Compact, compression-free, displaceable, and resealable vacuum feedthrough with built-in strain relief for sensitive components such as optical fibers.

For the direct fiber coupling of small optical measurement cells, we developed a new compact vacuum feedthrough for glass fibers and other similarly shaped objects that are compact and that offer the possibility of adjusting the fiber in longitudinal and in circular direction. The feedthrough assembly avoids compression or torsion on the fiber and thus protects, e.g., highly frangible fiber materials. In the following, we will present a brief simulation of the tightness requirements for low-pressure and low-concentration water vapor measurements and we will explain an integrated concept for a displaceable and self-adjustable, compression-free, compact, ultra-high vacuum, resealable feedthrough with good strain relief. The feedthrough has been successfully tested in a laboratory test facility and in several extractive airborne tunable diode laser absorption spectroscopy hygrometers. The leakage rate of the feedthrough presented here was tested via a helium leak searcher and was quantified further in an 8-week vacuum measurement campaign. The leakage rate is determined to be 0.41 ± 0.04 × 10(-9) hPa l/s, which--to our knowledge--is the first time a leakage rate for such a feedthrough has been quantified.

VCSEL-based, high-speed, in situ TDLAS for in-cylinder water vapor measurements in IC engines.

We report the first application of a vertical-cavity surfaceemitting laser (VCSEL) for calibration- and sampling-free, high-speed, in situ H2O concentration measurements in IC engines using direct TDLAS (tunable diode laser absorption spectroscopy). Measurements were performed in a single-cylinder research engine operated under motored conditions with a time resolution down to 100 µs (i.e., 1.2 crank angle degrees at 2000 rpm). Signal-to-noise ratios (1σ) up to 29 were achieved, corresponding to a H2O precision of 0.046 vol.% H2O or 39 ppm · m. The modulation frequency dependence of the performance was investigated at different engine operating points in order to quantify the advantages of VCSEL against DFB lasers.

[Occupational disease 2108. Degenerative changes of the cervical spine as a causality criterion in the assessment of discogenic diseases according to BeKV 2108]. / Berufserkrankung 2108. Degenerative Veränderungen der Halswirbelsäule als Kausalitätskriterium in der Begutachtung bandscheibenbedingter Erkrankungen gemäss BeKV 2108.

With the second amendment to the Ordinance on Occupational Diseases (BeKV) of 18 December 1992, discogenic diseases of the spine are included in the disease register of occupational diseases for the first time. If occupations that impose stress on the spine have been practised for many years, the possibility exists of recognizing degenerative diseases as an occupational disease. In assessment practice, the radiological data on the spine exposed to stress is compared with that of regions which are remote from the stress (cervical/thoracic spine). This pattern of the distribution of degenerative disease is then used as the basis for determining a causal relationship between the occupation causing the stress and disease of the axial skeleton. The pattern of degeneration of the cervical spine was investigated in two groups, one with ( n =153) and one without ( n =333) occupations that impose stress on the lumbar spine. A cumulative score of degenerative changes was elaborated and presented as a new classification. No differences were found between the groups with regard to either the frequency of occurrence, segmental distribution or severity of disease. In both groups, degenerative changes correlated with age. The prevailing assessment practice is discussed on the basis of these data.

In situ detection of potassium atoms in high-temperature coal-combustion systems using near-infrared-diode lasers.

