Infralimbic Prefrontal Cortex Is Responsible for Inhibiting Cocaine Seeking in Extinguished Rats

The rat prelimbic prefrontal cortex and nucleus accumbens core are critical for initiating cocaine seeking. In contrast, the neural circuitry responsible for inhibiting cocaine seeking during extinction is unknown. The present findings using inhibition of selected brain nuclei with GABA agonists show that the suppression of cocaine seeking produced by previous extinction training required activity in the rat infralimbic cortex. Conversely, the reinstatement of drug seeking by a cocaine injection in extinguished animals was suppressed by increasing neuronal activity in infralimbic cortex with the glutamate agonist AMPA. The cocaine seeking induced by inactivating infralimbic cortex resembled other forms of reinstated drug seeking by depending on activity in prelimbic cortex and the basolateral amygdala. A primary efferent projection from the infralimbic cortex is to the nucleus accumbens shell. Akin to infralimbic cortex, inhibition of the accumbens shell induced cocaine seeking in extinguished rats. However, bilateral inhibition of the shell also elicited increased locomotor activity. Nonetheless, unilateral inhibition of the accumbens shell did not increase motor activity, and simultaneous unilateral inactivation of the infralimbic cortex and shell induced cocaine seeking, suggesting that an interaction between these two structures is necessary for extinction training to inhibit cocaine seeking. The infralimbic cortex and accumbens shell appear to be recruited by extinction learning because inactivation of these structures before extinction training did not alter cocaine seeking. Together, these findings suggest that a neuronal network involving the infralimbic cortex and accumbens shell is recruited by extinction training to suppress cocaine seeking.

[1]  L. Swanson The Rat Brain in Stereotaxic Coordinates, George Paxinos, Charles Watson (Eds.). Academic Press, San Diego, CA (1982), vii + 153, $35.00, ISBN: 0 125 47620 5 , 1984 .

[2]  R. Roth,et al.  Topographical organization of the efferent projections of the medial prefrontal cortex in the rat: An anterograde tract‐tracing study with Phaseolus vulgaris leucoagglutinin , 1989, The Journal of comparative neurology.

[3]  M Ennis,et al.  Connections between the central nucleus of the amygdala and the midbrain periaqueductal gray: Topography and reciprocity , 1991, The Journal of comparative neurology.

[4]  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.

[5]  JaneR . Taylor,et al.  Impulsivity resulting from frontostriatal dysfunction in drug abuse: implications for the control of behavior by reward-related stimuli , 1999, Psychopharmacology.

[6]  M. Reivich,et al.  Limbic activation during cue-induced cocaine craving. , 1999, The American journal of psychiatry.

[7]  C. Ghez,et al.  Pharmacological inactivation in the analysis of the central control of movement , 1999, Journal of Neuroscience Methods.

[8]  J. Price,et al.  The organization of networks within the orbital and medial prefrontal cortex of rats, monkeys and humans. , 2000, Cerebral cortex.

[9]  P. Kalivas,et al.  The Circuitry Mediating Cocaine-Induced Reinstatement of Drug-Seeking Behavior , 2001, The Journal of Neuroscience.

[10]  G. Di Chiara Nucleus accumbens shell and core dopamine: differential role in behavior and addiction. , 2002, Behavioural brain research.

[11]  H. Eichenbaum,et al.  Dissociable Effects of Lidocaine Inactivation of the Rostral and Caudal Basolateral Amygdala on the Maintenance and Reinstatement of Cocaine-Seeking Behavior in Rats , 2002, The Journal of Neuroscience.

[12]  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.

[13]  J. Stewart,et al.  A role for the prefrontal cortex in stress- and cocaine-induced reinstatement of cocaine seeking in rats , 2003, Psychopharmacology.

[14]  Rita Z. Goldstein,et al.  Drug addiction and its underlying neurobiological basis: neuroimaging evidence for the involvement of the frontal cortex. , 2002, The American journal of psychiatry.

[15]  D. Paré,et al.  Stimulation of Medial Prefrontal Cortex Decreases the Responsiveness of Central Amygdala Output Neurons , 2003, The Journal of Neuroscience.

[16]  P. Kalivas,et al.  Prefrontal Glutamate Release into the Core of the Nucleus Accumbens Mediates Cocaine-Induced Reinstatement of Drug-Seeking Behavior , 2003, The Journal of Neuroscience.

