Neuronal and behavioral correlates of intrastriatal infusions of amphetamine in freely moving rats

When injected systemically in rats, amphetamine routinely activates striatal neurons that increase firing rate in close temporal association with movement but suppresses nonmotor-related neurons. To assess the role of striatal mechanisms in these opposing effects, D-amphetamine (20 micrograms/microliters) was infused (10 microliters/h) directly into the striatum of awake, behaving rats and single-unit activity was recorded simultaneously at the infusion site. Intrastriatal amphetamine reliably activated motor-related, but suppressed nonmotor-related neuronal activity shortly after infusion onset. These changes in firing rate preceded overt behavioral changes, in most cases by several minutes. When they did emerge, behavioral responses were characterized mainly by focused sniffing and head bobbing. Interestingly, the strongest behavioral responses, as measured by onset latency and response magnitude, were likely to result from infusions into motor-related rather than nonmotor-related recording sites. Systemic injection of haloperidol (1.0 mg/kg) shortly after infusion offset suppressed both behavior and striatal neuronal activity. Control infusions of intrastriatal saline had no consistent effect on either striatal neuronal activity or behavior. Collectively, these results indicate that the divergence in firing rate between motor- and nonmotor-related striatal neurons reflects an intrinsic action of amphetamine in the striatum rather than a secondary effect of behavioral feedback. Moreover, the linkage of motor-related striatal areas with the strongest behavioral responses to amphetamine suggests important functional differences between motor- and nonmotor-related striatal neurons.

[1]  O. Hikosaka,et al.  Neural activities in the monkey basal ganglia related to attention, memory and anticipation , 1986, Brain and Development.

[2]  R. Christopher Pierce,et al.  A simple micromanipulator for multiple uses in freely moving rats: electrophysiology, voltammetry, and simultaneous intracerebral infusions , 1993, Journal of Neuroscience Methods.

[3]  G. Rebec,et al.  Heterogenous responses of neostriatal neurons to amphetamine in freely moving rats , 1988, Brain Research.

[4]  A. Mele,et al.  Striatal extracellular dopamine in conscious vs. anesthetized rats: effects of chloral hydrate anesthetic on responses to drugs of different classes , 1992, Brain Research.

[5]  P. Solomon,et al.  Microinjections of d-amphetamine into the nucleus accumbens and caudate-putamen differentially affect stereotypy and locomotion in the rat , 1984 .

[6]  M. Desban,et al.  Distinct presynaptic control of dopamine release in striosomal and matrix areas of the cat caudate nucleus. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[7]  P. Groves,et al.  Antidromically identified striatonigral projection neurons in the chronically implanted behaving rat: relations of cell firing to amphetamine-induced behaviors. , 1989, Behavioral neuroscience.

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

[9]  George V. Rebec,et al.  Striatal single-unit responses to amphetamine and neuroleptics in freely moving rats , 1993, Neuroscience & Biobehavioral Reviews.

[10]  C. Gerfen The neostriatal mosaic: multiple levels of compartmental organization in the basal ganglia. , 1992, Annual review of neuroscience.

[11]  D J Woodward,et al.  A region in the dorsolateral striatum of the rat exhibiting single-unit correlations with specific locomotor limb movements. , 1990, Journal of neurophysiology.

[12]  C. D. Stern,et al.  Handbook of Chemical Neuroanatomy Methods in Chemical Neuroanatomy. Edited by A. Bjorklund and T. Hokfelt. Elsevier, Amsterdam, 1983. Cloth bound, 548 pp. UK £140. (Volume 1 in the series). , 1986, Neurochemistry International.

[13]  G. Rebec,et al.  The involvement of D1 and D2 dopamine receptors in amphetamine-induced changes in striatal unit activity in behaving rats , 1993, Brain Research.

[14]  G. Rebec,et al.  Responses of rat striatal neurons during performance of a lever-release version of the conditioned avoidance response task , 1993, Brain Research.

[15]  D. Segal,et al.  Concomitant characterization of behavioral and striatal neurotransmitter response to amphetamine using in vivo microdialysis , 1989, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  G. Rebec,et al.  Responses of Motor- and Nonmotor-Related Neostriatal Neurons to Amphetamine and Neuroleptic Drugs , 1991 .

[17]  Gerard P. Smith,et al.  Relationships between selective denervation of dopamine terminal fields in the anterior forebrain and behavioral responses to amphetamine and apomorphine , 1980, Brain Research.

