Role of Primate Substantia Nigra Pars Reticulata in Reward-Oriented Saccadic Eye Movement

To test the hypothesis that the basal ganglia are related to reward-oriented saccades, we examined activity of substantia nigra pars reticulata (SNr) neurons by using a one-direction-rewarded version of the memory-guided saccade task (1DR). Many SNr neurons changed (decreased or increased) their activity after and before a visual cue (post-cue and pre-cue activity). Post-cue decreases or increases tended to be larger to a contralateral cue. They were often modulated prospectively by the presence or absence of reward, either positively (enhanced in the rewarded condition) or negatively (enhanced in the nonrewarded condition). The positive reward modulation was more common among decreasing type neurons, whereas no such preference was observed among increasing type neurons. The reward-contingent decrease in SNr neuronal activity would facilitate rewarded saccades by inducing disinhibition in superior colliculus (SC) neurons. In contrast, the increase in SNr activity would suppress a saccade less selectively (rewarded or nonrewarded) by augmenting inhibition of SC neurons. The post-cue activity was often preceded by anticipatory pre-cue activity. Most typically, post-cue decrease was preceded by pre-cue decrease, selectively when the contralateral side was rewarded. This would reinforce the reward-oriented nature of SNr neuronal activity. The decreases and increases in SNr activity may be derived directly and indirectly, respectively, from the caudate (CD), where neurons show reward-contingent pre-cue and post-cue activity. These results suggest that the CD–SNr–SC mechanism would promote saccades oriented to reward.

[1]  B. Richmond,et al.  Implantation of magnetic search coils for measurement of eye position: An improved method , 1980, Vision Research.

[2]  M. Mishkin,et al.  Responses of cells in the tail of the caudate nucleus during visual discrimination learning. , 1995, Journal of neurophysiology.

[3]  O. Hikosaka,et al.  Role of Tonically Active Neurons in Primate Caudate in Reward-Oriented Saccadic Eye Movement , 2001, The Journal of Neuroscience.

[4]  Joel L. Davis,et al.  A Model of How the Basal Ganglia Generate and Use Neural Signals That Predict Reinforcement , 1994 .

[5]  O. Hikosaka,et al.  Reward-dependent spatial selectivity of anticipatory activity in monkey caudate neurons. , 2002, Journal of neurophysiology.

[6]  P. Glimcher,et al.  Contextual modulation of substantia nigra pars reticulata neurons. , 2000, Journal of neurophysiology.

[7]  O. Hikosaka,et al.  Role of the basal ganglia in the control of purposive saccadic eye movements. , 2000, Physiological reviews.

[8]  O. Hikosaka,et al.  Visual and oculomotor functions of monkey subthalamic nucleus. , 1992, Journal of neurophysiology.

[9]  Y. Smith,et al.  The output neurones and the dopaminergic neurones of the substantia nigra receive a GABA‐Containing input from the globus pallidus in the rat , 1990, The Journal of comparative neurology.

[10]  J. Joseph,et al.  Activity in the caudate nucleus of monkey during spatial sequencing. , 1995, Journal of neurophysiology.

[11]  H. Kita,et al.  Intracellular study of rat substantia nigra pars reticulata neurons in an in vitro slice preparation: electrical membrane properties and response characteristics to subthalamic stimulation , 1987, Brain Research.

[12]  D. Robinson,et al.  A METHOD OF MEASURING EYE MOVEMENT USING A SCLERAL SEARCH COIL IN A MAGNETIC FIELD. , 1963, IEEE transactions on bio-medical engineering.

[13]  P. Glimcher,et al.  Quantitative analysis of substantia nigra pars reticulata activity during a visually guided saccade task. , 1999, Journal of neurophysiology.

[14]  M. Delong,et al.  Functional and pathophysiological models of the basal ganglia , 1996, Current Opinion in Neurobiology.

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

[16]  O. Hikosaka,et al.  Feature-Based Anticipation of Cues that Predict Reward in Monkey Caudate Nucleus , 2002, Neuron.

[17]  O. Hikosaka,et al.  Function of the Indirect Pathway in the Basal Ganglia Oculomotor System: Visuo-Oculomotor Activities of External Pallidum Neurons , 1995 .

[18]  D. Surmeier,et al.  Coordinated Expression of Dopamine Receptors in Neostriatal Medium Spiny Neurons , 1996, The Journal of Neuroscience.

[19]  C. Gerfen,et al.  D1 and D2 dopamine receptor-regulated gene expression of striatonigral and striatopallidal neurons. , 1990, Science.

[20]  M. Williams,et al.  The striatonigral projection and nigrotectal neurons in the rat. A correlated light and electron microscopic study demonstrating a monosynaptic striatal input to identified nigrotectal neurons using a combined degeneration and horseradish peroxidase procedure , 1985, Neuroscience.

[21]  J. Deniau,et al.  Electrophysiological demonstration of an excitatory subthalamonigral pathway in the rat , 1978, Brain Research.

[22]  Toshio Kusama,et al.  Stereotaxic atlas of the brain of Macaca fuscata , 1970 .

[23]  R. Wurtz,et al.  Visual and oculomotor functions of monkey substantia nigra pars reticulata. III. Memory-contingent visual and saccade responses. , 1983, Journal of neurophysiology.

[24]  R. Wurtz,et al.  Visual and oculomotor functions of monkey substantia nigra pars reticulata. I. Relation of visual and auditory responses to saccades. , 1983, Journal of neurophysiology.

[25]  R Iansek,et al.  Motor functions of the basal ganglia , 1993, Psychological research.

[26]  T. Ono,et al.  Caudate unit activity during operant feeding behavior in monkeys and modulation by cooling prefrontal cortex , 1984, Behavioural Brain Research.

[27]  G. E. Alexander,et al.  Functional architecture of basal ganglia circuits: neural substrates of parallel processing , 1990, Trends in Neurosciences.

[28]  S. Thorpe,et al.  Responses of striatal neurons in the behaving monkey. 1. Head of the caudate nucleus , 1983, Behavioural Brain Research.

[29]  D. Pinault,et al.  Single striatofugal axons arborizing in both pallidal segments and in the substantia nigra in primates , 1995, Brain Research.

[30]  O. Hikosaka,et al.  Functional properties of monkey caudate neurons. III. Activities related to expectation of target and reward. , 1989, Journal of neurophysiology.

[31]  O. Hikosaka,et al.  Modulation of saccadic eye movements by predicted reward outcome , 2001, Experimental Brain Research.

[32]  Elsevier Biomedical Press RESPONSES OF STRIATAL NEURONS IN THE BEHAVING MONKEY. 1. HEAD OF THE CAUDATE NUCLEUS , 1983 .

[33]  O Hikosaka,et al.  Functional properties of monkey caudate neurons. II. Visual and auditory responses. , 1989, Journal of neurophysiology.

[34]  J. Féger,et al.  The unitary activity of the substantia nigra following stimulation of the striatum in the awake monkey , 1975, Brain Research.

[35]  J. Joseph,et al.  Role of the cat substantia nigra pars reticulata in eye and head movements I. Neural activity , 2004, Experimental Brain Research.

[36]  W. Precht,et al.  Monosynaptic inhibition of neurons of the substantia nigra by caudato-nigral fibers. , 1971, Brain research.

[37]  O. Hikosaka,et al.  Functional properties of monkey caudate neurons. I. Activities related to saccadic eye movements. , 1989, Journal of neurophysiology.

[38]  O. Hikosaka,et al.  Effects of caudate nucleus stimulation on substantia nigra cell activity in monkey , 2004, Experimental Brain Research.