[17]  K. Berridge,et al.  Glutamate motivational ensembles in nucleus accumbens: rostrocaudal shell gradients of fear and feeding , 2003, The European journal of neuroscience.

[18]  David W. Self,et al.  Extinction-induced upregulation in AMPA receptors reduces cocaine-seeking behaviour , 2003, Nature.

[19]  P. Kalivas,et al.  Limbic and Motor Circuitry Underlying Footshock-Induced Reinstatement of Cocaine-Seeking Behavior , 2004, The Journal of Neuroscience.

[20]  B. Everitt,et al.  Direct Interactions between the Basolateral Amygdala and Nucleus Accumbens Core Underlie Cocaine-Seeking Behavior by Rats , 2004, The Journal of Neuroscience.

[21]  A. Kelley Ventral striatal control of appetitive motivation: role in ingestive behavior and reward-related learning , 2004, Neuroscience & Biobehavioral Reviews.

[22]  T. Robbins,et al.  Putting a spin on the dorsal–ventral divide of the striatum , 2004, Trends in Neurosciences.

[23]  D. Paré,et al.  Infralimbic cortex activation increases c-fos expression in intercalated neurons of the amygdala , 2005, Neuroscience.

[24]  A. Kelley,et al.  Differential behavioral effects following microinjection of an NMDA antagonist into nucleus accumbens subregions , 1994, Psychopharmacology.

[25]  Y. Yanagawa,et al.  A Specialized Subclass of Interneurons Mediates Dopaminergic Facilitation of Amygdala Function , 2005, Neuron.

[26]  M. P. Witter,et al.  Intrinsic connections of the cingulate cortex in the rat suggest the existence of multiple functionally segregated networks , 2005, Neuroscience.

[27]  A. Bechara Decision making, impulse control and loss of willpower to resist drugs: a neurocognitive perspective , 2005, Nature Neuroscience.

[28]  Gregory J. Quirk,et al.  Prefrontal Mechanisms in Extinction of Conditioned Fear , 2006, Biological Psychiatry.

[29]  R. A. Fuchs,et al.  Different Neural Substrates Mediate Cocaine Seeking after Abstinence versus Extinction Training: A Critical Role for the Dorsolateral Caudate–Putamen , 2006, The Journal of Neuroscience.

[30]  H. Schmidt,et al.  Administration of the D2 Dopamine Receptor Antagonist Sulpiride into the Shell, but not the Core, of the Nucleus Accumbens Attenuates Cocaine Priming-Induced Reinstatement of Drug Seeking , 2006, Neuropsychopharmacology.

[31]  A. Bonci,et al.  Cocaine self-administration selectively abolishes LTD in the core of the nucleus accumbens , 2006, Nature Neuroscience.

[32]  S. Rauch,et al.  Microstimulation reveals opposing influences of prelimbic and infralimbic cortex on the expression of conditioned fear. , 2006, Learning & memory.

[33]  H. Schmidt,et al.  Stimulation of D1‐like or D2 dopamine receptors in the shell, but not the core, of the nucleus accumbens reinstates cocaine‐seeking behaviour in the rat , 2006, The European journal of neuroscience.

[34]  T. Curran,et al.  Prefrontal Regions Orchestrate Suppression of Emotional Memories via a Two-Phase Process , 2007, Science.

[35]  H. Schmidt,et al.  When administered into the nucleus accumbens core or shell, the NMDA receptor antagonist AP-5 reinstates cocaine-seeking behavior in the rat , 2007, Neuroscience Letters.

[36]  C. Pennartz,et al.  Pharmacological Manipulation of Neuronal Ensemble Activity by Reverse Microdialysis in Freely Moving Rats: A Comparative Study of the Effects of Tetrodotoxin, Lidocaine, and Muscimol , 2007, Journal of Pharmacology and Experimental Therapeutics.

[37]  A. Zangen,et al.  Repeated Electrical Stimulation of Reward-Related Brain Regions Affects Cocaine But Not “Natural” Reinforcement , 2007, The Journal of Neuroscience.

[38]  P. Kalivas,et al.  Drug Addiction as a Pathology of Staged Neuroplasticity , 2008, Neuropsychopharmacology.