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Plasticity of Circadian Behavior and the Suprachiasmatic Nucleus Following Exposure to Non-24-Hour Light Cycles

Department of Biology, Washington University, St. Louis, MO, sjaton{at}artsci.wustl.edu

Gene D. Block

Department of Biology, University of Virginia, Charlottesville, VA

Hajime Tei

Human Genome Center, University of Tokyo, Japan

Shin Yamazaki

Department of Biological Sciences, Vanderbilt University, Nashville, TN

Erik D. Herzog

Department of Biology, Washington University, St. Louis, MO

Period aftereffects are a form of behavioral plasticity in which the free-running period of circadian behavior undergoes experience-dependent changes. It is unclear whether this plasticity is age dependent and whether the changes in behavioral period relate to changes in the SCN or the retina, 2 known circadian pacemakers in mammals. To determine whether these changes vary with age, Per1-luc transgenic mice (in which the luciferase gene is driven by the Period1 promoter) of different ages were exposed to short (10 h light: 10 h dark, T20) or long (14 h light: 14 h dark, T28) light cycles (T cycles). Recordings of running-wheel activity in constant darkness (DD) revealed that the intrinsic periods of T20 mice were significantly shorter than of T28 mice at all ages. Aftereffects following the shorter light cycle were significantly smaller in mice older than 3 months, corresponding with a decreased ability to entrain to T20. Age did not diminish entrainment or aftereffects in the 28-h light schedule. The behavioral period of pups born in DD depended on the T cycle experienced in utero, showing maternal transference of aftereffects. Recordings of Per1-luc activity from the isolated SCN in vitro revealed that the SCN of young mice expressed aftereffects, but the periods of behavior and SCN were negatively correlated. Enucleation in DD had no effect on behavioral aftereffects, indicating the eyes are not required for aftereffects expression. These data show that circadian aftereffects are an age-dependent form of plasticity mediated by stable changes in the SCN and, importantly, extra-SCN tissues.

Key Words: SCN • oscillator • aftereffects • T cycle • Period gene • mPer1 • entrainment • aging

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