The Caudal Part of Putamen Represents the Historical Object Value Information

The basal ganglia, especially the circuits originating from the putamen, are essential for controlling normal body movements. Notably, the putamen receives inputs not only from motor cortical areas but also from multiple sensory cortices. However, how these sensory signals are processed in the putamen remains unclear. We recorded the activity of tentative medium spiny neurons in the caudal part of the putamen when the monkey viewed many fractal objects. We found many neurons that responded to these objects, mostly in the ventral region. We called this region “putamen tail” (PUTt), as it is dorsally adjacent to “caudate tail” (CDt). Although PUTt and CDt are mostly separated by a thin layer of white matter, their neurons shared several features. Almost all of them had receptive fields in the contralateral hemifield. Moreover, their responses were object selective (i.e., variable across objects). The object selectivity was higher in the ventral region (i.e., CDt > PUTt). Some neurons above PUTt, which we called the caudal–dorsal putamen (cdPUT), also responded to objects, but less selectively than PUTt. Next, we examined whether these visual neurons changed their responses based on the reward outcome. We found that many neurons encoded the values of many objects based on long-term memory, but not based on short-term memory. Such stable value responses were stronger in PUTt and CDt than in cdPUT. These results suggest that PUTt, together with CDt, controls saccade/attention among objects with different historical values, and may control other motor actions as well. SIGNIFICANCE STATEMENT Although the putamen receives inputs not only from motor cortical areas but also from sensory cortical areas, how these sensory signals are processed remains unclear. Here we found that neurons in the caudal–ventral part of the putamen (putamen tail) process visual information including spatial and object features. These neurons discriminate many objects, first by their visual features and later by their reward values as well. Importantly, the value discrimination was based on long-term memory, but not on short-term memory. These results suggest that the putamen tail controls saccade/attention among objects with different historical values and might control other motor actions as well.

[1]  M. Delong,et al.  Putamen: Activity of Single Units during Slow and Rapid Arm Movements , 1973, Science.

[2]  D. Denny-Brown,et al.  The role of the basal ganglia in the initiation of movement. , 1976, Research publications - Association for Research in Nervous and Mental Disease.

[3]  E. Yeterian,et al.  Cortico-striate projections in the rhesus monkey: The organization of certain cortico-caudate connections , 1978, Brain Research.

[4]  G. V. Van Hoesen,et al.  Widespread corticostriate projections from temporal cortex of the rhesus monkey , 1981, The Journal of comparative neurology.

[5]  F. N. Dempster,et al.  Memory Span: Sources of Individual and Developmental Differences , 1981 .

[6]  G. E. Alexander,et al.  Microstimulation of the primate neostriatum. II. Somatotopic organization of striatal microexcitable zones and their relation to neuronal response properties. , 1985, Journal of neurophysiology.

[7]  G. E. Alexander,et al.  Parallel organization of functionally segregated circuits linking basal ganglia and cortex. , 1986, Annual review of neuroscience.

[8]  M. Kimura Behaviorally contingent property of movement-related activity of the primate putamen. , 1990, Journal of neurophysiology.

[9]  G. E. Alexander,et al.  Basal ganglia-thalamocortical circuits: parallel substrates for motor, oculomotor, "prefrontal" and "limbic" functions. , 1990, Progress in brain research.

[10]  Leslie G. Ungerleider,et al.  Organization of visual cortical inputs to the striatum and subsequent outputs to the pallido‐nigral complex in the monkey , 1990, The Journal of comparative neurology.

[11]  Y. Smith,et al.  Convergence of synaptic inputs from the striatum and the globus pallidus onto identified nigrocollicular cells in the rat: A double anterograde labelling study , 1991, Neuroscience.

[12]  Mitsuo Yoshida The neuronal mechanism underlying parkinsonism and dyskinesia: differential roles of the putamen and caudate nucleus , 1991, Neuroscience Research.

