Responses of midbrain dopamine neurons to behavioral trigger stimuli in the monkey.

Destruction of the midbrain dopamine (DA) system in Parkinsonian man and experimental animals leads to deficits in initiation of behavior, motor performance, and cognitive mechanisms. We have investigated the extracellular impulse activity of single midbrain DA neurons in unlesioned monkeys performing in a controlled behavioral task that was designed to paradigmatically test behavioral reactivity. Animals were trained to execute natural forelimb reaching movements for food reward in response to a trigger stimulus. Presumptive DA neurons were histologically located in the pars compacta of substantia nigra and in neighboring areas A8 and A10. They spontaneously discharged polyphasic impulses of relatively long duration (1.4-3.6 ms) and at low frequencies (0.5-8.5/s). Systemic injections of low doses of the DA autoreceptor agonist apomorphine (0.05-0.2 mg/kg) depressed the activity of virtually all thus tested DA neurons. In following established criteria, these characteristics strongly suggest the DAergic nature of the recorded neurons. The majority of midbrain DA neurons (70 of 128) responded to the behavioral trigger stimulus of the task with a short burst of impulses. Latencies ranged from 39 to 105 ms (median 65 ms) for onset and from 65 to 165 ms (median 95 ms) for peak of responses. Responses occurred before arm movement and at the time of or before onset of electromyographic (EMG) activity in prime mover muscles. Responses were time-locked to the stimulus and not to the onset of movement or EMG. Responses remained present in most neurons but were reduced when vision of the behavioral trigger stimulus was prevented while maintaining the associated acoustic signals. In another variation of the task, most neurons also responded to a stimulus that was physically identical to the behavioral trigger but to which the animal made no movement. The activity of a few DA neurons (11 of 128) was reduced following presentation of the behavioral trigger stimulus, with latencies comparable to those of activations. The activity of many DA neurons was increased (40 of 128) or reduced (22 of 128) during execution of the forelimb reaching movement. These changes were of a slow and moderate nature, and were minor compared with responses to the behavioral trigger stimulus. About half of movement-related neurons also responded to the behavioral trigger. The activity of a few DA neurons was increased (11 to 128) or reduced (1 to 128) when the food reward reached the mouth. These changes did not occur with spontaneous mouth movements. About half of these neurons also responded to the behavioral trigger.(ABSTRACT TRUNCATED AT 400 WORDS)

[1]  L. Poirier Experimental and histological study of midbrain dyskinesias. , 1960, Journal of neurophysiology.

[2]  P. Teitelbaum,et al.  Sensory Neglect Produced by Lateral Hypothalamic Damage , 1971, Science.

[3]  F. Mcdowell,et al.  Intellectual impairment in Parkinson's syndrome. , 1972, Brain : a journal of neurology.

[4]  K. E. Moore,et al.  Release of endogenously synthesized catechols from the caudate nucleus by stimulation of the nigro-striatal pathway and by the administration of d-amphetamine. , 1973, Brain research.

[5]  R. Roth,et al.  Dopaminergic neurons: effect of antipsychotic drugs and amphetamine on single cell activity. , 1973, The Journal of pharmacology and experimental therapeutics.

[6]  R. Roth,et al.  Comparison of effects of L-dopa, amphetamine and apomorphine on firing rate of rat dopaminergic neurones. , 1973, Nature: New biology.

[7]  E. Stricker,et al.  Activation-induced restoration of sensorimotor functions in rats with dopamine-depleting brain lesions. , 1976, Journal of comparative and physiological psychology.

[8]  F. Hefti,et al.  A quantitative correlation between single unit activity and fluorescence intensity of dopamine neurones in zona compacta of substantia nigra, as demonstrated under the influence of nicotine and physostigmine , 1976, Brain Research.

[9]  Michel Jouvet,et al.  The raphe nuclei of the cat brain stem: A topographical atlas of their efferent projections as revealed by autoradiography , 1976, Brain Research.

[10]  M. Besson,et al.  Involvement of cholinergic presynaptic receptors of nicotinic and muscarinic types in the control of the spontaneous release of dopamine from striatal dopaminergic terminals in the rat. , 1977, The Journal of pharmacology and experimental therapeutics.

[11]  M. Brownstein,et al.  Evidence for substance P in the striato-nigral tract , 1977, Brain Research.

[12]  H. Künzle An autoradiographic analysis of the efferent connections from premotor and adjacent prefrontal regions (areas 6 and 9) in macaca fascicularis. , 1978, Brain, behavior and evolution.

[13]  N. Sharif,et al.  Effects ofl-glutamate and related amino acids upon the release of [3H]dopamine from rat striatal slices , 1978, Brain Research.

[14]  P. Teitelbaum,et al.  Role of activation and sensory stimuli in recovery from lateral hypothalamic damage in the cat. , 1978, Journal of comparative and physiological psychology.

[15]  J. Glowinski,et al.  Release of dopamine evoked by electrical stimulation of the motor and visual areas of the cerebral cortex in both caudate nuclei and in the substantia nigra in the cat , 1978, Brain Research.

[16]  G. P. Smith,et al.  Efferent connections and nigral afferents of the nucleus accumbens septi in the rat , 1978, Neuroscience.

[17]  L. Chiodo,et al.  Reciprocal influences of activating and immobilizing stimuli on the activity of nigrostriatal dopamine neurons , 1979, Brain Research.

[18]  H. E. Rosvold,et al.  Cognitive deficit caused by regional depletion of dopamine in prefrontal cortex of rhesus monkey. , 1979, Science.

