System Analysis of the Circadian Rhythm of Euglena gracilis, II: Masking Effects and Mutual Interactions of Light and Temperature Responses

1984 ◽  
Vol 39 (7-8) ◽  
pp. 801-811 ◽  
Author(s):  
T. Kreuels ◽  
R. Joerres ◽  
W. Martin ◽  
K. Brinkmann

Abstract Motility of Euglena gracilis shows free running circadian rhythms. The circadian system is sensitive to light and temperature signals, but it is always masked by direct responses of motility to light (photokinesis) and temperature (thermokinesis). By means of a compartimental model which defines the interrelations between the pathways of thermokinesis, photokinesis and the circadian system a unifying view of effects of temperature and light input signals is outlined. According to the model, and using double sine input signals the dynamics of thermokinesis is described by a differential amplifier with constant gain. Although thermokinesis heavily masks circadian responses to temperature signals, the limited range of circadian entrainment is indirectly demonstrated by a limited reappearance of free running circadian oscillations after stopping the temperature program. Free running circadian oscillations do reappear only after pretreatment with temperature periods near the circadian eigenperiod.A white mutant lacking photosynthesis is used to investigate the role of photosynthesis in the signal processing. Although light synchronizes the circadian rhythms of the white mutant if applied as single input, it does not affect the motility if applied together with temperature inputs near the circadian eigenperiod. These results indicate frequency dependent mutual interactions between the model compartments.

Plants ◽  
2021 ◽  
Vol 10 (7) ◽  
pp. 1475
Author(s):  
Shota Kato ◽  
Hong Gil Nam

In unicellular photosynthetic organisms, circadian rhythm is tightly linked to gating of cell cycle progression, and is entrained by light signal. As several organisms obtain a fitness advantage when the external light/dark cycle matches their endogenous period, and aging alters circadian rhythms, senescence phenotypes of the microalga Euglena gracilis of different culture ages were characterized with respect to the cell division cycle. We report here the effects of prolonged-stationary-phase conditions on the cell division cycles of E. gracilis under non-24-h light/dark cycles (T-cycles). Under T-cycles, cells established from 1-month-old and 2-month-old cultures produced lower cell concentrations after cultivation in the fresh medium than cells from 1-week-old culture. This decrease was not due to higher concentrations of dead cells in the populations, suggesting that cells of different culture ages differ in their capacity for cell division. Cells from 1-week-old cultures had a shorter circadian period of their cell division cycle under shortened T-cycles than aged cells. When algae were transferred to free-running conditions after entrainment to shortened T-cycles, the young cells showed the peak growth rate at a time corresponding to the first subjective night, but the aged cells did not. This suggests that circadian rhythms are more plastic in younger E. gracilis cells.


1982 ◽  
Vol 37 (11-12) ◽  
pp. 1240-1252
Author(s):  
Wolfram Lork ◽  
Til Kreuels ◽  
Wolfgang Martin ◽  
Klaus Brinkmann

Abstract The approach of control theory is used to describe the structure of the circadian system of Euglena gracilis. As a first step we discriminate linear and non linear properties of the dynamics. The cellular motility as measured via long time records of sedimentation parameters in cultures is defined as the system output; sinusoidal temperature signals are used as input. By means of non stationary signal processing procedures we estimate gain and phase of the output signal. The problem of defining an appropiate gain of a cell suspension with an undefinite number of cells is solved by using the superimposition of two different input signals and by keeping one of them fixed as a reference signal. Linear properties are shown with a linear frequency transfer and with the validity of the superposition principle at least within distinct regions of amplitude and frequency. Non linear properties are the signal distortion, the restriction of linear amplification to a distinct range of input temperature and the ambiguity of phase coupling near the circadian eigenfrequency. The apparent lack of a limit of entrainment -an unexpected linear property - is explained by the masking effect of thermokinesis. A model is proposed describing the simultaneous control of motility by thermokinesis and the circadian system. On the base of that model further experiments are outlined.


2000 ◽  
Vol 164 (1) ◽  
pp. R1-R6 ◽  
Author(s):  
SW Lockley ◽  
DJ Skene ◽  
K James ◽  
K Thapan ◽  
J Wright ◽  
...  

