Exponential distribution of interimpulse current intervals in lipid bilayer membrane at phase transition temperature

The statistical analysis of current fluctuations in unmodified bilayer lipid membranes at the phase transition temperature was made. An exponential distribution of current fluctuations was revealed.     

Interfacial tension of aqueous biopolymer mixtures close to the critical point

Proteins and polysaccharides, being the main constructional materials in many biological structures, have a limited compatibility in aqueous media. At sufficiently high concentrations, they form water-in-water emulsions. Interfacial tension is an important parameter in such systems since it is a controlling factor in the morphology development during processing. In this work a rheo-optical methodology, based on the analysis of small angle light scattering (SALS) patterns during fibril break-up, is used to study the interfacial tension of water-sodium caseinate-sodium alginate systems located close to and relatively far from the binodal. The interfacial tension close to the critical point was approximately 10(-8) N/m, and it increased considerably, to a value of up to 5.2 x 10(-6) N/m farther from the critical point. For the scaling of the interfacial tension with the density difference between the phases, a scaling exponent of 3.1 +/- 0.3 was found, in agreement with the critical mean-field scaling exponent of 3.     

Spectral Analysis of Long Electroencephalographic Records

Spectral analysis of a 10-min electroencephalogram (EEG) record has made it possible to describe the behavior of EEG rhythms as a dynamic spectrum and find a distinct periodic pattern in this behavior. The data on the dynamic spectra of long EEGs offer a new insight into the estimation of the stability of EEG electrical processes in healthy subjects, inter- and intrahemispheric relationships between the electrical activities of different cortical regions, and estimation of phase relations, which were previously performed on the basis of comparison between single EEG spectral patterns.     

Characteristics of EEG signs of anxiety in human

Influence of anxiety (tested by Luscher) on the spatial organization of brain electrical activity was studied using multichannel EEG recording. In subjects with a high-level of anxiety, the level of coherence and spectral power of some high-frequency EEG components was higher in the parieto-temporal regions of both hemispheres than that in the opposite group. Solving the inverse problem (classification of individuals with one of the groups) made it possible to work out the criteria of automated evaluation of the anxiety level at the preclinic state of neuropsychic disorders. The EEG signs of the influence of increased anxiety on psychophysiological and cognitive processes and autonomic functions were analyzed. The EEG signs of increased anxiety in animals (rats) and humans were compared and some similarity of the spatial-frequency organization was revealed. The main difference consists in a greater activation of the left parieto-temporal area in humans, which is interpreted as a morphofunctional basis of verbalization of anxiogenic stimuli.     

Capacitive and ionic currents in BLM from phosphatidic acid in Ca2+-induced phase transition

The development of electric current with time in a bilayer lipid membrane (BLM) formed from dipalmitoylphosphatidic acid on introducing Ca2+ ions into the medium was studied at constant temperature and pH. The phase transition in the Ca2+-induced BLM is accompanied by the initial capacitive current followed by the occurrence of single ionic channels. The amount of transported charges in the capacitive current is 5 C/ microF. The conductivity of the single ionic channels ranges from 50 to 100 pSm.     

Stellate cells of aortic intima: II. Arborization of intimal cells in culture.

The present study analyzed effects of different cAMP-elevators on cell morphology in primary culture of human intimal and medial cells from grossly normal and atherosclerotic areas. In primary culture of human aortic cells adenylate cyclase activator forskolin and other cAMP elevators induced arborization of cells, i.e. they reversibly changed the shape of cells. This resulted in the formation of thin branching processes and in the concentration of cytoplasm around the nucleus. In the culture, the shape of the arborized cells resembled that of stellate ones detected in the aortic intima in situ. The arborization of cells was accompanied by destruction of myofilaments. Due to cAMP elevators' effect, most of the arborized cells were exhibited in the cultures isolated from the elastic-hyperplastic layer of the intima. The number of arborized cells was significantly less in the cultures isolated from the musculo-elastic layer and still lesser in those isolated from media. We failed to reveal any significant difference in the number of arborized cells cultured from fatty streaks, atherosclerotic plaques and grossly normal aortic areas. Obtained results suggest that the previously revealed polymorphism of human aortic intimal cells may be accounted for by the cell shape transformations underlined by the mechanism similar to that of arborization in vitro.     

Ca2+ ions induce successive capacity and ion currents in BLM from phosphatidic acid as a result of phase transition

Time dependence of Ca2+-induced electric current in BLM formed from DPPA was studied at constant temperature and pH. The phase transition in BLM is accompanied by capacity current and following appearance of single ionic channels. It was shown that transferred charge was 5 nC/F, conductivity of single ionic channels--500-100 pSm.     

Study of the structural and functional properties of fibronectin--a high molecular weight plasma glycoproteins--by using monoclonal antibodies

Functional and structural properties of fibronectin--high molecular weight glyco-protein from human plasma--were studied by monoclonal antibodies against fibronectin. It was shown that monoclonal antibodies against human plasma fibronectin exhibit a certain species specificity. Antigenic determinant for our monoclonal antibody is located in the central part of the protein polypeptide chain--in the structural domain. The monoclonal antibodies studied do not inhibit any tested functions of fibronectin. In contrast, polyclonal antibodies are not species specific and inhibit all fibronectin functions.