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T V Davydova

Publications and source records attributed to T V Davydova.

At least 73 records · Page 4Linked to original sources

[Different types of secondary degeneration of visual nerve endings in the midbrain tectum of the steppe turtle].

Along with the commonly known patterns of terminal destruction ("dark", "light", "neurofilamentous"), new types of changes have been revealed, referred to as "vesicular" and "glycogen" trasformation types. Vesicular transformation which may develop according to the dark or light type is characterized by a sharp deformation of synaptic vesicles; glycogen transformation is distinguished by agglutination and disappearance of synaptic vesicles, the inside of the terminal being filled up with glycogen granules. Ultrastructural differences of the terminal degeneration process in different groups of nerve fibers reflect the morpho-functional heterogeneity of the retina ganglion cells and of their axons.

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[Laminar analysis of neuronal ultrastructure in the midbrain tectum of the steppe turtle].

A layer-to-layer study of the neuronal ultrastructure in the mesencephalic optic centre of T. horsfieldi has been made, the results being compared to those of similar experments with Emys orbicularis L. Neurons of the efferent type (layers IV, V), in contrast to short axon elements (layers, I, 22) are characterized by a greater amount of cytoplasm and by a variety of cytoplasmatic organelles. A few morphological types of neurons are distinguished: light, dark and neurons with a light nucleus and a dark cytoplasm. In two systems of horizontal neurons dark cells predominate to be assumed as being an independent morphofunctional neuronal type. In contrast to E. orbicularis, the neurons of T. horsfieldi show a large amount of axo-somatic synapses on the surface, and a deficiency in spiny outgrowths, both on the apical and basal dendrites.

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Retinotectal system of the tortoise, Testudo horsfieldi, Gray (morpho-functional study in the norm and after enucleation).

The optic nerve and mesencephalic optic centre (tectum opticum, TO) of the tortoise, Testudo horsfieldi, Gray, in the norm and after the enucleation have been studies using Golgi's method, electron microscopy and the electrophysiological technique. The optic nerve comprises about 400,000 fibres represented by two classes of axons: myelinated (10%) and unmyelinated (90%). The diameters of the former vary within 0.3-3 mum, of the latter within 0.3-1.1 mum. The neurogramms of the optic nerve contain two components corresponding to the two rates of conduction through different groups of fibres (1.3 musec and 0.5 musec). The stratified synaptic organization of the TO has been investigated. The optic terminals are shown to join in complex synaptic formations at certain levels of the upper layers of the TO (Strata I, II and III). The process of degeneration in the optic system of Testudo is drastically stretched in time. It was demonstrated by the electrophysiological control that the TO potentials induced in response to the nerve stimulation were not registered any longer only 6-6.5 months after the enucleation. Certain groups of retinal fibres of the optic nerve and their terminals in the TO are shown to degenerate differently and asynchronously. Earlier unknown types of destructive changes of the terminals (vesicular, neurofilamentous, glycogen and others) are described. It is suggested that the different types of degeneration of the optic fibres and their terminals are the result of possible biochemical heterogeneity of the retinal ganglious cells. The comparison of the terms and types of degeneration of different groups of nervous fibres in the optic nerve and their terminals in the TO has revealed some correlations suggesting that the myelinated optic fibres produce nervous terminals degenerating by the "dark" type, whereas the unmyelinated optic axons may be subdivided into several groups, each producing nervous terminals subjected to a definite type of destruction ("clear", "vesicular", "neurofilamentous" etc.). The localization of certain groups of therminals at certain levels of the cortical plate of the TO confirms the electrophysiological data on the stratified organization of the retino-tectal projections in the TO of lower vertebrates. It has been shown by the comparison of the results obtained with those reported for Emys orbicularis, L. that the two species have marked differences in the morpho-functional characteristics of the retino-tectal system, neuronic composition of the TO, the character of destructive changes of the terminals after the enucleation and the component composition of polysynaptic complexes and glomerules. Probably these differences may come from the peculiarities of the perception and transformation of visual information in the species.

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[Period of degeneration and features of the laminar distribution of the visual nerve endings in the midbrain tectum of the steppe turtle (Testudo horsfieldi, Gray)].

A study of ultrastructural changes in the neuronal terminals of optic fibres at the level of tectum opticum (TO) in different periods after unilateral enucleation has revealed the process of degeneration in the optic system of Testudo horsfieldii as well as in Emysorbicularis L. to take a considerable time: from two weeks to six months. The character of destructive changes and the mode of utilization of desintegrated elements are dissimilar in different groups of retinal axons in the optic nerve and their terminals in TO. A comparison of the degeneration periods and the character of the changes in the optic fibres has made it possible to establish the following approximate correlations: all the nerve terminals of myelinated fibres degenerate after the "dark" type, whereas the terminals of non-myelinated axons are subjected to other kinds of transformations ("light", vesicular", neurofilamentous", "glycogen"). The analysis of the distribution of degenerating nerve terminals in the TO layers has demonstrated that there is a regularity in localization of different nerve terminals at certain levels of TO which is indicative of the layered organization of retino-tectile connections. Considerable differences in the neuronal and synaptic organization of TO have been revealed as well as in the character and the time of destructive changes of retino-tectile fibres after enucleation in T. horsfieldii and E. orbicularis.

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[Morpho-functional changes in the tegmentum mesencephali of turtles following enucleation].

Morpho-functional changes in the mesencephalic centre of the turtle (Emys orbicularis L.) were studied during optic nerve degeneration. It was observed that synaptic terminals in this centre undergoing the "dark" degeneration are associated with myelinated optic fibres and terminals undergoing the "light" one are associated with unmyelinated fibres. The first low amplitude component of the evoked potential disappears with degeneration of myelinated fibres of large diameter during the "dark" degeneration (4-5 months after enucleation). The first high amplitude component disappears with degeneration of the middle-sized myelinated fibres and the end of the "dark" degeneration (7 months after enucleation). The characteristics of the second high amplitude component which reflects the excitation of both thin myelinated and all unmyelinated fibres, begin to change with degeneration of unmyelinated fibres during "light" degeneration (2.5-3.5 months). This component disappears with degeneration of the thin myelinated fibres (7 months).

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[Dark and light neurons in the cortical plate of the forebrain of the swamp turtle].

Electron microscopic study of the neuronal composition of Emys orbicularis cortical zones as compared with the light microscopy data has revealed that the distinctions in the cell cytoplasm ultrastructure with respect to the dendrite branching pattern and the peculiarities of their localization in the cortical plate are suggestive of a possible metabolic heterogeneity and can serve as a foundation of the morpho-functional characteristics of the neurons. A few neuronal types of neurons have been revealed: 1. light neurons distinguished by the cytoplasm matrix devoid of any electron density, a poorly developed endoplasmic reticulum and a few cytoplasmatic organells and inclusions; 2. light neurons having slight osmophility of the cytoplasm matrix, a more developed endoplasmic reticulum with elongated cisternae, a great number of organells including neurofilaments; 3. dark neurons having a high degree of cytoplasm matrix and the nucleus, a large number of the nuclei, cytoplasm, dendrites and axons in contrast to the above described patterns.

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