ArticleFeeding cycles entrain circadian rhythms of locomotor activity in CS mice but not in C57BL/6J mice
References (26)
- et al.
Feeding schedules and the circadian organization of behavior in the rat
Behav. Brain Res.
(1980) - et al.
Persistent mean-associated rhythms in SCN-lesioned rats
Physiol. Behav.
(1986) - et al.
Evidence for a separate meal-associated oscillator in the rat
Physiol. Behav.
(1982) - et al.
Food and light as entrainers of circadian running activity in the rat
Physiol. Behav.
(1977) - et al.
The multiplicity of biological oscillators in the control of circadian running activity in the rat
Physiol. Behav.
(1977) Ventromedial hypothalamic lesions eliminate anticipatory activities of restricted daily feeding schedule in the rat
Brain Res.
(1982)- et al.
Restricted feeding and circadian activity rhythms of a predatory marsupial, Dasyuroides byrnei
Physiol. Behav.
(1986) - et al.
The effects of restricted food access upon locomotor activity in rats with suprachiasmatic nucleus lesions
Physiol. Behav.
(1979) - et al.
Memory for feeding time: Possible dependence on coupled circadian oscillators
Physiol. Behav.
(1984) - et al.
Entrainment of circadian rhythms by feeding schedules in rats with suprachiasmatic lesions
Behav. Neural Biol.
(1979)
Phase shifts of circadian rhythms in activity entrained to food access
Physiol. Behav.
The role of period and phase in interactions between feeding- and light-entrainable circadian rhythms
Physiol. Behav.
Circadian rhythms of small carnivores and the effect of restricted feeding on daily activity
Physiol. Behav.
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Insulin/IGF-1 Drives PERIOD Synthesis to Entrain Circadian Rhythms with Feeding Time
2019, CellCitation Excerpt :Here, we identify insulin and related insulin-like growth factor 1 (IGF-1) as such a signal, delineate a mechanism for its action on circadian rhythms in vitro and in vivo, and test its functional consequences in cellular and mouse models of circadian disruption. Restricted feeding cycles are sufficient to determine timing of locomotor activity and clock gene activity in peripheral tissues (Abe et al., 1989; Damiola et al., 2000). As potential timing cues, the postprandial rise in circulating glucose and insulin are obvious candidates, both being competent to affect clock gene transcription (Balsalobre et al., 2000a; Hirota et al., 2002).
Neural activity in the suprachiasmatic circadian clock of nocturnal mice anticipating a daytime meal
2016, NeuroscienceCitation Excerpt :However, the result is limited to the one case, and FAA in this mouse was unremarkable. The phase of the SCN circadian clock, as defined by rhythms of clock gene expression, is assumed to be impervious to daytime feeding schedules, but modulations of phase have been observed when feeding schedules are maintained for several weeks or longer (Challet et al., 1997; Pavlovski and Mistlberger, unpublished), especially in the absence of a competing LD cycle (Abe et al., 1989; Castillo et al., 2004). Whether or not the change in MUA waveform in this mouse reflects a shift in the SCN molecular clock, it is possible that the effect is limited to a particular subgroup of SCN neurons sampled by the electrode in this mouse.
Feedback actions of locomotor activity to the circadian clock
2012, Progress in Brain ResearchCitation Excerpt :While daytime restricted feeding under an LD cycle is effective in entraining a component of behavioral rhythms and can alter SCN function (Verwey and Amir, 2009), it does not entrain the SCN (Damiola et al., 2000). However, daytime restricted feeding does entrain peripheral oscillators (Damiola et al., 2000; Stokkan et al., 2001) and scheduled feeding in DD in the absence of other timing cues does entrain the SCN and major SCN-controlled circadian systems, at least in some mouse strains (Abe et al., 1989, 2007; Castillo et al., 2004). The timing of feeding during scheduled locomotor activity entrainment has yet to be recorded though is likely to be high around the times of increased locomotor activity.
Competing clocks: Metabolic status moderates signals from the master circadian pacemaker
2012, Neuroscience and Biobehavioral ReviewsCitation Excerpt :Interestingly, there are also cases where the absence of light as a zeitgeber, under conditions of constant darkness, produce free-running behavioural rhythms that can be shifted to the time of meal presentation. This has been observed in certain mouse strains, a carnivorous marsupial, and the rat (Abe et al., 1989; Castillo et al., 2004; O’Reilly et al., 1986). Crucially, several arousal inducing procedures can suppress cFOS induction within the hamster SCN, indicating a reduction in neural activation (Antle and Mistlberger, 2000; Mikkelsen et al., 1998).
Neurobiology of food anticipatory circadian rhythms
2011, Physiology and BehaviorCitation Excerpt :Nonetheless, when spontaneous feeding behavior is controlled by the SCN in animals housed in LD, the entire circadian system is synchronized to the phase of the SCN, and is thereby light-entrained. Similarly, when rodents are maintained on a 24 h restricted feeding schedule in constant light or dark, the entire circadian system, including the SCN, can come under control of mealtime, and adopt a stable phase of entrainment rather than free-run [28–30]. This occurs commonly in some species, such as Syrian hamsters (Fig. 2c) and mice (albeit with strain differences), and less commonly in other species, such as Norway rats, which in constant dark or dim light more typically exhibit both a free-running, non-24 h activity rhythm driven by the SCN, and a food-anticipatory 24-h activity rhythm coupled to mealtime (i.e., two rhythms in the same behavioral variables; Fig. 2d).
Circadian Rhythms in Mammals. Formal Properties and Environmental Influences
2010, Principles and Practice of Sleep Medicine: Fifth Edition