A supervised, home-based, flexible training program has significant effect on CRF in young and middle-aged cancer patients shortly after curative chemotherapy, but it has no favorable effect on patients' experience of fatigue, mental distress, or HRQOL.
Six male and six female runners were chosen on the basis of age (20-30 years) and their performance over the marathon distance (mean time = 199.4, SEM 2.3 min for men and 201.8, SEM 1.8 min for women). The purpose was to find possible sex differences in maximal aerobic power (VO2max), anaerobic threshold, running economy, degree and utilization of VO2max (when running a marathon) and amount of training. The results showed that performance-matched male and female marathon runners had approximately the same VO2max (about 60 ml.kg-1.min-1). For both sexes the anaerobic threshold was reached at an exercise intensity of about 83% of VO2max, or 88%-90% of maximal heart rate. The females' running economy was poorer, i.e. their oxygen uptake during running at a standard submaximal speed was higher (P less than 0.05). The heart rate, respiratory exchange ratio and blood lactate concentration also confirmed that a given running speed resulted in higher physiological strain for the females. The percentage utilization of VO2max at the average marathon running speed was somewhat higher for the females, but the difference was not significant. For both sexes the oxygen uptake at average speed was 93%-94% of the oxygen uptake corresponding to the anaerobic threshold. Answers to a questionnaire showed that the females' training programme over the last 2 months prior to running the actual marathon comprised almost twice as many kilometers of running per week compared to the males (60 and 33 km, respectively).(ABSTRACT TRUNCATED AT 250 WORDS)
The role of the hypothalamic and skin temperatures in controlling the thermal response of a resting animal was studied by measurements of 1) hypothalamic, rectal, ear skin, and trunk skin temperatures on the resting dog and rhesus monkey in hot, neutral, and cold environments; and 2) the thermal and metabolic responses of a dog in neutral and cold environments during and immediately after holding the hypothalamus at approximately 39.0 C by means of six thermodes surrounding the hypothalamus and perfused with water. The results indicate that 1) a resting animal shivers in a cold environment with the same or higher hypothalamic temperature as the same animal in a neutral environment; 2) a resting animal pants in a hot environment with the same or lower hypothalamic temperature as the same animal in a neutral environment; 3) the hypothalamus is nonetheless strongly responsive to an increase or decrease of 1 C; 4) the rate of heat loss increases at the onset of sleep while the hypothalamic temperature is falling; 5) the hypothalamic temperature is 1–2 C lower during sleep even though thermoregulatory responses are the same as when awake; 6) the rate of heat loss decreases upon awakening while the hypothalamic temperature is rising. The discussion of these results includes a suggestion that the set point for temperature regulation is 1) decreased by a rising or elevated skin and extrahypothalamic core temperature, 2) increased by a falling or lowered skin and extrahypothalamic core temperature, 3) decreased upon entering and during sleep and is increased upon awakening. hypothalamic temperature; temperature set point; hypothalamic stimulation; dog temperature regulation; monkey temperature regulation Submitted on October 15, 1962
Maximal aerobic power of 37 athletes (14 females and ten male cross-country skiers, eight male rowers and five male cyclists) was determined during uphill running on the treadmill and during maximal performance of their specific sport activity. For the skiers a significantly (P less than 0.005) higher VO2max was found during uphill skiing than during running, the differences being 2.9 and 3.1% for the females and males, respectively. The rowers and cyclists obtained a difference of 4.2 and 5.6%, respectively (P less than 0.01). The largest individual differences between the two test procedures were 12.2, 5.4, 14.3, and 7.9% for female and male cross-country skiers, rowers, and cyclists, respectively. It is concluded that in evaluation of maximal aerobic power of atheletes, it becomes important to select a work situation which allows optimal use of the specifically trained muscle fibres. This means that the test preferably should be identical with the subjects' specific sport activity, under the assumption that a reasonably large muscle mass is engaged during the performance.
Changes in the testosterone concentrations after single sessions of endurance and strength training were measured in seven well trained men, experienced in both forms of training. Both training sessions were rated as hard to very hard on the Borg scale. Blood samples for testosterone measurements were taken before, immediately after, and 2, 4 and 6 h after the training sessions as well as the next morning. The mean testosterone concentration increased 27% (P less than 0.02) and 37% (P less than 0.02) during the strength and endurance training session, respectively. Two hours after the training sessions the mean testosterone concentration had returned to the pre-training level and remained at that level for the length of the observation period. There were no significant differences in the changes in testosterone concentration after strength and endurance training but there were large differences in the testosterone response at the level of the individual. A high correlation (r = 0.98; P less than 0.001) for individuals was found between increases in testosterone concentration after strength and after endurance training. It was concluded that the changes in mean testosterone values followed the same timecourse after single sessions of strength and endurance training of the same duration and perceived exertion. The interindividual differences in testosterone response may be of importance for individual adaptation to training.
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