Literature DB >> 10357435

Nonphotic entrainment of activity and temperature rhythms in anophthalmic mice.

L K Laemle1, J E Ottenweller.   

Abstract

Although it is more common to study the effects of light on circadian systems, nonphotic stimuli can also influence and entrain circadian clocks. Because anophthalmic mice (ZRDCT-AN) have a genetic mutation that prevents the development of the eyes, they do not respond to light or entrain to light-dark cycles. Thus, entrainment of anophthalmic mice requires a nonphotic zeitgeber (entraining stimulus). In the current study we attempted to entrain sighted and anophthalmic mice of the same strain, using restricted access to an unlocked running wheel as the zeitgeber. First, free-running rhythms were established. The running wheels were then locked, and unlocked only from 0930-1130 h each day. Finally, a postentrainment free run was measured. In one group of animals, body temperature and general activity were measured using a Minimitter telemetry system. In another, general activity was measured by a sensitive force plate beneath the cage. Running-wheel activity was recorded in both groups. The force plate proved satisfactory for observing the behavior of the circadian system during wheel locking, and preferable to the temperature transmitters for long-term studies because the battery life of the mouse temperature transmitters was limited. Both sighted and anophthalmic mice were able to entrain to restricted wheel access, although not all animals responded. Mice that did not entrain showed either no effect of wheel locking or exhibited masking.

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Mesh:

Year:  1999        PMID: 10357435     DOI: 10.1016/s0031-9384(98)00318-7

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  6 in total

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5.  Forced rather than voluntary exercise entrains peripheral clocks via a corticosterone/noradrenaline increase in PER2::LUC mice.

Authors:  Hiroyuki Sasaki; Yuta Hattori; Yuko Ikeda; Mayo Kamagata; Shiho Iwami; Shinnosuke Yasuda; Yu Tahara; Shigenobu Shibata
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6.  Circadian clock network desynchrony promotes weight gain and alters glucose homeostasis in mice.

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  6 in total

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