Direct tunable diode laser absorption spectroscopy at 769.9 and 767.5 nm was used to measure potassium (K) atom concentrations in situ in the high temperature (up to 1650 K) flue gas of two different pulverized coal dust combustion systems (atmospheric or pressurized (12 bar)). Two laser types (Fabry-Pérot (FP) and vertical-cavity surface-emitting lasers (VCSEL)) were used for the spectrometer and characterized with respect to the magnitude and linearity of their static and dynamic wavelength tuning properties. The wide continuous current-induced tuning range of the VCSEL of 20 cm(-1) (compared to 1 cm(-1) for the FP) make this laser ideal for species monitoring in high pressure processes. Two VCSELs were time-multiplexed to realize the simultaneous detection of the potassium D1 and D2 lines. Several oxygen absorption lines in the A-band, which are in close spectral vicinity of the K lines, were detected simultaneously, showing the possibility of multi-species detection with one laser. Using the FP-DL for the atmospheric process and the VCSEL for the high pressure process, the pressure-dependent coefficients for spectral broadening as well as a shift of the K line in the flue gas were determined to be (0.18 +/- 0.01) and (-0.060 +/- 0.003) cm(-1) per atm (at 1540 K and 11.2 bar). The total width and shift of the D1 line (11.2 bar/1540 K) were 60 and -20 GHz, respectively. The K atom concentration was determined continuously for several days in both plants under various operation conditions. Typical concentrations in the atmospheric plant were around 2 microg m(-3) with a range of 50 ng m(-3)-30 microg m(-3). Averaging 100 scans for each concentration value, we achieved a time resolution of 1.7 s and a detection limit of 10 ng m(-3), which corresponds to a fractional absorption in the 10(-3)-10(-4) range. A strong anti-correlation with the oxygen concentration could be verified. At the 12 bar plant, the concentration was again typically around 2 microg m(-3) but K levels up to 60 microg m(-3) were observed. Here, a strong dependence of the K-signal on the type of fuel could be verified.

Surface electromyography-verified muscular damage associated with the open dorsal approach to the lumbar spine.

The dorsal approach is increasingly preferred in the surgical treatment of vertebral fractures. However, the access and the implant's position cause muscle loss, which can lead to instability and a reduced capacity for rehabilitation. Morphological factors (bones, intervertebral discs) are typically blamed for chronic pain syndromes in the literature, while less importance is attached to functional factors (muscles). The objective of this study was therefore to investigate the isolated influence of dorsal spinal instrumentation on the back muscles by means of electromyography (EMG). A total of 32 patients with conditions after dorsal spondylodesis following the fracture of a vertebral body and 32 subjects with healthy backs were enrolled in this study. The EMG signal was recorded in three different muscle groups during isometric extension exercise. The evaluation was performed by comparing the mean rectified amplitudes of the three muscle groups in the patients and controls. The patients had significantly lower amplitudes in the multifidus muscle (MF) and significantly higher amplitudes in the iliocostal muscle (IL). Patients with severe pain were found to have lower electric muscle potentials in all investigated muscle groups than patients with mild pain. The muscle damage which was established in the multifidus muscle is compensated by increased activity in the iliocostal muscle. On the basis of anatomical considerations, the damage pattern can be identified as having been caused by surgery. It is extremely unlikely that trauma is the cause.

Detection and binding properties of GABA(A) receptor assembly intermediates.

Density gradient centrifugation of native and recombinant gamma-aminobutyric acid, type A (GABA(A)) receptors was used to detect assembly intermediates. No such intermediates could be identified in extracts from adult rat brain or from human embryonic kidney (HEK) 293 cells transfected with alpha(1), beta(3), and gamma(2) subunits and cultured at 37 degrees C. However, subunit dimers, trimers, tetramers, and pentamers were found in extracts from the brain of 8-10-day-old rats and from alpha(1)beta(3)gamma(2) transfected HEK cells cultured at 25 degrees C. In both systems, alpha(1), beta(3), and gamma(2) subunits could be identified in subunit dimers, indicating that different subunit dimers are formed during GABA(A) receptor assembly. Co-transfection of HEK cells with various combinations of full-length and C-terminally truncated alpha(1) and beta(3) or alpha(1) and gamma(2) subunits and co-immunoprecipitation with subunit-specific antibodies indicated that even subunits containing no transmembrane domain can assemble with each other. Whereas alpha(1)gamma(2), alpha(1)Ngamma(2), alpha(1)gamma(2)N, and alpha(1)Ngamma(2)N, combinations exhibited specific [(3)H]Ro 15-1788 binding, specific [(3)H]muscimol binding could only be found in alpha(1)beta(3) and alpha(1)beta(3)N, but not in alpha(1)Nbeta(3) or alpha(1)Nbeta(3)N combinations. This seems to indicate that a full-length alpha(1) subunit is necessary for the formation of the muscimol-binding site and for the transduction of agonist binding into channel gating.

Structure and subunit composition of GABA(A) receptors.

