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[Abstract Title]. - Society for Neuroscience

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corticosterone, brain monoamine utilization, and brain cytokine mRNA expression are<br />

exaggerated. As behavioral variations following an immune challenge are often dependent on<br />

environmental context, it was of interest to investigate whether synergistic or additive effects<br />

would also be present when the immune challenge preceded the social stressor. In fact, there was<br />

reason to believe that sickness behavior represents a luxury that animals cannot af<strong>for</strong>d in the face<br />

of ongoing threat, and hence would be less pronounced under these conditions. Mice received<br />

acute LPS (10 κg) treatment immediately be<strong>for</strong>e or following a 1-hour social disruption stressor<br />

(e.g., regrouping mice after a prolonged period of isolation) and the effects on sickness behavior,<br />

and on neuroendocrine, cytokine and monoamine variations were assessed. As predicted, when<br />

LPS was administered following the social stressor, sickness behavior, corticosterone as well as<br />

monoamine utilization within the hippocampus and prefrontal cortex were markedly increased.<br />

However, when the stressor was applied after LPS administration, the sickness behavior<br />

ordinarily elicited by LPS was abolished. In addition, plasma corticosterone levels were<br />

dramatically increased by the social stressor, to the degree that a ceiling effect largely precluded<br />

detection of further elevations by LPS treatment. Identical findings were also obtained with<br />

norepinephrine utilization within the prefrontal cortex. Together, these findings suggest that<br />

synergistic effects between psychosocial stressors and LPS treatment are only apparent when the<br />

immune challenge is administered following the social stressor. Although the interaction<br />

between LPS and psychosocial stressors produce dramatic behavioral and neurochemical effects,<br />

these appear to be mediated by the context in which the challenge is administered, and is<br />

influenced by the timing and order of the treatments.<br />

Disclosures: J.E. Gibb , None; M. Audet, None; B.P. Wann, None; H. Anisman, None.<br />

Poster<br />

280. Stress and the Brain: Stress and Neuroimmunology I<br />

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

Program#/Poster#: 280.3/NN3<br />

Topic: E.06.c. Stress and neuroimmunology<br />

Support: NSF IOS-05-54514 (to RS)<br />

NICHD 05751-33 (to DP)<br />

NIMH 67782 (to RS)<br />

<strong>Title</strong>: Mast cells in the brain influence anxiety-like behaviors

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