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E A Lebedev

Publications and source records attributed to E A Lebedev.

8 recordsLinked to original sources

Constancy and variability in the content of DNA in cerebellar Purkinje cell nuclei. A cytophotometric study.

A cytophotometric study of DNA content in Purkinje cells of the cerebellum of rats, cats, chicken and humans (Feulgen staining) revealed that in a certain number of cells the amount of NDA ranged between the diploid and tetraploid level (H2C cells). The incidence of H2C Purkinje cells varied among the species studied. In rats, which were studied most thoroughly, these cells amounted on average to 3%. In some rats, as well as in some cats and chickens H2C Purkinje cells were entirely absent. In the group of animals possesing H2C Purkinje cells, great interindividual differences were observed. In rats for instance, the incidence of these cells varied from 1 to 23 per cent. Topographic analyses carried out in rat and human cerebellum revealed that H2C Purkinje cells occurred more frequently in the hemispheres than in the vermis. No significant differences were found in the number of H2C Purkinje cells in healthy and Kilham-DNA-virus infected rats. Densitometric analysis of the distribution of nuclear chromatin showed that H2C Purkinje cells were richer in condensed chromatin, especially in the region of the nucleolus, which apparently contains the hyperploid surplus of DNA. It is proposed that the phenomenon of DNA hyperdiploidy arises as a result of either incomplete S-phase in some immature Purkinje cell precursors or the amplification of some DNA sequences particularly those localized in the nucleolar region.

Aged

[Ultraviolet cytophotometry of a single live neuron in the crayfish mechanoreceptor].

Measurements of ultra-violet absorption by a live neuron, with 5-minutes' intervals, have shown variations in RNP content amounting almost 20% with a period of 30 min. The fact that these variations and their phase were independent from changes in the volume of RNP zone allows to relate them to the rhythm of macromolecule synthesis. When ultra-violet radiation was delivered in large doses, mean RNP content decreased with a latency 20 to 40 min, and 30- minutes' variations of RNP content were suppressed.

Animals

[Changes in the activity of 3beta-OH-steroid dehydrogenase in the adrenals of rat fetuses following decapitation in utero].

The activity of 3beta-OH-steroid dehydrogenase in the adrenal cortex of 21-day fetuses in control and 3 days after decapitation in utero was estimated quantitatively by microspectrophotometry. The enzyme activity calculated as per conditioned cell in the fascicular zone exceeded that in the forming glomerular zone. After hypophysectomy the activity of the 3beta-OH-steroid dehydrogenase decreased in both the fascicular and glomerular zones.

Adrenal Cortex

[Histochemical studies of the sensitivity of frog retinal cells to stimulus movement and flashes].

The technique of quantitative UV-cytophotometry of RNA was used for comparative study of the sensitivity of frog retina cells to the movement of stimuli and flashings. A corresponding set of stimulators which includes the movement of mounted stimuli and heterogenous flashings of diffuse light showed that a type of cells exists in the interior nuclear layer of the retina which is specifically sensitive to the movement. It is suggested that in the formation of this property a dynamic reciprocal lateral inhibition on the level between bipolar and amacrine cells takes place. Application of heterogenous flashing light allowed also to reveal functional variety of bipolar cells.

Animals

Life span of lymphocytes in cattle in the norm and during lymphatic leukemia.

Comparison was made of the rate of in vivo elimination from blood and organs of cattle of lymphocytes labeled with 3H-thymidine in the course of seven days in the norm and during lymphatic leukemia. Significant delay in the elimination of labeled lymphocytes, and especially of lymphocyte precursors, from the blood, spleen, and lymph glands of the animal was established in the stage of lymphatic leukemia that was examined.

Animals