GABA(A) receptors are the major inhibitory neurotransmitter receptors in the brain and are the site of action of many clinically important drugs. These receptors are composed of five subunits that can belong to eight different subunit classes. If all GABA(A) receptor subunits could randomly combine with each other, an extremely large number of GABA(A) receptor subtypes with distinct subunit composition and arrangement would be formed. Depending on their subunit composition, these receptors would exhibit distinct pharmacological and electrophysiological properties. Recent evidence, however, indicates that not all subunits can assemble efficiently with each other and form functional homo- or hetero-oligomeric receptors. In addition, the efficiency of formation of hetero-oligomeric assembly intermediates determines the subunit stoichiometry and subunit arrangement for each receptor and thus further reduces the possible heterogeneity of GABA(A) receptors in the brain. Studies investigating the subunit composition of native GABA(A) receptors support this conclusion, but also indicate that receptors composed of one, two, three, four, or five different subunits might exist in the brain. Using a recently established immunodepletion technique, the subunit composition and quantitative importance of native GABA(A) receptor subtypes can be determined. This information, together with studies on the regional, cellular and subcellular distribution of these receptor subtypes, will be the basis for a rational development of drugs that specifically affect the GABAergic system.

Identification of subunits mediating clustering of GABA(A) receptors by rapsyn.

Human embryonic kidney 293 cells transfected with alpha1beta1gamma2, alpha1beta2gamma2, alpha1beta3gamma2, alpha1beta1, alpha1beta2, alpha1beta3, beta3gamma2, or beta3 subunits formed gamma-aminobutyric acidA receptors on the cell surface that could be clustered by rapsyn. In contrast, alpha1, beta1, beta2, or gamma2 subunits, or alpha1gamma2 subunit combinations could not be detected on the surface of transfected cells and could not be clustered by rapsyn. Experiments investigating the ability of rapsyn to cluster chimeras consisting of the N-terminus of the beta3 subunit and the remaining part of the alpha1, beta2 or gamma2 subunits indicated that the intracellular domains of beta1, beta2, beta3 or gamma2 subunits, but not those of alpha1 subunits are able to form sites mediating clustering by rapsyn. These results demonstrate that rapsyn has the potential to cluster the majority of GABA(A) receptor subtypes via beta or gamma2 subunits. Further experiments will have to clarify the physiological importance of this observation.

A significant part of native gamma-aminobutyric AcidA receptors containing alpha4 subunits do not contain gamma or delta subunits.

Using a novel antibody directed against the alpha4 subunit of gamma-aminobutyric acidA (GABAA) receptors, 5% of all [3H]muscimol but only about 2% of all [3H]Ro15-4513 binding sites present in brain membrane extracts could be precipitated. This indicated that part of the alpha4 receptors containing [3H]muscimol binding sites did not contain [3H]Ro15-4513 binding sites. Immunoaffinity purification and Western blot analysis of alpha4 receptors demonstrated that not only alpha1, alpha2, alpha3, beta1, beta2, and beta3 subunits but also gamma1, gamma2, gamma3, and delta subunits can be colocalized with alpha4 subunits in native GABAA receptors. Quantification experiments, however, indicated that only 7, 33, 4, or 7% of all alpha4 receptors contained gamma1, gamma2, gamma3, or delta subunits, respectively. These data not only explain the low percentage of [3H]Ro15-4513 binding sites precipitated by the anti-alpha4 antibody but also indicate that approximately 50% of the alpha4 receptors did not contain gamma1, gamma2, gamma3, or delta subunits. These receptors, thus, either are composed of alpha4 and beta1-3 subunits only, or additionally contain epsilon, pi, or so far unidentified GABAA receptor subunits.

Mission accomplished: a system for discharge planning.

A brief pilot study has shown how efficient and effective an integrated one-page documentation tool can be in utilizing admissions data to facilitate discharge planning. This manual form makes immediate interdisciplinary documentation possible.

Affinity of various ligands for GABAA receptors containing alpha 4 beta 3 gamma 2, alpha 4 gamma 2, or alpha 1 beta 3 gamma 2 subunits.