[13]  M. Kimura,et al.  Effects of reversible blockade of basal ganglia on a voluntary arm movement. , 1992, Journal of neurophysiology.

[14]  Y. Smith,et al.  The striatum and the globus pallidus send convergent synaptic inputs onto single cells in the entopeduncular nucleus of the rat: A double anterograde labelling study combined with postembedding immunocytochemistry for GABA , 1992, The Journal of comparative neurology.

[15]  C. Marsden,et al.  The behavioural and motor consequences of focal lesions of the basal ganglia in man. , 1994, Brain : a journal of neurology.

[16]  Leslie G. Ungerleider,et al.  Transient subcortical connections of inferior temporal areas TE and TEO in infant macaque monkeys , 1995, The Journal of comparative neurology.

[17]  A. Graybiel,et al.  Temporal and spatial characteristics of tonically active neurons of the primate's striatum. , 1995, Journal of neurophysiology.

[18]  R. Ridley,et al.  Functional integration of striatal allografts in a primate model of Huntington's disease , 1998, Nature Medicine.

[19]  O. Hikosaka,et al.  Expectation of reward modulates cognitive signals in the basal ganglia , 1998, Nature Neuroscience.

[20]  M. Land,et al.  The Roles of Vision and Eye Movements in the Control of Activities of Daily Living , 1998, Perception.

[21]  S. Gathercole Cognitive approaches to the development of short-term memory , 1999, Trends in Cognitive Sciences.

[22]  Martin Lévesque,et al.  Single‐axon tracing study of neurons of the external segment of the globus pallidus in primate , 2000 .

[23]  P. Lavallée,et al.  Single-axon tracing study of neurons of the external segment of the globus pallidus in primate. , 2000, The Journal of comparative neurology.

[24]  R. Johansson,et al.  Eye–Hand Coordination in Object Manipulation , 2001, The Journal of Neuroscience.

[25]  P. Hare Advance Online Publication , 2002, Nature Medicine.

[26]  A. Nambu,et al.  Organization of corticostriatal motor inputs in monkey putamen. , 2002, Journal of neurophysiology.

[27]  J. Assad,et al.  Putaminal activity for simple reactions or self-timed movements. , 2003, Journal of neurophysiology.

[28]  Optimal response of eye and hand motor systems in pointing at a visual target , 1979, Biological Cybernetics.

[29]  N. Mizuno,et al.  Topographical projections from the posterior thalamic regions to the striatum in the cat, with reference to possible tecto-thalamo-striatal connections , 2004, Experimental Brain Research.

[30]  G. E. Alexander Selective neuronal discharge in monkey putamen reflects intended direction of planned limb movements , 2004, Experimental Brain Research.

[31]  C. Gross,et al.  A bimodal map of space: somatosensory receptive fields in the macaque putamen with corresponding visual receptive fields , 1993, Experimental Brain Research.

[32]  N. Swindale,et al.  Diffusion tensor fiber tracking shows distinct corticostriatal circuits in humans , 2004, Annals of neurology.

[33]  M. Jeannerod,et al.  The coordination of eye, head, and arm movements during reaching at a single visual target , 2004, Experimental Brain Research.

[34]  W. Schultz,et al.  Neuronal activity in the monkey striatum during the initiation of movements , 2004, Experimental Brain Research.

[35]  M. Kawato,et al.  Different neural correlates of reward expectation and reward expectation error in the putamen and caudate nucleus during stimulus-action-reward association learning. , 2006, Journal of neurophysiology.

[36]  N. Logothetis,et al.  A combined MRI and histology atlas of the rhesus monkey brain in stereotaxic coordinates , 2007 .

[37]  Richard L. Lewis,et al.  The mind and brain of short-term memory. , 2008, Annual review of psychology.

[38]  M. D’Esposito Working memory. , 2008, Handbook of clinical neurology.

[39]  Jessica A. Grahn,et al.  The cognitive functions of the caudate nucleus , 2008, Progress in Neurobiology.

