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[Abstract Title]. - Society for Neuroscience

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present study we tested the hypothesis that striatal dopamine is particularly important <strong>for</strong> the<br />

manipulation of in<strong>for</strong>mation in working memory in a pharmacological, event-related fMRI<br />

study. Twenty healthy human subjects were scanned twice, once after placebo and once after<br />

sulpiride 400 mg, a selective DA D2 receptor antagonist, while per<strong>for</strong>ming a working memory<br />

task requiring different levels of manipulation. We found a significant correlation between<br />

sulpiride plasma levels and process-specific BOLD signal bilaterally in the striatum, suggesting a<br />

dose-dependent effect of D2 antagonism on a striatally-based manipulation process. When<br />

subjects with high sulpiride plasma levels were examined separately we observed the predicted<br />

interaction between drug and condition, whereby striatal BOLD signal was lower during<br />

manipulation trials than during simple retrieval trials after sulpiride but not after placebo. No<br />

significant drug effects were observed in the PFC. These results support models of dopamine<br />

function which posit a „gating‟ function <strong>for</strong> dopamine D2 receptors in the striatum, which<br />

enables the flexible updating and manipulation of in<strong>for</strong>mation in working memory.<br />

Disclosures: C.M. Dodds , None; U. Muller, None; L. Clark, None; T.W. Robbins, None.<br />

Poster<br />

288. Working Memory: Disorders, Genes and Connectivity<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm<br />

Program#/Poster#: 288.10/RR17<br />

Topic: F.01.f. Working memory<br />

Support: DAAD research scholarship<br />

<strong>Title</strong>: An fMRI study of transcranial direct current stimulation effects on planning per<strong>for</strong>mance<br />

and associative learning<br />

Authors: *C. DOCKERY, T. GABER, B. VARKUTI, R. HÜCKEL-WENG, N.<br />

BIRBAUMER;<br />

Inst. Med. Psychology, Univ. Tuebingen, Tuebingen, Germany<br />

<strong>Abstract</strong>: Transcranial direct current stimulation (tDCS) applied over the cortex transiently<br />

modifies cortical excitability via altering the membrane potential of underlying neurons.<br />

Different cortical areas can be targeted by tDCS, and it‟s pairing with fMRI imaging supports<br />

further understanding of the effect by providing a tool to evaluate neuropathologies,<br />

pathophysiology of disease and tDCS mechanisms of action. Baudewig et al. (2001) reported<br />

reduced motor cortex activity after cathodal tDCS on sensorimotor activity shown by fMRI<br />

BOLD signal changes post-stimulation. Combined fMRI and tDCS to study cognitive function<br />

can expand knowledge about the efficacy of tDCS.

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