Cognitive Impairment in Pain through Amygdala-Driven Prefrontal Cortical Deactivation

Cognitive deficits such as impaired decision-making can be a consequence of persistent pain. Normal functions of the intact amygdala and prefrontal cortex are required for emotion-based decision-making that relies on the ability to assess risk, attribute value, and identify advantageous strategies. We tested the hypothesis that pain-related cognitive deficits result from amygdala-driven impairment of medial prefrontal cortical (mPFC) function. To do this, we used electrophysiological single-unit recordings in vivo, patch clamp in brain slices, and various behavioral assays to show that increased neuronal activity in the amygdala in an animal model of arthritis pain was accompanied by decreased mPFC activation and impaired decision-making. Furthermore, pharmacologic inhibition (with a corticotropin-releasing factor 1 receptor antagonist) of pain-related hyperactivity in the basolateral amygdala (BLA), but not central amygdala (CeA), reversed deactivation of mPFC pyramidal cells and improved decision-making deficits. Pain-related cortical deactivation resulted from a shift of balance between inhibitory and excitatory synaptic transmission. Direct excitatory transmission to mPFC pyramidal cells did not change in the pain model, whereas polysynaptic inhibitory transmission increased. GABAergic transmission was reduced by non-NMDA receptor antagonists, suggesting that synaptic inhibition was glutamate driven. The results are consistent with a model of BLA-driven feedforward inhibition of mPFC neurons. In contrast to the differential effects of BLA versus CeA hyperactivity on cortical-cognitive functions, both amygdala nuclei modulate emotional-affective pain behavior. Thus, this study shows that the amygdala contributes not only to emotional-affective but also cognitive effects of pain. The novel amygdalo-cortical pain mechanism has important implications for our understanding of amygdala functions and amygdalo-cortical interactions.

[1]  D. Kahneman,et al.  Functional Imaging of Neural Responses to Expectancy and Experience of Monetary Gains and Losses tasks with monetary payoffs , 2001 .

[2]  J. Besson,et al.  The organization of the efferent projections from the pontine parabrachial area to the amygdaloid complex: A phaseolus vulgaris leucoagglutinin (PHA‐L) study in the rat , 1993, The Journal of comparative neurology.

[3]  P. Goldman-Rakic,et al.  Correlated discharges among putative pyramidal neurons and interneurons in the primate prefrontal cortex. , 2002, Journal of neurophysiology.

[4]  T. Gray,et al.  Corticotropin releasing factor neurons are innervated by calcitonin gene-related peptide terminals in the rat central amygdaloid nucleus , 1994, Brain Research Bulletin.

[5]  S. Nicola,et al.  Contributions of the amygdala and medial prefrontal cortex to incentive cue responding , 2008, Neuroscience.

[6]  J. D. McGaugh The amygdala modulates the consolidation of memories of emotionally arousing experiences. , 2004, Annual review of neuroscience.

[7]  V. Neugebauer,et al.  Techniques for assessing knee joint pain in arthritis , 2007, Molecular pain.

[8]  M. Heinricher,et al.  Microinjection of morphine into various amygdaloid nuclei differentially affects nociceptive responsiveness and RVM neuronal activity , 2002, Pain.

[9]  B. Myers,et al.  Corticosteroid receptor-mediated mechanisms in the amygdala regulate anxiety and colonic sensitivity. , 2007, American journal of physiology. Gastrointestinal and liver physiology.

[10]  P. Shinnick‐Gallagher,et al.  A novel rat medial prefrontal cortical slice preparation to investigate synaptic transmission from amygdala to layer V prelimbic pyramidal neurons , 2006, Journal of Neuroscience Methods.

[11]  Michel Baudry,et al.  The amygdala modulates prefrontal cortex activity relative to conditioned fear , 1999, Nature.

[12]  G. Alheid Amygdala and extended amygdala , 1995 .

[13]  A. Apkarian,et al.  Chronic Back Pain Is Associated with Decreased Prefrontal and Thalamic Gray Matter Density , 2004, The Journal of Neuroscience.

[14]  P. Shinnick‐Gallagher,et al.  Loss of long-lasting potentiation mediated by group III mGluRs in amygdala neurons in kindling-induced epileptogenesis. , 1997, Journal of neurophysiology.

[15]  P. Shinnick‐Gallagher,et al.  Long-Lasting Changes in the Pharmacology and Electrophysiology of Amino Acid Receptors in Amygdala Kindled Neurons , 1998 .

