Teaching the basic principles of electrocardiography experimentally.

Electrocardiography (ECG) is one of the most widely used methods in clinical diagnosis. Here we describe an experimental approach that offers hands-on learning of its basic principles. An experimental model that consists of a rubber foil with a low electrical conductivity and a DC power unit is used to simulate the body and the electric dipole of the heart.

Cell Volume Changes and Membrane Ruptures Induced by Hypotonic Electrolyte and Sugar Solutions.

The cell volume changes induced by hypotonic electrolyte and sucrose solutions were studied in Chinese-hamster-ovary epithelial cells. The effects in the solutions with osmolarities between 32 and 315 mosM/L and distilled water were analyzed using bright-field and fluorescence confocal microscopy. The changes of the cell volume, accompanied by the detachment of cells, the formation of blebs, and the occurrence of almost spherical vesicle-like cells ("cell-vesicles"), showed significant differences in the long-time responses of the cells in the electrolyte solutions compared with the sucrose-containing solutions.

The pore-forming action of polyenes: From model membranes to living organisms.

The incidence of resistant fungal pathogens has been increasing, especially in immuno-compromised people. As such, considerable research has been focused on discovering anti-fungal agents with new mechanisms of action and on optimizing the use of existing agents. In this context, interest in the polyene group of anti-fungals has recently been renewed, since they are known to be effective against a broad spectrum of fungal pathogens that only rarely develop a resistance to them.

Osmotic Effects Induced by Pore-Forming Agent Nystatin: From Lipid Vesicles to the Cell.

The responses of Chinese hamster ovary epithelial cells, caused by the pore-forming agent nystatin, were investigated using brightfield and fluorescence microscopy. Different phenomena, i.e.

The influence of very low illumination on the postural sway of young and elderly adults.

The purpose of the present study was to evaluate the influence of very low ambient illumination and complete darkness on the postural sway of young and elderly adults. Eighteen healthy young participants aged 23.8 ± 1.

The role of sterols in the lipid vesicle response induced by the pore-forming agent nystatin.

The influences of ergosterol and cholesterol on the activity of the nystatin were investigated experimentally in a POPC model membrane as well as theoretically. The behavior of giant unilamellar vesicles (GUVs) under osmotic stress due to the formation of transmembrane pores was observed on single vesicles at different nystatin concentrations using phase-contrast microscopy. A significant shift of the typical vesicle behavior, i.

Role of red blood cell elastic properties in capillary occlusions.

The shape transformations of red blood cells stuck in capillary narrowings with radii close to the critical radius where the maximum deformations occur are analyzed. The membrane skeleton deformations are studied within the effective network model and the continuum elastic model, whereas the area-difference elasticity model is applied to describe the phospholipid bilayer. A minimization of the total free energy is performed to determine the cell shapes in a stopped flow, which are calculated by a triangulated representation of the membrane surface.

Effects of the pore-forming agent nystatin on giant phospholipid vesicles.

The effects of the polyene pore-forming agent nystatin were investigated on individual giant unilamellar phospholipid vesicles (GUVs), made of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), in different methanol-water solutions using phase-contrast optical microscopy. Three characteristic effects were detected in three different nystatin concentration ranges: vesicle shape changes (between 150 and 250μM); transient, nonspecific, tension pores (between 250 and 400μM); and vesicle ruptures (above 400μM). Both the appearance of the transient tension pores and the vesicle ruptures were explained as being a consequence of the formation of size-selective nystatin channels, whose membrane area density increases with the increasing nystatin concentrations.

Shapes of phospholipid [correction of phosholipid] vesicles with beadlike protrusions.

Giant phospholipid vesicles obtained by the method of electroformation were observed by the phase contrast microscope. Most of these vesicles contain a protrusion which shortens in a slow shape transformation process until it is absorbed into the main vesicle body. We are concerned with the last stages of this shape transformation process, where the protrusions attain a beadlike shape.

Asymmetrical labeling of giant phospholipid vesicles.

The method for labeling of inner membrane leaflet in unilamellar giant POPC vesicles was developed and characterised. Symmetrically NBD-PC labeled vesicles were treated by sodium dithionite, which undergoes an irreversible chemical reaction with NBD-PC molecule making it non-fluorescent. After the addition of dithionite the fluorescence on single vesicles as well as on vesicle suspension showed a 50% decrease of its initial value corresponding to marker quenching in the outer leaflet.

Rotation of giant phospholipid vesicles in an uniform shear flow.

Rotation of giant "point attached" phospholipid (POPC) vesicles in a shear flow was studied. The dependence of the angular velocity on the flow gradient was measured and the experimental results were compared to the predictions of a theoretical model. A good linear correlation between the angular velocity of the vesicle and the flow gradient, as predicted, was observed.

Rotation of giant phospholipid vesicles in an uniform shear flow.

Rotation of giant "point attached" phospholipid (POPC) vesicles in a shear flow was studied. The dependence of the angular velocity on the flow gradient was measured and the experimental results were compared to the predictions of a theoretical model. A good linear correlation between the angular velocity of the vesicle and the flow gradient, as predicted, was observed.

