ABSTRACT
UNLABELLED: The aim of this study was to determine the effects of prolonged exercise in hot conditions on saliva IgA (s-IgA) responses in trained cyclists. On two occasions, in random order and separated by 1 week, 12 male cyclists cycled for 2 h on a stationary ergometer at 62 (3)% V(.)O(2 max) [194 (4) W; mean (SEM)], on one occasion (HOT: 30.3 degrees C, 76% RH) and on another occasion ( CONTROL: 20.4 degrees C, 60% RH). Water was available ad-libitum. Venous blood samples and 2-min whole unstimulated saliva samples were collected at pre, post and 2 h post-exercise. The s-IgA concentration was determined using a sandwich-type ELISA. Exercising heart rate, rating of perceived exertion, rectal temperature, corrected body mass loss (P<0.01) and plasma cortisol (P<0.05) were greater during HOT. The decrease in plasma volume post-exercise was similar on both trials [HOT: -6.7 (1.1) and CONTROL: -6.6 (1.3)%; P<0.01]. Saliva flow rate decreased post-exercise by 43% returning to pre-exercise levels by 2 h post-exercise (P<0.05) with no difference between trials. Saliva IgA concentration increased post-exercise (P<0.05) with no difference between trials. Saliva IgA secretion rate decreased post-exercise by 34% returning to pre-exercise levels by 2 h post-exercise (P<0.05) with no difference between trials. These data show that a prolonged bout of exercise results in a reduction in s-IgA secretion rate. Additionally, these data demonstrate that performing prolonged exercise in the heat, with ad libitum water intake, does not influence s-IgA responses to prolonged exercise.
Subject(s)
Bicycling/physiology , Hot Temperature , Immunoglobulin A/analysis , Adaptation, Physiological , Adult , Humans , Male , Saliva/immunology , SalivationABSTRACT
We have derived risk figures for fra(X) syndrome carrier mothers based on their DNA status. Clinical and molecular information was analysed in 200 carrier mothers and their offspring. Individuals were classified as affected by a requirement for special education. Risk figures were calculated using the genotype of the intellectually normal offspring in order to reduce ascertainment bias. Analysis was made on women with differing mutation size to predict the proportion of affected offspring. Using this method the following risk figures were derived: 1. For carrier women with an increase (delta) of 0.06-0.14 Kb, the risk for having an affected son was 29% (1 in 3.5) and 25% for daughters (1 in 4). This predicts an overall 73% chance of a normal child. 2. For delta size 0.15-0.24 Kb, the risk of having an affected son was 46% (1 in 2.2) and 32% for daughters (1 in 3.1), predicting a 61% chance of a normal child. 3. For delta size > 0.24 Kb, normal transmitting male offspring were not seen, i.e., the risk for males was 50% (1 in 2) and for females 32% (1 in 3.1) which predicts a 59% chance of a normal child.
Subject(s)
Fragile X Syndrome/genetics , Genetic Counseling , Heterozygote , Adult , Child, Preschool , Chromosome Banding , DNA Mutational Analysis , DNA Primers , Female , Fragile X Syndrome/epidemiology , Gene Dosage , Humans , Male , Polymerase Chain Reaction , Pregnancy , Pregnancy Outcome/genetics , Repetitive Sequences, Nucleic Acid , Risk Assessment , Sex FactorsABSTRACT
Formaldehyde was found to off-gas from flint sandpaper that contained an urea-formaldehyde resin as the minor component in a double glue system. Approximately 2000 sheets of sandpaper in a 115 m3 (4050 ft3) ship's storeroom with no mechanical ventilation produced a formaldehyde concentration of at least 4.5 ppm that was uniform throughout the compartment. A contributing factor was elevated compartment temperature due to high ambient temperature and the heating of the ship's steel hull by direct exposure to the sun.