The potency of 30 benzodiazepine binding site ligands from 14 different structural classes for inhibition of [3H]Ro 15-4513 (ethyl-8-azido-5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4] benzodiazepine-3-carboxylate) binding to human embryonic kidney (HEK) 293 cells transiently transfected with alpha 4 beta 3 gamma 2S or alpha 1 beta 3 gamma 2S subunits of GABAA receptors was investigated. Most of these compounds were unable to significantly inhibit [3H]Ro 15-4513 binding to alpha 4 beta 3 gamma 2S receptors under conditions where they potently inhibited binding to alpha 1 beta 3 gamma 2S receptors. Nevertheless, compounds from four different structural classes were identified which exhibited a high affinity for alpha 4 beta 3 gamma 2S receptors. Variation of the structure of these compounds could lead to new ligands selectively interacting with alpha 4 beta 3 gamma 2S receptors. Compounds interacting with alpha 4 beta 3 gamma 2S receptor were also able to inhibit [3H]Ro 15-4513 binding to receptors consisting of alpha 4 gamma 2S subunits with comparable potency. These results support the conclusion that the alpha subunit is a major determinant of the benzodiazepine binding site properties of GABAA receptors containing alpha and gamma subunits.

Extensive heterogeneity of recombinant gamma-aminobutyric acidA receptors expressed in alpha 4 beta 3 gamma 2-transfected human embryonic kidney 293 cells.

Human embryonic kidney 293 cells transiently transfected with alpha 4-, beta 3- and gamma 2-subunits of gamma-aminobutyric acidA (GABAA) receptors from the rat exhibited specific high affinity binding sites for [3H]muscimol, [3H]Ro 15-4513 and [35S]t-butylbicyclophosphorothionate (TBPS). Bmax values obtained, however, were dramatically different for these compounds. In addition, GABA was able to inhibit only 20% of specific [35S]TBPS binding to membranes from alpha 4 beta 3 gamma 2-transfected cells. In order to investigate possible receptor heterogeneity, receptors were extracted from alpha 4 beta 3 gamma 2-transfected cells and were fractionated by chromatography on an anti-gamma 2-, followed by an anti-alpha 4- and an anti-beta 3-immunoaffinity column. Western blot analysis of the column eluates indicated the separate existence of GABAA receptors consisting of alpha 4 beta 3 gamma 2-, alpha 4 beta 3- or beta 3-subunits in alpha 4 beta 3 gamma 2-transfected cells. This, and the finding that only alpha 4 beta 3 gamma 2- but not alpha 4 beta 3- or beta 3-receptors possess high affinity binding sites for all three radiolabeled ligands investigated, combined with the observation that [35S]TBPS binding to receptors consisting of beta 3-subunits cannot be inhibited by GABA, can explain most of the binding data obtained. The present results suggest an inefficient assembly of gamma 2- with alpha 4- and/or beta 3-subunits under the conditions used, and indicate that recombinant receptors expressed in HEK cells are not necessarily homogeneous.

Expression of a human monoclonal anti-HIV-1 antibody in CHO cells.

The cDNA coding for the light and heavy chains, respectively, of the human monoclonal antibody 3D6 (IgG1, kappa), which binds specifically to human immunodeficiency virus-1 (HIV-1) gp41, was inserted into three different mammalian expression vectors and transfected into Chinese hamster ovary (CHO) cells. Transcription was under the control of Rous sarcoma virus long terminal repeat (RSV LTR), human cytomegalovirus major immediate early (CMV IE) promoter, and mouse mammary tumor virus long terminal repeat (MMTV LTR), respectively. Antibody productivity was monitored in the supernatants of selected clones. The binding characteristics of the CHO-derived antibody to HIV-1 gp41 were found to be identical to that of the original antibody produced by hybridoma cells.

[ Problems of wound dressing after gingivectomy in the periodontally diseased incomplete dentition (report of treatment) ]. / Zur Problematik der Verbandanlage nach Gingivektomie im parodontarlerkrankten Lückengebiss (Behandlungsbericht).

After some remarks upon the value and the importance of periodontal surgical dressing in general and in case of incomplete dentition in particular, the author reports of a case in which a temporary plastic bridge had been combined with a dressing plate. This combination may also be recommended as a model to busy stomatological practices.