Dopamine release is heterogeneous within microenvironments of the rat nucleus accumbens

Many individual neurons within the intact brain fire in stochastic patterns that arise from interactions with the neuronal circuits that they comprise. However, the chemical communication that is evoked by these firing patterns has not been characterized because sensors suitable to monitor subsecond chemical events in micron dimensions have only recently become available. Here we employ a voltammetric sensor technology coupled with principal component regression to examine the dynamics of dopamine concentrations in the nucleus accumbens (NAc) of awake and unrestrained rats. The sensor has submillimeter dimensions and provides high temporal (0.1 s) resolution. At select locations spontaneous dopamine transient concentration changes were detected, achieving instantaneous concentrations of ∼50 nm. At other locations, transients were absent even though dopamine was available for release as shown by extracellular dopamine increases following electrical activation of dopaminergic neurons. At sites where dopamine concentration transients occur, uptake inhibition by cocaine enhances the frequency and magnitude of the rapid transients while also causing a more gradual increase in extracellular dopamine. These effects were largely absent from sites that did not support ongoing transient activity. These findings reveal an unanticipated spatial and temporal heterogeneity of dopamine transmission within the NAc that may depend upon the firing of specific subpopulations of dopamine neurons.

[1]  R. A. Davidoff From Neuron to Brain , 1977, Neurology.

[2]  R. Adams,et al.  Voltammetry in brain tissue: chronic recording of stimulated dopamine and 5-hydroxytryptamine release. , 1978, Life sciences.

[3]  Michel Jouvet,et al.  In vivo electrochemical detection of catechols in the neostriatum of anaesthetized rats: dopamine or DOPAC? , 1980, Nature.

[4]  H. Groenewegen,et al.  The pre- and postnatal development of the dopaminergic cell groups in the ventral mesencephalon and the dopaminergic innervation of the striatum of the rat , 1988, Neuroscience.

[5]  E. Richfield,et al.  Anatomical and affinity state comparisons between dopamine D1 and D2 receptors in the rat central nervous system , 1989, Neuroscience.

[6]  Ina Ruck,et al.  USA , 1969, The Lancet.

[7]  Ralph N. Adams,et al.  In vivo electrochemical measurements in the CNS , 1990, Progress in Neurobiology.

[8]  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.

[9]  A. Grace,et al.  Activation of dopamine cell firing by repeated L-DOPA administration to dopamine-depleted rats: its potential role in mediating the therapeutic response to L-DOPA treatment , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[10]  G. Rebec,et al.  Transient increases in catecholaminergic activity in medial prefrontal cortex and nucleus accumbens shell during novelty , 1996, Neuroscience.

[11]  P. Garris,et al.  Real‐Time Measurement of Electrically Evoked Extracellular Dopamine in the Striatum of Freely Moving Rats , 1997, Journal of neurochemistry.

[12]  V. Pickel,et al.  The Dopamine Transporter: Comparative Ultrastructure of Dopaminergic Axons in Limbic and Motor Compartments of the Nucleus Accumbens , 1997, The Journal of Neuroscience.

[13]  R. Wightman,et al.  Color images for fast-scan CV measurements in biological systems. , 1998, Analytical chemistry.

[14]  R. Mark Wightman,et al.  Peer Reviewed: Color Images for Fast-Scan CV Measurements in Biological Systems , 1998 .

[15]  D R Walt,et al.  Randomly ordered addressable high-density optical sensor arrays. , 1998, Analytical chemistry.

[16]  S. Ikemoto,et al.  The role of nucleus accumbens dopamine in motivated behavior: a unifying interpretation with special reference to reward-seeking , 1999, Brain Research Reviews.

[17]  B. Hyland,et al.  Firing modes of midbrain dopamine cells in the freely moving rat , 2002, Neuroscience.

[18]  A. Phillips,et al.  Glutamate Receptor-Dependent Modulation of Dopamine Efflux in the Nucleus Accumbens by Basolateral, But Not Central, Nucleus of the Amygdala in Rats , 2002, The Journal of Neuroscience.

[19]  R. Wightman,et al.  Response times of carbon fiber microelectrodes to dynamic changes in catecholamine concentration. , 2002, Analytical chemistry.

[20]  R. Wightman,et al.  Transient changes in mesolimbic dopamine and their association with ‘reward’ , 2002, Journal of neurochemistry.

[21]  P. Garris,et al.  Frequency of Dopamine Concentration Transients Increases in Dorsal and Ventral Striatum of Male Rats during Introduction of Conspecifics , 2002, The Journal of Neuroscience.