Although melatonin treatment has been shown to phase shift human circadian rhythms, it still remains ambiguous as to whether exogenous melatonin can entrain a free-running circadian system. We have studied seven blind male subjects with no light perception who exhibited free-running urinary 6-sulphatoxymelatonin (aMT6s) and cortisol rhythms. In a single-blind design, five subjects received placebo or 5 mg melatonin p.o. daily at 2100 h for a full circadian cycle (35-71 days). The remaining two subjects also received melatonin (35-62 days) but not placebo. Urinary aMT6s and cortisol (n=7) and core body temperature (n=1) were used as phase markers to assess the effects of melatonin on the During melatonin treatment, four of the seven free-running subjects exhibited a shortening of their cortisol circadian period (tau). Three of these had taus which were statistically indistinguishable from entrainment. In contrast, the remaining three subjects continued to free-run during the melatonin treatment at a similar tau as prior to and following treatment. The efficacy of melatonin to entrain the free-running cortisol rhythms appeared to be dependent on the circadian phase at which the melatonin treatment commenced. These results show for the first time that daily melatonin administration can entrain free-running circadian rhythms in some blind subjects assessed using reliable physiological markers of the circadian system.


1989 ◽  
Vol 257 (5) ◽  
pp. R1241-R1250 ◽  
Author(s):  
E. M. Thomas ◽  
S. M. Armstrong

Sixteen rats were ovariectomized and given either a 1-cm implant of crystalline estradiol-17 beta (eight rats) or an empty implant (eight rats). A further six rats were sham ovariectomized and given empty implants, and eight rats were left unoperated. The rats were exposed to 70 days of constant dim light (LL) with a maximum illumination level of 20 lx, and circadian running and drinking rhythms were monitored. In LL, both the running and drinking activity rhythms of the ovariectomized, blank-implanted rats became markedly disrupted, whereas unoperated and sham-operated rats maintained unified rhythms. Estradiol-implanted rats developed fewer rhythm desynchronies, and the majority displayed a single band of free-running activity. Rather than being arrhythmic, the activity of the LL-exposed ovariectomized rats appeared to contain several free-running components. Thus these data are consistent with the concept of a multioscillatory basis to the circadian system and support a role for the ovary and its hormone estradiol in the maintenance of coherence between component oscillators.


1987 ◽  
Vol 253 (1) ◽  
pp. R46-R54 ◽  
Author(s):  
B. Jilge ◽  
H. Hornicke ◽  
H. Stahle

Without a zeitgeber the circadian rhythms of five physiological functions free-ran with a period length greater than 24 h. Restricted feeding time (RF) masked the free-running rhythms. In addition to masking, entrainment with RF occurred. This process was most evident in locomotor activity and visits to the food box. RF thus had zeitgeber properties in these rabbits. However, in most rabbits the RF zeitgeber was not strong enough to entrain the circadian rhythm completely. A small component free-ran during RF. Following return to continuous food access the whole circadian rhythm resumed to free-run again. In some animals its phase was determined by the RF zeitgeber and in others by the small free-running fraction present during RF. The results suggest that in addition to the light-dark-entrainable circadian oscillator system a feeding-entrainable oscillator exists that takes over phase control of the majority of the rhythm during RF.


1997 ◽  
Vol 273 (4) ◽  
pp. R1540-R1549 ◽  
Author(s):  
Norman F. Ruby ◽  
Tom Kang ◽  
H. Craig Heller

Body temperature (Tb) was recorded via a biotelemetry system from 28 adult male Siberian hamsters maintained in a light-dark (LD) cycle of 16 h light/day for several months. After Tb was recorded for 3 wk, the LD cycle was phase delayed by extending the light phase by 5 h for 1 day; animals remained on a 16:8 LD cycle for the remainder of the experiment. Hamsters were injected daily with melatonin or vehicle solution for several weeks, beginning either 2 mo after ( experiment 1) or on the day of ( experiment 2) the phase shift; injections occurred within 30 min of dark onset. In experiment 1, 75% of animals free ran with circadian periods >24 h, beginning on the day of the phase shift, and never reentrained to the LD cycle; no hamsters unambiguously entrained to daily injections. In contrast, 78% of animals in experiment 2 entrained to melatonin injections, and 71% of those animals subsequently reentrained to the photocycle when the injection regimen ended. No vehicle-treated animals entrained to the injection schedule. Melatonin had no effect on daily mean Tb and Tb rhythm amplitude in either experiment; however, melatonin doubled the duration of a hyperthermic response that occurred after each injection. Thus melatonin can prevent loss of entrainment induced by a phase shift of the LD cycle but cannot restore entrainment to free-running animals. Failure to reentrain in the presence of two appropriately coordinated entraining agents also suggests that a phase shift of the photocycle can diminish the sensitivity of the circadian system to both photic and nonphotic input.