Asymmetrical labeling of giant phospholipid vesicles.

The method for labeling of inner membrane leaflet in unilamellar giant POPC vesicles was developed and characterised. Symmetrically NBD-PC labeled vesicles were treated by sodium dithionite, which undergoes an irreversible chemical reaction with NBD-PC molecule making it non-fluorescent. After the addition of dithionite the fluorescence on single vesicles as well as on vesicle suspension showed a 50 % decrease of its initial value corresponding to marker quenching in the outer leaflet.

Field strength dependence of MRI contrast enhancement: phantom measurements and application to dynamic breast imaging.

Differences in MRI-measured contrast enhancement have been used for tissue characterization, particularly for the characterization of mammary tumours. T1 weighted spoiled gradient echo sequences have usually been acquired for this purpose and relative signal intensity increase (Srel) has been determined to quantify contrast uptake. The field strength dependence of this technique is evaluated in this paper by phantom measurements.

Comparing localization of conventional functional magnetic resonance imaging and magnetoencephalography.

The technique of functional magnetic resonance imaging (FMRI) allows the measurement of functional cerebral blood flow changes occurring with specific tasks. However, the spatial relationship between neuronal activity and functional cerebral blood flow changes is not known yet. This study compares the centre of neuronal activation (measured by magnetoencephalography) with that of the blood flow response (measured by FMRI) to unilateral motor stimulation in eight subjects.

[Correlation of results of localization by functional magnetic resonance tomography with magnetoencephalography].

Functional magnetic resonance imaging (FMRI) allows the measurement of functional cerebral blood flow changes occurring with specific tasks. However, the spatial relationship between neuronal activity and functional cerebral blood flow changes is not yet known. This study compares the center of neuronal activation (measured by magnetoencephalography) with that of the blood-flow response (measured by FMRI) to unilateral motor stimulation in eight subjects.

Method for the quantitative assessment of contrast agent uptake in dynamic contrast-enhanced MRI.

In previous papers relative signal intensity increase was used as a quantitative assessment parameter for contrast uptake in contrast-enhanced MRI. However, relative signal intensity increase does not only reflect contrast uptake but depends also on tissue parameters (native T1 relaxation time) and sequence parameters (repetition time and flip angle); thus, the contrast uptake cannot be assessed accurately using relative signal intensity increase. Based on an analysis of the contrast behavior of spoiled gradient echo sequences, a method is described in this paper that overcomes the limitations of relative signal intensity increase measurement.

Magnetic resonance angiography and selective angiography following extra-intracranial bypass operations.

Magnetic resonance angiography (MRA) was compared with conventional angiography in 14 patients following extra-intracranial arterial anastomosis. In 13 patients the bypass was shown by MRA and confirmed by conventional angiography. In five of these, the anastomosed vessels, in particular the superficial temporal artery, was of the same calibre or smaller than the same vessels on the contralateral, healthy side.

Liver tissue characterization by in vitro NMR: tissue handling and biological variation.

The extraction of reliable and useful relaxation time data for tissue characterization by NMR requires strict protocols, optimized for each type of biological tissue, which include parameters like storage duration and temperature as well as measurement parameters. Spin-lattice relaxation times in liver tissue vary not only with NMR frequency but also with their "time-after-excision characteristics," while spin-spin relaxation times are almost independent of most parameters which influence T1 at 20 MHz in normal liver tissue (e.g.

In vitro NMR investigation of controlled single and repeated isoflurane anesthesia.

Immobilization of laboratory animals is a basic requirement for experimental in vivo NMR measurements. The effect of single and repeated isoflurane anesthesia on proton NMR relaxation times T1 and T2 in rat liver was studied. Furthermore, physiological monitoring was performed to evaluate the influence of isoflurane anesthesia (up to 2 hr) on biological parameters.

Systematic investigation of degradation effects on spin-lattice relaxation times in mouse-liver by low resolution NMR.

In spite of numerous work on in vitro proton relaxation time investigations of biological tissue, many questions still remain open. In this study we focused on spin-lattice (T1) relaxation time measurements of mouse liver tissue in order to estimate the time-after-excision effects. The post mortem behaviour of excised tissue was measured up to four hours in intervals of about nine minutes.

Systematic investigation of degradation effects on spin-spin relaxation times in mouse-liver by low resolution NMR.

Despite numerous work on spin-lattice (T1) relaxation in vitro, not much attention has been paid on spin-spin (T2) relaxation until now. In this study we are presenting spin-spin relaxation time measurements of mouse liver tissue in order to estimate the time-after-excision effects. The post mortem behaviour of excised tissue was investigated up to four hours in intervals of about nine minutes.

Analysis of relaxation time data from a low-resolution 1H-NMR-pulse-spectrometer.

Systematic investigations have been undertaken in order to evaluate the potential of low resolution NMR for characterization of biological tissue (in vitro) during early post mortem period. Test measurements from corn-oil samples are compared with computer simulated data. Furthermore, time-after-excision dependence of mouse-liver tissue is presented using the in vitro protocol developed in our laboratory.