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Biomedical subjects

F Zsuppán

Publications and source records attributed to F Zsuppán.

4 recordsLinked to original sources

Nerve cells with irregular processes: demonstration of anisotropic core geometry of a pyramidal cell.

An analytical, recursive method has been developed to demonstrate the anisotropic electrotonic geometry of nerve cells containing varicose or spiny dendrites. The procedure has been based on the distribution of the core geometry of dendrites into modules which consist of module elements where the physical length is much shorter than the actual space constant. The unambiguous representation of the anisotropic core geometry has been possible by plotting the decomposed geometries separated under the condition of the unidirectional spread of the wave front of dendritic potentials. This decomposition has revealed the bidirectional, "smoothed" core geometries as a function of irregular distribution of varicosities or spines. The shape of decomposed core geometries may change according to the position of the input site. The shaping of core geometry reflects the electrotonic effectiveness of a synaptic site to any arbitrary locations which may lead to considerable savings in computations on synaptic effects. The detailed, computer-reconstructed geometry of the apical dendritic field of the pyramidal cell has been analysed by the proposed method. The frequency-dependence of input impedances has been compared between the original and the transformed core geometries assuming that the current is injected into the soma. The significance of dendritic irregularities in the impedance matching has been studied when the shaping of the core geometry has been induced by laminar inputs. The proposed approach may be useful in comparing the input dependence of the receptive fields of different non-smooth cells. The mismatch of the core geometries induced by the opposite travelling waves from the same anatomical location has also been studied and the possible control of the preferred, direction-sensitive activities will be discussed. The important differences between the compartmental modelings based on the known isotropic treatment of dendrites and the more realistic anisotropic approach will be illustrated.

Animals

A computer reconstruction system for biological macro- and microstructures traced from serial sections.

A system of programs for building three-dimensional (3D) models of biological macro- and microstructures has been developed. A PDP 11/34 laboratory minicomputer with graphical output devices, and a QUANTIMET image analyzer are used for the reconstruction. The contours of the features can be digitized directly from tissue sections mounted on the stage of an OPTON research light microscope, or indirectly from microphotographs, and from camera lucida drawings. The operator selects contours of features in question from the image by using Quantimet's interactive input devices and commands the Quantimet system to record the image. The 3D models are built from a series of 2D outlines. In the visualization phase the reconstructed objects can be investigated from different viewpoints with their hidden lines removed. Additional calculations (volume and surface area) help in quantitative classification of the reconstructed structures.

Animals

A new approach to merging neuronal tree segments traced from serial sections.

The merging process which is one of the most significant problems in computer-aided reconstruction of neuronal trees has been investigated. This paper reports a new approach in merging tree segments traced from serial sections. The research was motivated by the fact that in most cases users can distinguish connectable cut ends of the different tree segments without any interaction, and with this knowledge merging can be easily solved by a computer program added to the neuron reconstruction program system at Semmelweis University Medical School, Budapest. Then, the merged neuron trees can be handled as if they had been digitized from one histological section.

Data Display

Approximation of missing sections in computer reconstruction of serial EM pictures.

Replacing missing contours or completing a series of contours of biological structures has been investigated. The paper reports on a method for approximating lateral surfaces between adjacent contours and generating new artificial outlines by slicing the interpolated surface parallel with the original sections. The research method was developed mainly due to the need to fill in damaged or missing ultrathin sections in longer series, since their absence may impede the three-dimensional visualization of selected components. The new program attached to the shape reconstruction program system existing at Second Department of Anatomy, Semmelweis University Medical School, Budapest, Hungary also permits new contours to be generated into the models of single or branching objects. Besides replacing missing contours, the program makes the reconstructed model more precise.

Animals