Subjective localization of electrocutaneous stimuli

Studying the perception of spatiotemporal stimulus patterns in various modalities may yield important information on the way in which humans process sensory information. The perception of tactile and nociceptive cutaneous stimulus patterns have been studied by Stolle et al. [1] and Trojan et al. [2][4] respectively. Among other things, both authors studied subjective localization of single stimuli. In Trojan et al. [4], two types of mislocalization patterns were observed for nociceptive single stimuli when comparing the localization reports with the stimulus locations: (1) overall proximal or distal displacement and (2) expansion or contraction of the stimulus area.\ud It is unknown whether tactile and nociceptive stimuli at the same skin site are perceived as being at the same site. Therefore, comparing the spatial perception of tactile and nociceptive cutaneous stimuli may provide new insights into their processing. This comparison can only be successfully made by applying nociceptive and tactile stimuli at the same skin site in the same experiment. This can be done by using a device which has recently been developed at our institute and which we refer to as the bimodal stimulation electrode [3]. \ud Recording the perceived locations of stimuli can be done by letting subjects report these on a scale. The most intuitive scale for this is the stimulated arm itself. However, this would bias the perception of stimulus location by providing visual information of the electrode locations. The goal of the present research was to (1) create and (2) test a setup which allows subjects to report perceived stimulus locations on their own arm without seeing the electrode positions. This was achieved by building a setup consisting of a touch screen (Provision Visboard) which presents a digital image of the subject’s own arm (without electrodes) and which is positioned over this arm after the electrodes have been attached. Subjects can report the localizations by pointing at the screen using a pointer

The Metallicity and Dust Content of HVC 287.5+22.5+240: Evidence for a Magellanic Clouds Origin

We estimate the abundances of S and Fe in the high velocity cloud HVC 287.5+22.5+240, which has a velocity of +240 km/s with respect to the local standard of rest and is in the Galactic direction l~287, b~23. The measurements are based on UV absorption lines of these elements in the Hubble Space Telescope spectrum of NGC 3783, a background Seyfert galaxy, as well as new H I 21-cm interferometric data taken with the Australia Telescope. We find S/H=0.25+/-0.07 and Fe/H=0.033+/-0.006 solar, with S/Fe=7.6+/-2.2 times the solar ratio. The S/H value provides an accurate measure of the chemical enrichment level in the HVC, while the super-solar S/Fe ratio clearly indicates the presence of dust, which depletes the gas-phase abundance of Fe. The metallicity and depletion information obtained here, coupled with the velocity and the position of the HVC in the sky, strongly suggest that the HVC originated from the Magellanic Clouds. It is likely (though not necessary) that the same process(es) that generated the Magellanic Stream is also responsible for HVC 287.5+22.5+240.Comment: AASTEX, 3 postscript figures, AJ, 1998, Jan issu

Microarray screening of Guillain-Barré syndrome sera for antibodies to glycolipid complexes

Objective: To characterize the patterns of autoantibodies to glycolipid complexes in a large cohort of Guillain-Barré syndrome (GBS) and control samples collected in Bangladesh using a newly developed microarray technique. Methods: Twelve commonly studied glycolipids and lipids, plus their 66 possible heteromeric complexes, totaling 78 antigens, were applied to polyvinylidene fluoride–coated slides using a microarray printer. Arrays were probed with 266 GBS and 579 control sera (2 μL per serum, diluted 1/50) and bound immunoglobulin G detected with secondary antibody. Scanned arrays were subjected to statistical analyses. Results: Measuring antibodies to single targets was 9% less sensitive than to heteromeric complex targets (49.2% vs 58.3%) without significantly affecting specificity (83.9%–85.0%). The optimal screening protocol for GBS sera comprised a panel of 10 glycolipids (4 single glycolipids GM1, GA1, GD1a, GQ1b, and their 6 heteromeric complexes), resulting in an overall assay sensitivity of 64.3% and specificity of 77.1%. Notable heteromeric targets were GM1:GD1a, GM1:GQ1b, and GA1:GD1a, in which exclusive binding to the complex was observed. Conclusions: Rationalizing the screening protocol to capture the enormous diversity of glycolipid complexes can be achieved by miniaturizing the screening platform to a microarray platform, and applying simple bioinformatics to determine optimal sensitivity and specificity of the targets. Glycolipid complexes are an important category of glycolipid antigens in autoimmune neuropathy cases that require specific analytical and bioinformatics methods for optimal detection

Weak decays of 4He-Lambda

We measured the lifetime and the mesonic and non-mesonic decay rates of the 4He-Lambda hypernucleus. The hypernuclei were created using a 750 MeV/c momentum K- beam on a liquid 4He target by the reaction 4He(K-,pi-)4He-Lambda. The 4He-Lambda lifetime was directly measured using protons from Lambda p -> n p non-mesonic decay (also referred to as proton-stimulated decay) and was found to have a value of tau = 245 +/- 24 ps. The mesonic decay rates were determined from the observed numbers of pi-'s and pi0's as Gamma_pi-/Gamma_tot = 0.270 +/- 0.024 and Gamma_pi0/Gamma_tot = 0.564 +/- 0.036, respectively, and the values of the proton- and neutron-stimulated decay rates were extracted as Gamma_p/Gamma_tot = 0.169 +/- 0.019 and Gamma_n/Gamma_tot <= 0.032 (95% CL), respectively. The effects of final-state interactions and possible 3-body Lambda N N decay contributions were studied in the context of a simple model of nucleon-stimulated decay. Nucleon-nucleon coincidence events were observed and were used in the determination of the non-mesonic branching fractions. The implications of the results of this analysis were considered for the empirical Delta I = 1/2 rule and the decay rates of the 4H-Lambda hypernucleus.Comment: 15 pages, 11 figures, published in PRC, revised content to match published versio