[19]  G. A. Howell,et al.  Activity of substantia nigra units across the sleep-waking cycle in freely moving cats , 1981, Neuroscience Letters.

[20]  J. D. Miller,et al.  Mesencephalic dopaminergic unit activity in the behaviorally conditioned rat. , 1981, Life sciences.

[21]  J. Rehfeld,et al.  Peptide-monoamine coexistence: Studies of the actions of cholecystokinin-like peptide on the electrical activity of midbrain dopamine neurons , 1981, Neuroscience.

[22]  P. Somogyi,et al.  Monosynaptic input from the nucleus accumbens-ventral striatum region to retrogradely labelled nigrostriatal neurones , 1981, Brain Research.

[23]  G. Arbuthnott,et al.  Altered paw preference after unilateral 6-hydroxy-dopamine injections into lateral hypothalamus , 1981, Neuropsychologia.

[24]  B. Jacobs,et al.  Raphe unit activity in freely moving cats: Effects of phasic auditory and visual stimuli , 1982, Brain Research.

[25]  D. Felten,et al.  Monoamine distribution in primate brain. V. Monoaminergic nuclei: Anatomy, pathways, and local organization , 1982, Brain Research Bulletin.

[26]  T. Hökfelt,et al.  Immunohistochemical evidence for a dynorphin immunoreactive striato-nigral pathway. , 1982, European journal of pharmacology.

[27]  Wolfram Schultz,et al.  Depletion of dopamine in the striatum as an experimental model of parkinsonism: direct effects and adaptive mechanisms , 1982, Progress in Neurobiology.

[28]  P. Goldman-Rakic,et al.  Brainstem innervation of prefrontal and anterior cingulate cortex in the rhesus monkey revealed by retrograde transport of HRP , 1982, The Journal of comparative neurology.

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

[30]  D. German,et al.  Activity of mesencephalic dopamine and non-dopamine neurons across stages of sleep and waking in the rat , 1983, Brain Research.

[31]  Y. Agid,et al.  Reduction of cortical dopamine, noradrenaline, serotonin and their metabolites in Parkinson's disease , 1983, Brain Research.

[32]  B. Jacobs,et al.  Behavioral correlates of dopaminergic unit activity in freely moving cats , 1983, Brain Research.

[33]  A. Björklund,et al.  Conditioned turning in rats: Dopaminergic involvement in the initiation of movement rather than the movement itself , 1983, Neuroscience Letters.

[34]  R. Wightman,et al.  Direct in vivo monitoring of dopamine released from two striatal compartments in the rat. , 1983, Science.

[35]  M. Zigmond,et al.  Environmental stimuli but not homeostatic challenges produce apparent increases in dopaminergic activity in the striatum: An analysis by in vivo voltammetry , 1983, Brain Research.

[36]  M. D. Crutcher,et al.  Relations between movement and single cell discharge in the substantia nigra of the behaving monkey , 1983, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[37]  J. Brown,et al.  The electrophysiology of dopamine (D2) receptors: A study of the actions of dopamine on corticostriatal transmission , 1983, Neuroscience.

[38]  A. Jackson,et al.  Nucleus tegmenti pedunculopontinus: Efferent connections with special reference to the basal ganglia, studied in the rat by anterograde and retrograde transport of horseradish peroxidase , 1983, Neuroscience.

[39]  A. Grace,et al.  Intracellular and extracellular electrophysiology of nigral dopaminergic neurons—1. Identification and characterization , 1983, Neuroscience.

[40]  E. Rolls,et al.  Activity of neurons in the ventral tegmental region of the behaving monkey , 1983, Behavioural Brain Research.

[41]  A. Parent,et al.  The striatopallidal and striatonigral projections: two distinct fiber systems in primate , 1984, Brain Research.

[42]  W. Schultz,et al.  The activity of pars compacta neurons of the monkey substantia nigra is depressed by apomorphine , 1984, Neuroscience Letters.

[43]  G. Percheron,et al.  A Golgi analysis of the primate globus pallidus. III. Spatial organization of the striato‐pallidal complex , 1984, The Journal of comparative neurology.

[44]  W. Schultz PRIMATE DOPAMINE CELL ACTIVITY IN RELATION TO BEHAVIORAL ACTS , 1984 .

[45]  W. Schultz,et al.  Responses of rat pallidum cells to cortex stimulation and effects of altered dopaminergic activity , 1985, Neuroscience.

[46]  T. Robbins,et al.  Depletion of unilateral striatal dopamine impairs initiation of contralateral actions and not sensory attention , 1985, Nature.

[47]  F. Gonon,et al.  Regulation of dopamine release by impulse flow and by autoreceptors as studied by in vivo voltammetry in the rat striatum , 1985, Neuroscience.

[48]  W. Schultz,et al.  Deficits in behavioral initiation and execution processes in monkeys with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism , 1985, Neuroscience Letters.

[49]  R. Romo,et al.  In vivo presynaptic control of dopamine release in the cat caudate nucleus—III. Further evidence for the implication of corticostriatal glutamatergic neurons , 1986, Neuroscience.

[50]  R. Romo,et al.  In vivo presynaptic control of dopamine release in the cat caudate nucleus—II. Facilitatory or inhibitory influence ofl-glutamate , 1986, Neuroscience.

[51]  W. Schultz Activity of pars reticulata neurons of monkey substantia nigra in relation to motor, sensory, and complex events. , 1986, Journal of neurophysiology.

[52]  E. Scarnati,et al.  Neuronal responses to iontophoretically applied dopamine, glutamate, and GABA of identified dopaminergic cells in the rat substantia nigra after kainic acid-induced destruction of the striatum , 2004, Experimental Brain Research.