[16]  T. Robbins,et al.  Effects of excitotoxic lesions of the central amygdaloid nucleus on the potentiation of reward-related stimuli by intra-accumbens amphetamine. , 1996, Behavioral neuroscience.

[17]  R. Gereau,et al.  Activation of the Extracellular Signal-Regulated Kinase in the Amygdala Modulates Pain Perception , 2007, The Journal of Neuroscience.

[18]  P. Shinnick‐Gallagher,et al.  Epileptogenesis In Vivo Enhances the Sensitivity of Inhibitory Presynaptic Metabotropic Glutamate Receptors in Basolateral Amygdala Neurons In Vitro , 1997, The Journal of Neuroscience.

[19]  E. Koechlin,et al.  Motivation and cognitive control in the human prefrontal cortex , 2009, Nature Neuroscience.

[20]  H. Markram,et al.  Interneurons of the neocortical inhibitory system , 2004, Nature Reviews Neuroscience.

[21]  T. Salt,et al.  Latest eruptions in metabotropic glutamate receptors. , 1996, Trends in pharmacological sciences.

[22]  O. Manzoni,et al.  Decreased Presynaptic Sensitivity to Adenosine after Cocaine Withdrawal , 1998, The Journal of Neuroscience.

[23]  Alberto Granato,et al.  Analgesia and hyperalgesia from GABA-mediated modulation of the cerebral cortex , 2003, Nature.

[24]  P. Conn,et al.  Protein Kinase C and A3 Adenosine Receptor Activation Inhibit Presynaptic Metabotropic Glutamate Receptor (mGluR) Function and Uncouple mGluRs from GTP-Binding Proteins , 1998, The Journal of Neuroscience.

[25]  T. Nakagawa,et al.  Differential contributions of the basolateral and central nuclei of the amygdala in the negative affective component of chemical somatic and visceral pains in rats , 2003, The European journal of neuroscience.

[26]  Heather L. Urry,et al.  Amygdala and Ventromedial Prefrontal Cortex Are Inversely Coupled during Regulation of Negative Affect and Predict the Diurnal Pattern of Cortisol Secretion among Older Adults , 2006, The Journal of Neuroscience.

[27]  A. McDonald,et al.  Organization of amygdaloid projections to the prefrontal cortex and associated striatum in the rat , 1991, Neuroscience.

[28]  Robert P. Vertes,et al.  Interactions among the medial prefrontal cortex, hippocampus and midline thalamus in emotional and cognitive processing in the rat , 2006, Neuroscience.

[29]  B. Lumb,et al.  The representation of prolonged and intense, noxious somatic and visceral stimuli in the ventrolateral orbital cortex of the cat , 1992, Pain.

[30]  D. Schoepp,et al.  Anxiolytic and side-effect profile of LY354740: a potent, highly selective, orally active agonist for group II metabotropic glutamate receptors. , 1998, The Journal of pharmacology and experimental therapeutics.

[31]  J. Pin,et al.  Pharmacology and functions of metabotropic glutamate receptors. , 1997, Annual review of pharmacology and toxicology.

[32]  G. Quirk,et al.  Neuronal signalling of fear memory , 2004, Nature Reviews Neuroscience.

[33]  M. Heinricher,et al.  Noradrenergic agonist administration into the central nucleus of the amygdala increases the tail-flick latency in lightly anesthetized rats , 2007, Neuroscience.

[34]  A. Mcgregor,et al.  Dopaminergic antagonism within the nucleus accumbens or the amygdala produces differential effects on intravenous cocaine self-administration under fixed and progressive ratio schedules of reinforcement , 1993, Brain Research.

[35]  Hillel Adesnik,et al.  Neocortical Disynaptic Inhibition Requires Somatodendritic Integration in Interneurons , 2009, The Journal of Neuroscience.

[36]  B. Balleine,et al.  Parallel incentive processing: an integrated view of amygdala function , 2006, Trends in Neurosciences.

[37]  W. Willis,et al.  Protein kinase A‐dependent enhanced NMDA receptor function in pain‐related synaptic plasticity in rat amygdala neurones , 2005, The Journal of physiology.

[38]  M. Gallagher,et al.  The amygdala complex: multiple roles in associative learning and attention. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[39]  Yumiko Yoshimura,et al.  Specialized Inhibitory Synaptic Actions Between Nearby Neocortical Pyramidal Neurons , 2007, Science.

[40]  A. Lüthi,et al.  Switching on and off fear by distinct neuronal circuits , 2008, Nature.

[41]  R. Anwyl Metabotropic glutamate receptors: electrophysiological properties and role in plasticity , 1999, Brain Research Reviews.

