Orbitofrontal and Anterior Cingulate Cortex Neurons Selectively Process Cocaine-Associated Environmental Cues in the Rhesus Monkey

Encounters with stimuli associated with drug use are believed to contribute to relapse. To probe the neurobiology of environmentally triggered drug use, we have conducted single-unit recordings in rhesus monkeys during presentation of two distinct types of drug paired cues that differentially support drug-seeking. The animals were highly conditioned to these cues via exposure during self-administration procedures conducted over a 4 year period. The cues studied were a discriminative cue that signaled response-contingent availability of cocaine, and a discrete cue that was temporally paired with the cocaine infusion (0.1 or 0.5 mg/kg). Two cortical regions consistently activated by cocaine-associated cues in human imaging studies are the orbitofrontal (OFC) and anterior cingulate cortex (ACC), though little is known about cortical neuronal activity responses to drug cues. We simultaneously recorded single-unit activity in OFC and ACC as well as in dorsal striatum in rhesus monkeys during cocaine self-administration. Dorsal striatal neurons were less engaged by drug cues than cortical regions. Between OFC and ACC, distinct functionality was apparent in neuronal responses. OFC neurons preferentially responded to the discriminative cue, consistent with a role in cue-induced drug-seeking. In contrast, the ACC did not respond more to the discriminative cue than to the discrete cue. Also distinct from the OFC, ACC showed sustained firing throughout the 18 s duration of the discrete cue. This pattern of sustained activation in ACC is consistent with a role in reward expectation and/or in mediating behavioral effects of discrete cues paired with drug infusions.

[1]  Rita Z. Goldstein,et al.  Anterior cingulate cortex hypoactivations to an emotionally salient task in cocaine addiction , 2009, Proceedings of the National Academy of Sciences.

[2]  R. Passingham How good is the macaque monkey model of the human brain? , 2009, Current Opinion in Neurobiology.

[3]  E. Rolls,et al.  The orbitofrontal cortex and beyond: From affect to decision-making , 2008, Progress in Neurobiology.

[4]  T. Robbins,et al.  Neural mechanisms underlying the vulnerability to develop compulsive drug-seeking habits and addiction , 2008, Philosophical Transactions of the Royal Society B: Biological Sciences.

[5]  T. Robbins,et al.  Drug Addiction and the Memory Systems of the Brain , 2008, Annals of the New York Academy of Sciences.

[6]  K. Berridge Faculty Opinions recommendation of Review. Neural mechanisms underlying the vulnerability to develop compulsive drug-seeking habits and addiction. , 2008 .

[7]  N. Logothetis,et al.  Neurophysiology of the BOLD fMRI Signal in Awake Monkeys , 2008, Current Biology.

[8]  Geoffrey Schoenbaum,et al.  The Role of Orbitofrontal Cortex in Drug Addiction: A Review of Preclinical Studies , 2008, Biological Psychiatry.

[9]  Hugh Garavan,et al.  The Role of Cognitive Control in Cocaine Dependence , 2007, Neuropsychology Review.

[10]  Walter Schneider,et al.  The cognitive control network: Integrated cortical regions with dissociable functions , 2007, NeuroImage.

[11]  Timothy Edward John Behrens,et al.  Contrasting roles for cingulate and orbitofrontal cortex in decisions and social behaviour , 2007, Trends in Cognitive Sciences.

[12]  M. Paulus,et al.  Location, location: using functional magnetic resonance imaging to pinpoint brain differences relevant to stimulant use. , 2007, Addiction.

[13]  Rita Z. Goldstein,et al.  Role of the anterior cingulate and medial orbitofrontal cortex in processing drug cues in cocaine addiction , 2007, Neuroscience.

[14]  K. Johnston,et al.  Top-Down Control-Signal Dynamics in Anterior Cingulate and Prefrontal Cortex Neurons following Task Switching , 2007, Neuron.

[15]  S. Haber,et al.  Reward-Related Cortical Inputs Define a Large Striatal Region in Primates That Interface with Associative Cortical Connections, Providing a Substrate for Incentive-Based Learning , 2006, The Journal of Neuroscience.

[16]  George V Rebec,et al.  Repeated Cocaine Self-Administration Alters Processing of Cocaine-Related Information in Rat Prefrontal Cortex , 2006, The Journal of Neuroscience.

[17]  C. Padoa-Schioppa,et al.  Neurons in the orbitofrontal cortex encode economic value , 2006, Nature.

[18]  Rajita Sinha,et al.  Cue-Induced Brain Activity Changes and Relapse in Cocaine-Dependent Patients , 2006, Neuropsychopharmacology.

[19]  N. Volkow,et al.  The neural basis of addiction: a pathology of motivation and choice. , 2005, The American journal of psychiatry.

