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  <item rdf:about="http://hdl.handle.net/10090/810">
    <title>N400 ERP Response as a Measurement of Semantic Expectancy in Trauma Survivors</title>
    <link>http://hdl.handle.net/10090/810</link>
    <description>Title: N400 ERP Response as a Measurement of Semantic Expectancy in Trauma Survivors
&lt;br/&gt;
&lt;br/&gt;Authors: Batterink, Laura
&lt;br/&gt;
&lt;br/&gt;Abstract: Semantic biases in trauma survivors were assessed using the N400 ERP response as a&#xD;
measurement of expectancy. Eighteen trauma survivors were recruited from the community.&#xD;
Subjects were interviewed and their post-traumatic stress disorder diagnosis was determined by a&#xD;
clinical psychologist. Ambiguous sentences that could be sensibly completed with a military or&#xD;
non-military ending were presented to subjects one word at a time. The sentences ended with&#xD;
expected, unexpected, or military words. Subjects&amp;#8217; EEG was continuously recorded throughout&#xD;
the task. Subjects with PTSD were found to have a reduced N400 response across all three&#xD;
conditions compared to subjects with no PTSD. The PTSD group also trended toward an&#xD;
inverted N400 pattern than normally seen in a healthy population. War veterans with PTSD&#xD;
showed a nearly significant reduction in N400 amplitude to the trauma condition relative to the&#xD;
unexpected condition. These findings provide more evidence for general cognitive deficiencies&#xD;
associated with PTSD, such as attentional problems, rather than differences in semantic&#xD;
expectancy in this population. However, there is some evidence to suggest that informationprocessing&#xD;
biases may also play a role in these differences. Future research should repeat this&#xD;
experimental design with a larger and less variable subject pool to substantiate these initial&#xD;
findings.
&lt;br/&gt;
&lt;br/&gt;Description: Submitted in Partial Fulfillment of Requirements For the Degree of Bachelor of Arts, Program in Neuroscience, Middlebury College</description>
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    <title>Neurochemical Mechanisms of Glucose-induced Cognitive Enhancement:</title>
    <link>http://hdl.handle.net/10090/809</link>
    <description>Title: Neurochemical Mechanisms of Glucose-induced Cognitive Enhancement:
&lt;br/&gt;
&lt;br/&gt;Authors: Fong, Chui Ying (Rachel)
&lt;br/&gt;
&lt;br/&gt;Abstract: Extensive research has found that glucose enhances memory in healthy young&#xD;
adults as well as in elderly people. Rodent studies have also shown that administration of&#xD;
glucose, via intraseptal, intrahippocampal and systemic injections, facilitates learning and&#xD;
attenuates age-related cognitive deficits. A potential mechanism by which glucose may&#xD;
enhance memory is through interaction with the mesolimbic dopaminergic system. The&#xD;
mesolimbic dopamine system has long been suggested to mediate the brain reward&#xD;
pathway, which can induce learning and approach behavior. Moreover, recent theories also&#xD;
propose that dopamine may act as a marker for salient environmental stimuli and underlie&#xD;
motivated behavior. We hypothesized that different dopamine receptors would mediate the&#xD;
glucose-induced cognitive enhancement since ATP-sensitive potassium channels have&#xD;
been found to link glucose metabolism and neuronal excitability, which in turn modulates&#xD;
dopamine release. Spontaneous alternation was used to assess male Sprague-Dawley rats&amp;#8217;&#xD;
spatial working memory after systemic administrations of glucose and selective D1&#xD;
antagonist, SCH 23390, or D2 antagonist, eticlopride. Glucose was found to improve&#xD;
alternation performance compared to control rats. SCH 23390 and eticlopride blocked the&#xD;
glucose facilitation to a similar extent when injected with glucose, but they did not alter the&#xD;
subjects&amp;#8217; alternation scores when injected with saline. No significant treatment-dependent&#xD;
difference was observed in the total numbers of arm entries or the temporal pattern of arm&#xD;
entries between all groups, indicating that the selected doses of dopamine antagonists did&#xD;
not produce motor or motivational deficits; the drug effects were likely to be cognitive.
&lt;br/&gt;
&lt;br/&gt;Description: Submitted in Partial Fulfillment of Requirements For the Degree of Bachelor of Arts, Program in Neuroscience, Middlebury College</description>
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