Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:Q86TM3 (cage)
 29,987 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The impact of the combined effects of exposure time and hydrostatic pressure on pressure reduction is explored in this study. In Phase I of the study, excursion dives were made to 10, 20, and 30 ATA for 5, 10, 20, 40, or 80 min. In Phase II, the animals were saturated at 1.3, 10, or 20 ATA for 60 min; each saturation exposure was followed by a 10-atm excursion dive of either 1, 5, 10, 20, or 40 min. The chamber gas mixture during all pressure exposures was 0.51 ATA oxygen, 0.79 ATA nitrogen, and the remainder helium. The subjects were 655 rats; during each pressure exposure 5 rats were exercised in a rotating cage. After each exposure, the rats were abruptly decompressed to a lesser pressure for observation and tabulation of the decompression sickness incidence. Results suggest that neither the starting saturation pressure nor the differential excursion pressure alters the time required for an animal to reach equilibrium with the surrounding environment. Pressure-reduction values, however, vary with both the exposure pressure and exposure time. These results will have a direct impact on the formulation of future decompression models.
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PMID:Pressure reduction limits for rats subjected to various time/pressure exposures. 73

The purpose of the research was to determine if pregnant rats subjected to a maximum tolerated duration of exposure to air at 6 atmospheres absolute pressure (ATA) (50.3 meters seawater) would have an increased frequency fetal death, resorption, low birth-weight, or malformations. Ninety pregnant rats were assigned to one of three exposure schedules during organogenesis: days 9-11, 12-14, or 15-17, and were randomized between one treatment and two control groups. The treatment group was subjected to 6 ATA for 70 minutes with compression and decompression at 1.8 ATA (18.3 meters seawater)/minute. Control groups were exposed to either 1 ATA of air (surface) within the hyperbaric chamber, or 1 ATA of air outside the chamber. For 30 minutes following decompression, chamber-treated animals were placed in a slow, motor-driven rotating cage, and assessed for gait disturbances from decompression sickness. On Day 20 of gestation, laparotomy was performed, and corpora lutea, implantations, and resorptions were counted. Fetuses were weighed, sexed, and examined for gross malformations. Subsequently, they were fixed, sectioned, and examined for visceral anomalies. Minor visceral anomalies and anatomical variations were present in 16.3% of all fetuses; however, no significant differences existed between groups. Similarly there were no significant differences when number of resorptions, number of dead fetuses, mean fetal weights, and malformations were compared by analysis of variance. Finally, there was no relation between symptoms of decompression sickness and any of the above measures. These results indicate that exposing rats to air at increased atmospheric pressure does not affect fetal health or survival.
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PMID:Lack of teratogenic effects of air at high ambient pressure in rats. 733 60

The crystal structure of cyclo (D-Val-D-Hyi-D-Val-L-Hyi-L-Val-D-Hyi-L-Val-L-Hyi -L-Val-D-Hyi-D-Val-L-Hyi).2H2O has been solved by x-ray direct methods. The crystals (grown from a mixture of octane/CH2Cl2) are an orthorhombic, centrosymmetric space group Pbca, cell parameters a = 11.458 (2), b = 25.613 (3), c = 23.691 (3) A, Z = 4; therefore the molecule lies on a center of inversion in the cell. The atomic coordinates for the C, N, and O atoms were refined in the anisotropic thermal motion approximation (allowing for H-atom contribution to Fcal) to a standard R-factor value of 0.081. In contrast to meso-valinomycin, the analogue under study does not adopt an octahedral cage bracelet conformation. It has an unusual centrosymmetric elongated form with two type II terminal beta-bends formed by N-H ... C=O 4-->1 type intramolecular H bonds. Two symmetry-related water molecules reside in the elongated molecular cavity of the centrosymmetric depsipeptide ring.
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PMID:Crystal and molecular structure of the centrosymmetric meso-valinomycin analogue--cyclo (D-Val-D-Hyi-D-Val-L-Hyi-L-Val-D-Hyi-L-Val-L-Hyi-L-Val-D-Hyi-D-Val-L-Hy i) (C60H102N6O18). 757 53

OBJECTIVE: To determine the critical load of the osteoligamentous cervical spine in frontal plane. DESIGN: Whole human cervical spine specimens were loaded in axial compression with increasing force until the point of buckling. BACKGROUND: The osteoligamentous cervical spine and the surrounding muscles support the weight of the head and the external loads applied to it. Critical load is the maximum compressive force that the spinal column can sustain before buckling. Critical loads have been obtained for the osteoligamentous thoracolumbar spine (without the rib cage) and the lumbar spine. Critical load of the cervical spine has not yet been determined. METHODS: When a compressive force is applied to the cervical spine, it bends in the sagittal plane producing greater lordosis. The determination of critical load in Euler's sense requires blocking of this sagittal plane bending. A special apparatus was developed that constrained such bending in the sagittal plane, but allowed complete freedom of the spine motion in the frontal plane. Experiments were conducted to determine the axial force-lateral bending curves of whole cervical spine specimens. Critical load values were obtained from these curves. As an alternative to this method, bending stiffness in the frontal plane was experimentally determined and the critical load was computed using Euler's theory of columns. RESULTS: Based upon the study of seven spine specimens (CO-T1), the critical load for the human cervical spine was found to be 10.5 (3.8) N obtained by direct experimentation. The average critical load calculated with the Euler theory using bending stiffness data, was 11.9 (2.0), but there were large individual differences when compared with the experimental results. CONCLUSIONS: The critical load of the osteoligamentous human cervical spine is about one-fifth to one-quarter the weight of the average head.
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PMID:Critical load of the human cervical spine: an in vitro experimental study. 1141 66

