Scheduled exposure to daylight: a potential strategy to reduce "jet lag" following transmeridian flight.
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Biomedical subjects
Publications and source records attributed to S Daan.
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Castration of mice in freerunning conditions (total darkness, DD) causes a reduction of running wheel activity in the beginning of the active period (alpha) and stimulates activity at the end of alpha. Simultaneously, the period (tau) of the freerunning rhythm is increased. Both effects are abolished by implantation of a Silastic capsule from which a physiological dose of testosterone is released at a constant rate. The results are tentatively explained by differential endocrine influences on two oscillating components in the pacemaker of the circadian activity rhythm.
The circadian activity rhythms of golden hamsters and two species of deermouse, when released from a light-dark cycle of 12 hours light and 12 hours of darkness into constant darkness, had progressively shorter periods as the animals became older. A possible bearing of this fact on the aging process is briefly outlined.
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Spectral measurements of sunlight throughout the day show close correspondence between the timing of above ground activity of the European ground squirrel and the presence of ultraviolet light in the solar spectrum. However, in a standard entrainment experiment ground squirrels show no entrainment to ultraviolet light, while Syrian hamsters do entrain under the same protocol. Presented transmittance spectra for lenses, corneas, and vitreous bodies may explain the different results of the entrainment experiment. We found ultraviolet light transmittance in the colourless hamster lens (50% cut-off at 341 nm), but not in the yellow ground squirrel lens (50% cut-off around 493 nm). Ultraviolet sensitivity in the ground squirrels based upon possible fluorescence mechanisms was not evident. Possible functions of ultraviolet lens filters in diurnal mammals are discussed, and compared with nocturnal mammals and diurnal birds. Species of the latter two groups lack ultraviolet filtering properties of their lenses and their circadian system is known to respond to ultraviolet light, a feature that does not necessarily has to depend on ultraviolet photoreceptors. Although the circadian system of several species responds to ultraviolet light, we argue that the role of ultraviolet light as a natural Zeitgeber is probably limited.
The long-term consequences of social stress on daily rhythms of body temperature and activity in rats were studied by means of radiotelemetry with intraperitoneally implanted transmitters. Rats were subjected to a single social defeat by placing them into the territory of a male conspecific for 1 h. Social defeat caused a sharp subsequent reduction in the amplitude of the daily temperature rhythm, which lasted for at least 4 days. The reduced amplitude was mainly due to higher temperatures during the circadian rest phase, i.e., the light period. Movement activity was less affected, but the decrease in activity during the dark phase after defeat correlated significantly with the temperature increase during the light phase. The stress-induced changes in daily rhythms of body temperature and activity are discussed in terms of their relevance to the role of rhythm-disturbances in the pathogenesis of affective disorders.
Effect of photoperiod and food duration on body weight gain, energy intake, energy expenditure, and sexual development were investigated in two strains of Japanese quail (Coturnix c. japonica), bred for meat (broilers) or egg production (layers), from 7 to 71 days of age. In a first experiment chicks were subjected to 18L:6D, 15L:9D, 12L:12D, 9L:15D, or 6L:18D, with ad lib food during the light period. In a second experiment birds were exposed to a long photoperiod (18L:6D or 15L:9D) with ad lib food during part of the light period (first 6 or 9 h, respectively). Longer photoperiods were associated with larger weight gains. In 18L:6D broilers total body weight gain was 262 g compared to 213 g in 6L:18D broilers. In layers, corresponding values were 182 and 131 g. This effect of photoperiod on weight gain was primarily due to the effect of photoperiod on food availability. The photoperiod below which detrimental effects on weight gain occurred was 9L:15D for both strains. Chicks subjected to 9L:15D or 6L:18D exploited crop filling to enhance energy intake. They also decreased nocturnal metabolic rates to a greater extent compared to levels during the light phase than chicks subjected to light periods of 12 h or more. Sexual maturation was stimulated by photoperiod. At the age of 71 days, eight out of nine females subjected to 18L:6D were producing eggs, but none of the 6L:18D females. It is concluded that changes in feeding behavior and energy expenditure shown under short photoperiods are part of a strategy that allow chicks to gain weight continuously.
