Comparing different measures of energy expenditure in human subjects resident in a metabolic facility.

OBJECTIVE: To compare energy expenditure (EE) measured by doubly labeled water (DLW) with other measures, both physical and based on subjective questionnaires. DESIGN: A comparison of methods in a stratified sample of adult volunteers. SETTING: The feeding behaviour suite (FBS) at the Rowett Research Institute, Aberdeen. SUBJECTS: A total of 59 subjects, stratified for age, sex and body mass index (BMI). INTERVENTIONS: EE was assessed by DLW (validated using measurements of energy balance), heart rate monitor (HRM), activity monitor (Caltrac), 24-h physical activity diary (PAD) and 7-day physical activity recall. Energy intake was assessed using covert (investigator-weighed) food intake (EI). Data were collected over a 12-day period of residence in the Rowett's FBS. RESULTS: No methods correlated highly with physical activity assessed by DLW. Physical methods correlated more closely than did subjective recording. All methods (except EI) significantly underestimated EE, estimated by DLW. There were no significant differences in association between methods and sex, age, BMI or fat-free mass. CONCLUSION: EE is difficult to measure precisely or accurately with current approaches but physical methods are slightly better than subjective accounts.

Plausible self-reported dietary intakes in a residential facility are not necessarily reliable.

BACKGROUND/OBJECTIVES: Comparing reported energy intakes with estimated energy requirements as multiples of basal metabolic rate (Ein:BMR) is an established method of identifying implausible food intake records. The present study aimed to examine the validity of self-reported food intakes believed to be plausible. SUBJECTS/METHODS: One hundred and eighty men and women were provided with all food and beverages for two consecutive days in a residential laboratory setting. Subjects self-reported their food and beverage intakes using the weighed food diary method (WDR). Investigators covertly measured subjects' actual consumption over the same period. Subjects also reported intakes over four consecutive days at home. BMR was measured by indirect calorimetry. RESULTS: Average reported energy intakes were significantly lower than actual intakes (11.2 and 11.8 MJ/d, respectively, P<0.001). Two-thirds (121) of the WDR were under-reported to varying degrees. Only five of these were considered as implausible using an Ein:BMR cut-off value of 1.03*BMR. Under-reporting of food and beverage intakes, as measured by the difference between reported and actual intake, was evident at all levels of Ein;BMR. Reported energy intakes were lower still (10.2 MJ/d) while subjects were at home. CONCLUSIONS: Under-recording of self-reported food intake records was extensive but very few under-reported food intake records were identified as implausible using energy intake to BMR ratios. Under-recording was evident at all levels of energy intake.

Changes in plasma gonadotrophin and prolactin concentrations following castration of the pony stallion.

Concentrations of gonadotrophins and prolactin were recorded in pony stallions castrated during the early breeding season, to examine the regulatory role of the gonad at a time when testosterone has been postulated to exert positive feedback on LH secretion. Further, gonadotrophin concentrations in geldings are reported to return to values within the normal range of the entire stallion. In an attempt to characterize this species-specific reversal, the gonadotrophin concentrations of 6 male ponies castrated on 25 March were monitored for 4 months, and 4 stallions were used to generate control data. Blood samples were collected daily, from 3 d before to 10 d after castration (Day 0), and weekly thereafter until Day 122. The pituitary response to castration was immediate. Castration resulted in a previously unreported, dramatic (13-fold) but transient (3 d) surge in circulating concentrations of LH. Concentrations of LH and FSH increased in a logarithmically scaled (LH, R2 = 0.77; FSH, R2 = 0.93) manner over the subsequent 5 wk, during which temporal changes in concentrations of both hormones were strongly correlated (R2 = 0.97). The ratio of plasma gonadotrophin concentrations was consistent throughout (LH:FSH, 1.43 +/- 0.04). Maximal concentrations of LH (20.58 +/- 1.97 ng/mL, Day 34.8 +/- 3.2) were attained approximately 2 wk before the peak in FSH (16.99 +/- 1.97 ng/mL, Day 49.7 +/- 3.0). Plasma gonadotrophin concentrations exceeded those of entire stallions throughout the study. The equine testes inhibited LH secretion during the early breeding season, and no chronic decrease in plasma gonadotrophin concentrations was recorded. However, the LH surge evident for 3 d immediately afer castration, may be related to the dynamic seasonal interaction between gonadal steroids and the regulation of pituitary gonadotrophin release.

Optimized gating scheme for rapid lifetime determinations of single-exponential luminescence lifetimes.

The rapid lifetime method (RLD) for determining excited-state lifetimes uses the ratio of the areas under two regions of the decay. To get good precision with the standard method, prior knowledge of the lifetime is essential to selecting the integration regions. As will be shown, the usual method of selecting integration regions is far from optimal. An optimal gating scheme that is more precise and much more forgiving in the selection of integration region than any of the prior methods will be shown. Monte Carlo simulations were performed to determine the optimal gating. Experimental data was used to confirm the capabilities of the optimized RLD. The speed of the optimal RLD is similar to the standard RLD but without the necessity of matching the integration interval to the lifetime for precise results.

Photostability of luminescent ruthenium(II) complexes in polymers and in solution.

The effects of oxygen on the photochemical properties of ruthenium(II) complexes in solution and in polymers are reported. In solution, the complex is actually protected from decomposition by the presence of oxygen as a result of deactivation of the complex by oxygen quenching before it can undergo ligand loss by monomolecular dissociation; however, in polymers, the presence of oxygen increases photochemical decomposition. Singlet molecular oxygen, a product of the oxygen quenching process, may attack the ground state complex or triplet oxygen may directly attack the excited state of the complex. Both mechanisms may be involved in the photodestruction of the complex. The role of oxygen in the photodecomposition was examined by monitoring the photochemical decomposition of various complexes of different singlet oxygen reactivity, as well as absorption and mass spectroscopy studies. It is suggested that in polymers, unlike in solutions, the newly formed reactive singlet oxygen is not able to diffuse away from the complex. The singlet oxygen, trapped in close proximity to the metal complex, has an enhanced opportunity to attack it. This cage effect is supported by studies using tris(1,10-phenanthroline)ruthenium(II) in poly(ethylene glycol) of increasing molecular weight to create an increasingly constraining cage around the complex. Increased poly(ethylene glycol) molecular weight leads to increased oxygen attack of the complex, supporting the cage effect.