Search Results
Results 451 - 500 of 882
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Reebs S G - - 1997
In response to a light pulse, hamsters normally generate phase advances that are positively correlated with the length of their circadian period (tau). To determine whether this is a general property of the phase-shifting oscillator, the present study looked for a correlation between tau and phase-advance size not only for ...
Sharma V K - - 1997
The entrainment of the circadian rhythm of locomotor activity was studied in the field mouse Mus booduga in order to examine the relationship between the free-running period (tau) and minimum tolerable light pulse interval of the skeleton photoperiods. The animals were entrained under three different light/dark (LD) schedules, each out ...
Persinger M A - - 1997
The hypothesis was tested that compensatory susceptibility to electroencephalographic driving and entrainment by weak (1 microT) time-varying, externally applied complex magnetic fields would occur in normal subjects following successive stimulation by different patterns. 43% of the volunteers showed evidence of driving during the application of the complex magnetic fields and ...
Katona C - - 1997
Wheel-running behaviour of the Nile grass rat, Arvicanthis niloticus, was studied under a variety of lighting conditions to characterize circadian rhythms in this species. A series of lighting schedules was used to determine the nature of entrainment, the rates of reentrainment after 6-h phase shifts, and the stability of free-running ...
Samel A - - 1997
After time-zone flights, the environmental time is shifted abruptly. The sleep-wake cycle and the circadian system cannot follow this sudden phase shift. Therefore, some or several days are necessary to achieve complete adjustment to a new time zone. The effects resulting from the displacement between internal and external time are ...
Meerlo P - - 1997
Previous work has shown that social stress in rats (i.e., defeat by an aggressive male conspecific) causes a variety of behavioral and physiological changes including alterations in the daily rhythms of body temperature and activity. To study the role of the circadian pacemaker in these stress-induced changes, three experiments were ...
Mitchell P J - - 1997
This simulated night shift field study compared high-intensity ("bright") light exposures designed to either facilitate or conflict with adaptation to a 9-h phase shift of the sleep/dark schedule. There were 7 days of baseline with night sleep followed by 8 night shifts with day sleep in a 2 x 2 ...
Penev P D - - 1997
Recent findings have raised the possibility that some of the age-related changes in the circadian system and the response of the circadian pacemaker to environmental stimuli may involve central serotonergic mechanisms. The present study compared the effects ofpretreatment with the serotonin agonist 8-hydroxy-2(di-n-propylamino)tetralin (5 mg/kg ip) on the magnitude of ...
Khalsa S B - - 1997
In evaluation of whether extracellular ion concentrations or fluxes are involved in the mechanism of the circadian pacemaker in Bulla retinal neurons, previous studies have ruled out obligatory requirements for extracellular calcium and chloride. In this study, it is demonstrated that extracellular sodium and magnesium are also not requirements for ...
Vilaplana J - - 1997
For > 30 days Wistar rats were subjected to six dark pulses per day (T4 cycles; 3 h light, 1 h dark) to study the possibility of dissociating their motor activity rhythm into distinct circadian components. Rats of both sexes were used, one-half of which were pinealectomized to examine the ...
Vilaplana J - - 1997
Seven groups of 6 young male rats were exposed for 60 calendar days to symmetrical light/dark cycles with different periods (T = 22, 23, 24, 25, 26, 27, and 28 h), and subsequently to constant darkness for 30 days. During exposure to the light/dark cycles, all the animals in all ...
Puchalski W - - 1996
Neurons in the suprachiasmatic nucleus (SCN) of the hypothalamus exhibit a daily rhythm in spontaneous electrical activity. Essentially two methods have been employed to record this circadian rhythm: (1) an in vitro brain slice technique and (2) in vivo multiunit recordings. Reentrainment of a circadian output to a shifted light:dark ...
Sharma V K - - 1996
The circadian rhythm of locomotor activity of the field mouse Mus booduga was studied and single animal phase response curves (PRCs) (n = 8) were constructed for 15-min daylight pulses of 1000 lux intensity. The light pulses, presented at different phases of the circadian cycle, evoked advancing and delaying phase ...