[22]  Hui Zhang,et al.  Real‐time decoding of dopamine concentration changes in the caudate–putamen during tonic and phasic firing , 2003 .

[23]  Garret D Stuber,et al.  Real-time measurements of phasic changes in extracellular dopamine concentration in freely moving rats by fast-scan cyclic voltammetry. , 2003, Methods in molecular medicine.

[24]  R. Wightman,et al.  Subsecond dopamine release promotes cocaine seeking , 2003, Nature.

[25]  P. Garris,et al.  Real‐time decoding of dopamine concentration changes in the caudate–putamen during tonic and phasic firing , 2004, Journal of neurochemistry.

[26]  Garret D Stuber,et al.  Overoxidation of carbon-fiber microelectrodes enhances dopamine adsorption and increases sensitivity. , 2003, The Analyst.

[27]  M. D. Rooij,et al.  Electrochemical Methods: Fundamentals and Applications , 2003 .

[28]  R. Wise Dopamine, learning and motivation , 2004, Nature Reviews Neuroscience.

[29]  R. Wightman,et al.  Nomifensine amplifies subsecond dopamine signals in the ventral striatum of freely‐moving rats , 2004, Journal of neurochemistry.

[30]  R. Wightman,et al.  Dopamine Operates as a Subsecond Modulator of Food Seeking , 2004, The Journal of Neuroscience.

[31]  T. Robinson,et al.  The Rate of Cocaine Administration Alters Gene Regulation and Behavioral Plasticity: Implications for Addiction , 2004, The Journal of Neuroscience.

[32]  S. Cragg,et al.  DAncing past the DAT at a DA synapse , 2004, Trends in Neurosciences.

[33]  Erratum: Real-time decoding of dopamine concentration changes in the caudate-putamen during tonic and phasic firing (Journal of Neurochemistry (2003) 87 (1284-1295)) , 2004 .

[34]  R. Wightman,et al.  Resolving neurotransmitters detected by fast-scan cyclic voltammetry. , 2004, Analytical chemistry.

[35]  R. Wightman,et al.  Functional microcircuitry in the accumbens underlying drug addiction: insights from real-time signaling during behavior , 2004, Current Opinion in Neurobiology.

[36]  A. Hoffman,et al.  Marijuana and cannabinoid regulation of brain reward circuits , 2004, British journal of pharmacology.

[37]  R. Wightman,et al.  Extinction of Cocaine Self-Administration Reveals Functionally and Temporally Distinct Dopaminergic Signals in the Nucleus Accumbens , 2005, Neuron.

[38]  R. Wightman,et al.  Real-time measurement of dopamine fluctuations after cocaine in the brain of behaving rats. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[39]  J. Mayhew,et al.  How Visual Stimuli Activate Dopaminergic Neurons at Short Latency , 2005, Science.

[40]  P. Garris,et al.  Simultaneous dopamine and single-unit recordings reveal accumbens GABAergic responses: implications for intracranial self-stimulation. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[41]  R. Wightman,et al.  Rapid Dopamine Signaling in the Nucleus Accumbens during Contingent and Noncontingent Cocaine Administration , 2005, Neuropsychopharmacology.

[42]  Aaron R Wheeler,et al.  Microcontact printing-based fabrication of digital microfluidic devices. , 2006, Analytical chemistry.

[43]  P. Greengard,et al.  Cocaine Increases Dopamine Release by Mobilization of a Synapsin-Dependent Reserve Pool , 2006, The Journal of Neuroscience.

[44]  Robert T Kennedy,et al.  Monitoring dopamine in vivo by microdialysis sampling and on-line CE-laser-induced fluorescence. , 2006, Analytical chemistry.

[45]  Robert T Kennedy,et al.  In vivo measurements of neurotransmitters by microdialysis sampling. , 2006, Analytical chemistry.

[46]  R. Wightman,et al.  Phasic Dopamine Release Evoked by Abused Substances Requires Cannabinoid Receptor Activation , 2007, The Journal of Neuroscience.

[47]  R. Wightman,et al.  Coordinated Accumbal Dopamine Release and Neural Activity Drive Goal-Directed Behavior , 2007, Neuron.

[48]  J. Wickens,et al.  Space, time and dopamine , 2007, Trends in Neurosciences.

[49]  R. Wightman,et al.  Pharmacologically induced, subsecond dopamine transients in the caudate–putamen of the anesthetized rat , 2007, Synapse.