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[Abstract Title]. - Society for Neuroscience

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hyperpolarizes BLA neurons corresponding to the induction of an outward ionic current most<br />

likely through Gβγ activation of Kir3.x family channels. Based on our data, we speculate that<br />

somatostatin responses are through sst2 receptors, would be inhibitory to BLA projection cells,<br />

and that reduction in sst2 receptor expression by Ucn1-priming would bias these neurons toward<br />

hyperexcitability. Currently, experiments on primed animals are in progress to test this<br />

hypothesis.<br />

Disclosures: A. Molosh, None; W. Truitt, None; P. Kelley, None; A. Dietrich, None; S. Fitz,<br />

None; G. Ox<strong>for</strong>d, None; A. Shekhar, None.<br />

Poster<br />

283. Stress-Regulated Pathways II<br />

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

Program#/Poster#: 283.24/PP20<br />

Topic: E.06.f. Stress modulated pathways<br />

Support: NIMH MH60668<br />

NIMH MH069558<br />

<strong>Title</strong>: Chronic stress selectively reduces hippocampal volume in rats<br />

Authors: *F. J. HELMSTETTER 1,2 , T. LEE 1 , T. JAROME 1 , S.-J. LI 2 , J. J. KIM 3 ;<br />

1 Dept Psychol, Univ. of Wisconsin Milwaukee, Milwaukee, WI; 2 Med. Col. of Wisconsin,<br />

Milwaukee, WI; 3 Univ. of Washington, Seattle, WA<br />

<strong>Abstract</strong>: It is well-documented that stress can exert physiological changes in the hippocampus,<br />

a structure implicated in the <strong>for</strong>mation of long-term declarative memory in humans and spatial<br />

memory in rodents. As it increases in duration and/or intensity, uncontrollable stress will<br />

exacerbate neuronal endangerment in rodent hippocampus and correlate with hippocampal<br />

volume reduction in humans, particularly in posttraumatic stress disorder (PTSD) patients such<br />

as combat veterans. However, since human imaging studies cannot address the causal link<br />

between stress and hippocampal changes, the notion of stress-induced diminution of<br />

hippocampal volume remains controversial.<br />

To address these issues, the present study used a longitudinal, within-subjects design and<br />

compared hippocampal volumes in rats be<strong>for</strong>e and after exposure to chronic stress. Twenty<br />

Long-Evans rats (weight: 300-325 g) initially received a magnetic resonance imaging (MRI)<br />

scan to acquire T1-weighted brain images (spatial resolution: .068 x .068 x .75 mm) at 9.4T and<br />

then were divided into two groups: stress (n=10) and control (n=10). For 21 days, the stress

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