Sunday 19 june 2016
11:45 - 12:15h at Kilimanjaro
Categories: Neurobiology, Research
Parallel session: Research track: Addiction, Depression and Neurobiology
Disruption of fear processing seems to be at the core of posttraumatic stress disorders (PTSD). Indeed, mechanisms of fear conditioning, extinction and extinction recall have been found to be disrupted in PTSD patients. We have demonstrated that such deficits (especially fear extinction delay) disappear after EMDR therapy according to behavioral responses as well as psychophysiological measures (skin conductance, response, heart rate). In addition, using fMRI, we observed improvement of amygdala, hippocampus and ventro-medial prefrontal cortex functioning during extinction in PTSD after EMDR as compared to before EMDR therapy.
Considering these results, we used the fear conditioning, extinction and recall paradigm to test for the specific effect of bilateral alternating stimulations during extinction to mimic the EMDR therapy. In healthy human subjects as well as in PTSD patients, we found an effect of bilateral alternating stimulations in key structures involved in fear responses reduction (amygdala and the prefrontal cortex) as compared to without bilateral alternating stimulations.
The effect of the bilateral alternating stimulations during desensitization phase of the EMDR therapy may rely among others upon the prefrontal cortex and the amygdala.
● Demonstrate that bilateral alternating stimulations play a key role in desensitization
● Evaluate the brain structures involved in desensitization through the action of bilateral alternate stimulations
● Measure the effect of bilateral alternating stimulations in fear responses reduction