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Medication-Enhanced Learning In Therapy Important For Anxiety

Armen Hareyan's picture

A medication that enhances learning, taken just before an exposure therapy session, may aid cognitive behavior therapy (CBT) for anxiety disorders, say NIMH-funded researchers, who adapted the technique from studies in rats.

D-cycloserine, is used to "specifically enhance the efficacy of the emotional learning process that takes place in psychotherapy and hopefully make these new emotional memories more robust and long-lasting," explained psychologist Barbara Rothbaum, Ph.D., an NIMH grantee at Emory University, in an editorial in the March 2008 issue of the American Journal of Psychiatry (AJP). She heralded the new approach as "a paradigm shift."

So far, D-cycloserine enhanced psychotherapy has been found effective for social phobia in two studies, and for obsessive compulsive disorder (OCD) in two out of three studies, according to Rothbaum. A report on the second successful trial of the technique for OCD by Sabine Wilhelm, Ph.D., and colleagues at Massachusetts General Hospital is published in the same issue of AJP. With NIMH grant support, Rothbaum and colleagues are currently testing a D-cycloserine-enhanced virtual reality-based exposure therapy for Iraq veterans suffering from post-traumatic stress disorder (PTSD).

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D-cycloserine, an antibiotic, is normally prescribed at a 10-fold higher dose to treat tuberculosis. The effects of the single low dose given prior to CBT exposure therapy sessions are usually imperceptible to patients and last just a few hours. Yet animal studies show that the medication interacts with a receptor in the brain's fear hub to facilitate what is known as extinction learning - learning to be less fearful.

"This line of research crosses the boundaries of behavior and biology, revealing how understanding basic physiological processes underlying fear can translate into improving therapies for people with anxiety disorders," said NIMH grantee Michael Davis, Ph.D., of Emory University, whose pioneering studies in rats led to the clinical innovation.

Davis and colleagues had been exploring the workings of a pivotal receptor on cells in the brain's fear hub, the amygdala. The receptor controls the learning and extinction of fear in response to signals from the chemical messenger glutamate. D-cycloserine binds to this N-methyl-D-aspartate (NMDA) receptor.

The researchers taught rats to fear an initially neutral stimulus, a light, by repeatedly pairing it with an aversive stimulus, a mild shock. The animals then behaved fearfully when exposed to just the light. Extinguishing the fear response required repeated exposures to the light without the shock. Davis's team discovered that giving the rats just one dose of D-cycloserine just before these extinction training trials speeds up this safety learning process by making the NMDA receptor work better.

Davis then teamed up with Emory's Kerry Ressler, M.D., Ph.D., and Rothbaum for a 2004 pilot study in which D-cycloserine was shown to augment exposure therapy in which people learned to conquer their fear of heights (acrophobia) during trips in a virtual glass elevator. The results spurred similar trials for other anxiety disorders.