Zhang Y - - 1996
Recent studies indicate that the protein products of genes involved in transcriptional regulation play an important role in light-induced phase-shifting of the circadian clock, and suggest that protein synthesis may be necessary for some critical steps in the process by which light can induce a phase shift. In order to ...
Kerkhof G A - - 1996
In dealing with inter-individual phase differences in overt circadian rhythms, it is often difficult to distinguish the impact of the endogenous circadian oscillator from that of an individual's habitual lifestyle. In an attempt to resolve this uncertainty about the role of masking influences, two groups of subjects, morning-type and evening-types, ...
Boulos Z - - 1996
Entrainment patterns of the circadian rhythms of body temperature and locomotor activity were compared in 6 squirrel monkeys (Saimiri sciureus) exposed to daily illumination cycles with abrupt transitions between light and darkness (LD-rectangular) or with gradual dawn and dusk transitions simulating natural twilights at the equator (LD-twilight). Daytime light intensity ...
Walcott E C - - 1996
Aged rats often display abnormal circadian activity rhythms; the rhythm amplitude is low and entrainment to light-dark cycles is irregular. The activity rhythm of young rats can be entrained by both light and nonphotic cues, specifically food availability. In young rats, entrainment to restricted feeding cycles does not depend on ...
Scarbrough K - - 1996
The activity profiles of homozygous tau mutant hamsters bred in our colony exhibit several differences when compared to wildtype golden hamsters. In addition, tau mutant hamsters respond to saturating white light pulses presented between circadian time (CT) 11 and CT 16 with extremely large phase shifts (type 0 resetting) after ...
Ruby N F - - 1996
Body temperature (Tb) and locomotor activity were recorded telemetrically from male Siberian hamsters (Phodopus sungorus sungorus) that were 3 or 12 mo of age and maintained in a light-dark (LD) cycle of 16 h light/day for 2-4 mo. After 3 wk of Tb recording, the LD cycle was phase delayed ...
Pause B M - - 1996
In the present study we examined whether olfactory information processing depends on the phase of the menstrual cycle. Five female subjects were investigated during three phases (follicular, ovulatory, luteal) of their menstrual cycle. In each session chemosensory (olfactory) event-related potentials (CSERP) were recorded and olfactory thresholds and the hedonic tone ...
Iigo M - - 1996
Locomotor activities in the goldfish Carassius auratus were recorded under light-dark (LD) and constant light regimens. Under LD 12:12, all goldfish adjusted to given LD cycles. Activity patterns were classified into three types: L-type activity during the photophase (83%), LD-type activity both during the photophase and the scotophase (10%), and ...
Boulos Z - - 1996
Entrainment of wheel-running activity rhythms was compared in hamsters exposed to daily light-dark (LD) cycles with abrupt transitions between 0 and 10 lux or with artificial twilights simulating summer solstice conditions at 41 degrees N latitude but truncated at 10 lux. The photoperiod in LD-rectangular was set at 16.24 h, ...
Kennedy G A - - 1996
The effect of daily restricted feeding (RF) on the circadian wheel-running activity rhythms of the stripe-faced dunnart (Sminthopsis macroura) was examined. Dunnarts were presented with a 2-h meal in the middle of the light period of a 14:10 light:dark (LD) cycle and during constant dim light (LL). No meal-anticipatory activity ...
Boulos Z - - 1996
The upper limits of entrainment of the circadian activity rhythm were compared in hamsters initially exposed to daily light-dark (LD) cycles with either abrupt (LD-rectangular) or simulated twilight (LD-twilight) transitions. Daytime illuminance (10 lx) and the total amount of light emitted per day were the same under the two LD ...
Duffy J F - - 1996
1. Both the timing of behavioural events (activity, sleep and social interactions) and the environmental light-dark cycle have been reported to contribute to entrainment of human circadian rhythms to the 24 h day. Yet, the relative contribution of those putative behavioural synchronizers to that of light exposure remains unclear. 2. ...
