Effects of D-Cycloserine on Extinction: Translation From Preclinical to Clinical Work

Administration of benzodiazepines or serotonin reuptake inhibitors in combination with behavior therapy for the treatment of many anxiety disorders has generally lead to only modest gains. In this article we suggest that pharmacotherapy aimed not at treating the symptoms of anxiety but instead aimed at improving the learning that takes place in exposure therapy might actually improve the effectiveness of exposure therapy. This idea was based on animal work showing that the partial N-methyl-D-aspartate (NMDA) agonist D-cycloserine (DCS) facilitated extinction of fear when given either before or shortly after exposure to fearful cues, reduced return of fear that is normally seen when extinction training is followed by stress, and led to generalized extinction, where DCS given in combination with exposure to one fearful cue led to extinction to another cue previously paired with the same aversive event. These finding suggested that DCS might facilitate exposure-based psychotherapy, which was verified in a small clinical study showing that DCS facilitated exposure therapy for fear of heights in a well-controlled virtual reality environment.

[1]  J. Bisson,et al.  Randomised controlled trial of psychological debriefing for victims of acute burn trauma , 1997, British Journal of Psychiatry.

[2]  R. Morris,et al.  Hippocampal synaptic plasticity and NMDA receptors: a role in information storage? , 1990, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

[3]  B. Rothbaum,et al.  Virtual reality exposure therapy for Vietnam veterans with posttraumatic stress disorder. , 2001, The Journal of clinical psychiatry.

[4]  R. Richardson,et al.  Effects of D-cycloserine on extinction of conditioned freezing. , 2003, Behavioral neuroscience.

[5]  S. Hashtroudi,et al.  d-Cycloserine enhances implicit memory in Alzheimer patients , 1996, Neurology.

[6]  M. Bear,et al.  A synaptic basis for memory storage in the cerebral cortex. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[7]  R. Hales,et al.  J Neuropsychiatry Clin Neurosci , 1992 .

[8]  S. Ochs Integrative Activity of the Brain: An Interdisciplinary Approach , 1968 .

[9]  D. Olton,et al.  D-cycloserine, a novel cognitive enhancer, improves spatial memory in aged rats , 1994, Neurobiology of Aging.

[10]  R. F. Westbrook,et al.  The NMDA Receptor Antagonist MK-801 Blocks Acquisition and Extinction of Conditioned Hypoalgesic Responses in the Rat , 1994, The Quarterly journal of experimental psychology. B, Comparative and physiological psychology.

[11]  M. Bouton,et al.  State-dependent fear extinction with two benzodiazepine tranquilizers. , 1990, Behavioral neuroscience.

[12]  W. Schmidt,et al.  D-cycloserine reverses the working memory impairment of hippocampal-lesioned rats in a spatial learning task. , 1992, European journal of pharmacology.

[13]  B. Rothbaum,et al.  A controlled study of virtual reality exposure therapy for the fear of flying. , 2000, Journal of consulting and clinical psychology.

[14]  V. Cestari,et al.  NMDA receptors and learning and memory processes. , 2001, Current drug targets.

[15]  R. Richardson,et al.  d-cycloserine facilitates extinction of learned fear: Effects on reacquisition and generalized extinction , 2005, Biological Psychiatry.

[16]  John F. Disterhoft,et al.  Hippocampus-dependent learning facilitated by a monoclonal antibody or D-cycloserine , 1992, Nature.

[17]  R. Bolles,et al.  Role of conditioned contextual stimuli in reinstatement of extinguished fear. , 1979, Journal of experimental psychology. Animal behavior processes.

[18]  D. Quartermain,et al.  Acute but not chronic activation of the NMDA-coupled glycine receptor with D-cycloserine facilitates learning and retention. , 1994, European journal of pharmacology.

[19]  A. Ehlers,et al.  Psychological debriefing for road traffic accident victims , 2000, British Journal of Psychiatry.

[20]  R. Herting,et al.  Evaluation of Cycloserine in the Treatment of Alzheimer's Disease , 1995, Journal of geriatric psychiatry and neurology.

[21]  Naomi M Simon,et al.  Augmentation of exposure therapy with D-cycloserine for social anxiety disorder. , 2006, Archives of general psychiatry.

[22]  R. Muller,et al.  Consolidation of Extinction Learning Involves Transfer from NMDA-Independent to NMDA-Dependent Memory , 2001, The Journal of Neuroscience.

[23]  R. Bolles,et al.  Contextual control of the extinction of conditioned fear , 1979 .

[24]  R. Richardson,et al.  Effects of multiple exposures to d-cycloserine on extinction of conditioned fear in rats , 2005, Neurobiology of Learning and Memory.

[25]  R. Richardson,et al.  Facilitation of fear extinction by D-cycloserine: theoretical and clinical implications. , 2004, Learning & memory.

[26]  J. Krystal,et al.  NMDA receptor regulation of memory and behavior in humans , 2001, Hippocampus.

[27]  J. Konorski Integrative activity of the brain , 1967 .

[28]  R. Richardson,et al.  D-cycloserine and the facilitation of extinction of conditioned fear: consequences for reinstatement. , 2004, Behavioral neuroscience.

[29]  Michael Davis,et al.  Blocking of acquisition but not expression of conditioned fear-potentiated startle by NMDA antagonists in the amygdala , 1990, Nature.

[30]  Michael Davis,et al.  Behavioral and Neural Analysis of Extinction , 2002, Neuron.

[31]  Michael Davis,et al.  Facilitation of Conditioned Fear Extinction by Systemic Administration or Intra-Amygdala Infusions of d-Cycloserine as Assessed with Fear-Potentiated Startle in Rats , 2002, The Journal of Neuroscience.

[32]  Barbara O Rothbaum,et al.  Cognitive enhancers as adjuncts to psychotherapy: use of D-cycloserine in phobic individuals to facilitate extinction of fear. , 2004, Archives of general psychiatry.

[33]  Hongjoo J. Lee,et al.  Amygdalar NMDA Receptors are Critical for New Fear Learning in Previously Fear-Conditioned Rats , 1998, The Journal of Neuroscience.

[34]  C. Randolph,et al.  D‐Cycloserine Treatment of Alzheimer Disease , 1994, Alzheimer disease and associated disorders.

[35]  Yi Ling Yang,et al.  Facilitation of conditioned fear extinction by d-cycloserine is mediated by mitogen-activated protein kinase and phosphatidylinositol 3-kinase cascades and requires de novo protein synthesis in basolateral nucleus of amygdala , 2005, Neuroscience.

[36]  James C. Denniston,et al.  Massive extinction treatment attenuates the renewal effect , 2003 .

[37]  James L McGaugh,et al.  The role of NMDA glutamate receptors, PKA, MAPK, and CAMKII in the hippocampus in extinction of conditioned fear , 2003, Hippocampus.

[38]  R. Rescorla,et al.  Reinstatement of fear to an extinguished conditioned stimulus. , 1975, Journal of experimental psychology. Animal behavior processes.

[39]  E. Fischer Conditioned Reflexes , 1942, American journal of physical medicine.

[40]  Michael Davis,et al.  Extinction of fear-potentiated startle: blockade by infusion of an NMDA antagonist into the amygdala , 1992, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[41]  W. Falk,et al.  A preliminary study of D-cycloserine treatment in Alzheimer's disease. , 1998, The Journal of neuropsychiatry and clinical neurosciences.

[42]  J. Azorlosa,et al.  The NMDA antagonist MK-801 blocks the extinction of Pavlovian fear conditioning. , 1996, Behavioral Neuroscience.