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[Abstract Title]. - Society for Neuroscience

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day 20 to 40 (restricted-running), and access freely again from day 41 to 59 (unbound-running-<br />

2). Wheeling activity gradually increased from day 1 to 7, and stabilized around at 1,500 (an<br />

arbitrary unit) after day 8. During the restricted-running, wheeling activity decreased to<br />

approximately 300, however the wheeling activity jumped up to 700 during the unboundrunning-2,<br />

though the level was still lower than that in the unbound-running-1 period, which may<br />

probably be due to the change of set point of the wheel running during the running restriction.<br />

During the restricted-running period, food intake was significantly higher than that during both<br />

unbound-running-1 and -2 periods, suggesting that occasional running restriction changes<br />

regulation of food intake positively. This escalation is rather contradictory from the view of<br />

energy homeostasis, but <strong>for</strong> rats, they would have much time to eat foods instead of the time <strong>for</strong><br />

running. When they could run <strong>for</strong> 24 hrs again, food intake returned to the levels of unboundrunning-1.<br />

Thus, the complete running deprivation and restricted running differently affected the<br />

relation between running and food consumption. For the start or re-start of full running activity<br />

in rats, an introduction of anorexic stage must be indispensable. One possible explanation may be<br />

that rats try to find “running time” at expense of “eating time” until the putative flip-flop<br />

regulatory system is established. This regulation, if any, would have substantial influence on<br />

body weight control.<br />

Disclosures: M. Bannai, Ajinomoto Co., Inc., A. Employment (full or part-time); K. Kasuh,<br />

None; K. Nakahara, University of Miyazaki, A. Employment (full or part-time); N. Murakami,<br />

University of Miyazaki, A. Employment (full or part-time); M. Takahashi, Ajinomoto Co., Inc.,<br />

A. Employment (full or part-time).<br />

Poster<br />

285. Sleep: Molecular, Cellular and Pharmacology I<br />

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

Program#/Poster#: 285.1/QQ17<br />

Topic: E.08.c. Sleep: Molecular, cellular, and pharmacology<br />

Support: NIH Grant NS34004<br />

NIH Grant MH59839<br />

<strong>Title</strong>: Pontine-wave (P-wave) generator activation-dependent memory processing involves<br />

protein kinase A (PKA) activation-mediated brain-derived neurotrophic factor (BDNF)<br />

expression in the CA3 subfield of dorsal hippocampus<br />

Authors: *S. DATTA, J. L. SHEA;<br />

Dept Psychiatry, Boston Univ. Sch. Med., Boston, MA

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