[42]  D. Lovinger,et al.  Metabotropic glutamate receptor modulation of synaptic transmission in corticostriatal co-cultures: Role of calcium influx , 1995, Neuropharmacology.

[43]  M. Andresen,et al.  Reliability of monosynaptic sensory transmission in brain stem neurons in vitro. , 2001, Journal of neurophysiology.

[44]  Gregory P. Lee,et al.  Different Contributions of the Human Amygdala and Ventromedial Prefrontal Cortex to Decision-Making , 1999, The Journal of Neuroscience.

[45]  Arnold R. Kriegstein,et al.  Whole cell recording from neurons in slices of reptilian and mammalian cerebral cortex , 1989, Journal of Neuroscience Methods.

[46]  R. Dolan,et al.  Emotion, Decision Making, and the Amygdala , 2008, Neuron.

[47]  I. Módy,et al.  Decreased sensitivity to Group III mGluR agonists in the lateral perforant path following kindling , 1999, Neuropharmacology.

[48]  E. Nestler,et al.  Regulation of G proteins by chronic morphine in the rat locus coeruleus , 1989, Brain Research.

[49]  D. Mayer,et al.  The central nucleus of the amygdala contributes to the production of morphine antinociception in the rat tail-flick test , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  Joseph E LeDoux,et al.  Neural Circuitry Underlying the Regulation of Conditioned Fear and Its Relation to Extinction , 2008, Neuron.

[51]  P. Shinnick‐Gallagher,et al.  Cocaine and kindling alter the sensitivity of group II and III metabotropic glutamate receptors in the central amygdala. , 2000, Journal of neurophysiology.

[52]  G. Koob,et al.  Sensitization of cocaine-stimulated increase in extracellular levels of corticotropin-releasing factor from the rat amygdala after repeated administration as determined by intracranial microdialysis , 1995, Neuroscience Letters.

[53]  R. Post,et al.  The role of context and conditioning in behavioral sensitization to cocaine. , 1987, Psychopharmacology bulletin.

[54]  P. Dayan,et al.  Cortical substrates for exploratory decisions in humans , 2006, Nature.

[55]  A. Bonci,et al.  A Common Mechanism Mediates Long-Term Changes in Synaptic Transmission after Chronic Cocaine and Morphine , 1996, Neuron.

[56]  Martin P Paulus,et al.  Decision-Making Dysfunctions in Psychiatry—Altered Homeostatic Processing? , 2007, Science.

[57]  S. Rauch,et al.  Recall of Fear Extinction in Humans Activates the Ventromedial Prefrontal Cortex and Hippocampus in Concert , 2007, Biological Psychiatry.

[58]  F. J. White,et al.  Whole-Cell Plasticity in Cocaine Withdrawal: Reduced Sodium Currents in Nucleus Accumbens Neurons , 1998, The Journal of Neuroscience.

[59]  A. Damasio,et al.  Role of the Amygdala in Decision‐Making , 2003, Annals of the New York Academy of Sciences.

[60]  P. Shinnick‐Gallagher,et al.  Trans-ACPD and l-APB presynaptically inhibit excitatory glutamatergic transmission in the basolateral amygdala (BLA) , 1992, Neuroscience Letters.

[61]  池田 亮 NMDA receptor-independent synaptic plasticity in the central amygdala in the rat model of neuropathic pain , 2007 .

[62]  D. Amaral,et al.  The amygdala and autism: implications from non‐human primate studies , 2003, Genes, brain, and behavior.

[63]  S. Langer,et al.  Presynaptic receptors , 1978, Nature.

[64]  Dante R. Chialvo,et al.  Chronic pain patients are impaired on an emotional decision-making task , 2004, Pain.

[65]  M. Washburn,et al.  Electrophysiological and morphological properties of rat basolateral amygdaloid neurons in vitro , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[66]  Vasco Galhardo,et al.  Forebrain pain mechanisms , 2009, Brain Research Reviews.

[67]  V. Galhardo,et al.  Cognitive impairment of prefrontal-dependent decision-making in rats after the onset of chronic pain , 2009, Neuroscience.

[68]  V. Neugebauer,et al.  Differential sensitization of amygdala neurons to afferent inputs in a model of arthritic pain. , 2003, Journal of neurophysiology.

[69]  J. Power,et al.  The amygdaloid complex: anatomy and physiology. , 2003, Physiological reviews.

[70]  J. O'Doherty,et al.  The Role of the Ventromedial Prefrontal Cortex in Abstract State-Based Inference during Decision Making in Humans , 2006, The Journal of Neuroscience.

