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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Acetylcholinesterase and simple esterases distribution in squirrel monkey brain, examining activity in neuropil and postrema area neurons
Balloon-borne monkeys possible brain damage due to cosmic rays, discussing thindown tracks and acute vasculitis
Hypotensive effects of chlordiazepoxide, amobarbital and chlorpromazine on behaviorally induced elevated arterial blood pressure in squirrel monkey
Technique for exercise to counteract effect of zero gravity on skeletal muscles of rhesus monkeys during extended orbital spaceflight
Behaviorally induced hypertension in squirrel monkey following conditioned key-pressing response schedules
Oxidative and hydrolytic enzymes localization in rhesus monkey brain, investigating glutaraldehyde fixation effect with histochemistry
Biosatellite 3 onboard camera time lapse photography of monkey sleep/wake activity patterns during weightlessness
Orbiting Biosatellite 3 monkey environmental and physiological parameters circadian rhythms, investigating desynchronosis or arrhythmia
Biosatellite 3 monkey sleep and wake states based on visual and computer analysis of telemetered EEG data from earth orbital flight
In-flight monkey cardiovascular observations, discussing central venous pressure, urine volume, electrolyte imbalances and heart rate
Monkeys trained to observe and report two-member serial position sequences with delayed matching- to-sample procedure
Macaca nemestrina monkey bone density change during Biosatellite 3 mission
Observing behavior in squirrel monkeys under multiple schedule of reinforcement availability
Investigation of circadian rhythms in a number of variables related to sleep, EEG, temperature, and motor activity in rhesus monkeys on an LD 12:12 schedule. Circadian rhythms were found to appear in each of 15 variables investigated. Statistical procedures assessed the variables for evidence of common regulation in these aspects of their circadian rhythms: acrophase (timing), amplitude (extent of change), and level (24-hr mean value). Patterns appearing in the data suggested that the circadian rhythms of certain variables are regulated in common. The circadian modulation of activity in the beta and sigma frequency bands of the EEG was correlated with statistical significance in acrophase, level, and amplitude. The delta frequency band appeared to be under circadian rhythm regulation distinct from that of the other bands. The circadian rhythm of REM stage sleep was like that of beta activity in level and amplitude. The data indicate that REM stage may share some common regulation of circadian timing with both stage 3-4 sleep and with temperature. Generally, however, the circadian rhythm of temperature appeared to bear little relation to the circadian rhythms of motor activity, EEG, or sleep.
Study of the changes occurring in simian brain exposed to protons of varied energy, given in wide dose and dose-rate ranges. Results show that inflammatory reaction and glycogen accumulation in astrocytes occurred practically in all animals. Cerebral cortical necrosis, granule cell pyknosis, and inflammatory reaction occurred at doses far lower than effective for high-energy gamma radiation given other series of monkeys at comparable dose rates. Metallic impregnation, carried out in virtually all the animals tested, revealed a wide variation in glial response even at equal doses and dose rates in the same proton energy series. Proton energy effect, dose effect, dose-time effect, and dose-rate effect were evident in the various morphological categories investigated, but inconsistencies were encountered.
Two adult male pigtail monkeys were placed in an isolated, soundproofed chamber (entered for cleaning only) for a period of six months, during which time their deep body temperatures T sub DB, telemetered from transmitters implanted in the abdominal cavity), fluid intake, urinary output (UV), urinary sodium and potassium were continuously monitored. During the first 3 1/2 months, lights (L) were turned on at 0000 hours, off at 1200 hours. Photoperiod phase was then delayed (light span prolonged) 6 hours to a new schedule: L on at 0600 hours, off at 1800 hours. Six weeks later, photoperiod phase was advanced 6 hours to return to the original schedule. Prior to shift, T sub DB typically began a steep rise 0-5 hours prior to L on, a steep fall 3-4 hours prior to L off, relative plateaus in between. Urinary Na typically peaks 2 hours prior to L off, has a minimum 2-4 hours prior to L on; K tends both to peak and show a minimum 2-8 hours earlier than Na; in contrast, UV peaks at L on, has a minimum 2-6 hours after L off. Upon delaying photoperiod phase, T sub DB shift was completed in 8 days. UV shifted more rapidly but tended to overshoot the new phase. Within 5 days, UV and K completed their shifts, although Na did not fully resynchronize within the 6 week period monitored.
Progress report on a long-term experiment using rhesus monkeys and designed to study the effects of isolation up to one year, as well as the effects of bed rest simulated by immobilization in a plaster cast for six months. The investigation includes histopathological and histochemical studies of these effects on various internal organs and tissues, and some of the preliminary results of these studies are presented and discussed.
Quantitative investigation of the optokinetic nystagmus effect in rhesus monkeys. The results obtained are shown to parallel those found for the rabbit by Ter Braak (1936). Quantitative findings pertaining to the ratio between slow velocity of nystagmus and stimulus speed as a power function of pattern motion velocity and to other parameters are presented graphically and discussed.