Auditory frequency threshold comparisons of humans and pre-adolescent chimpanzees
Auditory frequency threshold comparisons of humans and pre-adolescent chimpanzees
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Auditory frequency threshold comparisons of humans and pre-adolescent chimpanzees
Cortical and subcortical electroencephalographic studies in chimpanzee in differing sleep stages
Cortical electroencephalographic activity /EEG/ RELATION to behavioral changes in chimpanzee following rapid decompression to near vacuum
Chimpanzee mesenteric artery blood flow for various activities during 24 hr period monitored by radio telemetry
Physiological assays, conditioned learning tasks, and visuomotor tracking using chimpanzees in simulated orbit
Circadian rhythms and biochemical analyses of urinary excretion of chimpanzees in simulated space environments
Sleep cycle and subcortical-cortical EEG relations in unrestrained chimpanzee
Unrestrained chimpanzees cortical and subcortical electrical activity during sleep recorded by telemetry and compared with human beings and other mammals
Subcortical-cortical EEG recording of unrestrained chimpanzees sleep cycles, using computer analysis and biotelemetry techniques
First and last rapid eye movement /REM/ sleep differences in unrestrained chimpanzee
The electroencephalogram and electro-oculogram of two unrestrained juvenile chimpanzees was monitored for 7 consecutive nights using telemetry methods. Of the sleeping time, 23% was spent in the rapid eye movement of REM type of sleep, whereas 8, 4, 15, and 10% were spent in non-REM stages 1 through 4, respectively. Seven to nine periods of REM sleep occurred per night. The average time from the beginning of one REM period to the beginning of the next was approximately 85 min.
An unrestrained chimpanzee was studied in an isolation chamber and in his home cage environment. The study consisted of 49 urine collection days (14 days pre-, 5 days post- and 30 days of isolation), and then of 10 days in the home cage. Dietary intake, urine and fecal data were obtained. The effect of isolation on various excretory parameters was studied. Urine samples were analyzed for volume, osmolarity, creatinine, creatine, urea-N, 17-hydroxy corticosteroids, VMA, calcium and inorganic phosphorus. One way analyses of variance performed on the urinary excretion parameters showed all except creatinine excretion to vary significantly during periods of the study. The changes observed in calcium and phosphorus were highly significant. The data suggests that the calcium to phosphorus excretion ratio might serve as a physiological stress indicator of Selye's adaptation syndrome (period of resistance).
A young male chimpanzee was subjected to 30 days of isolation. Urine volumes and voiding times were recorded every hour beginning 14 days prior to isolation, ending 6 days after isolation, and approximately 2 months later for 10 days as a control. Observed during most periods of the experiment were (1) clear circadian micturition rhythms with the voiding peak occurring immediately after the subject awoke and (2) urine flow rhythms with the maximum volume voided in the morning hours. A 24-hour rhythm was seen when the subject was entrained to 12L:12D treatments and 24.8-hour rhythm when he was exposed to continuous light. A possible underlying 24-hour micturition rhythm was also seen during the continuous light period. Distorted rhythm curves indicating possible stress were obtained for the pre-isolation adaptation period and the initial period of isolation. As time passed, the curves were more like the controls, perhaps indicating a decrease in stress.
Biorhythmic patterns of EEG activity - the sleep-wake cycle and the sleep cycle - were investigated in an unrestrained chimpanzee subjected to 30 days of isolation in a 4-ft cubical cage placed in a high performance sound isolation chamber. The animal received 10 days of 12 hours of light and 12 hours of dark, then 10 days of continuous light, followed by 10 more days of 12 hours of light and 12 hours of dark. The circadian sleep-wake rhythm and the wake and sleep phases of this rhythm during entrained and free running conditions were analyzed in terms of duration. The awake and nonREM sleep and REM sleep stages were also analyzed. In addition, the mean duration of the sleep cycle of the sleep phase was computed.
Major achievements and accomplishments are reported for the Physiology of Chimpanzees in Orbit Program. Scientific studies relate to behavior and physiology, and engineering studies cover telemetry, behavioral training, systems tests, life support subsystems, and program plan.
Interface requirements are presented for the design and development of an earth orbiting experiment to be known as POCO, Physiology of Chimpanzees in Orbit. The POCO experiment may be designed to operate within an orbiting space station (provided artificial gravity measures are not employed), a Saturn 4-B workshop, an Apollo command module or service module, a Saturn-1B spacecraft LM adapter, or aboard one of the presently conceived appendages connected by an umbilical to a space station. This document sets forth the experiment definition and requirements and describes the hardware under development to accomplish these objectives.
Early physiologic experiments using dogs and humans in centrifuges are reviewed. Because of the close similarity between the shape and dimensions of the thoraces of chimpanzees and humans, the former were used to obtain roentgenograms and photokymographic recordings of multiple physiologic variables before and during exposure to +5.8 Gy to study the effects of changes in the gravitational-inertial force environment on the cardiovascular and pulmonary systems during long duration space flight. A computer-controlled sciscanning system was used to obtain a two dimensional map of the amount of radiation emanating from the dorsal and ventricle surfaces after insertion of radioactive microspheres in the right ventricle. By using four different batches of microspheres tagged with isotopes of different energies, the spatial distribution of pulmonary blood flow under four conditions was determined.
Despite the phylogenetic similarities between chimpanzees and man, there exists a paucity of reliable data on normal cardiovascular function and the physiological responses of the system to standard interventions. Totally implanted biotelemetry systems or hardwire analog techniques were used to examine the maximum number of cardiovascular variables which could be simultaneously monitored without significantly altering the system's performance. This was performed in order to acquire base-line data not previously obtained in this species, to determine cardiovascular response to specific forcing functions such as ventricular pacing, drug infusions, and lower body negative pressure. A cardiovascular function profile protocol was developed in order to adjust independently the three major factors which modify ventricular performance, namely, left ventricular performance, left ventricular preload, afterload, and contractility. Cardiac pacing at three levels above the ambient rate was used to adjust end diastolic volume (preload). Three concentrations of angiotensin were infused continuously to evaluate afterload in a stepwide fashion. A continuous infusion of dobutamine was administered to raise the manifest contractile state of the heart.