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V A Brumberg

Publications and source records attributed to V A Brumberg.

At least 19 recordsLinked to original sources

Analysis of some histochemical colour reactions for cytospectrophotometry of basic and acidic proteins in nervous tissue cells.

Cytospectrophotometric analysis of model systems and of single cells in Carnoy-fixed paraffin sections of the nervous tissue has shown two histochemical colour reactions for basic proteins and two reactions for acidic proteins to obey Bouger-Lambert-Beer's law. Basic proteins can be stoichiometrically stained either with Fast Green FCF, pH 8.2, or with heparin-Alcian Blue; acidic proteins either with Fast Green, FCF, pH 2.6, or with Toluidine Blue o. basing on better reproducibility of cytochemical results and sufficiently good preservation of cell structure, heparine-Alcian Blue is recommended for cytospectrophotometric determinations of basic proteins. To stain acidic proteins both Fast Green, pH 2.6, and Toluidine Blue O are recommended, each of the dyes being characterized by its own advantages and disadvantages.

Animals↗

Cytospectrometric studies on the lactate dehydrogenase isoenzymes in functionally different neuron-neuroglia units. II. Species and strain differences and effects of histotoxic hypoxia and audiogenic convulsions.

Cytospectrophotometric determination of H- and M-forms of LDH has shown that in white mice as compared with Wistar rats the activity ratio of H- to M-forms is lower in cerebral cortex neurons but higher in spinal cord motoneurons. No statistically significant species difference has been found in cerebellum PURKINJE cells as well as in the perineuronal glia of all the areas studied. Rats of KRUSHINSKY-MOLODKINA strain with hereditary high sensitivity to audiogenic convulsions differed from Wistar rats only with higher H- to M-form activity ratio in cerebellum PURKINJE cells and in their glial satellite cells. Histotoxic hypoxia in mice due to KCN injection gave rise in 15 min to activation of M-forms of LDH in spinal cord motoneurons and spinal ganglia neurons, of H-forms in cerebral and cerebellar cortex neurons and of both forms in the neuroglial cells adjacent to cerebellum PURKINJE neurons. Audiogenic convulsions in KRUSHINSKY-MOLODKINA rats induced an increase of H-form activity of LDH in the perineuronal glia of spinal cord anterior horns and of M-form activity in cerebellum PURKINJE cells while decrease of M-forms of cerebellum neuroglia. An importance of multiple forms of enzymes for the fine functional regulation of the cell biochemical pattern is discussed.

Animals↗

[Cytospectrophotometric analysis of various color reactions for acid and basis proteins in nerve tissue cells].

Polyvinyl formal films soaked with various concentrations of proteins as well as Carnoy-fixed paraffin sections of rat brain were stained with various colour reactions for acidic and basic proteins. Sufficient specificity, reproductivity, sensitivity and applicability for cytospectrophotometric determinations have been shown for the staining of acidic proteins with Toluidine blue 0 (pH 9.0) or with Fast green FCF (pH 2.6), and for the staining of basic proteins with Alcian blue (pH 10.0), or with Fast green FCF (pH 8.2). Importance of cytophotometric analysis of individual protein fractions is outlined for the functional cytochemistry of the nervous system.

Albumins↗

[Effect of audiogenic convulsions on the activity of n- and m-forms of lactate dehydrogenase in the neurons and neuroglia of different sections of central nervous system].

It was shown spectrophotometrically that in Krushinsky-Molodkina and Wistar rats the ratio of the activity of the aerobic H-forms of lactic dehydrogenase (LDH) to the activity of the anaerobic M-forms was higher in the neurons of the cerebral cortex and the Purkinje's cells of the cerebellum and in their glial cells-satellites than in the motor neurons of the anterior horns of the spinal cord and their perineuronal glia. In Krushinsky-Molodkina rats (with genetically-determined high sensitivity to audiogenic convulsions) epileptiform attacks under the effect of sound were accompanied by a marked activation of both the H- and the M-forms of LDH in the cortical neurons in the absence of any shifts in the perineuronal glia. On the contrary, the activity of all the forms of LDH was unchanged in the spinal motor neurons, whereas in the neuroglia cells surrounding these neurons there was a distinct increase in the activity of the H-forms of LDH. In the Purkinje's cells of the cerebellum an increase and in the glial cells- satellites -- a reduction of the activity of the M-forms of LDH in case of convulsions was seen.

Acoustic Stimulation↗

Cytospectrophotometric studies on the lactate dehydrogenase isoenzymes in functionally different neuron-neuroglia units. I. Optimal procedure conditions and topochemical comparisons in normal mice.

Optimal conditions are described to reveal quantitatively the total activity of lactate dehydrogenase (LDH) and the activity of its H- and M-form in the nervous tissue sections when applying Brody and Engel's tetrazolium method modified by Gerebtzoff. This histochemical reaction has been shown to obey Bouger-Lambert-Beer's law which confirms the possibility of the quantitative determination of the activity of LDH and its isoenzymes by means of cytospectrophotometric method. In the neurons of different areas of the mouse nervous system (cerebral cortex, cerebellar cortex, spinal cord anterior horns, spinal ganglia), both the total LDH activity and the activities of its H- and M-forms were localized in the cytoplasm. Within the limits of the sensitivity and correctness of the cytospectrophotometric method, the ratio of H- to M-forms of LDH did not differ significantly in the majority of the neuron types studied as well as in the neurons as compared with their glial satellite cells.

Animals↗