Marchant E G - - 1996
Daily schedules of spontaneous, drug-, or novelty-induced running can entrain circadian rhythms in rodents. Forced running, by contrast, has been reported to have weak or no effects, although a thorough comparative study in a single species is lacking. To fill this gap, drinking or activity rhythms were monitored in C57 ...
Natelson B H - - 1996
In previous experiments we have shown that hamsters with inherited heart disease--cardiomyopathic hamsters (CMHs)--live longer if they spend their lives in an environment devoid of time cues. The purpose of this experiment was to test the several hypotheses by which life in constant light could extend life in CMHs. To ...
Sánchez-Vázquez F J - - 1996
In contrast to the common diurnal and nocturnal ways of life, some fish species have been shown to have a dual phasing behaviour. Therefore, the daily pattern of behaviour is not always rigidly confined to the light or dark phase and a diurnal fish may become nocturnal and vice versa. ...
Mrosovsky N - - 1996
Some of the main themes in this review are as follows. 1. The notion that non-photic zeitgebers are weak needs re-examining. Phase-shifts to some non-photic manipulations can be as large as those to light pulses. 2. As well as being able to phase-shift and entrain free-running rhythms, non-photic events have ...
Rosenwasser A M - - 1996
Chronic treatment of rats with clonidine, an alpha-adrenoceptor agonist, alters the period and amplitude of free-running circadian activity rhythms, as well as the level of home cage locomotor activity. Agents that alter free-running period are presumed to act directly on the circadian pacemaker or on its input pathways. Because shortening ...
Qiu J - - 1996
Circadian fluctuations in per mRNA and protein are central to the operation of a negative feedback loop that is necessary for setting the free-running period and for entraining the circadian oscillator to light-dark cycles. In this study, per mRNA cycling and locomotor activity rhythms were measured under different light and ...
Ikeda M - - 1996
Vitamin B12 (VB12) is a putative modulator of the human circadian clock, improving entrainability to the 24 h light-dark cycle. The present study was intended to elucidate the mechanism of VB12 action in an animal model. In male rats free-running under constant dim illumination, a single light pulse of 50-1000 ...
Subramanian P - - 1996
Experiments were carried out on the continuous action of diazepam (benzodiazepine) offered through drinking water in 2% ethanol on psi and tau of the activity rhythms under LD (12:12) and DD conditions. Under entraining conditions diazepam failed to evoke striking changes in psi. On the other hand, under free-running conditions ...
Benloucif S - - 1996
This study examines the effect of light pulses and administration of the pineal hormone melatonin on the circadian activity rhythm of C3H/HeN mice. Mice were housed in constant dark in cages equipped with running wheels. Phase shifts in the circadian rhythm of wheel-running activity were measured following treatment with a ...
Gillespie C F - - 1996
The present study investigated the effects of gamma-amino butyric acid (GABA)A-active drugs on the ability of light or coadministration of vasoactive intestinal peptide (VIP), peptide histidine isoleucine (PHI), and gastrin-releasing peptide (GRP) to phase delay hamster activity rhythms. Microinjection of the GABAA agonist, muscimol, significantly (p < .01) reduced the ...
Faillace M P - - 1996
Daily variations in cGMP, guanylate cyclase and phosphodiesterase activity in golden hamster retina were studied. Cyclic GMP content exhibited significant variations throughout the 24-hr cycle with maximal values during the dark phase. In order to establish the relative participation of nucleotide synthesis and breakdown during a 24-hr cycle, guanylate cyclase ...
Roberts M H - - 1996
To determine whether the ocular circadian pacemakers of the marine snail Bulla gouldiana exert phase control over the circadian rhythm in locomotor activity, we measured the phase angles for entrainment of the ocular pacemakers and the activity rhythm on four different photoperiods: L:D 15:9, 12:12, 9:15, and 4:20. We found ...
Deacon S - - 1996
The effects of melatonin (MT) and placebo (P) on adaptation to a rapid 9-h advance phase shift, in the presence and absence of inappropriate bright light (BL) exposure were examined. Volunteers were initially subjected to a gradual 9-h delay phase shift over 5 days (D1-D5) using a combination of bright ...
