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[Abstract Title]. - Society for Neuroscience

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Disclosures: R.S. Oosting , None; D. Meulendijks, None; T. Douma, None; E. Hendriksen,<br />

None; M. Breuer, None; K. Westphal, None; B. Olivier, None.<br />

Poster<br />

255. Mood Disorders: Animal Models and Treatment Effects II<br />

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

Program#/Poster#: 255.21/Z2<br />

Topic: C.15.h. Affective disorders: Animal models<br />

Support: University of Vermont<br />

<strong>Title</strong>: The 5-HT1A receptor antagonist WAY100635 dose-dependently decreases social<br />

interaction when infused into the bed nucleus of the stria terminalis (BNST)<br />

Authors: *K. M. RHODES, B. A. GRIMMIG, M. KOCHO-SCHELLENBERG, R. A.<br />

SUGARMAN, M. R. WILLIAMS, S. E. HAMMACK;<br />

Psychology, Univ. of Vermont, Burlington, VT<br />

<strong>Abstract</strong>: Substantial evidence suggests that serotonin (5-HT) activation within the brain<br />

modulates anxiety-like behavior. The bed nucleus of the stria terminalis (BNST) and<br />

serotonergic caudal dorsal raphe nucleus (DRN) have both been argued to mediate anxiety-like<br />

behavioral responding; hence, the activation of 5-HT neurons in the caudal DRN may modulate<br />

anxiety-like behavior via the release of 5-HT within the BNST. BNST neurons exhibit a complex<br />

response pattern to exogenous 5-HT, exhibiting both inhibitory and excitatory responses, which<br />

are mediated by different 5-HT receptor subtypes. Prior studies suggest that the 5-HT1,7 receptor<br />

agonist 5-carboxyamidotryptamine (5-CT) is anxiolytic, which is consistent with a reduction in<br />

BNST activity mediated by 5-HT1A postsynaptic receptor activation. However the anxiolytic<br />

effects of 5-CT could also be mediated by 5-HT7 receptor activation, due to high affinity of 5-<br />

CT to this receptor subtype. To determine the effects of 5-HT1A receptor activation on anxietylike<br />

behavior, we infused the 5-HT1A antagonist WAY-100635 (0, 0.04, 0.4 and 4 µg / 0.5 µl)<br />

into the BNST of rats immediately be<strong>for</strong>e social interaction testing. In order to observe a<br />

behavioral effect of the 5-HT1A antagonist against a background of elevated 5-HT, we<br />

administered two 5-sec 1-mA footshocks immediately after infusion, because this treatment has<br />

been shown to induce serotonin release in projection regions of the DRN. Rats were then tested<br />

<strong>for</strong> social interaction in a different room and testing apparatus. Two animals receiving the same<br />

drug treatment were placed into a testing box and social interaction was recorded <strong>for</strong> 10-min.<br />

Pairs were scored <strong>for</strong> the total amount of time interacting (i.e. sniffing, boxing, following,<br />

grooming, etc.) and locomotor activity (total number of line crosses). Social interaction was<br />

defined as the amount of time interacting per line cross. WAY-100635 dose dependently

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