[40]  M. Kimura,et al.  Neuronal encoding of reward value and direction of actions in the primate putamen. , 2009, Journal of neurophysiology.

[41]  C. Connor,et al.  Neural representations for object perception: structure, category, and adaptive coding. , 2011, Annual review of neuroscience.

[42]  Andrea Brovelli,et al.  Differential roles of caudate nucleus and putamen during instrumental learning , 2011, NeuroImage.

[43]  Stefan Everling,et al.  Neural Activity in the Macaque Putamen Associated with Saccades and Behavioral Outcome , 2012, PloS one.

[44]  O. Hikosaka,et al.  Robust Representation of Stable Object Values in the Oculomotor Basal Ganglia , 2012, The Journal of Neuroscience.

[45]  Roger Kurlan,et al.  Movement Disorders after Stroke in Adults: A Review , 2012, Tremor and other hyperkinetic movements.

[46]  Ilya E. Monosov,et al.  What and Where Information in the Caudate Tail Guides Saccades to Visual Objects , 2012, The Journal of Neuroscience.

[47]  Shinya Yamamoto,et al.  Reward Value-Contingent Changes of Visual Responses in the Primate Caudate Tail Associated with a Visuomotor Skill , 2013, The Journal of Neuroscience.

[48]  Carol A. Seger,et al.  The visual corticostriatal loop through the tail of the caudate: circuitry and function , 2013, Front. Syst. Neurosci..

[49]  Hyoung F. Kim,et al.  Distinct Basal Ganglia Circuits Controlling Behaviors Guided by Flexible and Stable Values , 2013, Neuron.

[50]  Hyoung F. Kim,et al.  Basal ganglia circuits for reward value-guided behavior. , 2014, Annual review of neuroscience.

[51]  Lawrence H Snyder,et al.  Movement order and saccade direction affect a common measure of eye-hand coordination in bimanual reaching. , 2014, Journal of neurophysiology.

[52]  Hyoung F. Kim,et al.  Parallel basal ganglia circuits for voluntary and automatic behaviour to reach rewards. , 2015, Brain : a journal of neurology.

[53]  O. Hikosaka,et al.  Functional territories in primate substantia nigra pars reticulata separately signaling stable and flexible values. , 2015, Journal of neurophysiology.

[54]  Ryuichi Matsuzaki,et al.  Characteristics of fast-spiking neurons in the striatum of behaving monkeys , 2016, Neuroscience Research.

[55]  Ali Ghazizadeh,et al.  Object-finding skill created by repeated reward experience , 2016, bioRxiv.

[56]  Philipp Sterzer,et al.  Priming in a shape task but not in a category task under continuous flash suppression. , 2016, Journal of vision.

[57]  Ali Ghazizadeh,et al.  Ecological Origins of Object Salience: Reward, Uncertainty, Aversiveness, and Novelty , 2016, Front. Neurosci..

[58]  Jinse Park Movement Disorders Following Cerebrovascular Lesion in the Basal Ganglia Circuit , 2016, Journal of movement disorders.

[59]  Hyoung F. Kim,et al.  Indirect Pathway of Caudal Basal Ganglia for Rejection of Valueless Visual Objects , 2017, Neuron.

[60]  David A. Leopold,et al.  Temporal–prefrontal cortical network for discrimination of valuable objects in long-term memory , 2018, Proceedings of the National Academy of Sciences.

[61]  Whitney S. Griggs,et al.  Visual Neurons in the Superior Colliculus Discriminate Many Objects by Their Historical Values , 2018, Front. Neurosci..

[62]  Hyoung F. Kim,et al.  Neuronal connections of direct and indirect pathways for stable value memory in caudal basal ganglia , 2018, The European journal of neuroscience.

[63]  Hyoung F. Kim,et al.  Direct and indirect pathways for choosing objects and actions , 2019, The European journal of neuroscience.