Relationship between free-running period and motor activity in blinded rats

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Abstract

The free-running rhythms of motor activity in blinded rats were measured by two different devices, an Automex or a running wheel. The period of free-running rhythm measured by a running wheel was likely to be shorter than that measured by an Automex, indicating that subtle environmental difference, such as whether a cage is equipped with a wheel or not, can affect the free-running period. In addition, we found a negative correlation not only between the free-running period measured by a running wheel and that measured by an Automex, but between the free-running period and the number of wheel revolutions per day. This is the first evidence that motor activity, other than the external factors such as light intensity and temperature, may be related to change in the free-running period.

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      In this study, running-wheel activity was used as an assay of circadian pacemaker function, as in many previous experiments. It has become increasingly clear, however, that running wheel access is not a behaviorally inert procedure, and housing with running wheels alters numerous neurobehavioral parameters, including both circadian activity rhythms [51,52] and voluntary ethanol intake [53,54], in both mice and rats. Further, it is plausible that running-wheel access interacts with strain to alter these processes [35].

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      The presence of a home-cage running wheel shortens tau in rats and mice (Benus et al., 1988; Edgar et al., 1991; Mistlberger and Holmes, 2000; Mistlberger et al., 1998; Yamada et al., 1986, 1988) and has been suggested, though not proven, to do so in hamsters (Pratt and Goldman, 1986; though see also Aschoff et al., 1973). In rats, the magnitude of tau shortening by wheel-running correlates with the number of wheel revolutions performed (Shioiri et al., 1991; Yamada et al., 1990), an effect also seen, though somewhat inconsistently, in hamsters (Mrosovsky, 1999; Weisgerber et al., 1997). To be of functional use for entrainment, however, feedback information from locomotor activity must demonstrate the ability to synchronize free-running rhythms through repeated phase adjustments when the opportunity to indulge in locomotor activity is either offered, induced, or forced repeatedly on sequential cycles.

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    Present address: Division of Mental Disorder Research, National Institute of Neuroscience, NCNP, Kodaira, Tokyo, Japan.

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