[71]  D. Buonomano,et al.  Differential Effects of Excitatory and Inhibitory Plasticity on Synaptically Driven Neuronal Input-Output Functions , 2009, Neuron.

[72]  G. V. Goddard,et al.  A permanent change in brain function resulting from daily electrical stimulation. , 1969, Experimental neurology.

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

[74]  M. Roesch,et al.  Cocaine-induced decision-making deficits are mediated by miscoding in basolateral amygdala , 2007, Nature Neuroscience.

[75]  Bruce S. McEwen,et al.  Stress, memory and the amygdala , 2009, Nature Reviews Neuroscience.

[76]  H. Kita,et al.  Amygdaloid projections to the frontal cortex and the striatum in the rat , 1990, The Journal of comparative neurology.

[77]  S. Cruikshank,et al.  Synaptic basis for intense thalamocortical activation of feedforward inhibitory cells in neocortex , 2007, Nature Neuroscience.

[78]  D. Schoepp,et al.  Group III human metabotropic glutamate receptors 4, 7 and 8: molecular cloning, functional expression, and comparison of pharmacological properties in RGT cells. , 1998, Brain research. Molecular brain research.

[79]  K. Follett,et al.  The effect of morphine on responses of ventrolateral orbital cortex (VLO) neurons to colorectal distension in the rat , 1998, Brain Research.

[80]  L. Benardo,et al.  Recruitment of GABAA inhibition in rat neocortex is limited and not NMDA dependent. , 1995, Journal of neurophysiology.

[81]  A. Vania Apkarian,et al.  Morphological and functional reorganization of rat medial prefrontal cortex in neuropathic pain , 2009, Proceedings of the National Academy of Sciences.

[82]  V. Neugebauer,et al.  Synaptic Plasticity in the Amygdala in a Model of Arthritic Pain: Differential Roles of Metabotropic Glutamate Receptors 1 and 5 , 2003, The Journal of Neuroscience.

[83]  R. Duvoisin,et al.  The metabotropic glutamate receptors: Structure and functions , 1995, Neuropharmacology.

[84]  W. Gehring,et al.  Medial Frontal Cortex Activity and Loss-Related Responses to Errors , 2006, The Journal of Neuroscience.

[85]  H. Markram,et al.  Disynaptic Inhibition between Neocortical Pyramidal Cells Mediated by Martinotti Cells , 2007, Neuron.

[86]  D. Lovinger,et al.  Metabotropic glutamate receptor modulation of voltage-gated Ca2+ channels involves multiple receptor subtypes in cortical neurons , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[87]  T. Knöpfel,et al.  Metabotropic glutamate receptors: novel targets for drug development. , 1995, Journal of medicinal chemistry.

[88]  Stephen Maren Synaptic transmission and plasticity in the amygdala , 1996, Molecular Neurobiology.

[89]  W. Willis,et al.  Role of metabotropic glutamate receptor subtype mGluR1 in brief nociception and central sensitization of primate STT cells. , 1999, Journal of neurophysiology.

[90]  V. Neugebauer,et al.  Pain-related anxiety-like behavior requires CRF1 receptors in the amygdala , 2007, Molecular pain.

[91]  V. Neugebauer,et al.  Differential Mechanisms of CRF1 and CRF2 Receptor Functions in the Amygdala in Pain-Related Synaptic Facilitation and Behavior , 2008, The Journal of Neuroscience.

[92]  A. D. Smith,et al.  Amygdala input to medial prefrontal cortex (mPFC) in the rat: A light and electron microscope study , 1996, Brain Research.

[93]  P. Kalivas,et al.  Neuroadaptations in Ionotropic and Metabotropic Glutamate Receptor mRNA Produced by Cocaine Treatment , 1999, Journal of neurochemistry.

[94]  V. Neugebauer,et al.  The Amygdala and Persistent Pain , 2004, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[95]  V. Neugebauer,et al.  Hemispheric lateralization of pain processing by amygdala neurons. , 2009, Journal of neurophysiology.

[96]  V. Galhardo,et al.  Orbitofrontal cortex lesions disrupt risk assessment in a novel serial decision-making task for rats , 2007, Neuroscience.

[97]  D. Schoepp,et al.  Design, synthesis, and pharmacological characterization of (+)-2-aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (LY354740): a potent, selective, and orally active group 2 metabotropic glutamate receptor agonist possessing anticonvulsant and anxiolytic properties. , 1997, Journal of medicinal chemistry.

