichenbaum,et al.  Hippocampal Formation Lesions Impair Performance in an Odor-Odor Association Task Independently of Spatial Context , 2002, Neurobiology of Learning and Memory.

[45]  David M. Bannerman,et al.  Effects of cytotoxic hippocampal lesions in mice on a cognitive test battery , 2002, Behavioural Brain Research.

[46]  R. J. McDonald,et al.  Multiple Parallel Memory Systems in the Brain of the Rat , 2002, Neurobiology of Learning and Memory.

[47]  Paul E. Gilbert,et al.  Role of rodent hippocampus in paired-associate learning involving associations between a stimulus and a spatial location. , 2002 .

[48]  George Paxinos,et al.  The Mouse Brain in Stereotaxic Coordinates , 2001 .

[49]  T. Robbins,et al.  Early Detection and Differential Diagnosis of Alzheimer’s Disease and Depression with Neuropsychological Tasks , 2001, Dementia and Geriatric Cognitive Disorders.

[50]  B. Balleine,et al.  The Role of the Hippocampus in Instrumental Conditioning , 2000, The Journal of Neuroscience.

[51]  Richard S. J. Frackowiak,et al.  Navigation-related structural change in the hippocampi of taxi drivers. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[52]  T. Robbins,et al.  Dissociation in Effects of Lesions of the Nucleus Accumbens Core and Shell on Appetitive Pavlovian Approach Behavior and the Potentiation of Conditioned Reinforcement and Locomotor Activity byd-Amphetamine , 1999, The Journal of Neuroscience.

[53]  R. Gerlai.  A new continuous alternation task in T-maze detects hippocampal dysfunction in mice A strain comparison and lesion study , 1998, Behavioural Brain Research.

[54]  M. Fanselow,et al.  Neurotoxic lesions of the dorsal hippocampus and Pavlovian fear conditioning in rats , 1997, Behavioural Brain Research.

[55]  T. Bussey,et al.  Triple dissociation of anterior cingulate, posterior cingulate, and medial frontal cortices on visual discrimination tasks using a touchscreen testing procedure for the rat. , 1997, Behavioral neuroscience.

[56]  Jennifer A. Mangels,et al.  A Neostriatal Habit Learning System in Humans , 1996, Science.

[57]  L. Rothblat,et al.  The hippocampus and long-term object memory in the rat , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[58]  J W Rudy,et al.  Rats with damage to the hippocampal-formation are impaired on the transverse-patterning problem but not on elemental discriminations. , 1995, Behavioral neuroscience.

[59]  H. Groenewegen,et al.  The specificity of the ‘nonspecific’ midline and intralaminar thalamic nuclei , 1994, Trends in Neurosciences.

[60]  T. Robbins,et al.  Comparative effects of excitotoxic lesions of the hippocampus and septum/diagonal band on conditional visual discrimination and spatial learning , 1993, Neuropsychologia.

[61]  J. N. P. Rawlins,et al.  Removal of the hippocampus and transection of the fornix produce comparable deficits on delayed non-matching to position by rats , 1992, Behavioural Brain Research.

[62]  Joseph E LeDoux,et al.  Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning. , 1992, Behavioral neuroscience.

[63]  T. Robbins,et al.  Dissociable roles of the ventral, medial and lateral striatum on the acquisition and performance of a complex visual stimulus-response habit , 1991, Behavioural Brain Research.

[64]  J. Duchek,et al.  Paired associate learning in senile dementia of the Alzheimer type. , 1991, Archives of neurology.

[65]  A. Mcgeorge,et al.  The organization of the projection from the cerebral cortex to the striatum in the rat , 1989, Neuroscience.

[66]  M. Packard,et al.  Differential effects of fornix and caudate nucleus lesions on two radial maze tasks: evidence for multiple memory systems , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[67]  I. Divac,et al.  Spontaneous alternation in rats with lesions in the frontal lobes: An extension of the frontal lobe syndrome , 1975 .

[68]  J. O'Keefe,et al.  The hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat. , 1971, Brain research.

[69]  R. Kirkby.  Caudate Nucleus Lesions Impair Spontaneous Alternation , 1969, Perceptual and Motor Skills.

[70]  W. N. Dember,et al.  Alternation and exploration in rats with hippocampal lesions. , 1962, Journal of comparative and physiological psychology.

[71]  W. Pelham,et al.  Reinforcement Enhances Vigilance Among Children With ADHD: Comparisons to Typically Developing Children and to the Effects of Methylphenidate , 2015, Journal of abnormal child psychology.

[72]  B. Balleine,et al.  Human and Rodent Homologies in Action Control: Corticostriatal Determinants of Goal-Directed and Habitual Action , 2010, Neuropsychopharmacology.

[73]  J. Rawlins,et al.  T-maze alternation in the rodent , 2006, Nature Protocols.

[74]  G. Desrosiers,et al.  Paired associate learning: form 1 and form 2 of the Wechsler Memory Scale. , 1988, Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists.