Daily exposure to a running wheel entrains circadian rhythms in mice in parallel with development of an increase in spontaneous movement prior to running-wheel access

2013 ◽  
Vol 305 (11) ◽  
pp. R1367-R1375 ◽  
Author(s):  
Yujiro Yamanaka ◽  
Sato Honma ◽  
Ken-ichi Honma
Keyword(s):  
Circadian Rhythms ◽  
Fixed Time ◽  
Time Of Day ◽  
Constant Darkness ◽  
Spontaneous Movement ◽  
Running Wheel ◽  
Daily Exposure ◽  
Free Running ◽  
Nonphotic Entrainment ◽  
Circadian Behavior

Entrainment of circadian behavior rhythms by daily exposure to a running wheel was examined in mice under constant darkness. Spontaneous movement was individually monitored for more than 6 mo by a thermal sensor. After establishment of steady-state free running, mice were placed in a different cage equipped with a running-wheel for 3 h once per day at 6 AM. The daily exchange was continued for 80 days. The number of wheel revolutions during exposure to the running wheel was also measured simultaneously with spontaneous movement. In 13 out of 17 mice, circadian behavior rhythm was entrained by daily wheel exposure, showing a period indistinguishable from 24 h. The entrainment occurred in parallel with an increase in spontaneous movement immediately prior to the daily wheel exposure. A similar preexposure increase was observed in only one of four nonentrained mice. The preexposure increase appeared in 19.5 days on average after the start of daily wheel exposure and persisted for 36 days on average after the termination of the exposure schedule. The preexposure increase was detected only when daily wheel exposure came into the activity phase of the circadian behavior rhythm, which was accompanied by an increase in the number of wheel revolutions. These findings indicate that a novel oscillation with a circadian period is induced in mice by daily exposure to a running wheel at a fixed time of day and suggest that the oscillation is involved in the nonphotic entrainment of circadian rhythms in spontaneous movement.

scholarly journals Free-running circadian breathing rhythms are eliminated by suprachiasmatic nucleus lesion

2020 ◽  
Vol 129 (1) ◽  
pp. 49-57
Author(s):  
Benton S. Purnell ◽  
Gordon F. Buchanan
Keyword(s):  
Sleep Apnea ◽  
Circadian Rhythms ◽  
Suprachiasmatic Nucleus ◽  
Time Of Day ◽  
Sudden Unexpected Death ◽  
Constant Darkness ◽  
Unexpected Death ◽  
Treatment And Prevention ◽  
Free Running

It has long been appreciated that breathing is altered by time of day. This study demonstrates that rhythmicity in breathing persists in constant darkness but is dependent on the suprachiasmatic nucleus in the hypothalamus. Understanding circadian rhythms in breathing may be important for the treatment and prevention of diseases such as sleep apnea and sudden unexpected death in epilepsy.

Organization of rat circadian rhythms during daily infusion of melatonin or S20098, a melatonin agonist

1999 ◽  
Vol 277 (3) ◽  
pp. R812-R828 ◽  
Author(s):  
B. Pitrosky ◽  
R. Kirsch ◽  
A. Malan ◽  
E. Mocaer ◽  
P. Pevet
Keyword(s):  
Body Temperature ◽  
Circadian Rhythms ◽  
Phase Response Curve ◽  
Constant Darkness ◽  
Time Interval ◽  
General Activity ◽  
Activity Peak ◽  
Free Running ◽  
Wheel Activity ◽  
Free Running Period

Daily administration of melatonin or S20098, a melatonin agonist, is known to entrain the free-running circadian rhythms of rats. The effects of the duration of administration on entrainment were studied. The animals demonstrated free-running circadian rhythms (running-wheel activity, body temperature, general activity) in constant darkness. Daily infusions of melatonin or S20098 for 1, 8, or 16 h entrained the circadian rhythms to 24 h. Two daily infusions of 1 h (separated by 8 h) entrained the activity peak within the shorter time interval. The entraining properties of melatonin and S20098 were similar and were affected neither by pinealectomy nor by infusion of 1- or 8-h duration. However, with 16-h infusion, less than half of the animals became entrained. Once entrained, the phase angle between the onset of infusion and the rhythms (onset of activity or acrophase of body temperature) increased with the duration of infusion. Before entrainment, the free-running period increased with the duration of infusion, an effect that was not predictable from the phase response curve.

