Verwey, Michael, Robinson, Barry and Amir, Shimon ORCID: https://orcid.org/0000-0003-1919-5023 (2013) Recording and Analysis of Circadian Rhythms in Running-wheel Activity in Rodents. Journal of Visualized Experiments (71). ISSN 1940-087X
Preview |
Text (application/pdf)
797kBAmir-Jove-2013.pdf - Published Version Available under License Spectrum Terms of Access. |
Official URL: http://dx.doi.org/10.3791/50186
Abstract
When rodents have free access to a running wheel in their home cage, voluntary use of this wheel will depend on the time of day1-5. Nocturnal rodents, including rats, hamsters, and mice, are active during the night and relatively inactive during the day. Many other behavioral and physiological measures also exhibit daily rhythms, but in rodents, running-wheel activity serves as a particularly reliable and convenient measure of the output of the master circadian clock, the suprachiasmatic nucleus (SCN) of the hypothalamus. In general, through a process called entrainment, the daily pattern of running-wheel activity will naturally align with the environmental light-dark cycle (LD cycle; e.g. 12 hr-light:12 hr-dark). However circadian rhythms are endogenously generated patterns in behavior that exhibit a ~24 hr period, and persist in constant darkness. Thus, in the absence of an LD cycle, the recording and analysis of running-wheel activity can be used to determine the subjective time-of-day. Because these rhythms are directed by the circadian clock the subjective time-of-day is referred to as the circadian time (CT). In contrast, when an LD cycle is present, the time-of-day that is determined by the environmental LD cycle is called the zeitgeber time (ZT).
Although circadian rhythms in running-wheel activity are typically linked to the SCN clock6-8, circadian oscillators in many other regions of the brain and body9-14 could also be involved in the regulation of daily activity rhythms. For instance, daily rhythms in food-anticipatory activity do not require the SCN15,16 and instead, are correlated with changes in the activity of extra-SCN oscillators17-20. Thus, running-wheel activity recordings can provide important behavioral information not only about the output of the master SCN clock, but also on the activity of extra-SCN oscillators. Below we describe the equipment and methods used to record, analyze and display circadian locomotor activity rhythms in laboratory rodents.
Divisions: | Concordia University > Faculty of Arts and Science > Psychology |
---|---|
Item Type: | Article |
Refereed: | Yes |
Authors: | Verwey, Michael and Robinson, Barry and Amir, Shimon |
Journal or Publication: | Journal of Visualized Experiments |
Date: | 2013 |
Funders: |
|
Digital Object Identifier (DOI): | 10.3791/50186 |
Keywords: | Neuroscience, Issue 71, Medicine, Neurobiology, Physiology, Anatomy, Psychology, Psychiatry, Behavior, Suprachiasmatic nucleus, locomotor activity, mouse, rat, hamster, light-dark cycle, free-running activity, entrainment, circadian period, circadian rhythm, phase shift, animal model |
ID Code: | 983745 |
Deposited By: | Danielle Dennie |
Deposited On: | 13 Apr 2018 15:47 |
Last Modified: | 13 Apr 2018 15:47 |
References:
Pittendrigh CS, Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents. V. Pacemaker Structure: A Clock for All Seasons. J. Comp. Physiol. 1976;106:333–355.Pittendrigh CS, Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents. IV. Entrainment: Pacemaker as Clock. J. Comp. Physiol. 1976;106:291–331.
Pittendrigh CS, Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents. III. Heavy Water and Constant Light: Homeostasis of Frequency? J. Comp. Physiol. 1976;106:267–290.
Pittendrigh CS, Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents. II. The Variability of Phase Response Curves. J. Comp. Physiol. 1976;106:253–266.
Pittendrigh CS, Daan S. A Functional Analysis of Circadian Pacemakers in Nocturnal Rodents. I. The Stability and Lability of Spontaneous Frequency. J. Comp. Physiol. 1976;106:223–252.
Ralph MR, Foster RG, Davis FC, Menaker M. Transplanted suprachiasmatic nucleus determines circadian period. Science. 1990;247:975–978.
Moore RY, Eichler VB. Loss of a circadian adrenal corticosterone rhythm following suprachiasmatic lesions in the rat. Brain Res. 1972;42:201–206.
Stephan FK, Zucker I. Circadian rhythms in drinking behavior and locomotor activity of rats are eliminated by hypothalamic lesions. Proc. Natl. Acad. Sci. U.S.A. 1972;69:1583–1586.
Abe M, et al. Circadian rhythms in isolated brain regions. J. Neurosci. 2002;22:350–356.
Yamazaki S, et al. Resetting central and peripheral circadian oscillators in transgenic rats. Science. 2000;288:682–685.
Lamont EW, Robinson B, Stewart J, Amir S. The central and basolateral nuclei of the amygdala exhibit opposite diurnal rhythms of expression of the clock protein Period2. Proc. Natl. Acad. Sci. U.S.A. 2005;102:4180–4184.
Amir S, Lamont EW, Robinson B, Stewart J. A circadian rhythm in the expression of PERIOD2 protein reveals a novel SCN-controlled oscillator in the oval nucleus of the bed nucleus of the stria terminalis. J. Neurosci. 2004;24:781–790.
Yoo SH, et al. PERIOD2::LUCIFERASE real-time reporting of circadian dynamics reveals persistent circadian oscillations in mouse peripheral tissues. Proc. Natl. Acad. Sci. U.S.A. 2004;101:5339–5346.
Guilding C, Piggins HD. Challenging the omnipotence of the suprachiasmatic timekeeper: are circadian oscillators present throughout the mammalian brain? Eur. J. Neurosci. 2007;25:3195–3216.
Boulos Z, Terman M. Food availability and daily biological rhythms. Neurosci. Biobehav. Rev. 1980;4:119–131
Boulos Z, Rosenwasser AM, Terman M. Feeding schedules and the circadian organization of behavior in the rat. Behav. Brain Res. 1980;1:39–65.
Verwey M, Amir S. Food-entrainable circadian oscillators in the brain. Eur. J. Neurosci. 2009;30:1650–1657.
Davidson AJ, Poole AS, Yamazaki S, Menaker M. Is the food-entrainable circadian oscillator in the digestive system? Genes Brain Behav. 2003;2:32–39.
Hara R, et al. Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus. Genes Cells. 2001;6:269–278.
Damiola F, et al. Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev. 2000;14:2950–2961.
Mrosovsky N. Phase response curves for social entrainment. J. Comp. Physiol. A. 1988;162:35–46.
Cain SW, et al. Reward and aversive stimuli produce similar nonphotic phase shifts. Behav. Neurosci. 2004;118:131–137
Antle MC, Mistlberger RE. Circadian clock resetting by sleep deprivation without exercise in the Syrian hamster. J. Neurosci. 2000;20:9326–9332.
Banjanin S, Mrosovsky N. Preferences of mice, Mus musculus, for different types of running wheel. Lab Anim. 2000;34:313–318
Verwey M, Lam GY, Amir S. Circadian rhythms of PERIOD1 expression in the dorsomedial hypothalamic nucleus in the absence of entrained food-anticipatory activity rhythms in rats. Eur. J. Neurosci. 2009;29:2217–2222
Gooley JJ, Schomer A, Saper CB. The dorsomedial hypothalamic nucleus is critical for the expression of food-entrainable circadian rhythms. Nat. Neurosci. 2006;9:398–407.
Repository Staff Only: item control page