Homozygous tau mutant Syrian hamsters (tau-/-) have a free-running circadian period (tau) around 20 h and a proportionally higher metabolic rate compared with wild-type hamsters (tau+/+) with a period of circa 24 h. In this study, we applied deuterium oxide (D(2)O) to hamsters to test whether deuteration affects the circadian period of locomotor activity and metabolic rate in both genotypes. Running wheel activity and the metabolic rate were measured in constant illumination before, during, and after administration of 25% deuterium in drinking water. Wild-type hamsters lengthened their circadian period by 1.19 h (SD=0.29 h) due to D(2)O application and tau-/- hamsters by 1.20 h (SD=0.39 h). Deuteration changed neither the amount of activity nor the duration of activity phase (alpha) in either genotype. The mass specific average metabolic rate (AMR, the oxygen consumption over 24 h) and the mass specific resting metabolic rate (RMR) did not differ during deuteration compared with non-deuteration conditions for either genotype. Both with and without D(2)O, tau-/- hamsters had higher metabolic rates than tau+/+ hamsters. There was no correlation between changes in the circadian period of locomotor activity and metabolic rates caused by D(2)O.
Food consumption was measured in six female and seven male hand-raised marsh harrier (Circus aeruginosus) nestlings. Females consumed on average 4,321 g and males consumed 3,571 g of food during the nestling stage from 0 to 36 d. Total consumption until 56 d was 6,960 g and 5,822 g for females and males, respectively. On the basis of Fisher's sex ratio theory, this food intake ratio of 0.46 (intake male/[intake male + female]) would explain the observed male-biased fledging sex ratio of 55% males in marsh harrier broods. Growth, gross energy intake, and metabolizable energy intake were measured, along with metabolism of the nestlings, enabling us to determine energy allocation. The assimilation quotient (Q = 0.72) did not differ systematically between the sexes. Differences in metabolic rates between males and females at 15 and 30 d of age were fully attributable to the difference in body mass. Sexual size dimorphism in marsh harriers (female body mass around 60 d of age is 1.28 times greater than male mass) did not fully explain the difference in food intake between male and female nestlings: an analysis of energy requirements for growth and body mass in 16 avian species shows that energy intake was less than proportional to the average body mass at release. The data presented in this study are in agreement with Fisher's theory of inverse proportionality between the sex-specific ratios of energy requirements for growth and of offspring numbers in the marsh harrier population.
Basal metabolic rate in the field vole (Microtus agrestis) was studied in relation to body composition and daily energy expenditure in the field. Daily energy expenditure was measured by means of doubly labelled water (D2 18O). In the same individuals, basal metabolic rate was subsequently derived from O2 consumption in an open-circuit system in the laboratory. Body composition was obtained by dissecting the animals and determining fresh, dry, and lean dry mass of different organs. Daily energy expenditure for free-living field voles ranged from 1.8 to 4.5 times basal metabolic rate, with an average of 2.9 times basal metabolic rate. Variation in both daily energy expenditure and basal metabolic rate was best explained by body mass. Gender or reproductive activity did not have significant additive effects. Daily energy expenditure and basal metabolic rate showed significant positive relationships to body mass with similar mass exponents of 0.493 and 0.526, respectively. Overall, there was a significant correlation between daily energy expenditure and basal metabolic rate, but the mass-independent residuals (deviations from the allometrically predicted values) did not correlate. Carcass analysis revealed that a number of organs were slightly better predictors for daily energy expenditure and basal metabolic rate than was fresh body mass. Mass-independent residuals of lean dry heart mass and basal metabolic rate were positively correlated, which is in agreement with the idea that basal metabolic rate reflects the size of metabolically active organs. The study does not provide support for an intraindividual association of basal metabolic rate with daily energy expenditure in the field.