[20]  P. Jatlow,et al.  Cocaine and cocaethylene: Effects on extracellular dopamine in the primate , 1995, Psychopharmacology.

[21]  M. Roesch,et al.  Neuronal Activity Related to Reward Value and Motivation in Primate Frontal Cortex , 2004, Science.

[22]  J. Kocsis,et al.  Local anesthetic effects of cocaethylene and isopropylcocaine on rat peripheral nerves , 2004, Brain Research.

[23]  H. Fields,et al.  Basolateral amygdala lesions impair both cue- and cocaine-induced reinstatement in animals trained on a discriminative stimulus task , 2003, Neuroscience.

[24]  E. Miller,et al.  Neuronal activity in primate dorsolateral and orbital prefrontal cortex during performance of a reward preference task , 2003, The European journal of neuroscience.

[25]  B. Everitt,et al.  Differential control over drug-seeking behavior by drug-associated conditioned reinforcers and discriminative stimuli predictive of drug availability. , 2003, Behavioral neuroscience.

[26]  Joselyn McLaughlin,et al.  Selective inactivation of the dorsomedial prefrontal cortex and the basolateral amygdala attenuates conditioned-cued reinstatement of extinguished cocaine-seeking behavior in rats , 2003, Psychopharmacology.

[27]  B. Richmond,et al.  Anterior Cingulate: Single Neuronal Signals Related to Degree of Reward Expectancy , 2002, Science.

[28]  T L Faber,et al.  Neural activity related to drug craving in cocaine addiction. , 2001, Archives of general psychiatry.

[29]  J C Gore,et al.  Functional magnetic resonance imaging of cocaine craving. , 2001, The American journal of psychiatry.

[30]  T. Robbins,et al.  Second-order schedules of drug reinforcement in rats and monkeys: measurement of reinforcing efficacy and drug-seeking behaviour , 2000, Psychopharmacology.

[31]  E. Stein,et al.  Cue-induced cocaine craving: neuroanatomical specificity for drug users and drug stimuli. , 2000, The American journal of psychiatry.

[32]  C. Bradberry Acute and Chronic Dopamine Dynamics in a Nonhuman Primate Model of Recreational Cocaine Use , 2000, The Journal of Neuroscience.

[33]  P. Janak,et al.  Neuronal and behavioral correlations in the medial prefrontal cortex and nucleus accumbens during cocaine self-administration by rats , 2000, Neuroscience.

[34]  C. Bradberry,et al.  Impact of Self-Administered Cocaine and Cocaine Cues on Extracellular Dopamine in Mesolimbic and Sensorimotor Striatum in Rhesus Monkeys , 2000, The Journal of Neuroscience.

[35]  L. Parsons,et al.  Control of cocaine-seeking behavior by drug-associated stimuli in rats: effects on recovery of extinguished operant-responding and extracellular dopamine levels in amygdala and nucleus accumbens. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[36]  R. A. Fuchs,et al.  Fos Protein Expression and Cocaine-Seeking Behavior in Rats after Exposure to a Cocaine Self-Administration Environment , 2000, The Journal of Neuroscience.

[37]  P. Janak,et al.  Comparison of Mesocorticolimbic Neuronal Responses During Cocaine and Heroin Self-Administration in Freely Moving Rats , 1998, The Journal of Neuroscience.

[38]  P F Renshaw,et al.  Functional magnetic resonance imaging of human brain activation during cue-induced cocaine craving. , 1998, The American journal of psychiatry.

[39]  D. Woodward,et al.  Single neuronal responses in medial prefrontal cortex during cocaine self‐administration in freely moving rats , 1997, Synapse.

[40]  S. Evans,et al.  Arterial and venous cocaine plasma concentrations in humans: relationship to route of administration, cardiovascular effects and subjective effects. , 1996, The Journal of pharmacology and experimental therapeutics.

[41]  V L Villemagne,et al.  Activation of memory circuits during cue-elicited cocaine craving. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[42]  B. Richmond,et al.  Neural signals in the monkey ventral striatum related to motivation for juice and cocaine rewards. , 1996, Journal of neurophysiology.

[43]  W. Schultz,et al.  Preferential activation of midbrain dopamine neurons by appetitive rather than aversive stimuli , 1996, Nature.

[44]  J. Price,et al.  Sensory and premotor connections of the orbital and medial prefrontal cortex of macaque monkeys , 1995, The Journal of comparative neurology.

[45]  W. Schultz,et al.  Neuronal activity in monkey ventral striatum related to the expectation of reward , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[46]  W. Schultz,et al.  Neuronal activity in monkey striatum related to the expectation of predictable environmental events. , 1992, Journal of neurophysiology.

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

[48]  S. Goldberg,et al.  Persistent behavior at high rates maintained by intravenous self-administration of nicotine. , 1981, Science.