Maternal-fetal communication of circadian phase in a precocious rodent, the spiny mouse

1987 ◽  
Vol 253 (4) ◽  
pp. E401-E409
Author(s):  
D. R. Weaver ◽  
S. M. Reppert
Keyword(s):  
Circadian Rhythms ◽  
Postnatal Period ◽  
Spiny Mouse ◽  
Constant Darkness ◽  
Suprachiasmatic Nuclei ◽  
Maternal Influences ◽  
Circadian Phase ◽  
Environmental Light ◽  
Running Activity ◽  
Free Running

The development of circadian rhythms was examined in a precocious rodent species, the spiny mouse. Spiny mouse pups born and reared in constant darkness expressed robust circadian rhythms in locomotor activity as early as day 5 of life. Free-running activity rhythms of pups born and reared in constant darkness were coordinated with the dam on the day of birth. Postnatal maternal influences on pup rhythmicity are minimal in this species, as pups fostered on the day of birth to dams whose circadian phases were opposite to the pups' original dams were coordinated with their original dams on the day of birth. Studies using 2-deoxy-D-[1-14C]-glucose autoradiography showed that there were synchronous (coordinated) rhythms in metabolic activity in the maternal and fetal suprachiasmatic nuclei, directly demonstrating prenatal coordination of maternal and fetal rhythmicity. Maternal-fetal coordination of circadian phase was not the result of direct entrainment of the fetuses to the environmental light-dark cycle. These results demonstrate that there is prenatal communication of circadian phase in this precocious species, without demonstrable postnatal maternal influences on pup circadian rhythmicity. Spiny mice therefore represent an important animal model in which circadian rhythms in the postnatal period can be used to precisely assess prenatal influences on circadian phase.

Circadian activity of the white sucker, Catostomus commersoni: comparison of individual and shoaling fish

1980 ◽  
Vol 58 (8) ◽  
pp. 1399-1403 ◽  
Author(s):  
Martin Kavaliers
Keyword(s):  
Locomotor Activity ◽  
Circadian Rhythms ◽  
Social Organization ◽  
Constant Darkness ◽  
White Sucker ◽  
Circadian Period ◽  
Circadian Activity ◽  
Catostomus Commersoni ◽  
Free Running ◽  
Precise Version

Individual and shoaling white suckers, Catostomus commersoni, displayed free running circadian rhythms of locomotor activity under conditions of constant darkness and temperature. The circadian activity of shoals was different from that of single fish. The activity of single fish was rhythmic initially with a period of less than 24 h, but became arrhythmic after 15–30 days. Shoals of white suckers had a less variable circadian period that was greater than 24 h, and showed no evidence of arrhythmicity. The circadian activity of shoals is determined by its behavioural and social organization; it is not simply a more precise version of the activity of single fish.

scholarly journals Transcriptional Structure of Petunia Clock in Leaves and Petals

Genes ◽  
2019 ◽  
Vol 10 (11) ◽  
pp. 860 ◽  
Author(s):  
Marta I. Terry ◽  
Marta Carrera-Alesina ◽  
Julia Weiss ◽  
Marcos Egea-Cortines
Keyword(s):  
Circadian Clock ◽  
Clock Genes ◽  
Time Of Day ◽  
Constant Darkness ◽  
Petunia X Hybrida ◽  
Environmental Signals ◽  
Expression Variability ◽  
Rhythmic Expression ◽  
Free Running ◽  
Maximum Expression

The plant circadian clock coordinates environmental signals with internal processes including secondary metabolism, growth, flowering, and volatile emission. Plant tissues are specialized in different functions, and petals conceal the sexual organs while attracting pollinators. Here we analyzed the transcriptional structure of the petunia (Petunia x hybrida) circadian clock in leaves and petals. We recorded the expression of 13 clock genes in petunia under light:dark (LD) and constant darkness (DD). Under light:dark conditions, clock genes reached maximum expression during the light phase in leaves and the dark period in petals. Under free running conditions of constant darkness, maximum expression was delayed, especially in petals. Interestingly, the rhythmic expression pattern of PhLHY persisted in leaves and petals in LD and DD. Gene expression variability differed among leaves and petals, time of day and photoperiod. The transcriptional noise was higher especially in leaves under constant darkness. We found that PhPRR7, PhPRR5, and PhGI paralogs showed changes in gene structure including exon number and deletions of CCT domain of the PRR family. Our results revealed that petunia petals presented a specialized clock.