Biello S M - - 1996
Neuropeptide Y (NPY)-containing fibers project from the intergeniculate leaflet to the suprachiasmatic nucleus. NPY has been shown to phase shift the circadian locomotor activity rhythm of wildtype hamsters, producing large phase advances in the subjective day and small delays in the subjective night. Previous studies have implicated this pathway in ...
Houpt T A - - 1996
The application of circadian principles has the potential to alleviate jet-lag in global travelers, but their application is hampered by the difficulty of determining light exposure along international flight routes. Computerized tools can solve this problem algorithmically. We have developed a program for Macintosh computers, called MidnightSun, which allows researchers ...
Cymborowski B - - 1996
Injection of S-antigen (arrestin) antibody into the brain of the blow fly, Calliphora vicina, appeared to reduce sensitivity to the photic effects of a light:dark cycle (LD; entrainment) or continuous "bright" light (LL; arrhythmicity). In LD, a proportion of the injected flies evaded entrainment or showed delayed entrainment. In bright ...
Geetha L - - 1996
The effect of pulses of different monochromatic light wavelengths was investigated on the circadian locomotor activity rhythm of the tropical rodent Mus booduga. Blue (480 nm), green (549 nm) and red (649 nm) light were used for pulses at circadian time (CT) 14 and 20, the maximum delay and advance ...
Boivin D B - - 1996
Since the first report in unicells, studies across diverse species have demonstrated that light is a powerful synchronizer which resets, in an intensity-dependent manner, endogenous circadian pacemakers. Although it is recognized that bright light (approximately 7,000 to 13,000 lux) is an effective circadian synchronizer in humans, it is widely believed ...
Knauth P - - 1996
The results of some intervention studies on the effects of the change from weekly rotating to quicker rotating shift systems are presented. Consequently, the following recommendations for the design of shift systems according to physiological, psychological and social criteria are discussed: (1) Nightwork should be reduced as much as possible. ...
Gattermann R - - 1997
The present paper describes the effects of animal house routine stressors on adult golden hamsters during activity time (2 hrs after lights off) and rest time (2 hrs after lights on). In addition, for determination of norm values, the circadian rhythms of the stress indicators heart rate, core body temperature ...
Klerman E B - - 1996
The sensitivity of the human circadian system to light has been the subject of considerable debate. Using computer simulations of a recent quantitative model for the effects of light on the human circadian system, we investigated these effects of light during different experimental protocols. The results of the simulations indicate ...
Kathiresan A - - 1996
Stem and leaf tissues of Stellaria longipes Goldie (prairie ecotype) exhibit circadian rhythmicity in the activity and mRNA abundance for 1-aminocyclopropane-1-carboxylic acid oxidase (EC 1.4.3). The steady-state mRNA levels and enzymatic activity levels fluctuated with a period of approximately 24 h and reached their maxima by the middle of the ...
Pereyra P - - 1996
A shadow moving overhead elicits an escape response in the crab Chasmagnathus that habituates promptly and for a long period. Experiments were done to test the effects of time of day (light-phase vs. dark-phase) on the acquisition and retention of the habituated response. The short-term habituation produced by the repetitive ...
Eaton S J - - 1996
Histamine may play a role in synchronizing endogenous circadian rhythms with exogenous photic cues. Direct application of histamine to the suprachiasmatic nucleus, the site of the mammalian circadian pacemaker, phase shifts the circadian rhythm in neural activity [7]. Intraventricular injections of histamine also phase shift circadian rhythms [14]. The magnitude ...
Pappert E J - - 1996
We defined the temporal stability characteristics of levodopa/carbidopa (LD/CD) solution, and determined the effects of temperature, ascorbate, and light on LD stability over 7 days. At room temperature and without ascorbate, LD levels significantly declined by 48 h. Ascorbate prolonged stability to 72 h. Refrigeration and freezing prevented a significant ...
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