[18]  G. Rebec,et al.  Critical issues in assessing the behavioral effects of amphetamine , 1984, Neuroscience & Biobehavioral Reviews.

[19]  J. Wayne Aldridge,et al.  The temporal structure of spike trains in the primate basal ganglia: afferent regulation of bursting demonstrated with precentral cerebral cortical ablation , 1991, Brain Research.

[20]  P. Worms,et al.  Predictability and specificity of behavioral screening tests for neuroleptics. , 1979, Pharmacology & therapeutics. Part B: General & systematic pharmacology.

[21]  P. Groves A theory of the functional organization of the neostriatum and the neostriatal control of voluntary movement , 1983, Brain Research Reviews.

[22]  A. Kelley,et al.  Amphetamine microinjections into distinct striatal subregions cause dissociable effects on motor and ingestive behavior , 1989, Behavioural Brain Research.

[23]  C. Gerfen The neostriatal mosaic: multiple levels of compartmental organization , 1992, Trends in Neurosciences.

[24]  M. Desban,et al.  Distinct presynaptic regulation of dopamine release through NMDA receptors in striosome- and matrix-enriched areas of the rat striatum , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[25]  G. Rebec,et al.  Bilateral cortical ablations attenuate amphetamine-induced excitations of neostriatal motor-related neurons in freely moving rats , 1991, Neuroscience Letters.

[26]  M. Lyon Animal Models with Parallels to Schizophrenia , 1991 .

[27]  A. Graybiel,et al.  Dopamine uptake sites in the striatum are distributed differentially in striosome and matrix compartments. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[28]  É. Dolbakyan,et al.  Skilled forelimb movements and unit activity in motor cortex and caudate nucleus in rats , 1977, Neuroscience.

[29]  Duncan P. Taylor,et al.  Potential antipsychotic BMY 14802 selectively binds to sigma sites , 1987 .

[30]  G. Rebec,et al.  Amphetamine-induced excitations predominate in single neostriatal neurons showing motor-related activity , 1989, Brain Research.

[31]  P. Herrling Pharmacology of the corticocaudate excitatory postsynaptic potential in the cat: Evidence for its mediation by quisqualateor kainate-receptors , 1985, Neuroscience.

[32]  J. Korf,et al.  A mosaic-like distribution of dopamine receptors in rat neostriatum and its relationship to striosomes , 1987, Brain Research.

[33]  Y. Katayama,et al.  Electrophysiological evidence favoring intracaudate axon collaterals of GABAergic caudate output neurons in the cat , 1981, Brain Research.

[34]  T. Ljungberg,et al.  A direct comparison of amphetamine-induced behaviours and regional brain dopamine release in the rat using intracerebral dialysis , 1987, Brain Research.

[35]  I. Grofová Extrinsic Connections of the Neostriatum , 1979 .

[36]  W. Nauta,et al.  Connections of the basal ganglia and of the cerebellum. , 1974, Confinia neurologica.

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

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

[39]  T. Lidsky,et al.  Caudate neuronal activity in cats during head turning: Selectivity for sensory-triggered movements , 1986, Brain Research Bulletin.

[40]  S. Gilman,et al.  A Comparison of Single Unit Activity in Primate Caudate Nucleus and Putamen in a Sensory Cued Motor Task , 1991 .

[41]  N. A. Buchwald,et al.  Aging reduces somatosensory responsiveness of caudate neurons in the awake cat , 1987, Brain Research.

[42]  G. Rebec,et al.  A simple device for the reliable production of varnish-insulated, high-impedance tungsten microelectrodes , 1989, Journal of Neuroscience Methods.

[43]  E. T. Rolls,et al.  Responses of striatal neurons in the behaving monkey. 3. Effects of iontophoretically applied dopamine on normal responsiveness , 1984, Neuroscience.

[44]  Charles J. Wilson,et al.  Spontaneous firing patterns of identified spiny neurons in the rat neostriatum , 1981, Brain Research.

[45]  Theodore W. Berger,et al.  Interactions between dopamine and amino acid-induced excitation and inhibition in the striatum , 1986, Brain Research.

[46]  G. Rebec,et al.  BMY‐14802, a sigma ligand and potential antipsychotic drug, reverses amphetamine‐induced changes in neostriatal single‐unit activity in freely moving rats , 1992, Synapse.

[47]  S. Iversen,et al.  The pharmacological and anatomical substrates of the amphetamine response in the rat , 1975, Brain Research.

[48]  G. Paxinos,et al.  The Rat Brain in Stereotaxic Coordinates , 1983 .