[98]  K. Yamada,et al.  Cocaine administered in vitro to brain slices from rats treated with cocaine chronically in vivo results in a gamma-aminobutyric acid receptor-mediated hyperpolarization recorded from the dorsolateral septum. , 1998, The Journal of pharmacology and experimental therapeutics.

[99]  A. Grace,et al.  Cannabinoids Potentiate Emotional Learning Plasticity in Neurons of the Medial Prefrontal Cortex through Basolateral Amygdala Inputs , 2006, The Journal of Neuroscience.

[100]  A. Walf,et al.  The use of the elevated plus maze as an assay of anxiety-related behavior in rodents , 2007, Nature Protocols.

[101]  Stephen J. Kish,et al.  Amygdala dopamine levels are markedly elevated after self- but not passive-administration of cocaine , 1994, Brain Research.

[102]  R. Nicoll,et al.  Pharmacology of metabotropic glutamate receptors at the mossy fiber synapses of the guinea pig hippocampus , 1995, Neuropharmacology.

[103]  Y. Humeau,et al.  Amygdala Inhibitory Circuits and the Control of Fear Memory , 2009, Neuron.

[104]  M. Patil,et al.  Behavioral / Systems / Cognitive Corticotrophin Releasing Factor-Induced Synaptic Plasticity in the Amygdala Translates Stress into Emotional Disorders , 2004 .

[105]  J. Ferreira,et al.  ACTH Modulates ERK Phosphorylation in the Adrenal Gland in a Time‐Dependent Manner , 2004, Endocrine research.

[106]  Paul Leonard Gabbott,et al.  Amygdala input monosynaptically innervates parvalbumin immunoreactive local circuit neurons in rat medial prefrontal cortex , 2006, Neuroscience.

[107]  M. Migliore,et al.  Feed-forward inhibition as a buffer of the neuronal input-output relation , 2009, Proceedings of the National Academy of Sciences.

[108]  D. Schoepp,et al.  LY354740 is a Potent and Highly Selective Group II Metabotropic Glutamate Receptor Agonist in Cells Expressing Human Glutamate Receptors , 1997, Neuropharmacology.

[109]  Joseph E LeDoux,et al.  Contributions of the Amygdala to Emotion Processing: From Animal Models to Human Behavior , 2005, Neuron.

[110]  P. Holland,et al.  Amygdala–frontal interactions and reward expectancy , 2004, Current Opinion in Neurobiology.

[111]  V. Neugebauer,et al.  Differential effects of CRF1 and CRF2 receptor antagonists on pain-related sensitization of neurons in the central nucleus of the amygdala. , 2007, Journal of neurophysiology.

[112]  S. Davis,et al.  Activation of metabotropic glutamate receptors induce differential effects on synaptic transmission in the dentate gyrus and CA1 of the hippocampus in the anaesthetized rat , 1996, Neuropharmacology.

[113]  N. Murakami,et al.  Enhancement of corticosterone release by repeated injections of ACTH in the dexamethasone pre-treated rat. , 1983, Acta endocrinologica.

[114]  J. Gallagher,et al.  Chronic Cocaine Enhances γ-Aminobutyric Acid and Glutamate Release by Altering Presynaptic and not Postsynaptic γ-Aminobutyric AcidB Receptors within the Rat Dorsolateral Septal Nucleus , 1997 .

[115]  C. Heyser,et al.  Substance dependence as a compulsive behavior , 1998, Journal of psychopharmacology.

[116]  E. Asprodini,et al.  Kindling-induced long-lasting changes in synaptic transmission in the basolateral amygdala. , 1992, Journal of neurophysiology.

[117]  P. Kalivas,et al.  Possible role for G-proteins in behavioral sensitization to cocaine , 1991, Brain Research.

[118]  C. Elger,et al.  Up‐regulation of the metabotropic glutamate receptor mGluR4 in hippocampal neurons with reduced seizure vulnerability , 2000, Annals of neurology.

[119]  G. Westbrook,et al.  Cloning and expression of rat metabotropic glutamate receptor 8 reveals a distinct pharmacological profile. , 1997, Molecular pharmacology.

[120]  F. Zheng,et al.  Metabotropic glutamate receptors are required for the induction of long-term potentiation , 1992, Neuron.

[121]  R. Adolphs,et al.  Electrophysiological correlates of reward prediction error recorded in the human prefrontal cortex. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[122]  G. Schoenbaum,et al.  Basolateral Amygdala Lesions Abolish Orbitofrontal-Dependent Reversal Impairments , 2007, Neuron.