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[Abstract Title]. - Society for Neuroscience

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predator) have been shown previously to reduce feeding and increase defensive behaviors in the<br />

rat. The mu-opioid peptide agonist DAMGO (D-Ala2, NMe-Phe4, Glyol5-enkephalin) was<br />

chronically microinfused directly into the Acb core of male Sprague-Dawley rats. Separate<br />

groups of animals received 4 daily microinfusions of either DAMGO or saline into the Acb core<br />

10 minutes be<strong>for</strong>e being placed in a test chamber with 5 grams of sweetened fat. After<br />

completion of these four chronic treatment days, all rats received a sham injection and were<br />

allowed to eat sweetened-fat ad-libitum. Enhancement of baseline fat intake was not observed in<br />

DAMGO-pretreated rats. Two days later, sham-injected animals were exposed to the ferret<br />

predator <strong>for</strong> 5 minutes and given the opportunity to eat sweetened-fat. Control rats showed a<br />

marked decrease in ad-libitum sweetened-fat intake immediately after ferret exposure whereas<br />

the prior chronic κ-opioid receptor stimulation by DAMGO prevented this stress-induced<br />

anorexic effect. Ad-libitum fat intake returned to pre-ferret baseline levels in all rats on a<br />

subsequent test day. Hence, chronic intra-Acb DAMGO pretreatment fundamentally alters the<br />

behavioral response to predator stress. These results establish a role <strong>for</strong> the nucleus accumbens in<br />

regulating stress-induced anorexia and may imply that individual differences in the effects of<br />

stress on palatable food intake may relate to nucleus accumbens opioid tone.<br />

Disclosures: L. Pascal , None; V.P. Bakshi, None; B.A. Baldo, None; R.C. Spencer,<br />

None; A.E. Kelley, None.<br />

Poster<br />

298. Neural Mechanisms of Reward: Self-Administration and Opioid Modulation<br />

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

Program#/Poster#: 298.12/TT45<br />

Topic: F.03.d. Reward<br />

Support: NIMH Grant MH63649<br />

<strong>Title</strong>: Hyperdopaminergic mice exhibit enhanced 'wanting' but normal modulation of 'liking'<br />

Authors: *G. M. SPROW 1 , S. V. MAHLER 1 , K. C. BERRIDGE 1 , J. A. BEELER 2 , X.<br />

ZHUANG 2 ;<br />

1 Psychology, Univ. Michigan, Ann Arbor, MI; 2 Neurobio., Univ. Chicago, Chicago, IL<br />

<strong>Abstract</strong>: Dopamine has long been thought to be a critical component of the natural reward<br />

pathway, although the exact role it plays in appetitive „wanting‟ versus hedonic „liking‟ remains<br />

undetermined. Mounting evidence points to a role of dopamine levels specifically in the<br />

„wanting‟ of rewards but neither the „liking‟ of them nor the „learning‟ about them. To further<br />

investigate this role, genetic and behavioral approaches were combined. Dopamine transporter

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