We have previously hypothesised that the number of bubbles evolving during decompression from a dive, and therefore the incidence of decompression sickness (DCS), might be reduced by pretreatment with hyperbaric oxygen (HBO). The inert gas in the gas micronuclei would be replaced by oxygen, which would subsequently be consumed by the mitochondria. This has been demonstrated in the transparent prawn. To investigate whether our hypothesis holds for mammals, we pretreated rats with HBO at 304, 405, or 507 kPa for 20 min, after which they were exposed to air at 1,013 kPa for 33 min and decompressed at 202 kPa/min. Twenty control rats were exposed to air at 1,013 kPa for 32 min, without HBO pretreatment. On reaching the surface, the rat was immediately placed in a rotating cage for 30 min. The animal's behaviour enabled us to make an early diagnosis of DCS according to accepted symptoms. Rats were examined again after 2 and 24 h. After 2 h, 65% of the control rats had suffered DCS (45% were dead), whereas 35% had no DCS. HBO pretreatment at 304, 405 and 507 kPa significantly reduced the incidence of DCS at 2 h to 40, 40 and 35%, respectively. Compared with the 45% mortality rate in the control group after 24 h, in all of the pretreated groups this was 15%. HBO pretreatment is equally effective at 304, 405 or 507 kPa, bringing about a significant reduction in the incidence of DCS in rats decompressed from 1,013 kPa.
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PMID:Hyperbaric oxygen pretreatment reduces the incidence of decompression sickness in rats. 1767 26

Divers are at risk of decompression sickness (DCS) when the ambient pressure decrease exceeds a critical threshold. Hyperbaric oxygen (HBO2) preconditioning has been used to prevent various injuries, but the protective effect on DCS has not been well explored. To investigate the prophylactic effect of HBO2 on DCS, rats were pretreated with HBO2 (250 kPa-60 minutes) (all the pressures described here are absolute pressure) for 18 hours before a simulated air dive (700 kPa-100 minutes) with fast decompression to the surface at the rate of 200 kPa/min (n=33). During the following 30 minutes, the rats walked in a 3 m/minute rotating cage and were monitored for signs of DCS. The control rats were pretreated with normobaric air (n=30), normoxic hyperbaric nitrox (250 kPa, 8.4% O2) (n=13), or N(G)-nitro-L-arginine methyl ester (L-NAME) 30 minutes before HBO2 exposure (n=13). Nitric oxide (NO) levels were recorded immediately and 18 hours after HBO2 exposure in the brain and spinal cord. The incidence of DCS in rats pretreated with HBO2 was 30.3%, which was significantly lower than those treated with normobaric air (63.3%) (p<0.05) or hyperbaric nitrox (61.5%) (p<0.05). The onset time of DCS of the rats pretreated with HBO2 was significantly delayed compared with those treated with air (p<0.05). L-NAME nullified the HBO2 preconditioning effect. HBO2 increased NO level in the rat brain and spinal cord right after exposure; this effect was inhibited by L-NAME. Taken together, HBO2 preconditioning reduced the incidence of DCS in rats, and NO was involved in the prophylactic effect.
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PMID:Hyperbaric oxygen preconditioning reduces the incidence of decompression sickness in rats via nitric oxide. 2056 47

The scoliometer is an inclinometer commonly used in scoliosis screening. The device is used during an Adam's forward bend test, in which a patient bends forward at the hips to measure deformity of the rib cage and spinal column. If a sufficient angle of rotation is measured, then the appropriate referrals and x-rays can be made and taken. This ubiquitous screening tool allows for a quick and simple scoliosis screening and is a mainstay of scoliosis management. With the advent and rapid improvement of smart phone technology, many scoliometer applications have become readily accessible. Our study was designed to test the accuracy, precision, and calibration of several scoliometer applications available on both the Apple iPhone and Samsung Galaxy platforms. Application cost was also analyzed to assess the plausibility of using a smartphone scoliometer application in place of a traditional scoliometer in a traditional scoliosis screening. Our data show that available smart phone applications can be used effectively and that, in a controlled environment, some applications performed better than a traditional scoliometer. Application price was not correlated with effectiveness; the cost-free application performed better than the for-purchase application.
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PMID:A Systematic Review of All Smart Phone Applications Specifically Aimed for Use as a Scoliosis Screening Tool. 2977 89