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[Abstract Title]. - Society for Neuroscience

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intracerebroventricular (i.c.v.) cannula guide. At least one week later, Mn 2+ (500mM, i.c.v.) was<br />

administered 1 h prior to a 15 min swim stress (n=10) in room temperature water (30 cm depth).<br />

Control rats (n=10) were handled 1 h after Mn 2+ administration. Rats were transcardially<br />

perfused with 4% para<strong>for</strong>maldehyde and sacrificed 6 h, 24 h, 48 h, or 72 h after swim stress and<br />

brains were removed. The brains were scanned with a 9.4 T vertical bore magnet and areas of<br />

increased activity were analyzed using a program written in IDL virtual machine. The presence<br />

of Mn 2+ was detected in brain in a time-dependent manner. Thus, at 6 h Mn 2+ was present<br />

primarily in the ventricles and there was little difference between swim stress and control rats.<br />

By 24 h and 48 h, Mn 2+ was visualized in specific brain nuclei, and fiber tracts became visible at<br />

48 h. By 72 h there was little enhancement left. Swim stress increased Mn 2+ labeling at both 24 h<br />

and 48 h in specific brain regions. Enhancements were observed in the bed nucleus of the stria<br />

terminalis and the dorsal hippocampus, areas that mediate stress related behaviors and regulate<br />

the hypothalamic-pituitary adrenal axis. Additionally, enhanced labeling was seen in the lateral<br />

periaqueductal gray (lPAG), a brain region that has been proposed to mediate escape behaviors<br />

and active coping strategies. This labeling is consistent with the escape behavior (climbing and<br />

swimming) observed during initial exposure to swim stress. Through these experiments we have<br />

found that MEMRI is a rapid way of identifying structures activated by stress in 3 dimensions.<br />

These are the first studies, to our knowledge, to use MEMRI to examine brain circuitry activated<br />

by an acute stressor. This technique has much promise <strong>for</strong> revealing the mechanisms by which<br />

stress impacts on the brain and how this might be altered by pharmacological agents.<br />

Disclosures: D.A. Bangasser , None; Y. Perez, None; B. Brockel, Full time employee of<br />

AstraZeneca, A. Employment (full or part-time); Stock options <strong>for</strong> AstraZeneca, E. Ownership<br />

Interest (stock, stock options, patent or other intellectual property); R.J. Valentino, None.<br />

Poster<br />

286. Imaging the Nervous System<br />

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

Program#/Poster#: 286.3/QQ43<br />

Topic: E.09.b. Blood flow<br />

Support: NIH Grant NS-051188<br />

NIH Grant EB00790<br />

<strong>Title</strong>: In vivo two-photon measurement of single vessel diameter changes using astrocytic<br />

indicator SR101

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