Behavioral and neurochemical sources of variability of circadian period and phase: studies of circadian rhythms of npy−/− mice

2007 ◽  
Vol 292 (3) ◽  
pp. R1306-R1314 ◽  
Author(s):  
Mary Harrington ◽  
Penny Molyneux ◽  
Stephanie Soscia ◽  
Cheruba Prabakar ◽  
Judy McKinley-Brewer ◽  
...  
Keyword(s):  
Locomotor Activity ◽  
Circadian Rhythms ◽  
Activity Patterns ◽  
Circadian Period ◽  
Running Wheel ◽  
Clock Period ◽  
A Value ◽  
Free Running ◽  
The Mean ◽  
Delayed Phase

The cycle length or period of the free-running rhythm is a key characteristic of circadian rhythms. In this study we verify prior reports that locomotor activity patterns and running wheel access can alter the circadian period, and we report that these treatments also increase variability of the circadian period between animals. We demonstrate that the loss of a neurochemical, neuropeptide Y (NPY), abolishes these influences and reduces the interindividual variability in clock period. These behavioral and environmental influences, from daily distribution of peak locomotor activity and from access to a running wheel, both act to push the mean circadian period to a value < 24 h. Magnitude of light-induced resetting is altered as well. When photoperiod was abruptly changed from a 18:6-h light-dark cycle (LD18:6) to LD6:18, mice deficient in NPY were slower to respond to the change in photoperiod by redistribution of their activity within the prolonged dark and eventually adopted a delayed phase angle of entrainment compared with controls. These results support the hypothesis that nonphotic influences on circadian period serve a useful function when animals must respond to abruptly changing photoperiods and point to the NPYergic pathway from the intergeniculate leaflet innervating the suprachiasmatic nucleus as a circuit mediating these effects.

Influence of running wheel activity on free-running sleep/wake and drinking circadian rhythms in mice

1991 ◽  
Vol 50 (2) ◽  
pp. 373-378 ◽  
Author(s):  
Dale M. Edgar ◽  
Thomas S. Kilduff ◽  
Connie E. Martin ◽  
William C. Dement
Keyword(s):  
Circadian Rhythms ◽  
Running Wheel ◽  
Free Running ◽  
Wheel Activity

scholarly journals Nitric Oxide Mediates Neuro-Glial Interaction that Shapes Drosophila Circadian Behavior

2019 ◽  
Author(s):  
Anatoly Kozlov ◽  
Emi Nagoshi
Keyword(s):  
Nitric Oxide ◽  
Circadian Rhythms ◽  
Neural Circuit ◽  
Critical Role ◽  
Constant Darkness ◽  
Molecular Clocks ◽  
Loss Of Function ◽  
Pacemaker Neurons ◽  
Circadian Behavior ◽  
First Time

AbstractDrosophila circadian behavior relies on the network of heterogeneous groups of clock neurons. Short -and long-range signaling within the pacemaker circuit coordinates molecular and neural rhythms of clock neurons to generate coherent behavioral output. The neurochemistry of circadian behavior is complex and remains incompletely understood. Here we demonstrate that the gaseous messenger nitric oxide (NO) is a signaling molecule linking circadian pacemaker to rhythmic locomotor activity. We show that two independent mutants lacking nitric oxide synthase (NOS) have severely disturbed locomotor behavior both in light-dark cycles and constant darkness, although molecular clocks in the main pacemaker neurons are unaffected. Behavioral phenotypes are due in part to the malformation of neurites of the main pacemaker neurons, s-LNvs. Using cell-type selective and stage-specific gain -and loss-of-function of NOS, we demonstrate that NO secreted from diverse cellular clusters non-cell-autonomously affect molecular and behavioral rhythms. We further identify glia as a major source of NO that regulates circadian locomotor output. These results reveal for the first time the critical role of NO signaling in the Drosophila circadian system and highlight the importance of neuro-glial interaction in the neural circuit output.Author summaryCircadian rhythms are daily cycles of physiological and behavioral processes found in most plants and animals on our planet from cyanobacteria to humans. Circadian rhythms allow organisms to anticipate routine daily and annual changes of environmental conditions and efficiently adapt to them. Fruit fly Drosophila melanogaster is an excellent model to study this phenomenon, as its versatile toolkit enables the study of genetic, molecular and neuronal mechanisms of rhythm generation. Here we report for the first time that gasotransmitter nitric oxide (NO) has a broad, multi-faceted impact on Drosophila circadian rhythms, which takes place both during the development and the adulthood. We also show that one of the important contributors of NO to circadian rhythms are glial cells. The second finding highlights that circadian rhythms of higher organisms are not simply controlled by the small number of pacemaker neurons but are generated by the system that consists of many different players, including glia.