1979 ◽  
Vol 34 (5-6) ◽  
pp. 470-473 ◽  
Author(s):  
A. Johnsson ◽  
W. Engelmann ◽  
W. Klemke ◽  
Aud Tveito Ekse

Abstract The body temperature, activity-rest time, electrolytes of urine samples and mood was measured in two persons during a 19 day period under continuous light conditions in the arctic (vicinity of Ny Ålesund, Svalbard-Spitsbergen). For temperature recording a new thermoprobe and a portable printer was used. Possible week Zeitgeber of the 24 hour day did not synchronize the circadian system, since circadian rhythms of about 26 hours were found. These results open up the pos­ sibility to study effects of drugs on the circadian system of humans under Svalbard conditions.


2021 ◽  
pp. 074873042199994
Author(s):  
Rosa Eskandari ◽  
Lalanthi Ratnayake ◽  
Patricia L. Lakin-Thomas

Molecular models for the endogenous oscillators that drive circadian rhythms in eukaryotes center on rhythmic transcription/translation of a small number of “clock genes.” Although substantial evidence supports the concept that negative and positive transcription/translation feedback loops (TTFLs) are responsible for regulating the expression of these clock genes, certain rhythms in the filamentous fungus Neurospora crassa continue even when clock genes ( frq, wc-1, and wc-2) are not rhythmically expressed. Identification of the rhythmic processes operating outside of the TTFL has been a major unresolved area in circadian biology. Our lab previously identified a mutation ( vta) that abolishes FRQ-less rhythmicity of the conidiation rhythm and also affects rhythmicity when FRQ is functional. Further studies identified the vta gene product as a component of the TOR (Target of Rapamycin) nutrient-sensing pathway that is conserved in eukaryotes. We now report the discovery of TOR pathway components including GTR2 (homologous to the yeast protein Gtr2, and RAG C/D in mammals) as binding partners of VTA through co-immunoprecipitation (IP) and mass spectrometry analysis using a VTA-FLAG strain. Reciprocal IP with GTR2-FLAG found VTA as a binding partner. A Δ gtr2 strain was deficient in growth responses to amino acids. Free-running conidiation rhythms in a FRQ-less strain were abolished in Δ gtr2. Entrainment of a FRQ-less strain to cycles of heat pulses demonstrated that Δ gtr2 is defective in entrainment. In all of these assays, Δ gtr2 is similar to Δ vta. In addition, expression of GTR2 protein was found to be rhythmic across two circadian cycles, and functional VTA was required for GTR2 rhythmicity. FRQ protein exhibited the expected rhythm in the presence of GTR2 but the rhythmic level of FRQ dampened in the absence of GTR2. These results establish association of VTA with GTR2, and their role in maintaining functional circadian rhythms through the TOR pathway.


1981 ◽  
Vol 241 (1) ◽  
pp. R62-R66 ◽  
Author(s):  
H. E. Albers

The circadian wheel-running rhythms of gonadectomized adult male, female, and perinatally androgenized female rats, maintained in constant darkness, were examined before and after implantation of Silastic capsules containing cholesterol (C) or estradiol-17 beta (E). The free-running period of the activity rhythm (tau) before capsule implantation tended to be shorter in animals exposed to perinatal androgen. Administration of C did not reliably alter tau in any group. E significantly shortened tau in 100% of females injected with oil on day 3 of life. In females, injected with 3.5 micrograms testosterone propionate on day 3, and males, E shortened or lengthened tau, with the direction and magnitude of this change in tau inversely related to the length of the individual's pretreatment tau. These data indicate that the presence of perinatal androgen does not eliminate the sensitivity of the circadian system of the rat to estrogen, since estrogen alters tau in a manner that depends on its pretreatment length.


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