Spontaneous Recovery of Circadian Organization in Mice Lacking a Core Component of the Molecular Clockwork

2021 ◽  
pp. 074873042110608
Author(s):  
Jonathan P. Riggle ◽  
Kenneth G. Onishi ◽  
Jharnae A. Love ◽  
Dana E. Beach ◽  
Irving Zucker ◽  
...  
Keyword(s):  
Circadian Rhythms ◽  
Spontaneous Recovery ◽  
Clock Genes ◽  
Feedback Loops ◽  
Constant Darkness ◽  
Core Component ◽  
Period 2 ◽  
Circadian Organization ◽  
Circadian Clock Genes ◽  
Free Running

Circadian rhythms are generated by interlocked transcriptional-translational feedback loops of circadian clock genes and their protein products. Mice homozygous for a functional deletion in the Period-2 gene ( Per2m/m mice) exhibit short free-running circadian periods and eventually lose behavioral circadian rhythmicity in constant darkness (DD). We investigated Per2m/m mice in DD for several months and identified a categorical sex difference in the dependence on Per2 for maintenance of circadian rhythms. Nearly all female Per2m/m mice became circadian arrhythmic in DD, whereas free-running rhythms persisted in 37% of males. Remarkably, with extended testing, Per2m/m mice did not remain arrhythmic in DD, but after varying intervals spontaneously recovered robust, free-running circadian rhythms, with periods shorter than those expressed prior to arrhythmia. Spontaneous recovery was strikingly sex-biased, occurring in 95% of females and 33% of males. Castration in adulthood resulted in male Per2m/m mice exhibiting female-like levels of arrhythmia in DD, but did not affect spontaneous recovery. The circadian pacemaker of many gonad-intact males, but not females, can persist in DD for long intervals without a functional PER2 protein; their circadian clocks may be in an unstable equilibrium, incapable of sustaining persistent coherent circadian organization, resulting in transient cycles of circadian organization and arrhythmia.

scholarly journals Drosophila clock cells use multiple mechanisms to transmit time-of-day signals in the brain

2020 ◽  
Author(s):  
Annika F. Barber ◽  
Shi Yi Fong ◽  
Anna Kolesnik ◽  
Michael Fetchko ◽  
Amita Sehgal
Keyword(s):  
Time Of Day ◽  
Insulin Producing Cells ◽  
Clock Network ◽  
Free Running ◽  
Output Neurons ◽  
Central Clock ◽  
Circadian Behavior ◽  
And Control ◽  
The Brain

AbstractRegulation of circadian behavior and physiology by the Drosophila brain clock requires communication from central clock neurons to downstream output regions, but the mechanism by which clock cells regulate downstream targets is not known. We show here that the pars intercerebralis (PI), previously identified as a target of the morning cells in the clock network, also receives input from evening cells. We determined that morning and evening clock neurons have time of day dependent connectivity to the PI, which is regulated by specific peptides as well as by fast neurotransmitters. Interestingly, PI cells that secrete the peptide DH44, and control rest:activity rhythms, are inhibited by clock inputs while insulin-producing cells are activated, indicating that the same clock cells can use different mechanisms to drive cycling in output neurons. Inputs of morning cells to the DILP2+ neurons are relevant for the circadian rhythm of feeding, reinforcing the role of the PI as a circadian relay that controls multiple behavioral outputs. Our findings provide mechanisms by which clock neurons signal to non-clock cells to drive rhythms of behavior.Significance StatementDespite our growing understanding of how the fly clock network maintains free-running rhythms of behavior and physiology, little is known about how information is communicated from the clock network to the rest of the brain to regulate behavior. We identify glutamate and acetylcholine as key neurotransmitters signaling from clock neurons to the pars interecerebralis (PI), a clock output region regulating circadian rhythms of sleep and metabolism. We report a novel link between Drosophila evening clock neurons and the PI, and find that the effect of clock neurons on output neuron physiology varies, suggesting that the same clock cells use multiple mechanisms simultaneously to drive cycling in output neurons.

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